Skip to main content

Titanium dioxide nanoparticles: a review of current toxicological data


Titanium dioxide (TiO2) nanoparticles (NPs) are manufactured worldwide in large quantities for use in a wide range of applications. TiO2 NPs possess different physicochemical properties compared to their fine particle (FP) analogs, which might alter their bioactivity. Most of the literature cited here has focused on the respiratory system, showing the importance of inhalation as the primary route for TiO2 NP exposure in the workplace. TiO2 NPs may translocate to systemic organs from the lung and gastrointestinal tract (GIT) although the rate of translocation appears low. There have also been studies focusing on other potential routes of human exposure. Oral exposure mainly occurs through food products containing TiO2 NP-additives. Most dermal exposure studies, whether in vivo or in vitro, report that TiO2 NPs do not penetrate the stratum corneum (SC). In the field of nanomedicine, intravenous injection can deliver TiO2 nanoparticulate carriers directly into the human body. Upon intravenous exposure, TiO2 NPs can induce pathological lesions of the liver, spleen, kidneys, and brain. We have also shown here that most of these effects may be due to the use of very high doses of TiO2 NPs. There is also an enormous lack of epidemiological data regarding TiO2 NPs in spite of its increased production and use. However, long-term inhalation studies in rats have reported lung tumors. This review summarizes the current knowledge on the toxicology of TiO2 NPs and points out areas where further information is needed.


With the development of nanotechnology, there has been a tremendous growth in the application of NPs for drug delivery systems, antibacterial materials, cosmetics, sunscreens, and electronics [1, 2]. In October 2011 the European Union defined nanomaterials as a natural, incidental or manufactured material containing particles, in an unbound state or as an aggregate or agglomerate; where 50% or more of the particles exhibited, one or more external dimensions in the size range 1–100 nm [3]. Others have defined NPs as objects with at least one of their three dimensions in the range of 1–100 nm [4, 5]. NPs generally possess dramatically different physicochemical properties compared to fine particles (FPs) of the same composition. The smaller size of NPs ensures that a large portion of atoms will be on the particle surface. Since surface properties, such as energy level, electronic structure, and reactivity are quite different from interior states, the bioactivity of NPs will likely differ from that of the fine size analogue.

Traditionally, TiO2 FPs have been considered as poorly soluble, low toxicity particles [6, 7]. Due to this reason, they have been traditionally used as a “negative control” in many in vitro and in vivo particle toxicological studies [8]. However, this view was challenged after lung tumors developed in rats after two years of exposure to high concentrations of fine TiO2 particles [9]. The International Agency for Research on Cancer (IARC), therefore, has classified TiO2 as a Group 2B carcinogen (possibly carcinogenic to humans) [10]. However, the tumorigenic effect of fine TiO2 has been questioned and attributed to lung overload rather than specific carcinogenicity of fine TiO2 [7]. In recent years, TiO2 NPs have been widely used in industrial and consumer products due to their stronger catalytic activity when compared to TiO2 FPs. This increase in catalytic activity has been attributed to their smaller sizes, which has allowed for larger surface area per unit mass. Concerns have been raised that these same properties of TiO2 NPs may present unique bioactivity and challenges to human health [11, 12]. The rapid growth in the number of published studies confirms that there is a high level of interest concerning the safety of TiO2 NPs. Different animal models employing multiple exposure routes of administration, including inhalation, dermal exposure, intra-tracheal instillation, oral gavage, intragastric, intraperitoneal or intravenous injection have been intensively used in these studies. Studies have revealed that TiO2 NPs are more toxic than FPs [8, 13, 14]. Oberdorster et al. [15] reported that TiO2 NPs (21 nm) caused a greater pulmonary inflammatory response than TiO2 at same mass burden, with greater amounts of TiO2 NPs entering the alveolar interstitium in the lungs. Sager et al. [16] have reported similar results after intra-tracheal instillation of well-dispersed suspensions of TiO2 NPs (80/20 anatase/rutile; 21 nm, P-25) and TiO2 FPs (100% rutile; 1μm) in rats. On an equal mass burden, nano TiO2 was 40 fold more potent in inducing lung inflammation and damage at 1 and 42 days post-exposure than fine TiO2. However, respective potencies were not significantly different when dose was expressed on the basis of total surface area of particles delivered to the lung.

Wide application of TiO2 NPs confers substantial potential for human exposure and environmental release, which inevitably allows for a potential health risk to humans, livestock, and the eco-system [17]. This paper will focus mainly on current knowledge concerning the toxicology of TiO2 NPs. Studies done with mixtures of TiO2 NPs with other compounds and studies that have focused on aquatic ecosystems and the environment will not be discussed in this review. Even though the nanoparticle (NP) size has recently been defined as <100 nm, we have also included some studies that have defined particle sizes that are >100 nm as NPs. The molecular mechanisms of carcinogenesis will also be reviewed, to address health concerns regarding carcinogenesis due to particle exposure.

Chemical and physical properties

Titanium (Ti), the ninth most abundant element in the earth's crust, is widely distributed. The average concentration of Ti in the earth's crust is 4400 mg/kg. Owing to its great affinity for oxygen and other elements, Ti does not exist in the metallic state in nature. The most common oxidation state of Ti is +4, but +3 and +2 states also exist. Metallic Ti, TiO2, and TiCl4 are the compounds most widely used in industry. TiO2 (CAS-No. 13463-67-7), also known as titanium (IV) oxide, titanic acid anhydride, titania, titanic anhydride, or Ti white, is the naturally occurring oxide of Ti. TiO2 is a white noncombustible and odorless powder with a molecular weight of 79.9 g/mol, boiling point of 2972°C, melting point of 1843°C, and relative density of 4.26 g/cm3 at 25°C. TiO2 is a poorly soluble particulate that has been widely used as a white pigment. Anatase and rutile are two crystal structures of TiO2, with anatase being more chemically reactive [18, 19]. For example, Sayes et al. [19] reported that NPs (80/20; anatase/rutile, 3–5 nm; 100 μg/ml) generated 6 fold more reactive oxygen species (ROS) than rutile after UV irradiation. Indeed, anatase generates ROS when irradiated by UV light [19]. It has been suggested that TiO2 anatase has a greater toxic potential than TiO2 rutile [20, 21]. However, anatase-generated ROS does not occur under ambient light conditions. TiO2 NPs are normally a mixture of anatase and rutile crystal forms. The principal parameters of particles affecting their physicochemical properties include shape, size, surface characteristics and inner structure. TiO2 FPs (the rutile form) are believed to be chemically inert. However, when the particles become progressively smaller, their surface areas, in turn, become progressively larger, and researchers have also expressed concerns about the harmful effects of TiO2 NPs on human health associated with the decreased size [22, 23]. Surface modification such as coating, influences the activity of TiO2 NPs. For example, diminished cytotoxicity was observed when the surface of TiO2 NPs was modified by a grafting-to polymer technique combining catalytic chain transfer and thiol–ene click chemistry [24]. Another study confirmed the effect of surface coating on biological response endpoints of TiO2 NPs [25].

In conclusion, TiO2 NPs possess different physicochemical properties compared to TiO2 FPs. These properties likely influence bioactivity. Based on this fact, adverse health effects and environmental bio-safety of TiO2 NPs should be carefully evaluated even if TiO2 FPs have been demonstrated to have low toxicity. It is recommended that researchers carefully characterize the physicochemical properties of TiO2 NPs not only in the bulk form but also as delivered to the test system.


TiO2 is a white pigment and because of its brightness and very high refractive index it is most widely used. Approximately four million tons of this pigment are consumed annually worldwide [26]. In addition, TiO2 accounts for 70% of the total production volume of pigments worldwide [27], and is in the top five NPs used in consumer products [28]. TiO2 can be used in paints, coatings, plastics, papers, inks, medicines, pharmaceuticals, food products, cosmetics, and toothpaste [2931]. It can even be used as a pigment to whiten skim milk. TiO2 NPs are also used in sunscreens [32]. In addition, TiO2 has long been used as a component for articulating prosthetic implants, especially for the hip and knee [33, 34]. These implants occasionally fail due to degradation of the materials in the implant or a chronic inflammatory response to the implant material [35].

Currently, TiO2 NPs are produced abundantly and used widely because of their high stability, anticorrosive and photocatalytic properties [4]. Some have attributed this increased catalytic activity to TiO2 NPs to their high surface area, while others attribute it to TiO2 NPs being predominantly anatase rather than rutile [18, 19]. TiO2 NPs can be used in catalytic reactions, such as semiconductor photocatalysis, in the treatment of water contaminated with hazardous industrial by-products [36], and in nanocrystalline solar cells as a photoactive material [37]. Industrial utilization of the photocatalytic effect of TiO2 NPs has also found its way into other applications, especially for self-cleaning and anti-fogging purposes such as self-cleaning tiles, self-cleaning windows, self-cleaning textiles, and anti-fogging car mirrors [38]. In the field of nanomedicine, TiO2 NPs are under investigation as useful tools in advanced imaging and nanotherapeutics [37]. For example, TiO2 NPs are being evaluated as potential photosensitizers for use in photodynamic therapy (PDT) [39]. In addition, unique physical properties make TiO2 NPs ideal for use in various skin care products. Nano-preparations with TiO2 NPs are currently under investigation as novel treatments for acne vulgaris, recurrent condyloma accuminata, atopic dermatitis, hyperpigmented skin lesions, and other non-dermatologic diseases [40]. TiO2 NPs also show antibacterial properties under UV light irradiation [37, 41].

Exposure routes and limits

Ti occurs in tissues of normal animals but only in trace amounts [42]. There is no evidence of Ti being an essential element for human beings or animals. The Ti compound concentration in drinking water is generally low. A typical diet may contribute 300–400 μg/day. TiO2 particles are produced and used in varying particle size fractions including fine (approximately 0.1-2.5 μm) and nanosize (<0.1 μm, primary particles) [43]. Human exposure to TiO2 NPs may occur during both manufacturing and use. TiO2 NPs can be encountered as aerosols, suspensions or emulsions. The major routes of TiO2 NP exposure that have toxicological relevance in the workplace are inhalation and dermal exposure. It is reported that more than 150 items of “manufacturer-identified nanotechnology-based consumer products would have long term dermal contact. The most common nanomaterials found in consumer products for dermal application are TiO2 NPs [2]. TiO2 NPs are also widely used for toothpaste, food colorants and nutritional supplements. Therefore, oral exposure may occur during use of such products. In a recent study by Weir et al. [44] found that candies, sweets and chewing gums contained the highest amount of TiO2 in the scale of <100 nm. In nanomedicine, intravenous or subcutaneous injection of TiO2 nano particulate carriers is a unique way to deliver TiO2 NPs into the human body [45]. In cases where TiO2 NPs were embedded into products such as household paint, they have been shown to be less harmful, unless liberated by sanding [46].

The United States Food and Drug Administration (FDA) approved TiO2 as a food color additive with the stipulation that the additive was "not to exceed 1% by body weight (BW) ". TiO2 was also approved by the United States FDA as a “food contact substance” in food packaging [47]. Due to the differences in the physicochemical properties of TiO2 FPs and NPs exposure and toxicity information for TiO2 NPs is needed to develop exposure limits specific for TiO2 NPs.

The American Conference of Governmental Industrial Hygienists (ACGIH) has assigned TiO2 FPs (total dust) a threshold limit value (TLV) of 10 mg/m3 as a time weighted average (TWA) for a normal 8 h workday and a 40 h workweek [48]. Permissible exposure limit (PEL)-TWA of the Occupational Safety & Health Administration (OSHA) for TiO2 FPs is 15 mg/m3 [49]. In November 2005, the United States National Institute for Occupational Safety and Health (NIOSH) proposed a recommended exposure limit (REL) for TiO2 NPs at 0.3 mg/m3, which was 10 times lower than the REL for TiO2 FPs [50]. In the “Risk Assessment of Manufactured Nanomaterials TiO2 Executive Summary” compiled by the New Energy and Industrial Technology Development Organization (NEDO) in Japan, the acceptable exposure concentration of TiO2 NPs was estimated to be 1.2 mg/m3 as a TWA for a 8 h workday and a 40 h workweek [51]. The no observed adverse effect level (NOAEL) for P25 TiO2 was extrapolated to be around 1.2 mg/m3 respirable dust as TWA in the case of a hypothetical 8-hour day, 5-day working week.

Worker exposure is possible during the handling process. However, a study showed that exposure during handling, transferring, bagging, mixing, and oven cleaning was well below the currently established limits [52]. Lee et al. [53] monitored the occupational exposure at workplaces in Korea that manufacture TiO2 NPs. Personal sampling, area monitoring, real-time monitoring, and dust monitoring were conducted at workplaces where the workers handled TiO2 NPs. The gravimetric concentrations of TiO2 NPs ranged from 0.10 to 4.99 mg/m3. The particle numbers concentration at the TiO2 NPs manufacturing workplaces ranged from 11,418 to 45,889 particles/cm3 with a size range of 15–710 nm. Occupational exposure to engineered nanomaterial oxides could be effectively reduced by proper local exhaust ventilation (LEV), filtration, containment, and good work practices [54].

In conclusion, the primary route of occupational exposure for TiO2 NPs is inhalation. Consumer inhalation is also possible during application of antimicrobial spray containing TiO2 NPs. Oral exposure may occur through food products which contain TiO2 NP-additives. Dermal contact may occur through applications of cosmetics and sunscreens. Intravenous injection of TiO2 NPs could occur in medical application. Further information is needed regarding airborne exposure levels of TiO2 NPs in the workplace and what processes are associated with high NP releases. It is recommended that workplace exposure assessment evaluate airborne mass particle concentrations, particle counts, and size distribution of TiO2 NPs. To date, the consumer or environmental exposure data for TiO2 NPs is inadequate. Therefore, it is recommended that exposure assessment be made throughout the life cycle of products containing TiO2 NPs.


Toxicokinetics is the description of the rate at which a substance (TiO2 NPs) enters the body through different exposure routes and its fate after entering the body. The level or concentration of TiO2 NPs in the body system depends on the rate (or kinetic) of absorption, distribution, metabolism, and excretion of TiO2 NPs. These processes may occur after exposure through inhalation, ingestion, dermal contact, and intraperitioneal or intravenous injection. The toxicokinetics of TiO2 NPs will be discussed in terms of the different kinetics.


Following deposition of NPs at the initial site of exposure, absorption and translocation to systemic sites is a critical step in toxicokinetics. It is often defined as migration of the NP to distal organs. For instance, at what rate are TiO2 NPs absorbed through the GIT, the skin (dermal), pulmonary system, or other exposure sites, as with intravenous exposure, intra-peritoneal exposure, or subcutaneous exposure.

Gastrointestinal absorption

GIT may be an important absorption route for TiO2 NPs since drug carriers, food products, water and liquid beverages may contain TiO2 NPs [55, 56]. In the field of nanomedicine, the GIT uptake of NPs has been the subject of recent efforts to develop effective carriers that enhance the oral uptake of drugs and vaccines [57]. TiO2 FPs (rutile; 500 nm; 12.5 mg/kg) have been shown to systemically translocate to other tissues from the rat GIT [58]. TiO2 particle uptake in GIT was proposed to take place via the peyers patches, due to the high presence of TiO2 FPs in the lymphoid tissues. TiO2 NPs have also been shown to be absorbed from the GIT (25, 80, and 155 nm; 5 g/kg BW; single oral dose; mice) [59]. TiO2 NPs may be absorbed through the GIT through the lymphoid tissues surrounding it. However, since the dose used in this study was high, the extent of absorption under relevant human exposures is in question.

Dermal absorption

Dermal absorption of TiO2 NPs is of interest because many consumer products, such as cosmetics and sunscreens may contain TiO2 NPs. The outer skin of human beings consists of a tough layer of SC that is difficult for inorganic particles to penetrate. Theoretically, only those materials with an appropriate octanol/water partition coefficient and low molecular weight (<ca. 500) should penetrate the intact human skin through the SC. Therefore, it is unlikely that inorganic particles would penetrate the intact skin under normal conditions [60]. It is worth noting that although cosmetics and sunscreens containing TiO2 are normally used on intact skin. Slight injuries to skin can occur under certain circumstances, such as physical force or sunburn. Thus, skin penetration studies of TiO2 particles are usually investigated in vivo and in vitro with both intact skin and stripped skin which mimics an injured skin [60]. Several studies have investigated dermal penetration by TiO2 NPs. Some of these studies [6165] concluded that TiO2 NPs did not penetrate the intact human skin. Senzui et al. [60] investigated the skin penetration of four types of rutile TiO2 particles (35 nm non-coated, 35 nm coated, 100 nm almina and silicon coated, and 250 nm non-coated) in intact or stripped skin of Yucatan micropigs in vitro (2 μl suspension, 1cm2 skin area). Results demonstrated that TiO2 particles did not penetrate viable skin, even though the particle size was less than 100 nm and the SC was damaged. Further observation with scanning electron microscopy (SEM) showed that although some TiO2 particles had lodged into vacant hair follicles, it did not penetrate the dermis or viable epidermis. Similar results were obtained previously by Lademann et al. [66], showing no penetration into live tissue. Tape stripping with adhesive tape is a widely accepted method to examine the localization and distribution of substances within the SC [67]. Tan et al. [68] investigated a sunscreen containing 8% TiO2 NPs (10–50 nm) applied twice a day for 2–6 weeks on the skin of human volunteers (age range 59–82 yr) and evaluated the epidermal penetration of TiO2 NPs into the epidermis using tape stripping. They found that levels of TiO2 NPs in the epidermis and dermis of subjects who applied TiO2 NPs to their skin were higher than the levels of TiO2 NPs found in controls. However, they pointed out that a larger sample size would be necessary to establish if this difference was significant. It is also worth noting that the morphology of the SC differs among different age groups, which also influences the results. Bennat and Müller-Goymann [69] showed that TiO2 NPs penetrated hairy skin when applied as an oil-in-water emulsion. They evaluated skin penetration of TiO2 NPs (20 nm, formulations with 5% TiO2 NPs) applied to human skin either as an aqueous suspension or as oil-in-water emulsion using the tape stripping method. The results suggest that TiO2 NPs maybe able to penetrate the surface through hair follicles or pores. However, no details were given regarding the fate of the particles that did penetrate. TiO2 NPs were also found to have no skin carcinogenesis promoting effects due to lack of penetration through the epidermis [70, 71] (details given in the section on carcinogenecity). Another study utilizing the time of flight secondary ion mass spectrometry (TOF-SIMS) showed the presence of silica coated TiO2 NPs (rutile; 14–16 nm) within epidermis and superficial dermis [72]. They concluded that ultraviolet-B (UVB) damaged skin (pigs; UVB sunburn; 250 μl of each sunscreen formulation) slightly enhanced TiO2 NPs penetration in sunscreen formulations but they did not detect transdermal absorption.

Similar results were obtained in an in vitro study [73]. In this study the cutaneous penetration and localization of TiO2 NPs (≥20 nm primary size; 24 h sunscreen application), included in a sunscreen was evaluated in intact, damaged, irradiated, and damaged/irradiated pig skin. Quantitative analysis was done using an inductively coupled plasma-mass spectrometry, qualitative analysis done using transmission electron microscopy (TEM) and elemental identity of the NPs was evaluated by TEM-coupled Energy Dispersive X-ray (TEM-EDX) analysis. In intact and damaged/irradiated skins, 102.35±4.20% and 102.84±5.67% of the Ti was deposited, respectively, at the surface and SC, whereas only 0.19±0.15% and 0.39±0.39% were found in the viable epidermis and dermis. No Ti was detected in the receptor fluid. TEM-EDX analysis confirmed the presence of TiO2 NPs at the SC surface, as already characterized in the sunscreen formulation. They concluded that TiO2 NPs included in a sunscreen remain in the uppermost layers of the SC, in intact skin, compromised skin, or skin exposed to simulated solar radiation. Filipe et al. [74] also noted that in normal human skin TiO2 NPs were unlikely to penetrate the SC towards the underlying keratinocytes (coated 20 nm; 2 and 48 h).

One study found that TiO2 NPs could possibly penetrate the SC depending on the particle coating and skin with or without hair. However, their claims may be questioned, due to lack of data on systemic evaluation of the NPs that did penetrate the SC. Apart from this, it should be noted that most other studies reported that TiO2 NPs did not penetrate into live tissue from the deposition sites. Therefore, it can be concluded that TiO2 NPs are not systemically available to a significant extant after dermal exposure.

Pulmonary absorption

The pulmonary system consists of the upper respiratory tract (nose and nasal passages, paranasal sinuses and pharynx) and the lower respiratory tract (larynx, trachea, bronchi and lungs). Here we include studies done through inhalation, intratracheal instillation and intra-nasal (oro-pharyngeal) exposure.

Inhalation exposure

Inhalation is one of the major routes for TiO2 NPs to gain entry into the human body especially in occupational settings. Numerous studies have used inhalation as the exposure route to determine the toxicokinetics and cyto- or genotoxicity of TiO2 NPs. The limit for FPs in the air is 50 μg/m3 for an average human of 70 kg [75].

Figure 1 shows the particulate distribution of TiO2 particles by size through the different regions of the respiratory tract after inhalation.

Figure 1

Particulate distribution of TiO 2 particles by size through different regions of the respiratory tract. This diagram was derived from an explanation of particulate distribution after inhalation given by Simko and Mattsson [75]. Arrows represent downward movement of particles through the respiratory tract. Most particles in the size range of 1–5 nm are distributed throughout the three regions. 1 nm and 20 nm particles are mostly distributed in the nasopharyngeal region and alveolar regions respectively. 0.5-10 μm particles remain on the epithelial surface of the airways and alveoli.

Human data related to absorption through inhalation of TiO2 NPs are currently not available. However, there are quantitative data available from rodent studies [76]. Muhlfeld et al.[77] suggested that a small fraction of TiO2 NPs (20 nm; 1 and 24 h; dose ranges differed according to compartment size) are transported from the airway lumen of adult male WKY/NCrl BR rats to the interstitial tissue and subsequently released into the systemic circulation.

Intratracheal instillation

Intratracheal instillation is a technique where single or repeated doses of precise volumes of particulate suspensions are administered directly to the lungs. It should be noted that there may be significant differences in distribution, clearance, and retention of materials administered by intratracheal instillation, especially at high bolus doses, compared to low dose rate inhalation. Although, inhalation studies are considered to be the gold standard, data from intratracheal instillation studies can be used for hazard assessment [78]. Sager et al. [16] reported that a significant portion of deposited TiO2 NPs (21 nm) migrated to the interstitial space by 42 days after intratracheal instillation in rats. TiO2 NPs migrated to the alveolar interstitium to a significantly greater extent than TiO2 FPs after either inhalation exposure [15] or intratracheal instillation [16]. Another study found that at 28 days after instillation, a small fraction of pulmonary TiO2 NPs were able to access the blood circulation and reach extrapulmonary tissues such as liver and kidneys [79].

Intranasal exposure

Breathing is mostly done through the nose, and is termed nasal breathing. The nasal cavity has two segments, the respiratory segment and the olfactory segment. The respiratory segment is lined with ciliated pseudostratified columnar epithelium, it has a very vascularized lamina propria allowing the venous plexuses of the conchal mucosa to engorge with blood, restricting airflow and causing air to be directed to the other side of the nose. The olfactory segment is lined with the olfactory epithelium, which contains receptors for the sense of smell. Olfactory mucosal cell types include bipolar neurons, supporting (sustentacular) cells, basal cells, and Bowman's glands. The axons of the bipolar neurons form the olfactory nerve (cranial nerve I) and enter the brain through the cribiform plate. Studies by Wang et al. [80, 81] on murine brain reported that intra-nasally instilled TiO2 NPs (80 nm rutile, 155 nm anatase; 500 μg/ml; 2, 10, 20, and 30 days) can be taken up by sensory nerves and translocate to the brain.

Even though the inhalation, intratracheal instillation and intranasal studies in regards to pulmonary absorption are few they suggest that TiO2 NPs can translocate from the lung into the circulatory system to systemic tissue and from the nasal cavity into sensory nerves to the nervous system. Available data suggest that the rate of NP migration to the circulatory system is low.


After the initial absorption of TiO2 NPs, the systemic circulation can distribute the particles to all organs and tissues in the body. After TiO2 NPs reach the systemic circulation, these particles potentially interact with plasma–proteins [82], coagulation factors, platelets and red or white blood cells. The binding to plasma components may have a substantial effect on the distribution, metabolism, and excretion of the NPs [55]. Binding to plasma components might neutralize or mask the adverse effects of TiO2 NPs in the systemic circulation. Therefore the biokinetics of the engineered NPs is also dependent on the local corona environment [83]. They might also contribute to disturbances in the corona environment as noted by Mikkelsen et al. [84]. In this study repeated exposure to TiO2 NPs (12–21.6 nm; 0.5 mg/kg BW) was associated with modest plaque progression in ApoE (−/−) mice. TiO2 NPs (20–30 nm, anatase 99.9%; 5 μg/ml) were also able to penetrate human red blood cells [85]. This cellular uptake of TiO2 NPs might not involve endocytosis, since erythrocytes do not have phagocytic receptors. These results imply that TiO2 NPs might be able to cross the cell membrane by processes other than phagocytosis and endocytosis. Diffusion or adhesive interactions may also play certain roles in this cellular uptake of TiO2 NPs [55, 86]. Wick et al. [87] used the ex vivo human placental perfusion model to determine whether NPs can cross the blood-placenta barrier and whether this process is size dependent. Fluroescent polystyrene particles were used as a model NP. They found that fluorescent polystyrene particles with diameter up to 240 nm were taken up by the placenta. Earlier studies by Shimizu et al. [88] and Takeda et al. [89] had shown that subcutaneous exposure of pregnant mice to TiO2 NPs affected gene expression and genital and cranial nerve systems of the offspring. In addition, a study using inhalation exposure has shown that TiO2 NPs can also penetrate the blood placenta barrier [8890].

Translocation refers to the way particles move from the site of absorption to other parts of the body. In humans it may occur in the alveolar region where the air-blood-barrier is approximately 2 μm thick. Geiser and Kreyling [91] in their review reported that NPs including TiO2 NPs in the size range of 5–100 nm could be translocated across the air-blood-barrier. When TiO2 NPs are translocated into the blood, generally they may be retained in the liver and lymphatic system, distributed to other organs and tissues, or eliminated out of the body. A 3-week inhalation study using nano- and fine TiO2 particles with 3, 28, and 90 days recovery time was performed in female Wistar rats [92]. This study observed that particles were mainly found in alveolar macrophages and, to a lesser extent, in type-I pneumocytes, and this was quantified using the relative deposition index (RDI). Particle-laden cells were rarely observed inside capillaries. They concluded that there was minimal translocation of particles into the blood stream.

The interactions between TiO2 NPs and alveolar macrophages and their associated pro-inflammatory effects in relation to particle size and physico-chemical properties was investigated in vitro by Scherbart et al. [93]. NR8383 rat lung alveolar macrophages were treated (10, 20, 40, and 80 μg/cm2; 1, 4, and 24 h) with TiO2 NPs (25 nm; 80/20; anatase/rutile), and FPs (250 nm). Alveolar macrophages rapidly took up both TiO2 NPs and FPs. Uptake inhibition experiments with cytochalasin D, chlorpromazine and a Fcγ receptor II (FcγRII) antibody revealed that the endocytosis of TiO2 FPs by the macrophages involved actin-dependent phagocytosis and macropinocytosis as well as clathrin-coated pit formation, whereas the uptake of TiO2 NPs was dominated by FcγIIR antibody. They suggested that the contrasting alveolar macrophage responses to TiO2 NPs and FPs relate to differences in the involvement of specific uptake mechanisms.

Ferin et al. [94] monitored pulmonary retention of TiO2 FPs and NPs in rats after a single intratracheal instillation or 12 week inhalation of different sizes of TiO2 particles (12, 21, 230, and 250 nm). They found that migration of particles to the interstitium appeared to be related to the particle size, the delivered dose, and the delivered dose rate. In addition, both acute instillation and sub-chronic inhalation studies showed that TiO2 NPs (20 nm) at equivalent masses access the pulmonary interstitium to a larger extent than TiO2 FPs (250 nm). A tracheal explants system study reported that TiO2 NPs (21 nm; 5 mg/ml; 1 h) enter the epithelium faster and are translocated in greater proportion to the subepithelial space compared with TiO2 FPs (0.12 μm) [95]. Li et al. [79] investigated the distribution and effects of TiO2 NPs (3 nm; 13.2 mg/kg; once a week for 4 weeks) in mice. They suggested that TiO2 NPs might pass through the blood–brain barrier.

Others have found that intra-nasally instilled TiO2 NPs could be translocated into the central nervous system via the olfactory nerves and cause potential brain lesions with the hippocampus being the main target [80]. These effects were mainly caused by the 155 nm anatase TiO2 particle, which they also defined as a NP. The same research group reported similar findings in another study (intranasal instillation; 80 nm rutile, 155 nm anatase; 30 days) [81]. The influence of intra-nasally instilled TiO2 NPs (25 nm, 80 nm and 155 nm; every other day in a dose of 50 mg/kg BW) on monoaminergic neurotransmitters (norepinephrine (NE), dopamine (DA), 5-hydroxytryptamine (5-HT), 5-hydroxyindole acetic acid (5-HIAA), 3, 4-dihydroxyphenylacetic acid (DOPAC), and homovanillic (HVA)) were investigated in CD female mice at 2, 10, 20, and 30 days post-exposure [62]. Due to the accumulation of TiO2 NPs in the brain, the contents of NE and 5-HT were significantly increased after exposure to 80 nm and 155 nm TiO2, while the concentrations of DA, DOPAC, HVA and 5-HIAA were decreased. They concluded that intranasally instilled TiO2 NPs could be translocated to and deposited in murine brain after absorption by nasal mucosa, and further influence the release and metabolism of monoaminergic neurotransmitters in the brain. Although these findings are intriguing, other studies are necessary to confirm these results.

Fabian et al. [13] investigated the tissue distribution of intravenously administered TiO2 NPs (70/30 anatase/rutile; 20–30 nm). Rats were treated with a single intravenous injection of a suspension of TiO2 NPs in serum (5 mg/kg BW), and the tissue content of TiO2 NPs was determined 1, 14, and 28 days later. The TiO2 NP levels were highest in the liver, followed in decreasing order by the levels in the spleen, lung, and kidneys, and the highest organ burdens were on day 1 post-exposure. TiO2 NP levels were retained in the liver for 28 days which was the duration of the experiment. There was a slight decrease in TiO2 NP levels from day 1 to days 14 and 28 in the spleen, and a return to control levels by day 14 in the lung and kidneys. In this study, there were no detectable levels of TiO2 NPs in blood cells, plasma, brain, or lymph nodes at 1, 14, and 28 days post-exposure, suggesting a rapid clearance of the TiO2 NPs from the blood into the lung, spleen, kidneys, and liver. TiO2 NPs had not been entirely cleared from the liver and spleen within the observation period, indicating that TiO2 NPs can accumulate in these organs after continuous intravenous exposure. It should be noted that these intravenous exposure levels were high, which may have influenced organ distribution by damaging the integrity of the endothelial barrier.

In a two week acute toxicity study [96], mice were intraperitoneally injected with different doses of TiO2 NPs (0, 324, 648, 972, 1296, 1944 or 2592 mg/kg BW). Examination of particle distribution demonstrated that at 1, 2, 7, and 14 days post-exposure accumulation of TiO2 NPs (80 nm, 100 nm, anatase) was highest in spleen, followed by liver, kidneys and lung in a decreasing order. Accumulation of TiO2 NPs in the spleen was the highest throughout the experimental period. Some of the particles were excreted from the kidneys (urine). These results indicated that TiO2 NPs could be transported to and deposited in other tissues or organs after intraperitoneal injection, although the use of extremely high intraperitoneal injection exposure doses may have affected the results. Liu et al. [97] investigated distribution of TiO2 anatase NPs (5 nm; 5, 10, 50, 100, and 150 mg/kg BW) after intraperitoneal injection in mice daily for 14 days. They found the order of the accumulation of TiO2 NPs in the organs was liver > kidneys > spleen > lung > brain > heart. The content of TiO2 NPs in the liver at the dose of 50 mg/kg was higher than that of TiO2 FPs at the same dose. A study by Ma et al. [98] found that TiO2 NPs (anatase, 5 nm; 5, 10, 50, 100, and 150 mg/kg BW; daily for 14 days) translocated from the site of injection, the abdominal cavity, to the brain causing oxidative stress and brain injury in ICR mice. Again, relevance of such injury is an issue due to the high exposure doses used.

These studies have shown that TiO2 NPs distributed to other organs after intravenous or intraperitoneal administration. Most of the NPs accumulated in the liver. TiO2 NPs were found in the brain after intranasal administration. However, these studies used high doses, which greatly exceed levels likely after anticipated exposures (occupational, medical, consumer use, etc.). Therefore, further investigation is necessary.


So far we have not found specific literature regarding the metabolism of TiO2 NPs.


Similar to other inorganic NPs, TiO2 NPs in the systemic circulation has two potential pathways for clearance, i.e., kidneys/urine and bile/feces. The International Program on Chemical Safety for TiO2 shows that most ingested TiO2 is excreted with urine [99]. Clearance of particles from the liver via the bile into the feces is well known in pharmaceutics and is also postulated for TiO2 NPs [100]. Furthermore, every NP not absorbed by the gut epithelium will presumably be eliminated from the body via this pathway. Similarly, inhaled TiO2 NPs which are deposited in the airways of the respiratory tract and phagocytized by alveolar macrophages may be transported by mucociliary action to the larynx from where they can be cleared via expiration of sputum or be swallowed entering the GIT. Although NPs deposited in the alveoli can either be translocated to the interstitium, lymph nodes, or pulmonary capillaries, the majority are cleared by macrophage-mediated transport to the distal end of the mucociliary escalator. A study found that alveolar clearance for TiO2 FPs (5.35, 10.7, and 21.41 mg/rat; Ti IV 100% rutile; 1 μm; 7 and 42 days post-exposure) via macrophage phagocytosis was greater than TiO2 NPs (0.26, 0.52, and 1.04 mg/kg; P-25, 80/20 anatase/rutile; 21 nm) [16]. This was attributed to the higher rate of interstitialization of TiO2 NPs. An in vivo inhalation study reported similar results. They found that clearance of TiO2 NPs (20 nm; 7.2 × 106 particles/ml; 1 h and 24 h post-exposure) from the lung by lung surface macrophages is relatively low [101]. This was based on data analysis which revealed an uptake of 0.06 to 0.12% TiO2 NPs by lung-surface macrophages within 24 h. Ineffective macrophage clearance of inhaled NPs from the peripheral lung would lead to bio-persistence of TiO2 NPs and/or favors their translocation into the lung interstitium and then to the vasculature, potentially enhancing adverse systemic effects [101]. Hydrogen-1 nuclear magnetic resonance spectroscopy (1H-NMR) was used to analyze urine metabolites of rats exposed by intratracheal instillation to low (0.8 mg/kg), medium (4 mg/kg) and high (20 mg/kg) doses of TiO2 NPs [102]. Significant metabolite (acetate, valine, dimethylamine, taurine, hippurate, and 2-oxoglutarate) changes were only observed in the low dose group. These compensatory changes resolve within seven days, and the results of serum biochemical assays also implied no parenchymal damages in the liver or kidney. They concluded that low dose instillation of TiO2 NPs resulted in a transient impact on metabolic function because the scattered NPs can migrate from the lung to liver or kidney. In contrast, TiO2 NPs form agglomerates at higher doses which decreases migration to systemic organs.

In summary, absorption, distribution, metabolism, and excretion of TiO2 NPs may be affected by various factors including routes of exposures and particle size, particle agglomeration and surface coating. The most frequently investigated exposure routes in the toxicokinetics studies of TiO2 NPs were pulmonary, lung inhalation, dermal and oral administrations. TiO2 NPs can be absorbed into the body through the lung and GIT. Further studies are needed to quantify the magnitude of such transport so that systemic risk can be assessed. There is no sufficient evidence available to indicate that TiO2 NPs have the ability to penetrate through the intact skin into the human body under normal conditions. TiO2 NPs injected intravenously or intra-peritoneally were found in different organs, such as liver, spleen, kidneys, lung, lymph nodes, and brain. TiO2 NPs may have the potential to penetrate the blood–brain barriers (BBB) and blood-placenta barriers. However, these studies employed very high doses of TiO2 NPs. Elimination of TiO2 NPs may be through kidneys/urine, and bile/feces. Though a large fraction of absorbed TiO2 NPs could be excreted rapidly, it is possible that not all of these particles will be eliminated from the body. As a result, accumulation of TiO2 NPs in some organs may take place in the human body after continuous exposure. A major site of accumulation seems to be the liver. However, there is a possibility that the accumulated TiO2 NPs can be completely cleared from these sites if the study time frame is increased. Therefore, further biokinetic studies are needed. Additionally, translocation of TiO2 NPs, at relevant lower doses, should be conducted to determine if the presence of TiO2 NPs at systemic sites alters their normal biological function and anatomical morphology. For example, pulmonary exposures of NPs did not cause extensive damage to the air/blood barrier, NP translocation was slow, representing less than 1% of the initial pulmonary burden at 1 week post-exposure [91]. The possible toxicokinetics of TiO2 NPs and accumulation sites are summarized in Figure 2.

Figure 2

Toxicokinetics and accumulation sites of TiO 2 NPs. The arrows in dotted lines represent uncertainties.

Toxicity of TiO2 NPs

The toxic effects of test substances are usually measured in terms of acute, sub-acute, sub-chronic or chronic exposure conditions. Studies with a maximum of 2 weeks (14 days) study duration are normally referred to as acute toxicity studies. Sub-acute toxicity studies last for a maximum of 4 weeks (28 days), sub-chronic toxicity studies for a maximum of 13 weeks (90 days) and chronic toxicity studies last longer than 4 months. The toxicity of TiO2 NPs will be discussed in terms of these types of studies.

Acute toxicity

Acute toxicity information for TiO2 NPs in humans is currently lacking. A value often given in animal toxicity studies is the median lethal dose (LD50)/median lethal concentration (LC50), which is defined as the dosage/concentration resulting in the death of 50% of the experimental animals. However, due to ethical reasons, this method of acute toxicity testing was abolished in 2002 from the Organization for Economic Co-operation and Development (OECD) acute toxicity guideline (TG 401) and is not recommended. However, there are other alternative methods such as fixed dose procedure (TG 420), up and down procedure (TG 423) and dose response method (TG 425) that can be used to determine the LD50. The acute toxicity studies are mentioned in the order; inhalation, intra-tracheal instillation, dermal, oral, intraperitoneal, and in vitro.

In an inhalation study, rats were exposed to aerosols of 0, 2, 10, or 50 mg/m3 TiO2 NPs by inhalation for 6 h/day for 5 days [103]. Necropsies were performed either immediately after the last exposure or after 3 and 16 days post-exposure. Lung inflammation was associated with dose-dependent increases in bronchoalveolar lavage fluid (BALF) total cell and neutrophil counts, total protein content, enzyme activities and levels of a number of cell mediators. No indications of systemic effects were found by measurement of appropriate clinical pathological parameters. An inhalation study on mice [104], exposed to TiO2 NPs (2–5 nm; 8.88 mg/m3; 4h/day for 10 days) showed higher counts of total cells and alveolar macrophages in the BALF. However, mice recovered by week 3 post-exposure. These inhalation studies showed that at sufficient lung burdens in both rats and mice TiO2 NPs can cause pulmonary inflammation. Nurkiewicz et al. [105] reported that inhalation of nano- or fine TiO2 (21 nm or 1 μm; 1.5 or 20 mg/m3; 24 h post-exposure) caused microvascular dysfunction in arterioles of the shoulder muscle, i.e., a failure to respond to dilators. On a mass basis, nano TiO2 was 6–7 times more potent than fine TiO2. However, the difference in potency was not present when dose was normalized to particle surface area delivered to the lungs. A recent study by the same research group found that the peripheral vascular effects associated with particulate matter (PM) exposure (TiO2 FP 710 nm and NP 100 nm; inhalation 1.5-16 mg/m3 for 4–12 h) are due to the activation of inflammatory and/or neurogenic mechanisms [106]. In addition, an increase in basal tone and a decreased responsiveness of coronary arterioles to dilators was noted 1 day after inhalation of nano TiO2 (21 nm; P-25:80/20 anatase/rutile; 6 mg/m3; at 24 h post-exposure) in another study [107]. It should be noted that microvascular dysfunction was reported at low lung burdens which did not significantly alter BALF measures of lung inflammation or damage. These findings are of interest because there are known associations between PM and cardiovascular diseases. PM exposure can result in significant changes in many cardiovascular indices, such as heart rate, heart rate variability, blood pressure, and blood coagulability [108].

Liu et al. [109] treated rats by intra-tracheal instillation with a single dose of 0.5, 5, or 50 mg/kg BW of TiO2 NPs (5, 21, or 50 nm, respectively). Rats were sacrificed one week post-exposure. Histopathological examinations of lung tissue indicated that exposure to TiO2 NPs induced dose-dependent inflammatory lesions in rats. In addition, on an equal mass basis, pulmonary toxicity induced by 5 nm TiO2 NPs was more severe than those induced by 21 and 50 nm TiO2 particles. The time course of pulmonary responses was reported in a study by Kobayashi et al. [110] at 1 and 7 days after rats were intra-tracheal instilled (19 and 28 nm; 5 mg/ml) with TiO2 NPs. The TiO2 NPs showed greater pulmonary inflammatory effect 24 h after exposure then 1 week after exposure. In these studies, the inflammatory effects of TiO2 NPs were locally distributed, dose dependent and recovery was probable. The effects of TiO2 NPs on the immune function were investigated by Liu et al. [111]. They evaluated immune function of rat alveolar macrophages (AM) exposed to TiO2 NPs (intratracheal instillation) and reported damage to the cell structure and AM dysfunction, leading to a reduction in both non-specific and specific immune responses in individuals exposed to TiO2 NPs (5 and 200 nm; 0.5, 5, or 50 mg/kg). The phagocytic ability of the macrophages increased when exposed to a low dose of TiO2 NPs and decreased when exposed to a high dose of TiO2 NPs. Exposure to TiO2 NPs also decreased the chemotactic ability of the macrophages and the expression of Fc receptors and MHC-class II on the cell surface. The mechanism responsible for these changes was mediated via altering nitric oxide (NO) and tumor necrosis factor-α (TNF-α) expression by the AM. The amount of NO and TNF-α secreted by macrophages was gradually increased when the dosage of TiO2 NPs increased. TiO2 NPs elicited greater NO and TNF-α production than FPs. This research group attributed the potency of TiO2 NPs to surface area and crystal structure [112]. The involvement of TNF-α in late airway hyper responsiveness (AHR) has recently been investigated. In a study, low pulmonary doses of TiO2 NPs were shown to aggravate pulmonary inflammation and AHR in a mouse model of toluene diisocyanate (TDI)-induced asthma [113]. To investigate the modulation of an asthmatic response by TiO2 NPs (99.9% anatase; 15 nm) in a murine model of diisocyanate-induced asthma, the investigators in this study treated mice on days 1 and 8 with 0.3% TDI or the vehicle acetone-olive oil (AOO) on the dorsum of both ears (20 μl). On day 14, the mice were oropharyngeally dosed with 40 μl of TiO2 NP suspension (0.8 mg/kg BW). One day later (day 15), the mice received an oropharyngeal challenge with 0.01% TDI (20 μl). On day 16, airway hyper-reactivity (AHR), BAL cell and cytokine levels, lung histology, and total serum immunoglobulin E were assessed. TiO2 NP exposure in sensitized mice led to a 2 fold increase in AHR, and a 3 fold increase in BAL total cell count, mainly comprising neutrophils and macrophages. Histological analysis revealed increased edema, epithelial damage and inflammation. These studies suggest TiO2 NPs can act as an airway irritant. Thus, if the compromised hosts are exposed to TiO2 NPs it may aggravate their condition.

Using acute dermal irritation studies in rabbits and the local lymph node assay in mice (CBA/JHsd mice), Warheit et al. [114] concluded that TiO2 NPs (129.4 nm in H2O; 80/20 anatase/rutile; 0%, 5%, 25%, 50%, or 100% TiO2 NPs, 3 consecutive days) were not a skin irritant or dermal sensitizer. Another study reported that acute dermal, eye and vaginal mucous membrane irritation tests revealed no significant irritation in TiO2 NP (size not given; 1000, 2,150, 4,640, and 10,000 mg/kg BW) treated mice at 1, 24, or 48 h post-exposure [115]. In a 14 days toxicity study, TiO2 NPs (20 nm; 14, 28, 42, and 56 mg/kg) applied topically on Wistar rat skin induced short term toxicity at the biochemical level [116]. Depletion in the levels of catalase and glutathione S-transferase (GST) activity were observed. In addition, there was an increase in the activity of lactate dehydrogenase (LDH) and lipid peroxidation (LPO). The levels of serum glutamic pyruvic transaminase (SGPT), serum glutamic oxaloacetic transaminase (SGOT), blood urea nitrogen (BUN), and creatinine were also increased. However, the histopathological studies did not show any observable effects at the tissue level. They concluded that short term dermal exposure to TiO2 NPs (42 mg/kg BW) can cause hepatic, as well as renal, toxicity in rats. The two studies cited here, in regards to dermal exposure, agree with a study mentioned earlier in the section on toxicokinetics. However, the findings of the latter study suggest that the hair follicles may be a way for TiO2 NPs to penetrate into live skin. It should be noted that the doses used in these studies are high and do not mimic likely human exposures.

Warheit et al. [114] reported in acute oral toxicity studies that TiO2 NPs (129.4 nm in H2O; 175, 550, 1750 or 5000 mg/kg; 80/20 anatase/rutile; 48 h intervals for 14 days) were very low in toxicity and produced short-term and reversible ocular conjunctiva redness in rabbits. In another study, the acute toxicity in mice was investigated after a single oral administration of TiO2 particles (25, 80, and 155 nm; 5 g/kg BW) [59]. Over two weeks post-exposure, TiO2 particles showed no obvious acute toxicity. However, the female mice showed high hepatic coefficients in the 25 and 80 nm groups. The changes of serum biochemical parameters (alanine aminotransferase (ALT), aspartate aminotransferase (AST), LDH, and BUN), and pathology of the liver and kidney indicated that hepatic renal injury was induced after exposure. Even though there were significant changes of serum LDH in TiO2 NP (25 and 80 nm) treated animals, indicating the presence of myocardial damage, the pathology results for the heart, lung, testicles (ovary), or spleen showed no abnormal changes. These oral exposure studies showed biochemical changes, but systemic toxicity was not demonstrated.

Intraperitoneal studies may be done to address the effects of possible TiO2 NP use in nanomedicine. At the higher doses of an intraperitoneal exposure study done on mice, TiO2 NPs (anatase, 5 nm; 5, 10, 50, 100, and 150 mg/kg BW; everyday for 14 days) caused serious damage to the liver, kidneys, and myocardium and disturbed the balance of blood sugar and lipid [97]. Furthermore, with increasing doses of TiO2 NPs, indicators of liver function, such as ALT, leucine acid peptide, pseudocholinesterase, total protein, and albumin levels, were enhanced significantly; the indicators of kidney function, such as uric acid and BUN, were decreased; and the activities of AST, creatine kinase (CK), LDH, and alpha-hydroxybutyrate dehydrogenase, indicators of the myocardium function, were increased. The contents of triglycerides, glucose, and high-density lipoprotein cholesterol were significantly elevated. The authors concluded that the accumulation of TiO2 NPs in the organs might be closely related to the differences in the coefficients of organs and the inflammatory responses of mice. In addition, they reported that the LD50 value of TiO2 NPs through intraperitoneal injection in mice was 150 mg/kg BW. Mice intraperitoneally injected with TiO2 NP (50 nm; 0, 324, 648, 972, 1296, 1944 or 2592 mg/kg; 24 h, 48 h, 7 days, and 14 days) showed signs of acute toxicity, such as passive behavior, loss of appetite, tremor, and lethargy. Slightly elevated levels of ALT and AST were observed. Histopathological examinations showed that some TiO2 NPs entered the spleen and caused lesions. Thrombosis was found in the pulmonary vascular system. In addition, hepatocellular necrosis and apoptosis, hepatic fibrosis, renal glomerular swelling and interstitial pneumonia associated with alveolar septal thickening were also observed in the high dose group. Ma et al. [117] stated that inflammatory responses and liver injury may be involved in TiO2 NP (5 nm; 5, 10, 50, 100, and 150 mg/kg BW; everyday for 14 days) induced liver toxicity. The real-time quantitative PCR (RT-PCR) and enzyme-linked immunosorbent assay (ELISA) analyses showed that TiO2 NPs can significantly alter the mRNA and protein expression of several inflammatory pathways, including nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), macrophage migration inhibitory factor (MMIF), TNF-α, interleukin(IL)-6 (IL-6), IL-1β, cross-reaction protein, IL-4, and IL-10. In addition to this, we have already mentioned some studies [19, 25, 118] that have also reported the inflammatory effects of TiO2 NPs. TiO2 NPs also induce some neurons to turn into filamentous shapes and others into inflammatory cells after translocating from the abdominal cavity [98]. Oxidative stress and injury of the brain triggered a cascade of reactions, such as LPO, decreases of the total anti-oxidation capacity and activities of antioxidative enzymes, the excessive release of NO, the reduction of glutamic acid, and the down-regulated level of acetylcholinesterase activity. The acute toxicity of intraperitoneally injected TiO2 NPs is systemic, it involves pathological and biochemical effects on the liver, kidney, heart and brain.

Since in vitro studies can be used as predictive indicators of acute toxicity, some are mentioned here. The influence TiO2 NPs on erythrocytes was systematically investigated by Li et al. [119]. Their results indicate that erythrocytes treated with TiO2 NPs underwent abnormal sedimentation, hemagglutination and dose dependent hemolysis, which totally differed from cells treated with TiO2 FPs. Another study reported that hemolysis (washed human erythrocytes, 37°C incubation for 1 h) caused by TiO2 FPs was 73 times greater than TiO2 NPs [120]. However, the hemolysis was abolished by plasma, indicating that in in vivo conditions the presence of plasma may prevent hemolysis. A study on mouse macrophages (Ana-1 and MH-S cells) found that TiO2 NPs (5, 10, 25, and 100 nm; anatase) caused low toxicity to MH-S cells [121]. Another study found TiO2 NPs (25 and 80 nm; 0, 10, 20, 40, and 80 mg/l; 24 h) inhibited gap junction intracellular communication between lung fibroblasts [122]. A number of in vitro studies also show toxic effects of TiO2 NPs on cells of the circulatory system.

In summary, the acute toxicity of TiO2 NPs have been frequently studied in rat and mouse models following multiple exposure routes of administration. The number of studies targeting the respiratory system outweighs the other exposure routes. Studies exposing the pulmonary system to TiO2 NPs produced both local and systemic symptoms and aggravate pre-existing symptoms. TiO2 NPs administered through the lung are more inflammatory than FPs of similar chemistry at equal mass concentrations. However, on an equal particle surface area basis, pulmonary inflammation to TiO2 NPs was similar to that of TiO2 FPs. The results from the other exposure routes cannot be ignored. For example, research evidence demonstrates that TiO2 NPs can be absorbed through the lung or GIT into the systemic circulation and then distributed in different organs such as the liver, kidneys, spleen, or even the brain. Distribution and accumulation of TiO2 NPs in the organs could induce organ injuries and inflammatory responses. However, most of the doses employed are too high to be realistic in occupational settings. In vitro studies also show effects of TiO2 NPs on the blood circulation system.

Sub- acute toxicity

Silicon dioxide (SiO2)-coated rutile TiO2 NPs (40 nm; 10 mg/m3; 2 h on 4 consecutive days, or 2 h on 4 consecutive days, 4 weeks) caused pulmonary neutrophilia, increased expression of TNF-α and neutrophil attracting chemokine (CXCL 1) in lung tissues [123]. However, they attributed the effects to the surface coating with SiO2. Others observed that TiO2 NPs caused minimal inflammatory changes in the lungs, leucopenia, and a decrease in β-glucuronidase after inhalation [92].

In another study [124], rats were intra-tracheally instilled with TiO2 NPs (1 or 10 mg/kg BW). At 10 mg/kg BW, LDH activity (1, 7, 14, and 28 days), malodialdehyde (MDA) (1, 7, and 14 days), total protein (1 and 7 days), as well as, the number of leukocytes (1 and 7 days) were all increased significantly when compared with the controls. Histopathological examination revealed a marked increase of pulmonary inflammation in the lungs in 10 mg/kg BW treated rats. While investigating dose–response relationships for intra-tracheal instillation of TiO2 NPs (20 nm) and FPs (250 nm), Oberdorster et al. [125] observed a significant pulmonary inflammatory response to TiO2 NPs in rats and mice, which included an increase of total protein in BALF, LDH activity, and acid-glucosidase. They concluded that the greater toxicity of the TiO2 NPs correlated well with their greater surface area per mass. Li et al. [79] investigated the effects of TiO2 NPs (3 nm) in mice after intra-tracheal instillation at a total dose of 13.2 mg/kg BW (once a week for 4 weeks). At 28 days after instillation, they found that instilled TiO2 NPs could induce lung damage, and change the permeability of the alveolar-capillary barrier. TiO2 NPs were able to access the blood circulation and reach extra-pulmonary tissues, such as the liver and kidneys, leading to different levels of tissue injury. In addition, TiO2 NPs might pass through the BBB and induce the injury through an oxidative stress response. At other sites, TiO2 NPs (1.0, 0.5, and 0.1 mg/ml; twice/week for 6 weeks) caused dyslipidemia and accelerated the development of atherosclerosis and plaque rupture in intra-tracheally instilled ApoE−/−mice [126]. In this study, viscera index, blood total cholesterol (TC), triglyceride (TG), high density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterin (LDL-C), and organic lipid ratio were assessed as biomarkers. Artery and aortic root issues were assessed by histopathology. Another study investigated whether photocatalytic TiO2 NPs (28 nm; rutile; 2, 10, 50, or 250 μg) exhibited an adjuvant effect, when administered through intraperitoneal injection in combination with ovalbumin (OVA) in mice [127]. The mice in this study were treated with OVA, OVA + TiO2 NPs or OVA + AlOH3 and challenged with aerosols of OVA. The TiO2 NPs promoted a Th2 dominant immune response with high levels of OVA-specific IgE and IgG1 in the serum, and influx of eosinophils, neutrophils and lymphocytes in BALF. Significantly higher levels of OVA-specific IgE were induced by TiO2 NPs than the standard adjuvant, AlOH3. However, the two substances were comparable regarding the level of eosinophilic inflammation and interleukins present in BALF.

The oral toxicological effects of TiO2 NPs (dosed at 0.16, 0.4, and 1 g/kg) were investigated using conventional approaches and metabolomic analysis in Wistar rats [128]. The urine and serum were analyzed by 1H-NMR using principal components and partial least squares discriminant analyses. The metabolic signature of urinalysis in TiO2 NPs-treated rats showed increases in the levels of taurine, citrate, hippurate, histidine, trimethylamine-N-oxide (TMAO), citrulline, alpha-ketoglutarate, phenylacetylglycine (PAG) and acetate. Decreases in the levels of lactate, betaine, methionine, threonine, pyruvate, 3-D-hydroxybutyrate (3-D-HB), choline and leucine were also observed. The metabolomics analysis of serum showed increases in TMAO, choline, creatine, phosphocholine and 3-D-HB as well as decreases in glutamine, pyruvate, glutamate, acetoacetate, glutathione and methionine after TiO2 NPs treatment. AST, CK and LDH were elevated and mitochondrial swelling in heart tissue was observed in TiO2 NPs-treated rats. They concluded that their findings indicated that disturbances in energy and amino acid metabolism, and the gut microflora environment may be attributable to slight injury to the liver and heart caused by TiO2 NPs. They proposed that the NMR-based metabolomic approach may be a reliable and sensitive method to study the biochemical effects of nanomaterials. What one can crudely deduce from these findings is that, in terms of occupational exposures, those with underlying health issues such as asthma and heart disease may be at risk of TiO2 NPs toxicity. However, since the studies were conducted in animals, there is a need for epidemiological studies in the workplace, to quantify the risks of TiO2 NPs in the workplace. This is further discussed in part IX, the epidemiological studies section.

Sub-chronic toxicity

A subchronic inhalation study comparing pulmonary responses to TiO2 NPs in several species was performed [129]. Female rats, mice, and hamsters were exposed to aerosol concentrations of 0.5, 2.0, or 10 mg/m3 TiO2 NPs (P-25; 21 nm; 6 h/day, 5 days/week, for 13 weeks). At each time point, TiO2 NPs burdens in the lung and lymph nodes and selected lung responses were examined. Retained lung burdens increased in a dose-dependent manner in all three species and were at a maximum at the end of exposures. There were significant species differences in the pulmonary responses to inhaled TiO2 NPs. Under conditions where the lung TiO2 NPs burdens were equivalent, rats developed a more severe inflammatory response than mice and, subsequently, developed progressive epithelial and fibroproliferative changes. Clearance of particles from the lung was markedly impaired in mice and rats exposed to 10 mg/m3 TiO2 NPs, whereas clearance in hamsters did not appear to be affected at any of the administered doses.

Warheit et al. [130] intra-tracheally instilled TiO2 NPs (25 and 100 nm; 1 or 5 mg/kg BW; 24 h, 1 week and 3 months) into rats to compare several types of TiO2 FPs and NPs with different sizes, surface areas, and crystal structures. In the comparison among these particles, even though the difference in surface areas was as large as 30 fold, the observed lung inflammatory responses were almost the same for the two particle sizes. They, therefore, concluded that toxicities of TiO2 particles through lung instillation are not dependent upon particle size and surface area. In addition, the same research group suggested that the toxicity was dependent on particle surface properties instead of surface areas. Roursgaard et al. [131] intratracheally instilled mice with single fixed doses of 5, 50, and 500 μg of TiO2 FPs and NPs (rutile). They found, in the acute phase, both FPs and NPs induced elevation of IL-6 and total protein in BALF at the highest doses. Similar effects were observed in acute (24 h) and sub-chronic (3 months) airway inflammation for two different sizes of TiO2 particles. These results suggest that TiO2 NPs may not be more cytotoxic or cause more inflammation to the lungs compared to FPs of similar composition. However, the results in both the Warheit et al. and Roursgaard et al. studies may be questioned due to poor dispersion of TiO2 NPs as suggested by Sager et al. [16]. Indeed, structural sizes of the different particles as delivered to the rats did not sifnificantly differ.

Wang et al. [132] investigated the influence of intranasally instilled TiO2 NPs on monoaminergic neurotransmitters at different times post-exposure (25, 80, and 155 nm; 50 mg/kg; 2, 10, 20, and 30 days) in CD female mice. They used ICP-MS to analyze the TiO2 NP contents in murine brain. The monoaminergic neurotransmitters such as NE, DA, 5-HT, 5-HIAA, DOPAC, and HVA, were determined by reversed-phase high performance liquid chromatography (RP-HPLC) with an electrochemical detector. TiO2 NPs in murine brain increased after 10 days for the 25 nm group ((1059.3+/−293.5) ng/g). It declined slowly at 20 days post-exposure ((654.7+/−269.2) ng/g). At 30 days post-exposure, the TiO2 NPs content remained the same as at 20 days. Due to the accumulation of TiO2 NPs in the brain, the levels of NE and 5-HT increased significantly after exposure to 80 and 155 nm TiO2 NPs, while decreases in the levels of DA, DOPAC, HVA and 5-HIAA were observed. The inhaled TiO2 NPs could be translocated to and deposited in murine brain after absorption through the nasal mucosa, and could influence the release and metabolism of monoaminergic neurotransmitters in brain.

Wu et al. [133] investigated the penetration and potential toxicity of TiO2 NPs after in vitro (porcine ears) and in vivo animal (domestic pig ears, BALB/c hairless mice) dermal exposure. They concluded that TiO2 NPs (various sizes) cannot penetrate through the SC 24 h after exposure to isolated porcine skin. However, after being topically applied on pig ear in vivo for 30 days, TiO2 NPs (4 and 60 nm; 24 mg of 5% TiO2 on an area of 3 cm2) could penetrate through the horny layer, and be located in the deep layer of the epidermis. Moreover, after 60 days dermal (400 μg/cm2) exposure in hairless mice, TiO2 NPs not only penetrated the skin, but also reached different tissues and induced diverse pathological lesions in several major organs. In addition, they found TiO2 NPs (21 nm, P-25) in the mouse brain without inducing any pathological changes.

Hu et al. [134] intragastrically instilled ICR mice with TiO2 NPs (5 nm anatase; 0, 5, 10, and 50 mg/kg BW; every day for 60 days). Their aim was to determine whether TiO2 NPs exposure results in persistent alterations in nervous system function. The Y-maze test showed that TiO2 NPs exposure could significantly impair the spatial recognition memory. TiO2 NPs also caused disturbances of the homeostasis of trace elements, enzymes and neurotransmitter systems in the mouse brain. They also found that there were significant alterations in the contents of Ca, Mg, Na, K, Fe, and Zn in the brain. TiO2 NPs also significantly inhibited the activities of Na+/K+-ATPase, Ca2 +-ATPase, Ca2 +/Mg2 +-ATPase, acetylcholine esterase, and nitric oxide synthase (NOS). The contents of some monoamines neurotransmitters, such as NE, DOPAC, 5-HT and its metabolite 5-HIAA, were significantly decreased, while acetylcholine, glutamate, and NO were significantly increased.

Chronic toxicity (excluding carcinogenicity)

In work environments, the potential chronic toxicity of TiO2 NPs is likely to be of more concern than acute effects. Early studies suggest that TiO2 is not highly toxic.

Chronic lung inhalation studies [9, 135] that exposed pigs or rats, respectively, to TiO2 FPs have reported findings of pulmonary pathology such as increased incidences of pneumonia, squamous metaplasia [135], sustained pulmonary responses [136], enhanced proliferation of pulmonary cells, defects in macrophage function [137], alveolar epithelial metaplasia, progressive fibroproliferative lesions [138] and accumulation of macrophages in interalveolar septa [9]. Some studies on TiO2 NPs show similar effects. Oberdorster et al. [15] investigated the correlation between particle size, in vivo particle persistence, and lung injury after a 12 week inhalation (23.5±2.9 mg/m3) experiment in rats (Fischer 344) exposed to TiO2 particles (20 and 250 nm). They reported inflammation and lung injury and concluded that the greater pulmonary effects of NPs, compared to FPs, can be explained by their larger specific surface area, the greater interstitial access, and their altered biopersistence, resulting in increased retention of NPs.

Exposure to TiO2 NPs (5–6 nm) resulted in chronic spleen injury, in a 90 day study done on ICR mice (intragastric administration; 2.5, 5, and 10 mg/kg; everyday) [139]. Blood cells, platelets, hemoglobin, immunoglobulin and lymphocyte subsets (such as CD3, CD4, CD8, B cell, and natural killer cell) of mice were significantly decreased. There was also a significant increase in the levels of NF-κB, TNF-α, MMIF, IL-2, IL-4, IL-6, IL-8, IL-10, IL-18, IL-1β, cross-reaction protein, transforming growth factor-β (TGF- β), interferon-γ, Bax, and CYP1A1 expression, and decreases in the levels of Bcl-2 and heat shock protein 70 (Hsp70) expression. Long-term exposure to low dose TiO2 NPs may cause spleen injury, resulting from alteration of inflammatory and apoptotic cytokines expression and reduction of immune capacity.

In conclusion, TiO2 NPs exhibit moderate toxicity, inducing pulmonary inflammatory response and enhanced proliferation of pulmonary cells at relatively high doses. TiO2 NPs are found to induce greater pulmonary inflammatory effects compared to TiO2 FPs. The modulatory effects of TiO2 NPs in asthmatic responses need to be confirmed. As evident in the acute toxicity studies, the chronic toxicity studies also focus on the respiratory system. However, with the increase in consumer use of sunscreens that contain TiO2 NPs, more effort should be put into carrying out chronic exposure studies for topically applied consumer goods.

In all the different types of toxicity study conditions, pulmonary toxicity seems to be a common finding. The number of studies on pulmonary toxicity also outweighs studies of other exposure routes, emphasizing its importance especially in reference to environmental and occupational exposures. Most of these studies also show that the endpoints of oxidative stress and inflammation seem to be most affected. This mechanistic information can be helpful in increasing the specificity and sensitivity of future in vitro and in vivo studies.


The genotoxicity of TiO2 NPs remains controversial [140]. Early studies suggest that TiO2 is not genotoxic in standard assays [141]. In recent years, in vivo and in vitro studies have examined the genotoxicity of TiO2 NPs. Test systems used frequently in in vivo studies of genotoxicity of TiO2 NPs include rat or mouse bone marrow cells. End points used in the in vitro studies include micronucleus (MN) test, Ames test, mammalian cell gene mutation, DNA breaks, chromosomal alterations, and cell transformation. These genotoxicity endpoints provide useful data for hazard identification of TiO2 NPs.

In vivo studies

A few in vivo studies have been carried out to investigate the genotoxicity of TiO2 NPs. A study by Yazdi et al. [142] found that inhalation of TiO2 NPs provoked lung inflammation which was strongly suppressed in IL-1R– and IL-1α– deficient mice. They concluded that the inflammation caused by TiO2 NPs in vivo was driven by IL-1α. The signaling of IL-1R by TiO2 NPs is similar to that of asbestos. TiO2 NPs (6 mg/m3; 4 h) also increased the phosphorylation of p38 and troponin 1 in cardiac muscle of rats exposed through inhalation, at 1 day post exposure [143]. These inhalation studies show that TiO2 NPs can affect the expression of certain genes in both the heart and lung.

An intratracheal instillation study showed that hypoxanthine phosphoribosyltransferase (HPRT) mutation frequency was increased in alveolar type II cells from rats exposed to TiO2 NPs (anatase; 18 nm; 100 mg/kg; 15 months) [144]. While in a study by Trouiller et al. [32], TiO2 NPs were genotoxic, clastogenic and caused moderate inflammation in vivo in mice exposed through drinking water (21 nm, P-25). TiO2 NPs at 500 mg/kg BW induced both DNA single and double-strand breaks and chromosomal damage. TiO2 NPs induced 8-hydroxy-2-deoxyguanosine, γ-H2AX foci, micronuclei, and DNA deletions. The formation of γ-H2AX foci is indicative of DNA double-strand breaks. They suggested that TiO2 NPs–induced genotoxicity in vivo in mice is possibly caused by a secondary genotoxic mechanism associated with inflammation and/or oxidative stress. RT-PCR and ELISA analysis showed that intra-gastrically administered TiO2 NPs (anatase; 5 nm; 5, 10, and 50 mg/kg; everyday for 60 days) significantly increased mRNA and protein expression of Toll-like receptor-2 (TLR2), TLR-4, IκB kinases (IKK-α, IKK-β), NF-κB, NF-κBP52, NF-κBP65, TNF-α, and NF-κB-inducible kinase (NIK), and decreased the expression of IκB and IL-2 in mice [145]. They stated that the signaling pathway of liver injury in the TiO2 NPs-stimulated mouse liver sequentially might occur via activation of TLRs → NIK → IκB kinase → NF-κB → TNF-α → inflammation → apoptosis → liver injury. Another intra-gastric administration study focusing on the molecular mechanisms of kidney injury of mice, found that TiO2 NPs (5–6 nm; 2.5, 5, and 10 mg/kg; everyday for 90 days) activated NF-κB, leading to increased expression of TNF-α, MMIF, Il-2, Il-4, Il-6, Il-10, Il-18, Il-1β, cross-reaction protein, TGF- β, interferon-γ, and CYP1A1, and a decrease in Hsp70 [146]. This showed that TiO2 NPs accumulate in the kidney, causing nephric inflammation, cell necrosis and dysfunction. Activation of NF-κB and increases in the expression of similar inflammatory cytokines were observed in a study by Sun et al. [147] after intratracheal instillation of TiO2 NPs (2.5, 5, and 10 mg/kg; 90 days) in mice. In addition, an increase in hemeoxygenase-1 (HO-1) expression and a decrease in NF-κB-inhibiting factor and Hsp70 expression were also observed. They suggested that the generation of pulmonary inflammation caused by TiO2 NPs (5–6 nm) in mice is closely related to oxidative stress and the expression of inflammatory cytokines. TiO2 NPs effectively activated caspase-3 and -9, decreased gene and protein levels of Bcl-2, Bax and cytochrome c, and promoted ROS accumulation in mice spleen [148]. In this study mice were intraperitoneally injected with TiO2 NPs for 45 days consecutively. TiO2 NPs accumulated in the mouse spleen, leading to congestion and lymph nodule proliferation of spleen tissue, and splenocyte apoptosis. Taken together, this study indicated that TiO2 NPs induce apoptosis in the mouse splenocyte via mitochondrial-mediated pathway.

In regards to in utero genotoxicity, Jackson et al. [149] analyzed hepatic gene expression in newborns of C57BL/6BomTac dames exposed to TiO2 (surface coated UV-Titan; 1 h/day; 42 mg UV-Titan/m3) using DNA microarrays. UV-Titan exposure did not induce DNA strand breaks in time-mated mice or their offspring. Even though there were changes in the expression of genes related to retinoic acid signaling in the females as indicated by transcriptional profiling of newborn livers. They concluded that the changes may be a secondary response to maternal inflammation although no direct link was evident through gene expression analysis. Another inhalation study on female C57BL/6BomTac mice (UV-Titan; 20 nm; 1h/day for 11 consecutive days; 42.4±2.9 mg surface-coated nanoTiO2/m3; sacrificed 5 days following the last exposure) showed that nanoTiO2 exposure resulted in increased levels of mRNA for acute phase markers. serum amyloid A-1 (Saa1) and serum amyloid A-3 (Saa3), several CXC and CC chemokines, and cytokine tumor necrosis factor genes [150]. Further protein analysis of Saa1 and 3 showed selective up-regulation of Saa3 in lung tissues. They also showed the up-regulation of miR-1, miR-449a and a 60-fold induction of miR-135b. They concluded that inhalation of surface-coated nanoTiO2 results in changes in the expression of genes associated with acute phase, inflammatory and immune response 5 days post exposure with concomitant changes in several miRNAs.

However, not all studies showed genotoxic effects. A study investigating the effects of NPs on the female germline found that TiO2 NPs (UV-Titan) do not induce expanded simple tandem repeat (ESTR) loci mutations in the germline of prenatally exposed female mice [151]. In this study, pregnant C57BL/6 mice were exposed by whole-body inhalation to the TiO2 NPs (UV-Titan L181; ~42.4mg/m3) on gestation days (GD) 8–18. F2 descendents were collected and ESTR germline mutation rates in this generation were estimated from full pedigrees (mother, father, and offspring) of F1 female mice (192 UV-Titan-exposed F2 offspring and 164F2 controls). Most of these studies were carried out on C57BL/6 mice strains. The positive endpoints of interest were polychromatic erythrocyte (PCE) micronuclei, γ-H2AX foci formation, DNA damage, HPRT mutation frequency and mRNA expression. However, some PCE micronuclei and ESTR mutations were not positive. An inhalation exposure (C57BL/6J mice; treated with 0.8, 7.2, and 28.5 mg/cm3 for 5 days; 4h/day) study by Lindberg et al. [152] showed no significant effect on the level of DNA damage in lung epithelial cells or micronuclei in bone marrow polychromatic erythrocytes (PCE’s) by freshly prepared TiO2 NPs (74% anatase; 26% brookite). In addition, the rate of PCE MN cells induced in mice after oral administration of TiO2 NPs (1, 2, and, 5 g/kg BW) were also not significantly different from controls [115]. Another study stated that DNA adduct formation in rat lungs was not detected following chronic inhalation for two years to TiO2 NPs (10.4 mg/m3) [153].

The in vivo genotoxicity studies targeted different organs as well as the reproductive system show that the TiO2 NPs increased the expression of the inflammatory cytokines, the mRNA expression of toll like receptors, gene mutations of the HPRT, induction of γ-H2AX foci, DNA deletions, and PCE. Increases in expression of HO-1, NF-κB, and Hsp70 were also observed. However, some studies also show that TiO2 NPs were not genotoxic. These disparities in results may be due to the differences in the physicochemical characteristics of the TiO2 NPs used, or the exposure metrics used by the investigators.

In vitro studies

Many in vitro studies have been conducted to investigate the genotoxicity of TiO2 NPs. TiO2 NPs have also been observed around the nuclei in the vicinity of the endoplasmic reticulum in cultured human-derived retinal pigment epithelial cells (ARPE-19) after exposure to high concentrations (30 μg/ml) [154]. The studies that have been conducted have tried to compare effects TiO2 NPs according to particle sizes, surface coatings, crystal structure, dose ranges, different cell lines, and exploratory studies.

Recently, a study by Jugan et al. [155] has shown that spherical TiO2 NPs (12–140 nm; both anatase and rutile) can induce single strand breaks, oxidative lesions to DNA and oxidative stress in A549 cells. They also showed that TiO2 NPs impair the cell’s ability to repair DNA by deactivation of both nucleotide excision repair (NER) and base excision repair (BER) pathways. Others have also found that TiO2 NPs cause increased extracellular ROS, HO-1, and NOS mRNA expression and TNF-α release in NR8383 rat lung alveolar macrophages [93]. TiO2 NPs demonstrated cytotoxic and genotoxic effects in human amnion epithelial (WISH) cells in another recent study [156]. In this study, polyhedral rutile TiO2 NPs (30.6 nm; 20 μg/ml) caused a 14 fold increase in olive tail moment (OTM), while cells treated with 0.625-10 μg/ml exhibited significant reduction in catalase activity and GSH level. There was a 1.87 fold increase in intracellular ROS generation and 7.3% increase in G2M cell cycle arrest.

Bhattacharya et al. [157] reported that human lung fibroblasts were more sensitive regarding cyto- and genotoxic effects caused by TiO2 NPs than human bronchial epithelial (BEAS-2B) cells. In this study, TiO2 NPs induced oxidative stress and DNA-adduct formation (8-OHdG) but not DNA-breakage in human lung fibroblasts. Hamster lung fibroblasts (V79 cells) were used in a study focusing on cyto- and genotoxic effects of TiO2 NPs (untreated anatase; 30–50 nm) and vanadium pentoxide (V2O5)-treated anatase particles [158]. V2O5-treated TiO2 NPs were capable of inducing greater DNA damage in mammalian cells through production of free radicals than untreated particles. V2O5-treated TiO2 NPs formed pronounced acellular and cellular radicals of interest. Surface-treated TiO2 NPs particles coated with V2O5 are used industrially for selective catalytic reactions such as the removal of nitrous oxide from exhaust gases of combustion power plants (SCR process) and in biomaterials for increasing the strength of implants.

Wang et al. [30] detected genotoxicity of TiO2 NPs in cultured human lymphoblastoid cells using the cytokinesis block micronucleus (CBMN) assay, the Comet assay, and the HPRT gene mutation assay. The cells were incubated for 6, 24 and 48 h with 0, 26, 65 or 130 μg/ml TiO2 NPs (7–8 nm). TiO2 NPs induced approximately a 2.5-fold increase in the frequency of micronucleated/binucleated cells (130 μg/ml), approximately a 5-fold increase in tail moment (65 μg/ml), and approximately a 2.5 fold increase in the HPRT mutation frequency (130 μg/ml). TiO2 anatase NPs and larger rutile particles provoked higher IL-1β production in macrophage-like human THP-1 cells [159]. A study on human monoblastoid cell line (U937) found that TiO2 NPs (<100 nm) induced both apoptotic and necrotic modifications at exposures of 0.005-4 mg/ml for 24 and 48 h [160]. Another study aimed at validating in vitro test systems for apoptosis induced by NPs found that TiO2 NPs induced DNA fragmentation in RAW264.7 macrophages [161]. While in cultured human lymphocytes TiO2 NPs increased the proportion of sub-G1 cells, activated caspase-9 and caspase-3, and induced caspase-3-mediated PARP cleavage [162]. Time-sequence analysis of the induction of apoptosis revealed that TiO2 NPs triggered apoptosis through caspase-8/Bid activation. They stated that TiO2 NPs induced apoptosis is mediated by the p38/JNK pathway and the caspase-8-dependent Bid pathway in human lymphocytes. However, in a study conducted on BEAS 2B cells, Shi et al. [163] noted that TiO2 NPs induced apoptosis via the mitochondrial apoptosis pathway independent of caspase 8/t-Bid pathway. These results show that different cell lines exhibit different responses to TiO2 NPs.

Another study on human lymphocytes showed that, TiO2 NPs significantly increased MN formation and DNA breakage [164]. The generation of ROS in TiO2 NP-treated cells was also observed. N-acetylcysteine (NAC) supplementation inhibited the level of TiO2 NP-induced DNA damage. The inhibitive nature of NAC on ROS formation in cells exposed to TiO2 was also noted by Xue et al. [165]. Shukla et al. [28] also demonstrated ROS involvement in oxidative DNA damage and MN formation in human epidermal cells. Ghosh et al. [166] investigated the genotoxicity of TiO2 NPs in plant and human lymphocytes using classical genotoxic endpoints: Comet assay and the DNA laddering technique. TiO2 NPs were found to be genotoxic at a low dose of 0.25 mM followed by a decrease in the extent of DNA damage at higher concentrations. In contrast, TiO2 FPs were consistently genotoxic at doses of 1.25 mM and above. This study concluded that the TiO2 NPs possess genotoxic potential in plant and human lymphocytes. These results imply that genotoxic effects of TiO2 NPs may occur through ROS generation in lymphocytes.

Uncoated TiO2 anatase NPs (99.7%; <25 nm) and TiO2 rutile FPs (99.9%; <5 μm) were shown to be more efficient than SiO2-coated TiO2 rutile NPs (>95%, <5% amorphous SiO2 coating; 10×40 nm) in inducing DNA damage, whereas only TiO2 anatase NPs were able to slightly induce micronuclei in a study by Falck et al. [167] on BEAS 2B cells (1–100 μg/cm2; 24, 48, and 72 h). The lower activity of nano sized rutile in genotoxicity is likely due to its coating. This conclusion is supported by Mano et al. [168]. They found that when TiO2 NPs (P25; 25 nm; 80/20 anatase/rutile) were coated with polyethylene glycol (PEG), their cytotoxic effects and induction of stress related genes in human pulmonary epithelial (NCI-H292) cells and human acute monocytic leukemia (THP-1) cells significantly decreased. Analysis of mRNA expression indicated that the expression of particular biomarkers depends upon the cell type, and that modification of TiO2 NPs with PEG reduces their cytotoxicity and reduces the induction of genes associated with stress and toxicity.

Petkovic et al. [21] investigated the genotoxic responses to two types of TiO2 NPs (<25 nm anatase: TiO2-An) and (<100 nm rutile: TiO2-Ru) in human hepatoma HepG2 cells. They found that TiO2-An, caused a persistent increase in DNA strand breaks (Comet assay) and oxidized purines (Fpg-Comet). Both types transiently upregulated mRNA expression of p53 and its downstream regulated DNA damage responsive genes (mdm2, gadd45α, and p21). A recent study conducted with Caco-2 cells found that in contrast to pure anatase TiO2 NPs, anatase/rutile TiO2 NPs induced significant LDH leakage and mild DNA damage as shown by the fpg-Comet assay [169]. The anatase/rutile NPs also showed higher toxicity per unit surface area. The investigators used the WST-1 assay to show that there was highly significant correlation between the specific surface area of anatase and cytotoxicity.

Gurr et al. [170] investigated the oxidative damage induced by TiO2 NPs in the absence of photo-activation in BEAS 2B cells. Results indicated that TiO2 NPs (anatase; 10 and 20 nm) in the absence of photo-activation induced oxidative DNA damage, LPO, and micronuclei formation. However, treatment with TiO2 FPs (anatase; >200 nm) did not. Huang et al. [171] investigated the cell transformation mediated by long-term exposure to TiO2 NPs and found that TiO2 NPs not only increased cell survival and growth in soft agar but also the numbers of multinucleated cells and MN. To study the potential of fine (>200 nm) and nano TiO2 particle (≤20 nm) to induce chromosomal changes, Rahman et al. [172] treated SHE cells with 1.0 μg/cm2 of TiO2 particle for 12–72 h. The micronuclei assay revealed a significant increase in MN induction in SHE cells after NP treatment, whereas TiO2 FPs did not show significant induction of MN formation. However, other investigators who used the same cell line have stated that cytotoxicity and genotoxicity induced by metal oxide NPs are not always higher than those induced by their FP counterparts (14–35 nm; 5,10, and 50 μg/cm2) [173]. Lu et al. [140] found TiO2 particles (sizes not reported) to be toxic to Chinese hamster ovary-K1 (CHO-K1) cells. The sister chromatid exchange (SCE) frequency and MN frequency in CHO-K1 cells treated with TiO2 particles (0–5 μM) for 24 h exhibited a significant and dose-dependent increase in genotoxicity. Their findings are supported by Di Virgilio et al. [174] who also had similar results in CHO-K1 cells. Genotoxic effects were shown by MN frequencies, which significantly increased at 0.5 and 1 μg/ml of TiO2 NPs. SCE frequencies were higher for cells treated with 1–5 μg/ml of TiO2 NPs. Conversely, a chronic (60 days) study with CHO cells (0, 10, 20, and 40 μg/cm2) showed no cyto or genotoxic effects by TiO2 NPs (100% anatase, 25 nm) [175]. They stated that CHO cells adapted to chronic exposure and detoxified the excess ROS possibly through upregulation of superoxide dismutase (SOD).

A recent study found that TiO2 NPs (aeroxide P-25 99.5% 73–85% anatase, 14–17% rutile, and 2–13% amorphous) were cytotoxic and genotoxic to human skin fibroblast cell line in a dose dependent manner (10, 25, 50, 100, 250, 500, and 1000 μg/ml) using the test for γ-H2AX expression [176]. Another study specifically targeted the relationship between TiO2 NPs and the DNA damage response pathways regulated by ATM/Chk2 and ATR/Chk1 in human dermal fibroblasts [177]. Their results showed increased phosphorylation of H2AX, ATM, and Chk2 after exposure. In addition, TiO2 NPs inhibited the overall rate of DNA synthesis and frequency of replicon initiation events in DNA-combed fibres. Taken together, these results demonstrate that exposure to TiO2 NPs activates the ATM/Chk2 DNA damage response pathway.

The interaction of TiO2 NPs with liver DNA from ICR mice was systematically studied in vivo using ICP-MS, various spectral methods and gel electrophoresis [178]. The results showed that the liver weights of the mice treated with higher amounts of anatase TiO2 NPs were significantly increased. They stated that anatase TiO2 NPs could have accumulated in liver DNA by inserting itself into DNA base pairs or binding to DNA nucleotide that bound with three oxygen or nitrogen atoms and two phosphorous atoms of DNA with the Ti-O(N) and Ti-P bond lengths of 1.87 and 2.38 A, respectively, and could alter the conformation of DNA. The gel electrophoresis showed that higher dose of nano-anatase TiO2 NPs could cause liver DNA cleavage in mice.

However, as stated in the in vivo studies section, there are also studies that imply the opposite. A recent study found that TiO2 NPs (28 nm; 90/10: anatase/rutile) did not induce ROS production or increase the expression of γ-H2AX in A549 cells (0, 2.5, 5, 10, 15, 20, and 40 μg/ml; 24h) [179]. The transcription and protein expression levels of two Hsp members, Grp78 and Hsp70, were evaluated to ascertain their suitability as biomarkers of TiO2 NP-induced toxicity in the respiratory system [180]. Even though the presence of TiO2 NPs (25 nm) was confirmed in the cells via ultra-structural observations leading to cell death and induction of intracellular ROS generation, the transcription and protein expression levels of Hsp70 and Grp78 did not change at the same dose range (25–500 μg/ml) in A549 cells. They concluded that Hsp70 and Grp78 are not suitable biomarkers for evaluating the acute toxicological effects of TiO2 NPs in the respiratory system.

A recent study by Woodruff et al. [181] found that TiO2 NPs (10 nm anatase spheres; non-coated; 0-200 μg/ml; 24 h) were not genotoxic under the conditions of the Ames test and Comet assay in the thymidine kinase heterozygote (TK6) cell lines. There was no significant DNA damage or oxidative DNA damage observed. Warheit et al. [114] also reported negative results for an in vitro mammalian chromosome aberration test on Chinese hamster ovary cells (CHO) treated with TiO2 NPs (metaphase at 750, 1250, and 2500 μg/ml 4 h non-activated test condition; at 62.5, 125, 250 μg/ml, 4 h activated test condition, and at 25, 50, 100 μg/ml 20 h non-activated test condition). Linnainmaa et al. [182] reported similar negative results in cultured rat liver epithelial cells using the MN assay. Their results suggest that both TiO2 FPs and NPs (5, 10, and 20 μg/cm2) have no direct clastogenic potential. Fisichella et al. [183] concluded in their study that surface treated TiO2 NPs (100 μg/ml of STNP for 4, 24, and 72 h) with a rutile core (7±2 nm × 50±10 nm) are not harmful to Caco-2 cells. In TiO2 NP-induced inflammation, NF-κB is thought to be activated in response to pro-inflammatory cytokines. However, a recent study by Wilson [184] showed that after 6 h incubation with P-25 (10, 50, and 250 μg/ml), NF-κB was not activated in A549 cells. They concluded that NF-κB DNA binding may not be the likely transcription pathway that leads to TiO2 NP-induced inflammation. TiO2 NPs also were found to have no effect on the regulation of plasminogen activator inhibitor-1 expression in endothelial cells [185]. TiO2 NPs did not cause an increase in pro-mitochondrial membrane potential (MMP)-2 and pro-MMP-9 gelatinolytic activities in conditioned media, there was no dose- and time-related decreases in tissue inhibitors of metalloproteinases 2 (TIMP-2) and no transcriptional change of TIMP-1 were observed in U937 cells [186].

In summary, many in vivo and in vitro studies were conducted to investigate the genotoxicity of TiO2 FPs and NPs, but results are conflicting. Some studies indicate that TiO2 NPs are genotoxic, whereas the others give negative results. Even though the rationale for these conflicting results is not clear, use of different cell types, exposure metrics, crystalline structure, particle dispersion and NP sizes may be an explanation. Most of the cell lines which show genotoxicity are cells associated with the respiratory system and the circulatory system. Overall, the studies indicating that TiO2 NPs are genotoxic outweigh the studies that state otherwise. Thus, TiO2 NPs can be treated as potential hazards. More studies are needed to determine the conditions in which TiO2 NPs genotoxicity occurs [32]. The possible mechanisms for TiO2 NP-induced genotoxicity involve DNA damage directly or indirectly via oxidative stress and/or inflammatory responses. Tables 1 and 2 give a summary of the genotoxicity studies mentioned in this paper.

Table 1 Genotoxicity of TiO 2 NPs in vivo studies
Table 2 Genotoxicity of TiO 2 NPs in vivo studies

Reproductive and developmental toxicity

Although experimental evidence shows that absorbed TiO2 particles may be able to move across the placenta into fetal tissue, it has not yet been established whether human exposure to TiO2 particles causes reproductive and developmental toxicities. Exposure of other species, such as zebra fish [187] and abalone embryo [113], to TiO2 particles have shown that it can impair reproduction, inhibit hatching, and cause malformations. However, in the case of zebra fish some disagree [188]. In mammals, limited animal data are available to define the developmental or reproductive toxicity of TiO2 NPs. With respect to in vivo studies, Takeda et al. [189] demonstrated that prenatal subcutaneous exposure of mice to TiO2 NPs (25 and 70 nm; 16 mg/kg) at day 3, 7, 10, and 14 can damage the genital and cranial nerve systems in the offspring. In this study, TiO2 NPs identified by energy-dispersive X-ray spectroscopy were found in the testes and brain of exposed 6-week-old male mice, which indicated that TiO2 NPs may penetrate both blood-testis and BBB. Shimizu et al. [88] reported that, in the brain tissue of male fetuses (embryonic day 16) and pups (postnatal days 2, 7, 14, and 21), subcutaneous injection of pregnant mice (100 μl TiO2 NPs suspended at 1 μg/μl) altered expression of genes associated with brain development, cell death, response to oxidative stress, and mitochondrial activity in the brain during the perinatal period [88]. Even though subcutaneous exposures may not be realistic, this study does show that the fetal nervous system is specifically sensitive to maternal TiO2 NPs exposure during pregnancy. Moderate alterations in neurobehavior were also noted by Hougaard et al. [90] in mated C57BL/6BomTac mice exposed (1 h/day) through inhalation (42 mg/m3) to surface coated TiO2 NPs (UV-Titan; 97 nm) on GD 8–18. Yamashita et al. [190] reported that silica and TiO2 NPs with diameters of 70 and 35 nm, respectively, can cause pregnancy complications when injected intravenously into pregnant mice. The TiO2 NPs were found in the placenta, fetal liver and fetal brain. Mice treated with TiO2 NPs had smaller uteri and smaller fetuses than untreated controls.

Komatsu et al. [191] investigated the effects of TiO2 NPs on mouse testis Leydig cells in vitro and found TiO2 NPs were more cytotoxic to Leydig cells than diesel exhaust and carbon black NPs. TiO2 NPs were taken up by Leydig cells, and affected viability, proliferation and gene expression.

In summary, limited in vivo and in vitro studies suggest that TiO2 NPs exposures may exert certain reproductive and developmental toxicities. Further studies are needed to clarify the mechanisms underlying these toxicity results.


The mechanisms of metal-induced carcinogenesis are not well understood. Both genetic and non-genetic factors elicited by TiO2 NPs in cells may predispose to carcinogenicity [176].

Experimental studies

Animal experimental studies show that high concentrations of TiO2 FPs (<2.5 um; 250 mg/m3; 2 yrs) and TiO2 NPs (<100 nm; 10 mg/m3; 2 yrs) can cause respiratory tract cancer in exposed rats [43, 192]. Chronic lung inhalation studies have shown that TiO2 NPs can cause bronchoalveolar adenomas and cystic keratinizing squamous cell carcinomas at high doses [9] and alveolar/bronchiolar adenoma [193]. Heinrich et al. [194] investigated the carcinogenicity of TiO2 NPs (15–40 nm) and found TiO2 NPs were tumorigenic in rats at a concentration of approximately 10 mg/m3 for 2 years, followed by a 6-month holding period. TiO2 NPs seem to have more carcinogenic potential in the rat than TiO2 FPs on an equal mass dose basis. This difference in carcinogenic potency suggests the need to develop separate risk estimates for TiO2 FPs and NPs exposures, and to develop separate recommendations for occupational exposures to each size range [43].

To assess the health risks of occupational exposure to TiO2 NPs, Kuempel et al. [76] extrapolated rodent data to humans using a lung dosimetry model. The rat-based estimates of the working lifetime airborne concentrations of TiO2 NPs associated with 0.1% excess risk of lung cancer were approximately 0.07 to 0.3 mg/m3. Using a similar model, Dankovic et al. [43] extrapolated rat threshold estimates to lifetime human occupational exposures and found a range of estimated occupational exposure levels of 0.8-5.8 mg/m3 for TiO2 FPs, and 0.09–0.66 mg/m3 for TiO2 NPs. Such risk analyses formed the basis for development of RELs of 0.3 and 2.4 mg/m3 for TiO2 NPs and FPs, respectively [50]. Due to the lack of human epidemiological information, these extrapolation models using animal experimental data are still useful in the prediction for risk assessment of occupational exposure to TiO2 NPs.

In an intratracheal instillation study female rats were administered TiO2 hydrophilic or anatase NPs (21–25 nm; 1/week for 30 weeks) of different doses [195]. The incidence of lung tumors (52–69.6%, adenomas/carcinomas and squamous cell epitheliomas/carcinomas combined) in rats receiving TiO2 hydrophilic or anatase NPs was significantly higher than controls (0%). Anatase NPs also significantly induced higher incidence of lung tumors (30–63.6%). The incidence of benign and malignant lung tumors in the TiO2 hydrophilic NPs groups (6.7%) was not significant. The incidences of cystic keratinizing epitheliomas (11.7%) and squamous cell carcinomas (4.8%) were significantly greater than the control group (0.5%) in another inhalation study with female rats treated with TiO2 particles (particle size not stated; 11.3 mg/m3; 24 months, followed by 6 months observation) [196]. Bernard et al. [197] conducted toxicological and carcinogenesis studies of dietary TiO2-coated mica in rats fed diets containing 0, 1.0, 2.0, or 5.0% TiO2-coated mica for up to 130 weeks. They found no evidence that TiO2-coated mica produced either toxicological or carcinogenic effects at dietary concentrations as high as 5.0%.

In regards to skin cancers, a two-stage skin model was used by Xu et al. [71] to examine the promoting/carcinogenic effect TiO2 NPs (rutile, 20 nm). C-Ha-ras proto-oncogene transgenic (Hras128) rats, which are sensitive to skin carcinogenesis and their wild-type siblings were exposed to UV-B radiation on shaved back skin twice weekly for 10 weeks. The shaved area was then painted with a 100 mg/ml TiO2 NP suspension twice weekly until sacrifice. The tumor incidence was not different from the UV-B controls. They suggested that TiO2 NPs does not cause skin carcinogenesis, which may be due to its inability to penetrate through the epidermis and reach underlying skin structures. The same conclusion was reached by Sagawa et al. [70] who studied the promoting effect of silicone coated TiO2 NPs (35 nm; 5 times a week for 8 and 40 weeks; 0, 10, or 20 mg) suspended in silicone oil and non-coated TiO2 NPs (20 nm; twice a week for 28 or 40 weeks; 0, 50, or 100 mg) suspended in Pentalan 408 on a two-stage skin chemical carcinogenesis model. Analysis of skin indicated that silicone coated TiO2 NPs and non-coated TiO2 NPs did not penetrate though either healthy or damaged skin. Newman et al. [65] also suggested that TiO2 NPs are not carcinogenic to the skin because they do not penetrate the intact dermal tissue. However, the authors emphasized that further studies for the safety evaluation of the TiO2 NPs in sunscreens must be done to simulate real-world conditions particularly in sunburned skin and under UV exposure.

Pulmonary studies support the carcinogenicity of TiO2 NPs in intratracheal and inhalation studies. However, exposure modes such as intragastric or dermal exposure do not indicate that TiO2 NPs are carcinogenic.

Epidemiological studies

Epidemiological studies on workers exposed to TiO2 particles, thus far, have not been able to detect an association between the occupational exposure and an increased risk for lung cancer. Furthermore, most studies were not designed to investigate the relationship between TiO2 particle size and lung cancer risk, which represents an important question for assessing the potential occupational carcinogenicity of TiO2 NPs [32]. The results from the epidemiological studies that have been conducted (no particle size defined) show that there are no significant associations between TiO2 exposure and risk of lung cancer [198, 199], elevated standardized mortality ratio (SMR) for cancer [200], and reduction in ventilatory capacity [119]. As a whole, these epidemiological studies imply that occupational exposures to TiO2 FPs (or total dust) are not associated with increasing risk of cancers. Unfortunately, epidemiological studies of adverse health effects induced by TiO2 NPs alone are lacking. The relatively short history in production and use seems to be the main reason for the lack of human epidemiological studies for TiO2 NPs. Furthermore, it is difficult to make reliable hazard assessments of manufactured NPs, because the NPs may form large agglomerates in both in vitro and in vivo studies [51]. Experimental evidence supports that TiO2 NP agglomeration increases when the surface area decreases at a constant pH and that the isoelectric point for TiO2 depends on the particle size [201]. The interaction of this increased surface area with the biological environment induces oxidative stress [8]. It is worth noting that although TiO2 NPs are prone to forming agglomerates of >100 nm in suspension, these agglomerates are not stable and may dissociate in bodily fluids and tissues. However, the extent of such dissociation has not yet been determined. To evaluate the health effects of TiO2 NPs on workers, further well designed epidemiological studies are needed. The animal studies that have been conducted (those mentioned in this paper) indicate potential risk factors that could be assessed in occupational settings. Examples of potential risk factors are the underlying health of the workers and co-exposures.

In summary, available epidemiological studies as well as in vivo animal experimental data concerning the carcinogenic effects of TiO2 particles are outlined above. Epidemiological studies on workers exposed to TiO2 FPs failed to detect an association between the occupational exposure and an increased risk for cancer. Available data from human studies on TiO2 NPs exposures alone are still lacking. Carcinogenicity studies in animals indicate that TiO2 NPs can produce tumors when exposed through inhalation or intratracheal instillation and are more carcinogenic on an equal mass basis than TiO2 FPs. The tumors preferentially include adenomas and squamous cell carcinomas. Based on the studies outlined above, TiO2 NPs were evaluated by World Health Organization (WHO)/IARC as a Group 2B compound [202]. An overview of currently available carcinogenicity data on TiO2 NPs from experimental animals raises serious questions as to their health and environmental safety. Therefore, all commercially available TiO2 NPs should be assessed and their production and application should be managed appropriately. At this stage, risk characterization of TiO2 NPs is hampered by incomplete or lack of data on human exposure and dose- response analysis.

Molecular mechanisms of carcinogenesis

Many studies have shown that TiO2 FPs and NPs induce cytotoxicity and genotoxicity in various cultured cell lines as well as tumorigenesis in animal models [171]. As stated above, DNA strand breaks, mutations, chromosomal damage and cell transformation have been observed in some in vitro or in vivo studies. However, the exact mechanisms of TiO2 NP-induced carcinogenesis are not clear. Recent evidence indicates that ROS formation, induction of inflammation and alterations in cell signal transduction induced by TiO2 NPs may play an important role in the etiology of their carcinogenesis. Elevated levels of ROS and down regulation of ROS scavengers and antioxidant enzymes are associated with various cancers [203]. ROS consist of a group of partially reduced forms of molecular oxygen, such as hydroxyl radical (•OH), superoxide anion (O2 −•), singlet oxygen (1O2), hydrogen peroxide (H2O2), lipid peroxides, and hypochlorous acid (HClO) [204]. Accumulation of ROS may be accompanied by the production of reactive nitrogen species [205], such as the highly reactive peroxynitrite anion, a strong oxidant formed by the reaction of O2 −• and NO•. The cumulative production of ROS through either endogenous or exogenous insults is termed oxidative stress. Oxidative stress induces a cellular redox imbalance found in various cancer cells. ROS could induce non-selective DNA damage, which may result in genetic changes in active genes. Oxidative damage to cellular DNA can lead to mutations. The mutations in DNA may be involved in the initiation of various cancers. Therefore, oxidative stress induced by ROS generation may play an important role in the initiation and progression of multistage carcinogenesis of TiO2 NPs. The generation of ROS and induction of inflammation leading to alterations of signaling components due to TiO2 NP exposures are reviewed in this paper.

Generation of ROS

It has been hypothesized that insoluble particle accumulation in the animal lungs is mechanistically linked to the development of lung tumors [43]. Accumulation of TiO2 NPs in the lung leads to chronic inflammation, which may further lead to the formation of ROS and epithelial proliferation, and eventually lead to mutations and tumor formation. Some of the studies cited previously have reported the involvement of free radicals in DNA damage [28, 157], ROS-induced activation of p53-mediated DNA damage check point signals [164], increased intracellular ROS leading to increased G2M cell cycle arrest or delay [156, 171], cell-derived oxidants involved in induction of mutagenesis [144], and increased extracellular ROS coupled with HO-1 and NOS mRNA expression and TNF-α release [93]. Others have linked TiO2 NPs (Wistar rats; 1, 5, 10, 25, and 50 μg/ml; <25 nm; 1 h) to ROS generation as a result of mitochondrial dysfunction in lung tissues [206]. Jaeger et al. [207] investigated whether ROS-induced mitochondrial DNA damage is the mode of action by which TiO2 NPs (≤20 nm) induce cytotoxic and genotoxic effects in human HaCaT keratinocytes in vitro. They demonstrated the induction of the mitochondrial "common deletion" in HaCaT cells following exposure to TiO2 NPs. They proposed a ROS-mediated (increased 16.7 fold of control; 4 h; 5 and 50 μg/ml) cytotoxic and genotoxic potential for TiO2 NPs. They also showed that TiO2 enters the cell by endocytosis. Another study with HaCaT cells also showed that TiO2 NPs (anatase, rutile and anatase/rutile; 4, 10, 21, 25, and 60 nm; 200 μg/ml) could induce the generation of ROS and damage the cells under ultraviolet-A (UVA) irradiation [20] . The induced ROS resulted in oxidative stress in the HaCat cells, reducing SOD and increasing MDA levels. The cell viability was also decreased in a dose dependent manner. Reduction of cell viability and increased ROS generation by TiO2 NPs under UVA irradiation was also noted by Sanders et al. [208]. Similar effects were seen in a recent study by Yin et al. [209] on HaCat cell cultures. Yoo et al. [210] also stated that sub-100 nm sized TiO2 treatment under UVA irradiation induces apoptotic cell death through ROS-mediated up regulation of the death receptor, Fas, and activation of the pre-apoptotic protein, Bax.

In addition to these, a long term study (intratracheal administration; 2.5, 5, and 10 mg/kg) found that TiO2 NPs (5–6 nm) caused oxidative damage in lungs and enhanced expression of (Nrf2), HO-1 and glutamate-cystine ligase catalytic subunit (GCLC) on days 15 and 75 which began to decrease on day 90 [211]. They suggested that induction of Nrf2 expression was an adaptive intracellular response to TiO2 NP-induced oxidative stress in mouse lung. Another study on PC12 cells found that TiO2 NPs (1, 10, 50, and 100 μg/ml; 6, 12, 24, and 48 h) caused generation of ROS in a dose and time-dependent manner, leading to apoptosis [212]. ROS-mediated oxidative stress, the activation of p53, Bax, and caspase-3, as well as oxidative DNA damage were found to be involved in the mechanistic pathways of apoptosis induced by TiO2 NPs (anatase; 25 nm; 50, 100, and 200 μg/ml; 24, 48, and 72 h) in human embryonic kidney (HEK) 293 cells [213]. These increases followed a dose-dependent pattern. Wu et al. [214] also showed the involvement of p53 and JNK activation in G2/M cell cycle arrest and apoptosis induced by anatase TiO2 NPs (20 nm; 25, 50, 100, and 200 μg/ml) in the neuronal cell, PC12. A study on dendritic cells also found that TiO2 NPs enhanced ROS production [215]. Wang et al. [216] found that TiO2 NPs (intragastric exposure; 30 consecutive days) exerted toxicity on the mouse spleen through oxidative stress with significant increases in ROS. This subsequently led to strong LPO and the significant expression of HO-1 via the p38-Nrf-2 signaling pathway.

Uchino et al. [217] showed that the crystal size of TiO2 NPs (anatase; 30 nm; 50μg/ml) had large influence on •OH generation, but the optimum size for the •OH generation was different between both crystalline forms (anatase and rutile). A significant relationship was observed between cytotoxicity and •OH generation in CHO cells. TiO2 NPs (rutile; 40–70 nm, minor axis; 200–300 nm, major axis; 40–55 g/100g) were also shown to have the potential to convert benign tumor cells into malignant ones through the generation of ROS in the target cells [218]. However, apart from all of these studies implicating TiO2 NP-generated ROS in cellular and molecular effects, a recent article by Toyooka et al. [219] demonstrated that TiO2 NPs could cause DNA damage without generating ROS. Their study examined the genotoxicity of two different sizes of TiO2 NPs in the A549 cells based on the phosphorylation of γ-H2AX. Flow cytometric analysis showed that the generation of γ-H2AX by TiO2 NPs was independent of cell cycle phases, and cells which incorporated larger amounts of TiO2 particles had more significant γ-H2AX.

Induction of inflammation

Most of the studies previously mentioned in other sections have also reported inflammatory effects due to TiO2 NPs exposure. The details of the molecular events involving inflammation for some of these studies will be discussed here. Cytokines are components of the immune system that are involved in these molecular events, either as agonists or antagonists of inflammation. TiO2 NPs (anatase; 20 nm; rutile, 80 nm; 7.5-30 mg/kg) signaled the interleukin 1 (IL-1α) family of cytokines in a mouse lung model [142]. The signaling of IL-1R by TiO2 NPs is similar to that of asbestos. Others showed that IL-1β production was depended on active cathepsin B and ROS production independent of the characteristics of TiO2 [159]. Another study showed increased expression of IL-1β, IL-2, IL-4, IL-6, IL-10, and IL-18, in nephritic inflammation caused by TiO2 NPs intragastrically administered to mice (5–6 nm; 2.5, 5, and 10mg/kg; everyday for 90 days) [146]. In addition, TiO2 NPs activated NF-κB, leading to increased expression of TNF-α, MMIF, cross-reaction protein, TGF-β, interferon-γ, and CYP1A1, and decreased Hsp70 expression. Moon et al. [220] showed that the levels of pro-inflammatory mediators, such as IL-1β, TNF-α, and macrophage inflammatory protein (MIP)-2, in BALF and mRNA expression of TNF-α and IL-1β in lung tissue were elevated post-exposure in mice (intraperitoneal; 40 mg/kg BW). TiO2 NP exposure increased neutrophil influx, protein levels in BALF, and ROS activity of BAL cells 4 h after exposure. In addition, TiO2 NP exposure resulted in significant activation of inflammatory signaling molecules, such as c-Src and p38 mitogen-activated protein kinase (MAPK), in lung tissue and alveolar macrophages. Activation of the NF-κB pathway in pulmonary tissue was also noted. Kan et al. [143] showed that TiO2 NPs increased phosphorylation of p38 and troponin 1 in cardiac muscle. It can be seen here that the induction of inflammation by TiO2 NPs involves a host of other molecular components and events including the signaling of cytokines. Additional evidence for this is shown by the following references [145, 154, 160, 162, 180].

Recent research indicates that TiO2 particle-induced alterations in signal transduction may also play an important role in the etiology of cancer. Goncalves et al. [221] investigated the in vitro effects of TiO2 NPs on human neutrophils. Kinetic experiments revealed no cell necrosis after a 24 h treatment with TiO2 NPs (0–100 μg/ml). However, TiO2 NPs markedly and rapidly induced tyrosine phosphorylation events, including phosphorylation of two key enzymes, p38 MAPK and extracellular signal-regulated kinases-1/2 (Erk-1/2). Supernatants from induced neutrophils were collected after 24 h and tested for the presence of 36 different analytes (cytokines, chemokines) using an antibody array assay. TiO2 NP treatment increased production of 13 (36%) analytes, including IL-8, which exhibited the greatest increase (approximately 16 fold increase compared to control). These results indicate TiO2 NPs exert important neutrophil agonistic properties in vitro which represents one of the characteristics of carcinogens. Chen et al. [118] pointed out that a mixture of anatase and rutile TiO2 NPs (<100 nm, anatase/rutile 99.5% trace metal basis; 0–0.75 mg/ml) induced histamine secretion in mast cells (RBL-2H3 cells). Mast cell exposure to TiO2 NPs activated membrane L-type Ca2+ channels, induce ROS production and stimulate PLC activity. Influx of extracellular Ca2+ raises [Ca2+] i, and when coupled with the IP3-IP3 receptor pathway can trigger the release of ER resident Ca2+ and subsequent histamine secretion. They stated that TiO2 NPs directly trigger inflammatory mediators, thus bypassing traditional immuno-stimulation by allergens. These results suggest that mast cell degranulation of histamine may be significantly augmented and intensified in TiO2 NP exposed tissues with or without IgE antibody-based sensitization.

In conclusion, research evidence seems to be sufficient to conclude that both TiO2 FPs and NPs generate ROS as demonstrated by both in vivo and in vitro studies. ROS-induced signaling and activation of the IL family of cytokines, Bax, caspases 3 and 9, NF-κB, and p53, as well as phosphorylation of p38 and G2M phase cell cycle arrest seem to be common findings. In regards to induction of inflammation leading to the production of ROS, inflammatory cytokines seem to play an influencing role. Furthermore, experimental data suggest that ROS generation and oxidative stress may be important in TiO2 NP-induced genotoxicity and carcinogenicity. The exact mechanisms of TiO2 NP induced carcinogenesis are not clear. Limited data show that ROS, oxidative stress, as well as, cell signaling alterations of carcinogenic genes may all play significant roles in the carcinogenicity of TiO2 NPs at relatively high doses. Further studies are needed employing lower, occupationally relevant doses, which avoid the confounding influence of possible overload.


Conventionally, TiO2 FPs have been considered as a low toxicity material. TiO2 NPs possess different physicochemical properties compared to TiO2 FPs, which would be expected to alter their biological properties. A full risk assessment for various routes of exposure to TiO2 NPs requires further data. Apart from the NIOSH recommended REL, to date, no occupational or environmental exposure limits for TiO2 NPs have been set by any other regulatory agency. Current understanding on their toxicity largely depends on a limited number of experimental animal or cell culture studies, where extrapolation to human exposures is required. Epidemiological studies thus far have not been able to detect an association between the occupational exposure to TiO2 particles and an increased risk for cancer. The physicochemical properties of TiO2 NPs may strongly influence their bioavailability and toxicity. Majority of data imply that TiO2 anatase NPs are cytotoxic or genotoxic. However, this conclusion was based on studies using TiO2 anatase NPs only. Under conditions of occupational exposure, inhalation of TiO2 NPs is normally the principal route for entry into the human body. Pulmonary inflammatory responses and lung cancers are the most important adverse effect observed in experimental animals due to TiO2 NP exposures. When only using realistic doses are considered, as in the case of some inhalation studies, inflammatory responses are still a prominent effect seen. TiO2 NPs can be absorbed through the lung or GIT into systematic circulation and then distributed in different organs such as liver, kidneys, spleen, or even brain causing localized effects. However, the rate of such translocation is currently uncertain. Some evidence has shown that TiO2 NPs cannot penetrate the intact skin into the human body. TiO2 NPs may have the potential to penetrate the blood–brain, blood-testis and blood-placenta barriers. However, the rate of translocation appears low and evidence is lacking which link systemic responses to translocation of particles to systemic sites. Many studies have been conducted in vitro and in vivo to investigate the genotoxicity of TiO2 NPs but the results are conflicting and doses employed were high. Certain reproductive and developmental toxicities in experimental animals or cell cultures have been observed in a few in vivo and in vitro studies. Whether human exposure to TiO2 NPs causes reproductive and developmental toxicities is unclear. Animal studies imply that accumulation of TiO2 NPs in organs or tissues may take place after continuous exposure. Responses to accumulation of TiO2 NPs in systemic organs need to be evaluated in further studies. In addition, TiO2 NP-induced generation of ROS and alterations in cell signal transduction pathways may play an important role in the etiology of carcinogenesis of TiO2 NPs at relatively high doses. However, these studies should be repeated at doses relevant to normal occupational or environmental exposure conditions where particle overload is not an issue. Despite this, the results currently available imply that TiO2 NPs exhibit greater toxicity than TiO2 FPs. These data should not be ignored, and development of prevention strategies to protect worker's health appears to be a prudent course of action.

In summary, although TiO2 NPs have been studied extensively in recent years, there is still much remaining to be elucidated concerning their possible health effects to support risk assessment and management.

First, to assure worker and consumer safety, it is urgently important to conduct exposure hazard assessment, which would allow the development of a framework enabling risk management for all commercial TiO2 NPs. This also includes bio-safety evaluation of TiO2 nanoparticulate carriers for drug delivery application.

Second, all future studies on TiO2 NPs should characterize the physicochemical properties of the NPs, such as size distribution, crystalline structure, surface area, surface coating, etc., as delivered to the biological system. This will allow for better comparison of data from different studies and assist in determination of appropriate dosimetry.

Third, long-term animal studies comparing the toxicity and carcinogenicity of TiO2 FPs and NPs are especially needed. The focus of these studies must be aimed at both occupational and consumer relevant doses and routes of exposure.

Fourth, detailed toxicokinetics studies that include absorption, distribution, metabolism, accumulation, and excretion of TiO2 NPs through different exposure routes into the human body are indispensable. In addition, future studies should focus on evaluating systemic responses distinct from the organ of exposure and biomarkers reflecting TiO2 NP exposure and toxic effects.

Finally, the molecular mechanisms by which TiO2 NPs may cause cancer are unclear. Limited data show that ROS generation and signal alterations of certain cancer-related genes may be involved in the carcinogenicity of TiO2 NPs. Therefore, further investigation is needed to elucidate the molecular mechanisms of carcinogenicity for TiO2 NPs.

Authors’ information

Miss Hongbo Shi and Ruth Magaye are graduate students at Ningbo University, China. Their current research focus is on nanotoxicology of nanomaterials. As authors or co-authors they have collectively published 7 scientific manuscripts.

Vincent Castranova, Ph.D., is the Chief of the Pathology and Physiology Research Branch in the Health Effects Laboratory Division of the National Institute for Occupational Safety and Health, Morgantown, West Virginia. Dr. Castranova’s research interests have been concentrated in pulmonary toxicology and occupational lung disease. He has been coordinator of the Nanotoxicology Program in NIOSH since its inception in 2005. He has been a co-editor of four books and has co-authored over 540 manuscripts and book chapters.

Dr. Jinshun Zhao works is a professor and director of the Public Health Department of Medical School of Ningbo University, Ningbo, Zhejiang, China. Dr. Jinshun Zhao’s research interests have been concentrated in occupational and environmental disease, toxicology and molecular mechanisms of chemical and metal-induced carcinogenesis. His current research is focused on the toxicology of nanomaterials. As an author or a co-author, he has published over 100 scientific manuscripts.





3,4-dihydroxyphenylacetic acid




5-hydroxyindole acetic acid


Acetone-Olive Oil


Airway hyper-reactivity


Alanine aminotransferase


American Conference of Governmental Industrial Hygienists


Aspartate aminotransferase


Base excision repair


Blood brain-barriers


Blood urea nitrogen


Body weight


Bronchoalveolar lavage fluid


Bronchial Epithelial


Chinese hamster ovary-K1


C-Ha-ras proto-oncogene transgenic


Creatine kinase


Cytokinesis block micronucleus




Enzyme-linked immunosorbent assay


Expanded simple tandem repeat


Fcγ receptor II


Fine particle


Fine particles


Food and Drug Administration


Gastrointestinal tract


Gestation days


Glutamate-cystine Ligase Catalytic Subunit


Glutathione S-transferase


Heat shock protein 70




High density lipoprotein cholesterol




Human embryonic kidney


Hydrogen-1 nuclear magnetic resonance spectroscopy


Hypochlorous acid


Hydrogen peroxide


Hydroxyl radical


Hypoxanthine phosphoribosyltransferase

(IKK-α IKK-β):

IκB kinases




International Agency for Research on Cancer


Lactate dehydrogenase


Lipid peroxidation


Local exhaust ventilation


Low density lipoprotein cholesterin


Macrophage inflammatory protein


Macrophage migration inhibitory factor




Median lethal dose


Median lethal concentration




Mitochondrial membrane potential


Mitogen-activated Protein Kinase








National Institute for Occupational Safety and Health


New Energy and Industrial Technology Development Organization


NF-κB-inducible kinase


Nitric oxide


Nitric oxide synthase


No Observed Adverse Effect Level




Nuclear factor kappa-light-chain-enhancer of activated B cells


Nucleotide excision repair


Occupational Safety & Health Administration


Olive tail moment


Organization for Economic Co-operation and Development




Particulate matter


Permissible exposure limit




Photodynamic therapy


Polychromatic erythrocyte


Polyethylene glycol


Reactive oxygen species


Recommended exposure limit


Relative deposition index


Reversed-phase high performance liquid chromatography


Real-time quantitative PCR


Scanning electron microscopy


Serum amyloid A-1


Serum amyloid A-3


Serum glutamic oxaloacetic transaminase


Serum glutamic pyruvic transaminase


Singlet oxygen


Silicon dioxide


Sister chromatid exchange


Standardized mortality ratio


Stratum corneum


Superoxide anion


Superoxide dismutase


TEM-coupled Energy Dispersive X-ray


Time of Flight Secondary Ion Mass Spectrometry


Time weighted average


Tissue inhibitors of metalloproteinases 2




Titanium dioxide


Threshold limit value


Toll-like receptor-2


Toluene diisocyanate


Total cholesterol

(TGF- β):

Transforming growth factor-β


Transmission electron microscopy






Tumor necrosis factor-α






Vanadium pentoxide


World Health Organization


  1. 1.

    Kisin ER, Murray AR, Keane MJ, Shi XC, Schwegler-Berry D, Gorelik O, Arepalli S, Castranova V, Wallace WE, Kagan VE, Shvedova AA: Single-walled carbon nanotubes: geno- and cytotoxic effects in lung fibroblast V79 cells. J Toxicol Environ Health A 2007, 70: 2071–2079. 10.1080/15287390701601251

    CAS  PubMed  Article  Google Scholar 

  2. 2.

    Robertson TA, Sanchez WY, Roberts MS: Are commercially available nanoparticles safe when applied to the skin? J Biomed Nanotechnol 2010, 6: 452–468. 10.1166/jbn.2010.1145

    CAS  PubMed  Article  Google Scholar 

  3. 3.

    EU - European Commission Recommendation on the definition of nanomaterial.

  4. 4.

    Riu J, Maroto A, Rius FX: Nanosensors in environmental analysis. Talanta 2006,69(2):288–301. 10.1016/j.talanta.2005.09.045

    CAS  PubMed  Article  Google Scholar 

  5. 5.

    Ruth Magaye JZ, Linda B, Min D: Genotoxicity and carcinogenicity of cobalt-, nickel- and copper-based nanoparticles (Review). Exp Ther Med 2012, 4: 551–561.

    PubMed Central  PubMed  Google Scholar 

  6. 6.

    American Conference of Governmental Industrial Hygienists (ACGIH): Threshold limit values and biological exposure indices for 1992–1993. Cincinnati: Ohio: American Conference of Governmental industrial hygienists; 1992.

    Google Scholar 

  7. 7.

    Participants IRSIW: The relevance of the rat lung response to particle overload for human risk assessment: a workshop consensus report. Inhal Toxicol 2000, 12: 1–17.

    Google Scholar 

  8. 8.

    Zhao J, Bowman L, Zhang X, Vallyathan V, Young SH, Castranova V, Ding M: Titanium dioxide (TiO2) nanoparticles induce JB6 cell apoptosis through activation of the caspase-8/Bid and mitochondrial pathways. J Toxicol Environ Health A 2009, 72: 1141–1149. 10.1080/15287390903091764

    CAS  PubMed  Article  Google Scholar 

  9. 9.

    Lee KP, Trochimowicz HJ, Reinhardt CF: Pulmonary response of rats exposed to titanium dioxide (TiO2) by inhalation for two years. Toxicol Appl Pharmacol 1985, 79: 179–192. 10.1016/0041-008X(85)90339-4

    CAS  PubMed  Article  Google Scholar 

  10. 10.

    IARC: Cobalt in Hard Metals and Cobalt Sulfate, Gallium Arsenide, Indium Phosphide and Vanadium Pentoxide. IARC Sci Publ 2006., 86:

    Google Scholar 

  11. 11.

    Maynard AD, Kuempel ED: Airborne nanostructured particles and occupational health. J Nanopart Res 2005, 6: 587–614.

    Article  CAS  Google Scholar 

  12. 12.

    Tsuji JS, Maynard AD, Howard PC, James JT, Lam CW, Warheit DB, Santamaria AB: Research strategies for safety evaluation of nanomaterials, part IV: risk assessment of nanoparticles. Toxicol Sci 2006, 89: 42–50.

    CAS  PubMed  Article  Google Scholar 

  13. 13.

    Fabian E, Landsiedel R, Ma-Hock L, Wiench K, Wohlleben W, van Ravenzwaay B: Tissue distribution and toxicity of intravenously administered titanium dioxide nanoparticles in rats. Arch Toxicol 2008, 82: 151–157. 10.1007/s00204-007-0253-y

    CAS  PubMed  Article  Google Scholar 

  14. 14.

    Oberdorster G: Pulmonary effects of inhaled ultrafine particles. Int Arch Occup Environ Health 2001, 74: 1–8.

    CAS  PubMed  Article  Google Scholar 

  15. 15.

    Oberdorster G, Ferin J, Lehnert BE: Correlation between particle size, in vivo particle persistence, and lung injury. Environ Health Perspect 1994,102(Suppl 5):173–179. 10.1289/ehp.94102s5173

    PubMed Central  PubMed  Article  Google Scholar 

  16. 16.

    Sager TM, Kommineni C, Castranova V: Pulmonary response to intratracheal instillation of ultrafine versus fine titanium dioxide: role of particle surface area. Part Fibre Toxicol 2008, 5: 17. 10.1186/1743-8977-5-17

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  17. 17.

    Long TC, Tajuba J, Sama P, Saleh N, Swartz C, Parker J, Hester S, Lowry GV, Veronesi B: Nanosize titanium dioxide stimulates reactive oxygen species in brain microglia and damages neurons in vitro. Environ Health Perspect 2007, 115: 1631–1637. 10.1289/ehp.10216

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  18. 18.

    Warheit DB, Webb TR, Reed KL, Frerichs S, Sayes CM: Pulmonary toxicity study in rats with three forms of ultrafine-TiO2 particles: differential responses related to surface properties. Toxicology 2007, 230: 90–104. 10.1016/j.tox.2006.11.002

    CAS  PubMed  Article  Google Scholar 

  19. 19.

    Sayes CM, Wahi R, Kurian PA, Liu Y, West JL, Ausman KD, Warheit DB, Colvin VL: Correlating nanoscale titania structure with toxicity: a cytotoxicity and inflammatory response study with human dermal fibroblasts and human lung epithelial cells. Toxicol Sci 2006, 92: 174–185. 10.1093/toxsci/kfj197

    CAS  PubMed  Article  Google Scholar 

  20. 20.

    Xue C, Wu J, Lan F, Liu W, Yang X, Zeng F, Xu H: Nano titanium dioxide induces the generation of ROS and potential damage in HaCaT cells under UVA irradiation. J Nanosci Nanotechnol 2010, 10: 8500–8507. 10.1166/jnn.2010.2682

    CAS  PubMed  Article  Google Scholar 

  21. 21.

    Petkovic J, Zegura B, Stevanovic M, Drnovsek N, Uskokovic D, Novak S, Filipic M: DNA damage and alterations in expression of DNA damage responsive genes induced by TiO2 nanoparticles in human hepatoma HepG2 cells. Nanotoxicology 2011, 5: 341–353. 10.3109/17435390.2010.507316

    CAS  PubMed  Article  Google Scholar 

  22. 22.

    Wang C, Li Y: Interaction and nanotoxic effect of TiO(2) nanoparticle on fibrinogen by multi-spectroscopic method. Sci Total Environ 2012, 429: 156–160.

    CAS  PubMed  Article  Google Scholar 

  23. 23.

    Andersson POLC, Ekstrand-Hammarstrom B, Akfur C, Ahlinder L, Bucht A, Osterlund L: Polymorph- and Size-Dependent Uptake and Toxicity of TiO2 Nanoparticles in Living Lung Epithelial Cells. Small 2011, 7: 514–523. 10.1002/smll.201001832

    CAS  PubMed  Article  Google Scholar 

  24. 24.

    Tedja R, Lim M, Amal R, Marquis C: Effects of serum adsorption on cellular uptake profile and consequent impact of titanium dioxide nanoparticles on human lung cell lines. ACS Nano 2012, 6: 4083–4093. 10.1021/nn3004845

    CAS  PubMed  Article  Google Scholar 

  25. 25.

    Saber AT, Jensen KA, Jacobsen NR, Birkedal R, Mikkelsen L, Moller P, Loft S, Wallin H, Vogel U: Inflammatory and genotoxic effects of nanoparticles designed for inclusion in paints and lacquers. Nanotoxicology 2012, 6: 453–471. 10.3109/17435390.2011.587900

    CAS  PubMed  Article  Google Scholar 

  26. 26.

    Ortlieb M: White Giant or White Dwarf?: Particle Size Distribution Measurements of TiO2. GIT Lab J Eur 2010, 14: 42–43.

    Google Scholar 

  27. 27.

    Baan R, Straif K, Grosse Y, Secretan B, El Ghissassi F, Cogliano V: Carcinogenicity of carbon black, titanium dioxide, and talc. Lancet Oncol 2006, 7: 295–296. 10.1016/S1470-2045(06)70651-9

    PubMed  Article  Google Scholar 

  28. 28.

    Shukla RK, Sharma V, Pandey AK, Singh S, Sultana S, Dhawan A: ROS-mediated genotoxicity induced by titanium dioxide nanoparticles in human epidermal cells. Toxicol In Vitro 2011, 25: 231–241. 10.1016/j.tiv.2010.11.008

    CAS  PubMed  Article  Google Scholar 

  29. 29.

    Kaida T, Kobayashi K, Adachi M, Suzuki F: Optical characteristics of titanium oxide interference film and the film laminated with oxides and their applications for cosmetics. J Cosmet Sci 2004, 55: 219–220.

    PubMed  Google Scholar 

  30. 30.

    Wang JJ, Sanderson BJ, Wang H: Cyto- and genotoxicity of ultrafine TiO2 particles in cultured human lymphoblastoid cells. Mutat Res 2007, 628: 99–106. 10.1016/j.mrgentox.2006.12.003

    CAS  PubMed  Article  Google Scholar 

  31. 31.

    Wolf R, Matz H, Orion E, Lipozencic J: Sunscreens–the ultimate cosmetic. Acta Dermatovenerol Croat 2003, 11: 158–162.

    PubMed  Google Scholar 

  32. 32.

    Trouiller B, Reliene R, Westbrook A, Solaimani P, Schiestl RH: Titanium dioxide nanoparticles induce DNA damage and genetic instability in vivo in mice. Cancer Res 2009, 69: 8784–8789. 10.1158/0008-5472.CAN-09-2496

    CAS  PubMed  Article  Google Scholar 

  33. 33.

    Jacobs JJ, Skipor AK, Black J, Urban R, Galante JO: Release and excretion of metal in patients who have a total hip-replacement component made of titanium-base alloy. J Bone Joint Surg Am 1991, 73: 1475–1486.

    CAS  PubMed  Google Scholar 

  34. 34.

    Sul YT: Electrochemical growth behavior, surface properties, and enhanced in vivo bone response of TiO2 nanotubes on microstructured surfaces of blasted, screw-shaped titanium implants. Int J Nanomedicine 2010, 5: 87–100.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  35. 35.

    Patri A, Umbreit T, Zheng J, Nagashima K, Goering P, Francke-Carroll S, Gordon E, Weaver J, Miller T, Sadrieh N: Energy dispersive X-ray analysis of titanium dioxide nanoparticle distribution after intravenous and subcutaneous injection in mice. J Appl Toxicol 2009, 29: 662–672. 10.1002/jat.1454

    CAS  PubMed  Article  Google Scholar 

  36. 36.

    Ni M, Leung MKH, Leung DYC, Sumathy K: A review and recent developments in photocatalytic water-splitting using TiO2 for hydrogen production. Renewable and Sustainable Energy Reviews 2007, 11: 401–425. 10.1016/j.rser.2005.01.009

    CAS  Article  Google Scholar 

  37. 37.

    Yuan Y, Ding J, Xu J, Deng J, Guo J: TiO2 nanoparticles co-doped with silver and nitrogen for antibacterial application. J Nanosci Nanotechnol 2010, 10: 4868–4874. 10.1166/jnn.2010.2225

    CAS  PubMed  Article  Google Scholar 

  38. 38.

    Montazer M, Seifollahzadeh S: Enhanced self-cleaning, antibacterial and UV protection properties of nano TiO2 treated textile through enzymatic pretreatment. Photochem Photobiol 2011, 87: 877–883. 10.1111/j.1751-1097.2011.00917.x

    CAS  PubMed  Article  Google Scholar 

  39. 39.

    Szacilowski K, Macyk W, Drzewiecka-Matuszek A, Brindell M, Stochel G: Bioinorganic photochemistry: frontiers and mechanisms. Chem Rev 2005, 105: 2647–2694. 10.1021/cr030707e

    CAS  PubMed  Article  Google Scholar 

  40. 40.

    Wiesenthal A, Hunter L, Wang S, Wickliffe J, Wilkerson M: Nanoparticles: small and mighty. Int J Dermatol 2011, 50: 247–254. 10.1111/j.1365-4632.2010.04815.x

    CAS  PubMed  Article  Google Scholar 

  41. 41.

    Montazer M, Behzadnia A, Pakdel E, Rahimi MK, Moghadam MB: Photo induced silver on nano titanium dioxide as an enhanced antimicrobial agent for wool. J Photochem Photobiol B 2011, 103: 207–214. 10.1016/j.jphotobiol.2011.03.009

    CAS  PubMed  Article  Google Scholar 

  42. 42.

    Schkroeder HA, Balassa JJ, Tipton IH: Abnormal trace metals in man: titanium. J Chronic Dis 1963, 16: 55–69. 10.1016/0021-9681(63)90019-5

    CAS  PubMed  Article  Google Scholar 

  43. 43.

    Dankovic D, Kuempel E, Wheeler M: An approach to risk assessment for TiO2. Inhal Toxicol 2007,19(Suppl 1):205–212.

    CAS  PubMed  Article  Google Scholar 

  44. 44.

    Weir A, Westerhoff P, Fabricius L, Hristovski K, von Goetz N: Titanium dioxide nanoparticles in food and personal care products. Environ Sci Technol 2012, 46: 2242–2250. 10.1021/es204168d

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  45. 45.

    Zhao J, Castranova V: Toxicology of nanomaterials used in nanomedicine. J Toxicol Environ Health B Crit Rev 2011, 14: 593–632. 10.1080/10937404.2011.615113

    CAS  PubMed  Article  Google Scholar 

  46. 46.

    Saber AT, Jacobsen NR, Mortensen A, Szarek J, Jackson P, Madsen AM, Jensen KA, Koponen IK, Brunborg G, Gutzkow KB: Nanotitanium dioxide toxicity in mouse lung is reduced in sanding dust from paint. Part Fibre Toxicol 2012, 9: 4. 10.1186/1743-8977-9-4

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  47. 47.

    FDA: Listing of color additives exempt from certification. In Code of Federal Regulations Title 21-Food and Drugs. 21 CFR 73.2575. Washington, DC: US Government Printing Office; 2002.

    Google Scholar 

  48. 48.

    ACGIH: Titanium dioxide. In Documentation of the threshold limit values for chemical substances. 7th edition. Cincinnati, OH: American Conference of Governmental Industrial Hygienists; 2001.

    Google Scholar 

  49. 49.

    Kitchin KT, Prasad RY, Wallace K: Oxidative stress studies of six TiO(2) and two CeO(2) nanomaterials: Immuno-spin trapping results with DNA. Nanotoxicology 2010, 5: 546–556.

    PubMed  Article  CAS  Google Scholar 

  50. 50.

    NIOSH: Occupational Exposure to Titanium Dioxide. In Current Intelligence Bulletin 63. Cincinnati: National Institute for Occupational Safety and Health; 2011.

    Google Scholar 

  51. 51.

    Morimoto Y, Kobayashi N, Shinohara N, Myojo T, Tanaka I, Nakanishi J: Hazard Assessments of Manufactured Nanomaterials. J Occup Health 2010, 52: 325–324. 10.1539/joh.R10003

    CAS  PubMed  Article  Google Scholar 

  52. 52.

    Curwin B, Bertke S: Exposure characterization of metal oxide nanoparticles in the workplace. J Occup Environ Hyg 2011, 8: 580–587. 10.1080/15459624.2011.613348

    CAS  PubMed  Article  Google Scholar 

  53. 53.

    Lee JH, Kwon M, Ji JH, Kang CS, Ahn KH, Han JH, Yu IJ: Exposure assessment of workplaces manufacturing nanosized TiO2 and silver. Inhal Toxicol 2011, 23: 226–236. 10.3109/08958378.2011.562567

    CAS  PubMed  Article  Google Scholar 

  54. 54.

    Methner MM: Effectiveness of a custom-fitted flange and local exhaust ventilation (LEV) system in controlling the release of nanoscale metal oxide particulates during reactor cleanout operations. Int J Occup Environ Health 2010, 16: 475–487. 10.1179/107735210799160039

    CAS  PubMed  Article  Google Scholar 

  55. 55.

    Hagens WI, Oomen AG, de Jong WH, Cassee FR, Sips AJ: What do we (need to) know about the kinetic properties of nanoparticles in the body? Regul Toxicol Pharmacol 2007, 49: 217–229. 10.1016/j.yrtph.2007.07.006

    CAS  PubMed  Article  Google Scholar 

  56. 56.

    Lomer MC, Thompson RP, Powell JJ: Fine and ultrafine particles of the diet: influence on the mucosal immune response and association with Crohn's disease. Proc Nutr Soc 2002, 61: 123–130. 10.1079/PNS2001134

    PubMed  Article  Google Scholar 

  57. 57.

    Hillyer JF, Albrecht RM: Gastrointestinal persorption and tissue distribution of differently sized colloidal gold nanoparticles. J Pharm Sci 2001, 90: 1927–1936. 10.1002/jps.1143

    CAS  PubMed  Article  Google Scholar 

  58. 58.

    Jania P, McCarthya D, Florence AT: Titanium dioxide (rutile) particle uptake from the rat GI tract and translocation to systemic organs after oral administration. Int J Pharm 1994, 105: 157–168. 10.1016/0378-5173(94)90461-8

    Article  Google Scholar 

  59. 59.

    Wang J, Zhou G, Chen C, Yu H, Wang T, Ma Y, Jia G, Gao Y, Li B, Sun J: Acute toxicity and biodistribution of different sized titanium dioxide particles in mice after oral administration. Toxicol Lett 2007, 168: 176–185. 10.1016/j.toxlet.2006.12.001

    CAS  PubMed  Article  Google Scholar 

  60. 60.

    Senzui M, Tamura T, Miura K, Ikarashi Y, Watanabe Y, Fujii M: Study on penetration of titanium dioxide (TiO(2)) nanoparticles into intact and damaged skin in vitro. J Toxicol Sci 2010, 35: 107–113. 10.2131/jts.35.107

    CAS  PubMed  Article  Google Scholar 

  61. 61.

    Schulz J, Hohenberg H, Pflucker F, Gartner E, Will T, Pfeiffer S, Wepf R, Wendel V, Gers-Barlag H, Wittern KP: Distribution of sunscreens on skin. Adv Drug Deliv Rev 2002,54(Suppl 1):S157–163.

    CAS  PubMed  Article  Google Scholar 

  62. 62.

    Pflucker F, Wendel V, Hohenberg H, Gartner E, Will T, Pfeiffer S, Wepf R, Gers-Barlag H: The human stratum corneum layer: an effective barrier against dermal uptake of different forms of topically applied micronised titanium dioxide. Skin Pharmacol Appl Skin Physiol 2001,14(Suppl 1):92–97.

    CAS  PubMed  Google Scholar 

  63. 63.

    Gamer AO, Leibold E, van Ravenzwaay B: The in vitro absorption of microfine zinc oxide and titanium dioxide through porcine skin. Toxicol In Vitro 2006, 20: 301–307. 10.1016/j.tiv.2005.08.008

    CAS  PubMed  Article  Google Scholar 

  64. 64.

    Sadrieh N, Wokovich AM, Gopee NV, Zheng J, Haines D, Parmiter D, Siitonen PH, Cozart CR, Patri AK, McNeil SE: Lack of significant dermal penetration of titanium dioxide from sunscreen formulations containing nano- and submicron-size TiO2 particles. Toxicol Sci 2010, 115: 156–166. 10.1093/toxsci/kfq041

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  65. 65.

    Newman MD, Stotland M, Ellis JI: The safety of nanosized particles in titanium dioxide- and zinc oxide-based sunscreens. J Am Acad Dermatol 2009, 61: 685–692. 10.1016/j.jaad.2009.02.051

    CAS  PubMed  Article  Google Scholar 

  66. 66.

    Lademann J, Weigmann H, Rickmeyer C, Barthelmes H, Schaefer H, Mueller G, Sterry W: Penetration of titanium dioxide microparticles in a sunscreen formulation into the horny layer and the follicular orifice. Skin Pharmacol Appl Skin Physiol 1999, 12: 247–256. 10.1159/000066249

    CAS  PubMed  Article  Google Scholar 

  67. 67.

    Escobar-Chavez JJ, Merino-Sanjuan V, Lopez-Cervantes M, Urban-Morlan Z, Pinon-Segundo E, Quintanar-Guerrero D, Ganem-Quintanar A: The tape-stripping technique as a method for drug quantification in skin. J Pharm Pharm Sci 2008, 11: 104–130.

    CAS  PubMed  Google Scholar 

  68. 68.

    Tan MH, Commens CA, Burnett L, Snitch PJ: A pilot study on the percutaneous absorption of microfine titanium dioxide from sunscreens. Australas J Dermatol 1996, 37: 185–187. 10.1111/j.1440-0960.1996.tb01050.x

    CAS  PubMed  Article  Google Scholar 

  69. 69.

    Bennat C, Muller-Goymann CC: Skin penetration and stabilization of formulations containing microfine titanium dioxide as physical UV filter. Int J Cosmet Sci 2000, 22: 271–283. 10.1046/j.1467-2494.2000.00009.x

    CAS  PubMed  Article  Google Scholar 

  70. 70.

    Sagawa Y, Futakuchi M, Xu J, Fukamachi K, Sakai Y, Ikarashi Y, Nishimura T, Suzui M, Tsuda H, Morita A: Lack of promoting effect of titanium dioxide particles on chemically-induced skin carcinogenesis in rats and mice. J Toxicol Sci 2012, 37: 317–327. 10.2131/jts.37.317

    CAS  PubMed  Article  Google Scholar 

  71. 71.

    Xu J, Sagawa Y, Futakuchi M, Fukamachi K, Alexander DB, Furukawa F, Ikarashi Y, Uchino T, Nishimura T, Morita A: Lack of promoting effect of titanium dioxide particles on ultraviolet B-initiated skin carcinogenesis in rats. Food Chem Toxicol 2011, 49: 1298–1302. 10.1016/j.fct.2011.03.011

    CAS  PubMed  Article  Google Scholar 

  72. 72.

    Monteiro-Riviere NA, Wiench K, Landsiedel R, Schulte S, Inman AO, Riviere JE: Safety evaluation of sunscreen formulations containing titanium dioxide and zinc oxide nanoparticles in UVB sunburned skin: an in vitro and in vivo study. Toxicol Sci 2011, 123: 264–280. 10.1093/toxsci/kfr148

    CAS  PubMed  Article  Google Scholar 

  73. 73.

    Miquel-Jeanjean C, Crepel F, Raufast V, Payre B, Datas L, Bessou-Touya S, Duplan H: Penetration Study of Formulated Nanosized Titanium Dioxide in Models of Damaged and Sun-Irradiated Skins. Photochem Photobiol 2012, 88: 1513–1521. 10.1111/j.1751-1097.2012.01181.x

    CAS  PubMed  Article  Google Scholar 

  74. 74.

    Filipe P, Silva JN, Silva R, Cirne de Castro JL, Marques Gomes M, Alves LC, Santus R, Pinheiro T: Stratum corneum is an effective barrier to TiO2 and ZnO nanoparticle percutaneous absorption. Skin Pharmacol Physiol 2009, 22: 266–275. 10.1159/000235554

    CAS  PubMed  Article  Google Scholar 

  75. 75.

    Simko M, Mattsson MO: Risks from accidental exposures to engineered nanoparticles and neurological health effects: a critical review. Part Fibre Toxicol 2010, 7: 42. 10.1186/1743-8977-7-42

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  76. 76.

    Kuempel ED, Tran CL, Castranova V, Bailer AJ: Lung dosimetry and risk assessment of nanoparticles: evaluating and extending current models in rats and humans. Inhal Toxicol 2006, 18: 717–724. 10.1080/08958370600747887

    CAS  PubMed  Article  Google Scholar 

  77. 77.

    Muhlfeld C, Geiser M, Kapp N, Gehr P, Rothen-Rutishauser B: Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature. Part Fibre Toxicol 2007, 4: 7. 10.1186/1743-8977-4-7

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  78. 78.

    Driscoll KE, Costa DL, Hatch G, Henderson R, Oberdorster G, Salem H, Schlesinger RB: Intratracheal instillation as an exposure technique for the evaluation of respiratory tract toxicity: uses and limitations. Toxicol Sci 2000, 55: 24–35. 10.1093/toxsci/55.1.24

    CAS  PubMed  Article  Google Scholar 

  79. 79.

    Li Y, Li J, Yin J, Li W, Kang C, Huang Q, Li Q: Systematic influence induced by 3 nm titanium dioxide following intratracheal instillation of mice. J Nanosci Nanotechnol 2010, 10: 8544–8549. 10.1166/jnn.2010.2690

    CAS  PubMed  Article  Google Scholar 

  80. 80.

    Wang J, Liu Y, Jiao F, Lao F, Li W, Gu Y, Li Y, Ge C, Zhou G, Li B: Time-dependent translocation and potential impairment on central nervous system by intranasally instilled TiO(2) nanoparticles. Toxicology 2008, 254: 82–90. 10.1016/j.tox.2008.09.014

    CAS  PubMed  Article  Google Scholar 

  81. 81.

    Wang J, Chen C, Liu Y, Jia F, Li W, Lao F, Lia Y, Lia B, Ge C, Zhou G: Potential neurological lesion after nasal instillation of TiO 2 nanoparticles in the anatase and rutile crystal phases. Toxicol Lett 2008, 183: 72–80. 10.1016/j.toxlet.2008.10.001

    CAS  PubMed  Article  Google Scholar 

  82. 82.

    Deng ZJ, Mortimer G, Schiller T, Musumeci A, Martin D, Minchin RF: Differential plasma protein binding to metal oxide nanoparticles. Nanotechnology 2009, 20: 455101. 10.1088/0957-4484/20/45/455101

    PubMed  Article  CAS  Google Scholar 

  83. 83.

    Cedervall T, Lynch I, Lindman S, Berggard T, Thulin E, Nilsson H, Dawson KA, Linse S: Understanding the nanoparticle-protein corona using methods to quantify exchange rates and affinities of proteins for nanoparticles. Proc Natl Acad Sci U S A 2007, 104: 2050–2055. 10.1073/pnas.0608582104

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  84. 84.

    Mikkelsen L, Sheykhzade M, Jensen KA, Saber AT, Jacobsen NR, Vogel U, Wallin H, Loft S, Moller P: Modest effect on plaque progression and vasodilatory function in atherosclerosis-prone mice exposed to nanosized TiO(2). Part Fibre Toxicol 2011, 8: 32. 10.1186/1743-8977-8-32

    PubMed Central  PubMed  Article  Google Scholar 

  85. 85.

    Rothen-Rutishauser BM, Schurch S, Haenni B, Kapp N, Gehr P: Interaction of fine particles and nanoparticles with red blood cells visualized with advanced microscopic techniques. Environ Sci Technol 2006, 40: 4353–4359. 10.1021/es0522635

    CAS  PubMed  Article  Google Scholar 

  86. 86.

    Geiser M: Update on macrophage clearance of inhaled micro- and nanoparticles. J Aerosol Med Pulm Drug Deliv 2010, 23: 207–217. 10.1089/jamp.2009.0797

    CAS  PubMed  Article  Google Scholar 

  87. 87.

    Wick P, Malek A, Manser P, Meili D, Maeder-Althaus X, Diener L, Diener PA, Zisch A, Krug HF, von Mandach U: Barrier capacity of human placenta for nanosized materials. Environ Health Perspect 2010, 118: 432–436. 10.1289/ehp.118-a432

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  88. 88.

    Shimizu M, Tainaka H, Oba T, Mizuo K, Umezawa M, Takeda K: Maternal exposure to nanoparticulate titanium dioxide during the prenatal period alters gene expression related to brain development in the mouse. Part Fibre Toxicol 2009, 6: 20. 10.1186/1743-8977-6-20

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  89. 89.

    Takeda K, Suzuki K, Ishihara A, Kubo-Irie M, Fujimoto R, Tabata M, Oshio S, Nihei Y, Ihara T, Sugamata M: Nanoparticles Transferred from Pregnant Mice to Their Offspring Can Damage the Genital and Cranial Nerve Systems. J Heal Sci 2009, 55: 95–102. 10.1248/jhs.55.95

    CAS  Article  Google Scholar 

  90. 90.

    Hougaard KS, Jackson P, Jensen KA, Sloth JJ, Loschner K, Larsen EH, Birkedal RK, Vibenholt A, Boisen AM, Wallin H, Vogel U: Effects of prenatal exposure to surface-coated nanosized titanium dioxide (UV-Titan). A study in mice. Part Fibre Toxicol 2010, 7: 16. 10.1186/1743-8977-7-16

    PubMed  Article  CAS  Google Scholar 

  91. 91.

    Geiser M, Kreyling WG: Deposition and biokinetics of inhaled nanoparticles. Part Fibre Toxicol 2010, 7: 2. 10.1186/1743-8977-7-2

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  92. 92.

    Eydner M, Schaudien D, Creutzenberg O, Ernst H, Hansen T, Baumgartner W, Rittinghausen S: Impacts after inhalation of nano- and fine-sized titanium dioxide particles: morphological changes, translocation within the rat lung, and evaluation of particle deposition using the relative deposition index. Inhal Toxicol 2012, 24: 557–569. 10.3109/08958378.2012.697494

    CAS  PubMed  Article  Google Scholar 

  93. 93.

    Scherbart AM, Langer J, Bushmelev A, van Berlo D, Haberzettl P, van Schooten FJ, Schmidt AM, Rose CR, Schins RP, Albrecht C: Contrasting macrophage activation by fine and ultrafine titanium dioxide particles is associated with different uptake mechanisms. Part Fibre Toxicol 2011, 8: 31. 10.1186/1743-8977-8-31

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  94. 94.

    Ferin J, Oberdorster G, Penney DP: Pulmonary retention of ultrafine and fine particles in rats. Am J Respir Cell Mol Biol 1992, 6: 535–542. 10.1165/ajrcmb/6.5.535

    CAS  PubMed  Article  Google Scholar 

  95. 95.

    Churg A, Stevens B, Wright JL: Comparison of the uptake of fine and ultrafine TiO2 in a tracheal explant system. Am J Physiol 1998, 274: L81–86.

    CAS  PubMed  Google Scholar 

  96. 96.

    Chen J, Dong X, Zhao J, Tang G: In vivo acute toxicity of titanium dioxide nanoparticles to mice after intraperitioneal injection. J Appl Toxicol 2009, 29: 330–337. 10.1002/jat.1414

    CAS  PubMed  Article  Google Scholar 

  97. 97.

    Liu H, Ma L, Zhao J, Liu J, Yan J, Ruan J, Hong F: Biochemical toxicity of nano-anatase TiO2 particles in mice. Biol Trace Elem Res 2009, 129: 170–180. 10.1007/s12011-008-8285-6

    CAS  PubMed  Article  Google Scholar 

  98. 98.

    Ma L, Liu J, Li N, Wang J, Duan Y, Yan J, Liu H, Wang H, Hong F: Oxidative stress in the brain of mice caused by translocated nanoparticulate TiO2 delivered to the abdominal cavity. Biomaterials 2010, 31: 99–105. 10.1016/j.biomaterials.2009.09.028

    CAS  PubMed  Article  Google Scholar 

  99. 99.

    World Health Organization (WHO): Environmental Health Criteria 24-Titanium. In International Programme on Chemical Safety. Geneva: World Health Organization; 1982.

    Google Scholar 

  100. 100.

    Huggins CB, Froehlich JP: High concentration of injected titanium dioxide in abdominal lymph nodes. J Exp Med 1966, 124: 1099–1106. 10.1084/jem.124.6.1099

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  101. 101.

    Geiser M, Casaulta M, Kupferschmid B, Schulz H, Semmler-Behnke M, Kreyling W: The role of macrophages in the clearance of inhaled ultrafine titanium dioxide particles. Am J Respir Cell Mol Biol 2008, 38: 371–376. 10.1165/rcmb.2007-0138OC

    CAS  PubMed  Article  Google Scholar 

  102. 102.

    Tang M, Zhang T, Xue Y, Wang S, Huang M, Yang Y, Lu M, Lei H, Kong L, Yuepu P: Dose dependent in vivo metabolic characteristics of titanium dioxide nanoparticles. J Nanosci Nanotechnol 2010, 10: 8575–8583. 10.1166/jnn.2010.2482

    CAS  PubMed  Article  Google Scholar 

  103. 103.

    Ma-Hock L, Burkhardt S, Strauss V, Gamer AO, Wiench K, van Ravenzwaay B, Landsiedel R: Development of a short-term inhalation test in the rat using nano-titanium dioxide as a model substance. Inhal Toxicol 2009, 21: 102–118. 10.1080/08958370802361057

    CAS  PubMed  Article  Google Scholar 

  104. 104.

    Grassian VH, O'Shaughnessy PT, Adamcakova-Dodd A, Pettibone JM, Thorne PS: Inhalation exposure study of titanium dioxide nanoparticles with a primary particle size of 2 to 5 nm. Environ Health Perspect 2007, 115: 397–402. 10.1289/ehp.10302R

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  105. 105.

    Nurkiewicz TR, Porter DW, Hubbs AF, Cumpston JL, Chen BT, Frazer DG, Castranova V: Nanoparticle inhalation augments particle-dependent systemic microvascular dysfunction. Part Fibre Toxicol 2008, 5: 1. 10.1186/1743-8977-5-1

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  106. 106.

    Nurkiewicz TR, Porter DW, Hubbs AF, Stone S, Moseley AM, Cumpston JL, Goodwill AG, Frisbee SJ, Perrotta PL, Brock RW: Pulmonary particulate matter and systemic microvascular dysfunction. Res Rep Health Eff Inst 2011, 3–48.

    Google Scholar 

  107. 107.

    LeBlanc AJ, Cumpston JL, Chen BT, Frazer D, Castranova V, Nurkiewicz TR: Nanoparticle inhalation impairs endothelium-dependent vasodilation in subepicardial arterioles. J Toxicol Environ Health A 2009, 72: 1576–1584. 10.1080/15287390903232467

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  108. 108.

    Sun Q, Hong X, Wold LE: Cardiovascular effects of ambient particulate air pollution exposure. Circulation 2010, 121: 2755–2765. 10.1161/CIRCULATIONAHA.109.893461

    PubMed Central  PubMed  Article  Google Scholar 

  109. 109.

    Liu R, Yin L, Pu Y, Liang G, Zhang J, Su Y, Xiao Z, Ye B: Pulmonary toxicity induced by three forms of titanium dioxide nanoparticles via intra-tracheal instillation in rats. Prog Nat Sci 2009, 19: 573–579. 10.1016/j.pnsc.2008.06.020

    CAS  Article  Google Scholar 

  110. 110.

    Kobayashi N, Naya M, Endoh S, Maru J, Yamamoto K, Nakanishi J: Comparative pulmonary toxicity study of nano-TiO(2) particles of different sizes and agglomerations in rats: different short- and long-term post-instillation results. Toxicology 2009, 264: 110–118. 10.1016/j.tox.2009.08.002

    CAS  PubMed  Article  Google Scholar 

  111. 111.

    Liu R, Zhang X, Pu Y, Yin L, Li Y, Liang G, Li X, Zhang J: Small-sized titanium dioxide nanoparticles mediate immune toxicity in rat pulmonary alveolar macrophages in vivo. J Nanosci Nanotechnol 2010, 10: 5161–5169. 10.1166/jnn.2010.2420

    CAS  PubMed  Article  Google Scholar 

  112. 112.

    Liu R, Yin LH, Pu YP, Li YH, Zhang XQ, Liang GY, Li XB, Zhang J, Li YF, Zhang XY: The immune toxicity of titanium dioxide on primary pulmonary alveolar macrophages relies on their surface area and crystal structure. J Nanosci Nanotechnol 2010, 10: 8491–8499. 10.1166/jnn.2010.2685

    CAS  PubMed  Article  Google Scholar 

  113. 113.

    Hussain S, Vanoirbeek JA, Luyts K, De Vooght V, Verbeken E, Thomassen LC, Martens JA, Dinsdale D, Boland S, Marano F: Lung exposure to nanoparticles modulates an asthmatic response in a mouse model. Eur Respir J 2011, 37: 299–309. 10.1183/09031936.00168509

    CAS  PubMed  Article  Google Scholar 

  114. 114.

    Warheit DB, Hoke RA, Finlay C, Donner EM, Reed KL, Sayes CM: Development of a base set of toxicity tests using ultrafine TiO2 particles as a component of nanoparticle risk management. Toxicol Lett 2007, 171: 99–110. 10.1016/j.toxlet.2007.04.008

    CAS  PubMed  Article  Google Scholar 

  115. 115.

    Liu Q, Hong Z, Guo B, Zhang Y, Li Y, Liu J: Experimental Study on Toxicity of Nanosized Titanium Dioxide. Mod Preventive Med 2006, 33: 1211–1212.

    CAS  Google Scholar 

  116. 116.

    Unnithan J, Rehman MU, Ahmad FJ, Samim M: Aqueous synthesis and concentration-dependent dermal toxicity of TiO2 nanoparticles in Wistar rats. Biol Trace Elem Res 2011, 143: 1682–1694. 10.1007/s12011-011-9010-4

    CAS  PubMed  Article  Google Scholar 

  117. 117.

    Ma L, Zhao J, Wang J, Liu J, Duan Y, Liu H, Li N, Yan J, Ruan J, Wang H, Hong F: The Acute Liver Injury in Mice Caused by Nano-Anatase TiO2. Nanoscale Res Lett 2009, 4: 1275–1285. 10.1007/s11671-009-9393-8

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  118. 118.

    Chen EY, Garnica M, Wang YC, Mintz AJ, Chen CS, Chin WC: A mixture of anatase and rutile TiO(2) nanoparticles induces histamine secretion in mast cells. Part Fibre Toxicol 2012, 9: 2. 10.1186/1743-8977-9-2

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  119. 119.

    Li SQ, Zhu RR, Zhu H, Xue M, Sun XY, Yao SD, Wang SL: Nanotoxicity of TiO(2) nanoparticles to erythrocyte in vitro. Food Chem Toxicol 2008, 46: 3626–3631. 10.1016/j.fct.2008.09.012

    CAS  PubMed  Article  Google Scholar 

  120. 120.

    Aisaka Y, Kawaguchi R, Watanabe S, Ikeda M, Igisu H: Hemolysis caused by titanium dioxide particles. Inhal Toxicol 2008, 20: 891–893. 10.1080/08958370802304123

    CAS  PubMed  Article  Google Scholar 

  121. 121.

    Zhang J, Song W, Guo J, Sun Z, Li L, Ding F, Gao M: Cytotoxicity of different sized TiO2 nanoparticles in mouse macrophages. Toxicol Ind Health 2012.

    Google Scholar 

  122. 122.

    Qi K, Deng FR, Guo XB: [Effects of nanoscale titanium dioxide on intercellular gap junction communication in human lung fibroblasts]. Beijing Da Xue Xue Bao 2009, 41: 297–301.

    CAS  PubMed  Google Scholar 

  123. 123.

    Rossi EMPL, Koivisto AJ, Vippopa M, Jensen KA, Miettinen M, Sirola K, Nykasenoja H, Karisola P, Stjernvall T, Vanhala E, Kiilunen M, Pasanen P, Makinen M, Hameri K, Joutsensaari J, Tuomi T, Jokiniemi J, Wolff H, Savolainen K, Matikainen S, Alenius H: Airway Exposure to Silica-Coated TiO2 Nanoparticles Induces Pulmonary Neutrophilia in Mice. Toxicol Sci 2010, 113: 422–433. 10.1093/toxsci/kfp254

    CAS  PubMed  Article  Google Scholar 

  124. 124.

    Zhang Y, Tao J, He P, Tang Y, Wang Y: Bio-effects of nano-TiO2 on lungs of mice. Sheng Wu Yi Xue Gong Cheng Xue Za Zhi 2009, 26: 803–806.

    CAS  PubMed  Google Scholar 

  125. 125.

    Oberdorster G, Finkelstein JN, Johnston C, Gelein R, Cox C, Baggs R, Elder AC: Acute pulmonary effects of ultrafine particles in rats and mice. Res Rep Health Eff Inst 2000, 95: 5–74.

    Google Scholar 

  126. 126.

    Hu JQ, Chen CY, Bai R, Zhen S, Du XM, Zang JJ, Li JC, Gu YQ, Jia G: [Effect of nano-TiO(2) intratracheal instillation on lipid metabolism of AopE gene-knockout mice]. Zhonghua Yu Fang Yi Xue Za Zhi 2010, 44: 780–784.

    CAS  PubMed  Google Scholar 

  127. 127.

    Larsen ST, Roursgaard M, Jensen KA, Nielsen GD: Nano titanium dioxide particles promote allergic sensitization and lung inflammation in mice. Basic Clin Pharmacol Toxicol 2010, 106: 114–117. 10.1111/j.1742-7843.2009.00473.x

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  128. 128.

    Bu Q, Yan G, Deng P, Peng F, Lin H, Xu Y, Cao Z, Zhou T, Xue A, Wang Y: NMR-based metabonomic study of the sub-acute toxicity of titanium dioxide nanoparticles in rats after oral administration. Nanotechnology 2010, 21: 125105. 10.1088/0957-4484/21/12/125105

    PubMed  Article  CAS  Google Scholar 

  129. 129.

    Bermudez E, Mangum JB, Wong BA, Asgharian B, Hext PM, Warheit DB, Everitt JI: Pulmonary responses of mice, rats, and hamsters to subchronic inhalation of ultrafine titanium dioxide particles. Toxicol Sci 2004, 77: 347–357. 10.1093/toxsci/kfh019

    CAS  PubMed  Article  Google Scholar 

  130. 130.

    Warheit DB, Webb TR, Sayes CM, Colvin VL, Reed KL: Pulmonary instillation studies with nanoscale TiO2 rods and dots in rats: toxicity is not dependent upon particle size and surface area. Toxicol Sci 2006, 91: 227–236. 10.1093/toxsci/kfj140

    CAS  PubMed  Article  Google Scholar 

  131. 131.

    Roursgaard M, Jensen KA, Poulsen SS, Jensen NE, Poulsen LK, Hammer M, Nielsen GD, Larsen ST: Acute and subchronic airway inflammation after intratracheal instillation of quartz and titanium dioxide agglomerates in mice. Sci World J 2011, 11: 801–825.

    CAS  Article  Google Scholar 

  132. 132.

    Wang JX, Li YF, Zhou GQ, Li B, Jiao F, Chen CY, Gao YX, Zhao YL, Chai ZF: [Influence of intranasal instilled titanium dioxide nanoparticles on monoaminergic neurotransmitters of female mice at different exposure time]. Zhonghua Yu Fang Yi Xue Za Zhi 2007, 41: 91–95.

    CAS  PubMed  Google Scholar 

  133. 133.

    Wu J, Liu W, Xue C, Zhou S, Lan F, Bi L, Xu H, Yang X, Zeng FD: Toxicity and penetration of TiO2 nanoparticles in hairless mice and porcine skin after subchronic dermal exposure. Toxicol Lett 2009, 191: 1–8. 10.1016/j.toxlet.2009.05.020

    CAS  PubMed  Article  Google Scholar 

  134. 134.

    Hu R, Gong X, Duan Y, Li N, Che Y, Cui Y, Zhou M, Liu C, Wang H, Hong F: Neurotoxicological effects and the impairment of spatial recognition memory in mice caused by exposure to TiO2 nanoparticles. Biomaterials 2010, 31: 8043–8050. 10.1016/j.biomaterials.2010.07.011

    CAS  PubMed  Article  Google Scholar 

  135. 135.

    Baskerville A, Fitzgeorge RB, Gilmour MI, Dowsett AB, Williams A, Featherstone AS: Effects of inhaled titanium dioxide dust on the lung and on the course of experimental Legionnaires' disease. Br J Exp Pathol 1988, 69: 781–792.

    PubMed Central  CAS  PubMed  Google Scholar 

  136. 136.

    Warheit DB, Yuen IS, Kelly DP, Snajdr S, Hartsky MA: Subchronic inhalation of high concentrations of low toxicity, low solubility particulates produces sustained pulmonary inflammation and cellular proliferation. Toxicol Lett 1996, 88: 249–253. 10.1016/0378-4274(96)82678-6

    CAS  PubMed  Article  Google Scholar 

  137. 137.

    Warheit DB, Hansen JF, Yuen IS, Kelly DP, Snajdr SI, Hartsky MA: Inhalation of high concentrations of low toxicity dusts in rats results in impaired pulmonary clearance mechanisms and persistent inflammation. Toxicol Appl Pharmacol 1997, 145: 10–22. 10.1006/taap.1997.8102

    CAS  PubMed  Article  Google Scholar 

  138. 138.

    Bermudez E, Mangum JB, Asgharian B, Wong BA, Reverdy EE, Janszen DB, Hext PM, Warheit DB, Everitt JI: Long-term pulmonary responses of three laboratory rodent species to subchronic inhalation of pigmentary titanium dioxide particles. Toxicol Sci 2002, 70: 86–97. 10.1093/toxsci/70.1.86

    CAS  PubMed  Article  Google Scholar 

  139. 139.

    Sang X, Zheng L, Sun Q, Li N, Cui Y, Hu R, Gao G, Cheng Z, Cheng J, Gui S: The chronic spleen injury of mice following long-term exposure to titanium dioxide nanoparticles. J Biomed Mater Res A 2012, 100: 894–902.

    PubMed  Article  CAS  Google Scholar 

  140. 140.

    Lu PJ, Ho IC, Lee TC: Induction of sister chromatid exchanges and micronuclei by titanium dioxide in Chinese hamster ovary-K1 cells. Mutat Res 1998, 414: 15–20. 10.1016/S1383-5718(98)00034-5

    CAS  PubMed  Article  Google Scholar 

  141. 141.

    IARC: Titanium dioxide. In IARC monographs on the evaluation of carcinogenic risks to humans, volume 47. Lyon; 1989:307–328.

    Google Scholar 

  142. 142.

    Yazdi AS, Guarda G, Riteau N, Drexler SK, Tardivel A, Couillin I, Tschopp J: Nanoparticles activate the NLR pyrin domain containing 3 (Nlrp3) inflammasome and cause pulmonary inflammation through release of IL-1alpha and IL-1beta. Proc Natl Acad Sci U S A 2010, 107: 19449–19454. 10.1073/pnas.1008155107

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  143. 143.

    Kan H, Wu Z, Young SH, Chen TH, Cumpston JL, Chen F, Kashon ML, Castranova V: Pulmonary exposure of rats to ultrafine titanium dioxide enhances cardiac protein phosphorylation and substance P synthesis in nodose ganglia. Nanotoxicology 2011, 6: 736–745.

    PubMed  Article  CAS  Google Scholar 

  144. 144.

    Driscoll KE, Deyo LC, Carter JM, Howard BW, Hassenbein DG, Bertram TA: Effects of particle exposure and particle-elicited inflammatory cells on mutation in rat alveolar epithelial cells. Carcinogenesis 1997, 18: 423–430. 10.1093/carcin/18.2.423

    CAS  PubMed  Article  Google Scholar 

  145. 145.

    Cui Y, Liu H, Zhou M, Duan Y, Li N, Gong X, Hu R, Hong M, Hong F: Signaling pathway of inflammatory responses in the mouse liver caused by TiO2 nanoparticles. J Biomed Mater Res A 2011, 96: 221–229.

    PubMed  Article  CAS  Google Scholar 

  146. 146.

    Gui S, Zhang Z, Zheng L, Cui Y, Liu X, Li N, Sang X, Sun Q, Gao G, Cheng Z: Molecular mechanism of kidney injury of mice caused by exposure to titanium dioxide nanoparticles. J Hazard Mater 2011, 195: 365–370.

    CAS  PubMed  Article  Google Scholar 

  147. 147.

    Sun Q, Tan D, Ze Y, Sang X, Liu X, Gui S, Cheng Z, Cheng J, Hu R, Gao G: Pulmotoxicological effects caused by long-term titanium dioxide nanoparticles exposure in mice. J Hazard Mater 2012, 235–236: 47–53.

    PubMed  Article  CAS  Google Scholar 

  148. 148.

    Li N, Duan Y, Hong M, Zheng L, Fei M, Zhao X, Wang J, Cui Y, Liu H, Cai J: Spleen injury and apoptotic pathway in mice caused by titanium dioxide nanoparticules. Toxicol Lett 2010, 195: 161–168. 10.1016/j.toxlet.2010.03.1116

    CAS  PubMed  Article  Google Scholar 

  149. 149.

    Jackson P, Halappanavar S, Hougaard KS, Williams A, Madsen AM, Lamson JS, Andersen O, Yauk C, Wallin H, Vogel U: Maternal inhalation of surface-coated nanosized titanium dioxide (UV-Titan) in C57BL/6 mice: effects in prenatally exposed offspring on hepatic DNA damage and gene expression. Nanotoxicology 2011, 7: 85–96.

    PubMed  Article  CAS  Google Scholar 

  150. 150.

    Halappanavar S, Jackson P, Williams A, Jensen KA, Hougaard KS, Vogel U, Yauk CL, Wallin H: Pulmonary response to surface-coated nanotitanium dioxide particles includes induction of acute phase response genes, inflammatory cascades, and changes in microRNAs: a toxicogenomic study. Environ Mol Mutagen 2011, 52: 425–439. 10.1002/em.20639

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  151. 151.

    Boisen AM, Shipley T, Jackson P, Hougaard KS, Wallin H, Yauk CL, Vogel U: NanoTIO2 (UV-Titan) does not induce ESTR mutations in the germline of prenatally exposed female mice. Part Fibre Toxicol 2012, 9: 19. 10.1186/1743-8977-9-19

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  152. 152.

    Lindberg HK, Falck GC, Catalan J, Koivisto AJ, Suhonen S, Jarventaus H, Rossi EM, Nykasenoja H, Peltonen Y, Moreno C: Genotoxicity of inhaled nanosized TiO(2) in mice. Mutat Res 2012, 745: 58–64. 10.1016/j.mrgentox.2011.10.011

    CAS  PubMed  Article  Google Scholar 

  153. 153.

    Gallagher J, Heinrich U, George M, Hendee L, Phillips DH, Lewtas J: Formation of DNA adducts in rat lung following chronic inhalation of diesel emissions, carbon black and titanium dioxide particles. Carcinogenesis 1994, 15: 1291–1299. 10.1093/carcin/15.7.1291

    CAS  PubMed  Article  Google Scholar 

  154. 154.

    Zucker RM, Massaro EJ, Sanders KM, Degn LL, Boyes WK: Detection of TiO2 nanoparticles in cells by flow cytometry. Cytometry A 2010, 77: 677–685.

    CAS  PubMed  Article  Google Scholar 

  155. 155.

    Jugan ML, Barillet S, Simon-Deckers A, Herlin-Boime N, Sauvaigo S, Douki T, Carriere M: Titanium dioxide nanoparticles exhibit genotoxicity and impair DNA repair activity in A549 cells. Nanotoxicology 2012, 6: 501–513. 10.3109/17435390.2011.587903

    CAS  PubMed  Article  Google Scholar 

  156. 156.

    Saquib Q, Al-Khedhairy AA, Siddiqui MA, Abou-Tarboush FM, Azam A, Musarrat J: Titanium dioxide nanoparticles induced cytotoxicity, oxidative stress and DNA damage in human amnion epithelial (WISH) cells. Toxicol In Vitro 2012, 26: 351–361. 10.1016/j.tiv.2011.12.011

    CAS  PubMed  Article  Google Scholar 

  157. 157.

    Bhattacharya K, Davoren M, Boertz J, Schins RP, Hoffmann E, Dopp E: Titanium dioxide nanoparticles induce oxidative stress and DNA-adduct formation but not DNA-breakage in human lung cells. Part Fibre Toxicol 2009, 6: 17. 10.1186/1743-8977-6-17

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  158. 158.

    Bhattacharya K, Cramer H, Albrecht C, Schins R, Rahman Q, Zimmermann U, Dopp E: Vanadium pentoxide-coated ultrafine titanium dioxide particles induce cellular damage and micronucleus formation in V79 cells. J Toxicol Environ Health A 2008, 71: 976–980. 10.1080/15287390801989218

    CAS  PubMed  Article  Google Scholar 

  159. 159.

    Morishige T, Yoshioka Y, Tanabe A, Yao X, Tsunoda S, Tsutsumi Y, Mukai Y, Okada N, Nakagawa S: Titanium dioxide induces different levels of IL-1beta production dependent on its particle characteristics through caspase-1 activation mediated by reactive oxygen species and cathepsin B. Biochem Biophys Res Commun 2010, 392: 160–165. 10.1016/j.bbrc.2009.12.178

    CAS  PubMed  Article  Google Scholar 

  160. 160.

    Vamanu CI, Cimpan MR, Hol PJ, Sornes S, Lie SA, Gjerdet NR: Induction of cell death by TiO2 nanoparticles: studies on a human monoblastoid cell line. Toxicol In Vitro 2008, 22: 1689–1696. 10.1016/j.tiv.2008.07.002

    CAS  PubMed  Article  Google Scholar 

  161. 161.

    Wilhelmi V, Fischer U, van Berlo D, Schulze-Osthoff K, Schins RP, Albrecht C: Evaluation of apoptosis induced by nanoparticles and fine particles in RAW 264.7 macrophages: facts and artefacts. Toxicol In Vitro 2012, 26: 323–334. 10.1016/j.tiv.2011.12.006

    CAS  PubMed  Article  Google Scholar 

  162. 162.

    Kang SJ, Kim BM, Lee YJ, Hong SH, Chung HW: Titanium dioxide nanoparticles induce apoptosis through the JNK/p38-caspase-8-Bid pathway in phytohemagglutinin-stimulated human lymphocytes. Biochem Biophys Res Commun 2009, 386: 682–687. 10.1016/j.bbrc.2009.06.097

    CAS  PubMed  Article  Google Scholar 

  163. 163.

    Shi Y, Wang F, He J, Yadav S, Wang H: Titanium dioxide nanoparticles cause apoptosis in BEAS-2B cells through the caspase 8/t-Bid-independent mitochondrial pathway. Toxicol Lett 2010, 196: 21–27. 10.1016/j.toxlet.2010.03.014

    CAS  PubMed  Article  Google Scholar 

  164. 164.

    Kang SJ, Kim BM, Lee YJ, Chung HW: Titanium dioxide nanoparticles trigger p53-mediated damage response in peripheral blood lymphocytes. Environ Mol Mutagen 2008, 49: 399–405. 10.1002/em.20399

    CAS  PubMed  Article  Google Scholar 

  165. 165.

    Xue C, Liu W, Wu J, Yang X, Xu H: Chemoprotective effect of N-acetylcysteine (NAC) on cellular oxidative damages and apoptosis induced by nano titanium dioxide under UVA irradiation. Toxicol In Vitro 2011, 25: 110–116. 10.1016/j.tiv.2010.09.014

    CAS  PubMed  Article  Google Scholar 

  166. 166.

    Ghosh M, Bandyopadhyay M, Mukherjee A: Genotoxicity of titanium dioxide (TiO2) nanoparticles at two trophic levels: plant and human lymphocytes. Chemosphere 2010, 81: 1253–1262. 10.1016/j.chemosphere.2010.09.022

    CAS  PubMed  Article  Google Scholar 

  167. 167.

    Falck GC, Lindberg HK, Suhonen S, Vippola M, Vanhala E, Catalan J, Savolainen K, Norppa H: Genotoxic effects of nanosized and fine TiO2. Hum Exp Toxicol 2009, 28: 339–352. 10.1177/0960327109105163

    CAS  PubMed  Article  Google Scholar 

  168. 168.

    Mano SSKK, Sonezaki S, Taniguchi A: Effect of Polyethylene Glycol Modification of TiO2 Nanoparticles on Cytotoxicity and Gene Expressions in Human Cell Lines. Int J Mol Sci 2012, 13: 3703–3717. 10.3390/ijms13033703

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  169. 169.

    Gerloff K, Fenoglio I, Carella E, Kolling J, Albrecht C, Boots AW, Forster I, Schins RP: Distinctive toxicity of TiO2 rutile/anatase mixed phase nanoparticles on Caco-2 cells. Chem Res Toxicol 2012, 25: 646–655. 10.1021/tx200334k

    CAS  PubMed  Article  Google Scholar 

  170. 170.

    Gurr JR, Wang AS, Chen CH, Jan KY: Ultrafine titanium dioxide particles in the absence of photoactivation can induce oxidative damage to human bronchial epithelial cells. Toxicology 2005, 213: 66–73. 10.1016/j.tox.2005.05.007

    CAS  PubMed  Article  Google Scholar 

  171. 171.

    Huang S, Chueh PJ, Lin YW, Shih TS, Chuang SM: Disturbed mitotic progression and genome segregation are involved in cell transformation mediated by nano-TiO2 long-term exposure. Toxicol Appl Pharmacol 2009, 241: 182–194. 10.1016/j.taap.2009.08.013

    CAS  PubMed  Article  Google Scholar 

  172. 172.

    Rahman Q, Lohani M, Dopp E, Pemsel H, Jonas L, Weiss DG, Schiffmann D: Evidence that ultrafine titanium dioxide induces micronuclei and apoptosis in Syrian hamster embryo fibroblasts. Environ Health Perspect 2002, 110: 797–800.

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  173. 173.

    Guichard Y, Schmit J, Darne C, Gate L, Goutet M, Rousset D, Rastoix O, Wrobel R, Witschger O, Martin A: Cytotoxicity and genotoxicity of nanosized and microsized titanium dioxide and iron oxide particles in Syrian hamster embryo cells. Ann Occup Hyg 2012, 56: 631–644.

    CAS  PubMed  Google Scholar 

  174. 174.

    Di Virgilio AL, Reigosa M, Arnal PM, Fernandez Lorenzo De Mele M: Comparative study of the cytotoxic and genotoxic effects of titanium oxide and aluminium oxide nanoparticles in Chinese hamster ovary (CHO-K1) cells. J Hazard Mater 2010, 177: 711–718. 10.1016/j.jhazmat.2009.12.089

    CAS  PubMed  Article  Google Scholar 

  175. 175.

    Wang S, Hunter LA, Arslan Z, Wilkerson MG, Wickliffe JK: Chronic exposure to nanosized, anatase titanium dioxide is not cyto- or genotoxic to Chinese hamster ovary cells. Environ Mol Mutagen 2011, 52: 614–622. 10.1002/em.20660

    CAS  PubMed  Article  Google Scholar 

  176. 176.

    Setyawati MI, Khoo PK, Eng BH, Xiong S, Zhao X, Das GK, Tan TT, Loo JS, Leong DT, Ng KW: Cytotoxic and genotoxic characterization of titanium dioxide, gadolinium oxide, and poly(lactic-co-glycolic acid) nanoparticles in human fibroblasts. J Biomed Mater Res A 2012, 101: 633–640.

    PubMed  Google Scholar 

  177. 177.

    Prasad RY, Chastain PD, Nikolaishvili-Feinberg N, Smeester L, Kaufmann WK, Fry RC: Titanium dioxide nanoparticles activate the ATM-Chk2 DNA damage response in human dermal fibroblasts. Nanotoxicology 2012. 10.3109/17435390.2012.710659

    Google Scholar 

  178. 178.

    Li N, Ma L, Wang J, Zheng L, Liu J, Duan Y, Liu H, Zhao X, Wang S, Wang H: Interaction Between Nano-Anatase TiO(2) and Liver DNA from Mice In Vivo. Nanoscale Res Lett 2009, 5: 108–115.

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  179. 179.

    Wan R, Mo Y, Feng L, Chien S, Tollerud DJ, Zhang Q: DNA damage caused by metal nanoparticles: involvement of oxidative stress and activation of ATM. Chem Res Toxicol 2012, 25: 1402–1411. 10.1021/tx200513t

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  180. 180.

    Aueviriyavit S, Phummiratch D, Kulthong K, Maniratanachote R: Titanium dioxide nanoparticles-mediated in vitro cytotoxicity does not induce hsp70 and grp78 expression in human bronchial epithelial a549 cells. Biol Trace Elem Res 2012, 149: 123–132. 10.1007/s12011-012-9403-z

    CAS  PubMed  Article  Google Scholar 

  181. 181.

    Woodruff RS, Li Y, Yan J, Bishop M, Jones MY, Watanabe F, Biris AS, Rice P, Zhou T, Chen T: Genotoxicity evaluation of titanium dioxide nanoparticles using the Ames test and Comet assay. J Appl Toxicol 2012, 32: 934–943. 10.1002/jat.2781

    CAS  PubMed  Article  Google Scholar 

  182. 182.

    Linnainmaa K, Kivipensas P, Vainio H: Toxicity and cytogenetic studies of ultrafine titanium dioxide in cultured rat liver epithelial cells. Toxicol In Vitro 1997, 11: 329–335. 10.1016/S0887-2333(97)00000-3

    CAS  PubMed  Article  Google Scholar 

  183. 183.

    Fisichella M, Berenguer F, Steinmetz G, Auffan M, Rose J, Prat O: Intestinal toxicity evaluation of TiO2 degraded surface-treated nanoparticles: a combined physico-chemical and toxicogenomics approach in caco-2 cells. Part Fibre Toxicol 2012, 9: 18. 10.1186/1743-8977-9-18

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  184. 184.

    Wilson D, Zaqout M, Heo JH, Park EK, Oak CH, Ueno S: Nuclear factor-kappa B is not involved in titanium dioxide-induced inflammation. J UOEH 2012, 34: 183–191.

    CAS  PubMed  Article  Google Scholar 

  185. 185.

    Yu M, Mo Y, Wan R, Chien S, Zhang X, Zhang Q: Regulation of plasminogen activator inhibitor-1 expression in endothelial cells with exposure to metal nanoparticles. Toxicol Lett 2010, 195: 82–89. 10.1016/j.toxlet.2010.02.010

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  186. 186.

    Wan R, Mo Y, Zhang X, Chien S, Tollerud DJ, Zhang Q: Matrix metalloproteinase-2 and −9 are induced differently by metal nanoparticles in human monocytes: The role of oxidative stress and protein tyrosine kinase activation. Toxicol Appl Pharmacol 2008, 233: 276–285. 10.1016/j.taap.2008.08.022

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  187. 187.

    Wang J, Zhu X, Zhang X, Zhao Z, Liu H, George R, Wilson-Rawls J, Chang Y, Chen Y: Disruption of zebrafish (Danio rerio) reproduction upon chronic exposure to TiO nanoparticles. Chemosphere 2011, 83: 461–467. 10.1016/j.chemosphere.2010.12.069

    CAS  PubMed  Article  Google Scholar 

  188. 188.

    Zhu X, Zhu L, Duan Z, Qi R, Li Y, Lang Y: Comparative toxicity of several metal oxide nanoparticle aqueous suspensions to Zebrafish (Danio rerio) early developmental stage. J Environ Sci Health, Part A: Tox Hazard Subst Environ Eng 2008, 43: 278–284. 10.1080/10934520701792779

    CAS  Article  Google Scholar 

  189. 189.

    Takeda K, Suzuki K, Ishihara A, Kubo-Irie M, Fujimoto R, Tabota M, Oshio S, Nihei Y, Ihara T, Sugamata M: Nanoparticles Transferred from Pregnent Mice to Their Offspring can Damage the Genital and Cranial Nerve Systems. J Health Sci 2009, 55: 95–102. 10.1248/jhs.55.95

    CAS  Article  Google Scholar 

  190. 190.

    Yamashita K, Yoshioka Y, Higashisaka K, Mimura K, Morishita Y, Nozaki M, Yoshida T, Ogura T, Nabeshi H, Nagano K: Silica and titanium dioxide nanoparticles cause pregnancy complications in mice. Nat Nanotechnol 2011, 6: 321–328. 10.1038/nnano.2011.41

    CAS  PubMed  Article  Google Scholar 

  191. 191.

    Komatsu T, Tabata M, Kubo-Irie M, Shimizu T, Suzuki K, Nihei Y, Takeda K: The effects of nanoparticles on mouse testis Leydig cells in vitro. Toxicol In Vitro 2008, 22: 1825–1831. 10.1016/j.tiv.2008.08.009

    CAS  PubMed  Article  Google Scholar 

  192. 192.

    Borm PJ, Schins RP, Albrecht C: Inhaled particles and lung cancer, part B: paradigms and risk assessment. Int J Cancer 2004, 110: 3–14. 10.1002/ijc.20064

    CAS  PubMed  Article  Google Scholar 

  193. 193.

    Trochimowicz HJ, Lee KP, Reinhardt CF: Chronic inhalation exposure of rats to titanium dioxide dust. J Appl Toxicol 1988, 8: 383–385.

    CAS  PubMed  Google Scholar 

  194. 194.

    Heinrich UF R, Rittinghausen S, Creutzenberg O, Bellmann B, Koch W, Levsen K: Chronic inhalation exposure of Wistar rats and two different strains of mice to diesel engine exhaust, carbon black, and titanium dioxide. Inhal Toxicol 1995, 7: 533–556. 10.3109/08958379509015211

    Article  Google Scholar 

  195. 195.

    Pott F, Roller M: Carcinogenicity study with nineteen granular dusts in rats. Eur J Oncol 2005, 10: 249.

    Google Scholar 

  196. 196.

    Rittinghausen S, Mohr U, Dungworth DL: Pulmonary cystic keratinizing squamous cell lesions of rats after inhalation/instillation of different particles. Exp Toxicol Pathol 1997, 49: 433–446. 10.1016/S0940-2993(97)80131-5

    CAS  PubMed  Article  Google Scholar 

  197. 197.

    Bernard BK, Osheroff MR, Hofmann A, Mennear JH: Toxicology and carcinogenesis studies of dietary titanium dioxide-coated mica in male and female Fischer 344 rats. J Toxicol Environ Health 1990, 29: 417–429. 10.1080/15287399009531402

    CAS  PubMed  Article  Google Scholar 

  198. 198.

    Boffetta P, Gaborieau V, Nadon L, Parent MF, Weiderpass E, Siemiatycki J: Exposure to titanium dioxide and risk of lung cancer in a population-based study from Montreal. Scand J Work Environ Health 2001, 27: 227–232. 10.5271/sjweh.609

    CAS  PubMed  Article  Google Scholar 

  199. 199.

    Fryzek JP, Chadda B, Marano D, White K, Schweitzer S, McLaughlin JK, Blot WJ: A cohort mortality study among titanium dioxide manufacturing workers in the United States. J Occup Environ Med 2003, 45: 400–409. 10.1097/01.jom.0000058338.05741.45

    CAS  PubMed  Article  Google Scholar 

  200. 200.

    Boffetta P, Soutar A, Cherrie JW, Granath F, Andersen A, Anttila A, Blettner M, Gaborieau V, Klug SJ, Langard S: Mortality among workers employed in the titanium dioxide production industry in Europe. Cancer Causes Control 2004, 15: 697–706.

    PubMed  Article  Google Scholar 

  201. 201.

    Suttiponparnit KJJ, Sahu M, Suvachittanont S, Charinpanitkul T, Biswas P: Role of Surface Area, Primary Particle Size, and Crystal Phase on Titanium Dioxide Nanoparticle Dispersion Properties. Nanoscale Res Lett 2011, 6: 27.

    PubMed Central  Google Scholar 

  202. 202.

    Baan RA: Carcinogenic hazards from inhaled carbon black, titanium dioxide, and talc not containing asbestos or asbestiform fibers: recent evaluations by an IARC Monographs Working Group. Inhal Toxicol 2007,19(Suppl 1):213–228.

    CAS  PubMed  Article  Google Scholar 

  203. 203.

    Waris G, Ahsan H: Reactive oxygen species: role in the development of cancer and various chronic conditions. J Carcinog 2006, 5: 14. 10.1186/1477-3163-5-14

    PubMed Central  PubMed  Article  CAS  Google Scholar 

  204. 204.

    Buechter DD: Free radicals and oxygen toxicity. Pharm Res 1988, 5: 253–260. 10.1023/A:1015914418014

    CAS  PubMed  Article  Google Scholar 

  205. 205.

    Susin SA, Daugas E, Ravagnan L, Samejima K, Zamzami N, Loeffler M, Costantini P, Ferri KF, Irinopoulou T, Prevost MC: Two distinct pathways leading to nuclear apoptosis. J Exp Med 2000, 192: 571–580. 10.1084/jem.192.4.571

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  206. 206.

    Freyre-Fonseca V, Delgado-Buenrostro NL, Gutierrez-Cirlos EB, Calderon-Torres CM, Cabellos-Avelar T, Sanchez-Perez Y, Pinzon E, Torres I, Molina-Jijon E, Zazueta C: Titanium dioxide nanoparticles impair lung mitochondrial function. Toxicol Lett 2011, 202: 111–119. 10.1016/j.toxlet.2011.01.025

    CAS  PubMed  Article  Google Scholar 

  207. 207.

    Jaeger A, Weiss DG, Jonas L, Kriehuber R: Oxidative stress-induced cytotoxic and genotoxic effects of nano-sized titanium dioxide particles in human HaCaT keratinocytes. Toxicology 2012, 296: 27–36. 10.1016/j.tox.2012.02.016

    CAS  PubMed  Article  Google Scholar 

  208. 208.

    Sanders K, Degn LL, Mundy WR, Zucker RM, Dreher K, Zhao B, Roberts JE, Boyes WK: In vitro phototoxicity and hazard identification of nano-scale titanium dioxide. Toxicol Appl Pharmacol 2012, 258: 226–236. 10.1016/j.taap.2011.10.023

    CAS  PubMed  Article  Google Scholar 

  209. 209.

    Yin JJ, Liu J, Ehrenshaft M, Roberts JE, Fu PP, Mason RP, Zhao B: Phototoxicity of nano titanium dioxides in HaCaT keratinocytes-Generation of reactive oxygen species and cell damage. Toxicol Appl Pharmacol 2012, 263: 81–88. 10.1016/j.taap.2012.06.001

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  210. 210.

    Yoo KC, Yoon CH, Kwon D, Hyun KH, Woo SJ, Kim RK, Lim EJ, Suh Y, Kim MJ, Yoon TH, Lee SJ: Titanium dioxide induces apoptotic cell death through reactive oxygen species-mediated Fas upregulation and Bax activation. Int J Nanomedicine 2012, 7: 1203–1214.

    PubMed Central  CAS  PubMed  Google Scholar 

  211. 211.

    Sun Q, Tan D, Zhou Q, Liu X, Cheng Z, Liu G, Zhu M, Sang X, Gui S, Cheng J: Oxidative damage of lung and its protective mechanism in mice caused by long-term exposure to titanium dioxide nanoparticles. J Biomed Mater Res A 2012, 100: 2554–2562.

    PubMed  Article  CAS  Google Scholar 

  212. 212.

    Liu S, Xu L, Zhang T, Ren G, Yang Z: Oxidative stress and apoptosis induced by nanosized titanium dioxide in PC12 cells. Toxicology 2010, 267: 172–177. 10.1016/j.tox.2009.11.012

    CAS  PubMed  Article  Google Scholar 

  213. 213.

    Meena R, Rani M, Pal R, Rajamani P: Nano-TiO2-induced apoptosis by oxidative stress-mediated DNA damage and activation of p53 in human embryonic kidney cells. Appl Biochem Biotechnol 2012, 167: 791–808. 10.1007/s12010-012-9699-3

    CAS  PubMed  Article  Google Scholar 

  214. 214.

    Wu J, Sun J, Xue Y: Involvement of JNK and P53 activation in G2/M cell cycle arrest and apoptosis induced by titanium dioxide nanoparticles in neuron cells. Toxicol Lett 2010, 199: 269–276. 10.1016/j.toxlet.2010.09.009

    CAS  PubMed  Article  Google Scholar 

  215. 215.

    Winter M, Beer HD, Hornung V, Kramer U, Schins RP, Forster I: Activation of the inflammasome by amorphous silica and TiO2 nanoparticles in murine dendritic cells. Nanotoxicology 2011, 5: 326–340. 10.3109/17435390.2010.506957

    CAS  PubMed  Article  Google Scholar 

  216. 216.

    Wang J, Li N, Zheng L, Wang S, Wang Y, Zhao X, Duan Y, Cui Y, Zhou M, Cai J: P38-Nrf-2 signaling pathway of oxidative stress in mice caused by nanoparticulate TiO2. Biol Trace Elem Res 2011, 140: 186–197. 10.1007/s12011-010-8687-0

    CAS  PubMed  Article  Google Scholar 

  217. 217.

    Uchino T, Tokunaga H, Ando M, Utsumi H: Quantitative determination of OH radical generation and its cytotoxicity induced by TiO(2)-UVA treatment. Toxicol In Vitro 2002, 16: 629–635. 10.1016/S0887-2333(02)00041-3

    CAS  PubMed  Article  Google Scholar 

  218. 218.

    Onuma K, Sato Y, Ogawara S, Shirasawa N, Kobayashi M, Yoshitake J, Yoshimura T, Iigo M, Fujii J, Okada F: Nano-scaled particles of titanium dioxide convert benign mouse fibrosarcoma cells into aggressive tumor cells. Am J Pathol 2009, 175: 2171–2183. 10.2353/ajpath.2009.080900

    PubMed Central  CAS  PubMed  Article  Google Scholar 

  219. 219.

    Toyooka T, Amano T, Ibuki Y: Titanium dioxide particles phosphorylate histone H2AX independent of ROS production. Mutat Res 2012, 742: 84–91. 10.1016/j.mrgentox.2011.12.015

    CAS  PubMed  Article  Google Scholar 

  220. 220.

    Moon C, Park HJ, Choi YH, Park EM, Castranova V, Kang JL: Pulmonary inflammation after intraperitoneal administration of ultrafine titanium dioxide (TiO2) at rest or in lungs primed with lipopolysaccharide. J Toxicol Environ Health A 2010, 73: 396–409. 10.1080/15287390903486543

    CAS  PubMed  Article  Google Scholar 

  221. 221.

    Goncalves DM, Chiasson S, Girard D: Activation of human neutrophils by titanium dioxide (TiO2) nanoparticles. Toxicol In Vitro 2010, 24: 1002–1008. 10.1016/j.tiv.2009.12.007

    CAS  PubMed  Article  Google Scholar 

Download references


The excellent assistance of Mrs. Linda Bowman, Prof. Gunter Oberdorster, Mrs Baobo Zou, Mr. Kui Liu and Miss Xia Yue in the preparation of this article is greatly appreciated. This work was partly supported by the National Nature Science Foundation of China (Grant No.81273111), the Foundations of Innovative Research Team of Educational Commission of Zhejiang Province (T200907), the Nature Science Foundation of Ningbo city (Grant No.2012A610185), the Ningbo Scientific Project (SZX11073 and 2012C5019), the Scientific Innovation Team Project of Ningbo (no. 2011B82014), Innovative Research Team of Ningbo (2009B21002) and K.C. Wong Magna Fund in Ningbo University.


The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the National Institute for Occupational Safety and Health.

Author information



Corresponding author

Correspondence to Jinshun Zhao.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

HS and RM were involved in writing the manuscript, JZ and VC helped to organize and proof read the final manuscript. All authors read and approved the final manuscript.

Hongbo Shi, Ruth Magaye contributed equally to this work.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Shi, H., Magaye, R., Castranova, V. et al. Titanium dioxide nanoparticles: a review of current toxicological data. Part Fibre Toxicol 10, 15 (2013).

Download citation


  • Titanium dioxide
  • Nanoparticle
  • Toxicology
  • Toxicokinetics
  • Acute toxicity
  • Chronic toxicity
  • Genotoxicity
  • Reproductive toxicity
  • Carcinogenicity