- Open Access
Particle characterization and toxicity in C57BL/6 mice following instillation of five different diesel exhaust particles designed to differ in physicochemical properties
Particle and Fibre Toxicology volume 17, Article number: 38 (2020)
Diesel exhaust is carcinogenic and exposure to diesel particles cause health effects. We investigated the toxicity of diesel exhaust particles designed to have varying physicochemical properties in order to attribute health effects to specific particle characteristics. Particles from three fuel types were compared at 13% engine intake O2 concentration: MK1 ultra low sulfur diesel (DEP13) and the two renewable diesel fuels hydrotreated vegetable oil (HVO13) and rapeseed methyl ester (RME13). Additionally, diesel particles from MK1 ultra low sulfur diesel were generated at 9.7% (DEP9.7) and 17% (DEP17) intake O2 concentration. We evaluated physicochemical properties and histopathological, inflammatory and genotoxic responses on day 1, 28, and 90 after single intratracheal instillation in mice compared to reference diesel particles and carbon black.
Moderate variations were seen in physical properties for the five particles: primary particle diameter: 15–22 nm, specific surface area: 152–222 m2/g, and count median mobility diameter: 55–103 nm. Larger differences were found in chemical composition: organic carbon/total carbon ratio (0.12–0.60), polycyclic aromatic hydrocarbon content (1–27 μg/mg) and acid-extractable metal content (0.9–16 μg/mg). Intratracheal exposure to all five particles induced similar toxicological responses, with different potency. Lung particle retention was observed in DEP13 and HVO13 exposed mice on day 28 post-exposure, with less retention for the other fuel types. RME exposure induced limited response whereas the remaining particles induced dose-dependent inflammation and acute phase response on day 1. DEP13 induced acute phase response on day 28 and inflammation on day 90. DNA strand break levels were not increased as compared to vehicle, but were increased in lung and liver compared to blank filter extraction control. Neutrophil influx on day 1 correlated best with estimated deposited surface area, but also with elemental carbon, organic carbon and PAHs. DNA strand break levels in lung on day 28 and in liver on day 90 correlated with acellular particle-induced ROS.
We studied diesel exhaust particles designed to differ in physicochemical properties. Our study highlights specific surface area, elemental carbon content, PAHs and ROS-generating potential as physicochemical predictors of diesel particle toxicity.
The classification of diesel exhaust as carcinogenic  and the reported diesel particle airway toxicity and systemic effects in both humans [2,3,4] and in mice [5,6,7,8,9,10,11,12] necessitates further studies. The ultrafine particle fraction has been suggested to be a main mediator of the carcinogenic effects and to contribute to other adverse health effects , but it is less known if it can be related to specific physicochemical particle properties.
Diesel engine exhaust consists of a particulate phase containing insoluble high surface area carbonaceous particles (elemental carbon; EC, also known as black carbon) with absorbed metal oxides and an adsorbed liquid fraction containing low volatility organic matter, including polycyclic aromatic hydrocarbons (PAH) formed in the combustion process and branched alkanes originating from the lubrication oil. In addition, diesel exhaust consists of gases including carbon monoxide, nitrogen oxides (NOx), and volatile organic compounds (VOCs) [14, 15]. Particulate matter and gas emissions can be reduced either by altering the combustion process or by installing after-treatment systems. Exhaust gas recirculation (EGR) is commonly used as a NOx reduction technique, but as the reduction of oxygen concentration and temperature reduce NOx emissions, soot emissions increase [13, 16]. Hence, the physicochemical characteristics of the emitted particles, such as content of PAH, metals and ratio of elemental and organic carbon [14, 17, 18], depend on engine combustion conditions. Particle size and thereby specific surface area (SSA) is a driver of pulmonary inflammation  and acute phase response [20, 21] whereas certain metals and PAH, as well as ROS formation are linked to genotoxicity [16, 22, 23]. Several PAH compounds including benzo[a]pyrene are classified as carcinogenic or possibly carcinogenic by IARC .
Emissions also depend on fuel type [18, 25,26,27], and recently, renewable diesel fuels have been introduced on large scales to replace fossil diesel [28,29,30]. There is incomplete knowledge on the potential adverse health effects of emissions from these new types of renewable diesel fuels, especially regarding gentoxicity and carcinogenicity . Renewable diesel fuels are based on vegetable oils, animal fats or waste products and are used in conventional engines as full substitution or in blends. Rapeseed methyl ester is a fatty acid methyl ester and differs from fossil diesel, as it has a high O2 content in the fuel (~ 10%). More recently, second generation renewable diesel fuels have become available where the oxygen content is removed by hydrogen treatment. One such example is hydrogen treated vegetable oil (HVO) which is a synthetic/paraffinic diesel produced from plant and animal sources and chemically similar to fossil diesel, except it has no aromatic content and shorter carbon chains .
In this study, we investigated the toxicological effects following pulmonary exposure to diesel exhaust particles collected without after-treatment from a controlled modern heavy-duty diesel engine in a laboratory environment. The particle production and collection was described in detail previously . Briefly, the engine was operated in different modes to vary the physical and chemical properties of five different diesel exhaust particles (DEP). Three different levels of EGR were chosen in order to generate diesel exhaust particles with a) high fraction of PAH and refractory organic carbon (OC) relative to EC, b) high fraction of EC and c) high fractions of lubrication oil related OC and metals relative to EC. The three EGR levels corresponded to engine intake O2 concentrations of 9.7% (DEP9.7), 13% (DEP13) and 17% (DEP17). For these EGR levels, the engine was fueled with petroleum-based ultralow-sulfur diesel of Swedish MK1 standard. In order to investigate the effect of renewable fuels, two additional particle types were generated by operating the engine on renewable rapeseed methyl ester (RME13) and hydrotreated vegetable/animal oil (HVO13) at an engine intake O2 concentration of 13%. Thus, the diesel exhaust particles were designed to differ in primary particle size and in content of PAHs, OC, EC and metals.
The aims of the study were: 1) to study the toxicity of five diesel exhaust particle samples designed to differ in physicochemical properties and 2) to identify physicochemical properties driving the toxicity of the particles. Toxicity was evaluated in terms of reactive oxygen species generation and inflammatory and genotoxic responses in mice on day 1, 28 and 90 after exposure to 6, 18 and 54 μg collected particles by single intratracheal instillation.
The characterization of the five different combustion particles in terms of particle mobility size in air, morphology by transmission electron microscopy (TEM), elemental carbon (EC)/organic carbon (OC) to total carbon (TC) ratio, PAH and metal contents are shown in Table 1 as previously reported . Overall, combustion conditions were the most important determinant for all particle characteristics. The combustion conditions heavily affected the mobility size, OC, EC, metal and PAH contents. The engine emissions measured as total PM1 were reduced by 65% for the renewable diesel fuels compared to the fossil diesel fuel (Table 1).
Analysis of OC, EC, metal- and PAH content was carried out on extracted particles, whereas TEM and mobility size distribution analyses was done on diluted exhaust particles.
The five different particle samples from experimental combustion emissions and the CB reference sample were visualized by transmission electron microscopy (Fig. 1). The morphology of the particles generated with 13% intake O2 concentration, namely DEP13, HVO13 and RME13 (Fig. 1 b, d, e) and DEP17 with 17% intake O2 concentration (Fig. 1 c) were all similar in appearance and showed typical soot agglomerates (diameter ~ 50–300 nm) of smaller primary particles (diameter ~ 10–30 nm). In contrast, the soot agglomerates from low temperature combustion (DEP9.7) had less defined primary particles and appeared more fused (bridging between primary particles) compared to the other samples (Fig. 1 a).
Organic and elemental carbon, primary particle size and specific surface area
Primary particle size and specific surface area (SSA) were estimated and calculated by measuring the diameters of well-defined spherical primary particles from the TEM images (assuming no voids inside the primary particles). The primary particle size decreased with the intake O2 concentration for the MK1 diesel samples. The largest primary particle size was found for HVO13, 23 nm, followed by 17 nm for DEP13 and 16 nm for RME13 (Table 1). Estimated SSA was overall rather similar, with the largest SSA for RME13 with 222 m2/g and the lowest for DEP9.7 with 152 m2/g. The EC fraction was highest for the particles generated at 13% intake O2, and the lowest for 9.7% intake O2. The EC fraction was higher for DEP13 compared to HVO13 and RME13.
The specific surface area (SSA) was estimated by using the primary particle size (d_pp) distribution and diesel soot density (ρ_pp) of 1.77 μg/m3  with the formula SSA =6/(ρ_pp · d_pp). Data from Gren et al. .
Semi-quantitative analysis of elemental contents by inductive coupled plasma mass spectrometry (ICP-MS) showed the highest mass fractions for Cu and Fe (Table 2). For Cu, Fe and several other trace elements, DEP17 showed 5–17 fold higher metal mass fractions compared to the other four samples. The emitted exhaust metal mass concentrations (μg/m3) were within a factor 2 for all operation points, however the PM1 mass emissions varied strongly (Table 1) and hence the metal mass fraction will be higher for the low mass emitting operation point (DEP17). DEP13 had the lowest mass fraction of Cu. RME13 and DEP13 had the lowest mass fraction of Fe.
Content of polycyclic aromatic hydrocarbons (PAHs) in the collected particles
The samples were analyzed for native PAHs and PAH derivatives by gas chromatography–mass spectrometry (GC-MS). In total, particle extracts were analyzed for 20 native PAHs, 13 alkylated PAHs (alkyl-PAHs), 14 nitrated PAHs (nitro-PAHs), 10 oxygenated (oxy-PAHs) and 6 dibenzothiophenes (DBTs). Table 3 shows the total amount of different groups of PAH derivatives in μg per g collected particle mass (PM). Values for the individual compounds are given in Additional file A. DEP9.7 showed the highest mass fractions of native PAHs, which was expected due to the low temperature combustion mode caused by the lower intake O2 concentration. DEP9.7 also contained the highest levels of nitro-PAHs.
The highest level of the sum of all PAHs were found in DEP9.7, followed by HVO13, DEP13, RME13 and DEP17. The PAH content decreased with increased intake O2 for DEP9.7, DEP13, and DEP17, which agrees well with a more complete combustion at higher intake O2 concentration.
Compared to DEP13, HVO13 particles contained higher amounts of all PAHs, especially native PAHs and oxy-PAHs, while RME particles contained lower mass fractions of total PAHs.
The levels of DBTs followed a different trend than the other PAH derivatives, by increasing with increasing intake O2 concentrations. DBT levels were highest for DEP17, followed by DEP13 and DEP9.7, while DBT levels were similar for DEP13, HVO13 and RME13.
Levels of native PAHs and PAH derivatives analyzed by GC-MS analysis (μg/g particles). Particle samples, blank control filters and standard reference material NIST2975 were analyzed for 20 native PAHs, 13 alkylated PAHs (alkyl-PAHs), 14 nitrated PAHs (nitro-PAHs), 10 oxygenated PAHs (oxy-PAHs) and 6 dibenzothiophenes (DBTs). PAH concentrations of blank control filters were substracted. A full list of all PAH derivatives can be found in Additional file A.
Reactive oxygen species (ROS) generation
Reactive oxygen species generation by the five different particle samples and by CB was measured acellularly, where generated ROS causes formation of 2′,7′ dichlorofluorescein (DCF) from DCFH2 which can be spectrofluorimetrically measured. The initial slope of the curve (alfa values) of measured fluorescence of the five particles are given in Table 4. In comparison, the alfa value of CB was 41,554. ROS data were reported previously . The ROS formation potential increased with the intake O2 concentration independently of fuel type. This indicates that engine operating conditions, combustion temperatures and the availability of O2 are important engine parameters that can alter the ROS formation potential of the soot .
Particle size distribution in dispersion
For the in vivo study, the diesel exhaust particles were collected on Teflon filters with a PM1 pre-separator, extracted using methanol, and dispersed in vehicle and diluted. The particles were dispersed in 0.1% Tween in Nanopure water and sonicated to achieve stable dispersions [35, 36]. The hydrodynamic number and intensity size distributions were measured by Dynamic Light Scattering (DLS). Similar distributions of particles sizes corresponding to agglomerates/aggregates were observed for the five particles, in the same size range as seen for CB and NIST2975 (Additional file B).
Pulmonary exposure of C57BL/6 mice
Mice were exposed by intratracheal instillation to 6, 18, and 54 μg of dispersed particles and euthanized on day 1, 28 and 90. Exposure to the vehicle (Nanopure water with 0.1% Tween) was included as exposure control (vehicle). In addition, exposure to blank filter extraction dispersed in 0.1%Tween was included as blank filter extraction control (extract). Carbon black Printex90 particles dispersed in the same vehicle (0.1% Tween) were included at a single dose level as reference particle (CB) to enable comparison with previous studies [12, 35, 37,38,39,40,41,42,43,44,45,46].
Pulmonary histopathology was evaluated on day 28 (Fig. 2) and day 90 (not shown). Generally, only minor histopathological changes were observed. Most particle retention on day 28 was observed in DEP13 and HVO13 exposed mice (Fig. 2b, d). Histopathological changes observed for these particles were related to macrophage and lymphocyte infiltration. For DEP9.7, DEP17 and RME13, particles were scarce and no apparent histological changes were observed (Fig. 2a, c, e). All five particle types appeared as black micron-sized agglomerates mainly phagocytized in macrophages (Fig. 2 a1-e1). In addition, some larger dense aggregates were observed for RME13 (Fig. 2 e2).
Cell composition in bronchoalveolar lavage (BAL) fluid
Pulmonary inflammation was evaluated 1, 28 and 90 days post-exposure by differential cell count of BAL fluid cell composition (Figs. 3 and 4, and Additional files C and D).
Day 1 post-exposure
Neutrophil influx was significantly increased in mice exposed to 54 μg of DEP9.7, DEP13, DEP 17, and HVO13 compared to vehicle control with similar, significant dose-response relationships. The 54 μg doses exceeded the level of response to the CB reference at the same dose level. DEP9.7 exposure induced high response (Fig. 3 a). In contrast, RME13 did not cause significantly increased neutrophil influx as compared to vehicle. No consistent differences were found for lymphocytes and macrophages compared to vehicle (Fig. 3 b and c). For eosinophils, only DEP13 at 54 μg significantly increased the influx compared to vehicle (Fig. 3 d).
Day 28 post-exposure
On day 28, some particle exposures seemingly resulted in reverse dose response relationships for neutrophil influx, with significant increase for 6 μg of RME13 and DEP13 compared to vehicle (Additional file, D 1). For 18 μg DEP13, there was a very low response, even significantly decreased compared to vehicle mice. CB exposure was not statistically different from vehicle for neutrophils. However, lymphocytes were significantly increased for CB exposed mice compared to vehicle (Additional file, D 2). No statistical differences were found for macrophages and eosinophils (Additional file, D 3 and 4).
Day 90 post-exposure
On day 90 following exposure, DEP13 had a significantly increased numbers of neutrophils and lymphocytes compared to vehicle (Fig. 4 a and b). Presence of macrophages was also observed for all exposed mice at levels around 40,000 cells, including vehicle mice, where HVO13 had a noteworthy lower cell numbers (Fig. 4 c). No statistically significant differences were seen for eosinophils (Fig. 4 d).
Serum amyloid A in lung
Day 1 post-exposure
Saa3 mRNA levels were used as biomarker of acute phase response [20, 46, 47] in lung tissue. On day 1, significant, dose-dependent increase in Saa3 mRNA levels compared to vehicle was observed in lung tissue for all exposures, except for RME13 (Fig. 5 a). DEP9.7 (p < 0.0003), DEP13 (p < 0.0003), DEP17 (p < 0.0003), and HVO13 (p < 0.0001) of 54 μg all exceeded the level of CB. DEP13 (p = 0.0110) and HVO13 (p = 0.0074) of 18 μg were also significantly increased compared to vehicle. Saa3 mRNA levels in lung correlated well with neutrophil influx (R2 = 0.5902, p = 0.0002) (Additional file E).
Test for linear dose-response was significant for all exposures, except for RME13 (Fig. 5 a).
Day 28 and 90 post-exposure
On day 28, DEP13 of 54 μg (p = 0.0034) and CB (p = 0.0007) were still increased compared to vehicle (Fig. 5 b). No significant differences were seen on day 90 (Fig. 5 c).
Genotoxicity was evaluated as DNA strand break levels in the comet assay, using comet tail length and % tail DNA in BAL derived cells, lung cells and liver cells on day 1, day 28 and day 90 post-exposure (Figs. 6 and 7, and Additional file F). Generally, variations were observed between exposures and within the vehicle control groups across doses and time points. No increases in DNA stand break levels were observed as compared to vehicle. There were no differences on day 1 (data not shown). There was a significant difference between vehicle and blank filter extraction control, especially for liver on day 28 (p = 0.0023), and for all tissues on day 90 (p-values: 0.0005–0.0305), with blank filter extraction control samples having significantly lower DNA strand break levels compared to vehicle (Figs. 6 and 7).
When compared to the blank filter extraction control, DEP13 at 6 μg was increased on day 28 for tail length in BAL cells (p = 0.078). For tail length in liver cells on day 28, RME13 (p = 0.0017), HVO (p = 0.004), DEP13 (6 and 18 μg: p = 0.0480), DEP17 (18 μg: p = 0.0072; 54 μg: p < 0.0001), and CB were increased (p = 0.0405) (Fig. 6). On day 90, DEP17 and HVO13 were increased in both lung (DEP17: p = 0.0008; HVO13: p = 0.0187) and liver cells (DEP17: p = 0.0026; HVO13: p = 0.0062) compared to blank filter extraction control (Fig. 7).
Linear regression analyses were carried out in order to assess physicochemical properties as predictors of inflammation and acute phase response. For this, the SSA of CB was estimated to 230 m2/g, although other values have been reported [5, 11, 48].
Neutrophil influx correlated well with estimated deposited SSA on day 1 (Fig. 8 a), where 50–60% of the variation in neutrophil influx could be explained by estimated deposited SSA. To compare with known reference particles, the plot was made with either inclusion (R2 = 0.6388, p < 0.0001) or exclusion (R2 = 0.5523, p = 0.0010) of previously published data on surface area and neutrophil influx on standard reference material (SRM) NIST2975 and NIST1650, which are diesel exhaust particles derived from a diesel-powered industrial forklift and a heavy duty truck, respectively. The vehicle used for these historical data was Nanopure water, without the addition of Tween80 . In a previous study comparing the effect of vehicle on carbon black-induced neutrophil influx, there was no differences between 0.1%Tween80 and Nanopure water . Similar significant correlations with neutrophil influx, with 40–50% of the variation explained, were seen when deposited elemental carbon (EC), organic carbon (OC) and total PAH dose were used as dose metrics (EC: R2 = 0.522, p = 0.0016; OC: R2 = 0.4688, p = 0.0049), Total PAHs: R2 = 0.4944, p = 0.0035) (Figs. 8 b-d). Deposited metals (sum of most abundant metals measured) were poorly correlated with neutrophil influx on day 1 (Additional file G a).
Saa3 mRNA levels in lung tissue on day 1 correlated well with deposited EC (R2 = 0.5041, p = 0.0021), but less with deposited surface area, OC, and PAHs (surface area: R2 = 0.3847, p = 0.0104; OC: R2 = 0.1771, p = 0.1182, PAHs: R2 = 0.3429, p = 0.0218) (Fig. 9 a-d).
As no significant differences were seen on day 28 for neutrophil influx and for genotoxicity on day 1, these data were not subjected to correlational analysis.
On day 28, ROS formation correlated with genotoxicity in lung (R2 = 0.3476, p = 0.0162) (Additional file H), whereas Total PAHs (Additional file I) and BaPeq (not shown) did not correlate well with genotoxicity, measured as Tail length in BAL, lung and liver in the Comet assay. On day 90, Tail length did not correlate with Total PAHs (Additional file J), or BaPeq (not shown) (Fig. 10 a-b). However, ROS correlated well with Tail length in the liver (Fig. 10 c) (R2 = 0.8348, p = 0.0301). On day 90, neutrophil influx did not correlate with surface area or deposited elemental carbon (Additional file G b-c).
Five diesel exhaust particles were designed to differ in regards to chemical and physical properties in order to assess the toxicity of the different particle properties. Toxicity was evaluated in terms of inflammation, acute phase response, DNA strand breaks and histopathological changes.
Organic and elemental carbon, primary particle size and surface area
A qualitative overview of the physicochemical properties and the toxicity parameters for the five different particle samples are shown in Table 5.
The obtained variations in the physical properties (primary particle size: 15–22 nm, SSA 152–222 m2/g and count median mobility diameter: 55–103 nm) were moderate, but are within the variations observed for the accumulation mode of real-world engine out emissions [49,50,51]. The renewable fuels reduced the PM1 emissions and the particle mobility size, which also have been found in previous studies [52,53,54].
Large variations were obtained for the organic carbon fraction (0.12–0.60), PAH fraction (1–27 μg/mg) and metal contents (0.9–16 μg/mg).
The combustion conditions strongly affected the exhaust emission composition. The particles generated at 13% intake O2 concentration had the highest EC fraction, while higher and lower intake O2 concentration increased the OC fraction. Organic carbon emissions in diesel exhaust are mainly lubrication oil-derived under lower/medium EGR (higher intake O2 concentrations)  and can therefore be expected to show less dependence on fuel type. This can also be seen as the renewable fuels had ~ 2.8 times lower PM1 mass emissions and a factor ~ 2.3–2.8 higher OC/EC fraction (Table 1). These observations are consistent with previously reported reduced EC/BC emissions from renewable diesel fuels .
The sample generated at low intake O2 concentration (DEP9.7) had the highest PAH mass fraction as a consequence of a higher degree of incomplete combustion process as the oxygen availability and combustion temperature were decreased .
All samples, except DEP9.7, were potent ROS producers, however all exhibited lower ROS formation potential per SSA than CB. The organic compounds were hypothesized to reduce the ROS formation compared to pure EC surfaces by reducing the physical particle size by filling pores in the soot agglomerate and/or by shielding of active solid soot surfaces . Gren et al.  dentified that the ROS potential per mass was highest for DEP17 and lowest for DEP 9.7 and correlated with increasing combustion temperature. In addition, a higher ROS formation potential was associated with an increasing refractory O:C ratio from aerosol mass spectrometry. These two observations suggested that increasing combustion temperature and O2 availability are linked to (1) more graphitic soot structures, and (2) increasing partial oxidation of soot surfaces. In turn, these processes appear to be strongly linked to the ROS formation potential  and, in this study, to particle-induced DNA strand-breaks.
The most abundant metals were Cu and Fe, with these and several other trace elements were increased 5–17 fold in DEP17 compared to the other four samples. Similarly, the metal fraction was 2.5–3.5 times higher for both renewable diesel fuels compared to DEP13. Increased concentrations of Cu and Fe in the used lubricating oil was found in a previous study using the same engine setup . The emissions of metals (μg/m3 in undiluted exhaust) are within a factor 2 for all samples, but as the PM emission was much lower for DEP17, and lower for HVO13 and RME 13, compared to DEP13, the relative metal fraction of the total collected PM was increased. The Zn and Mg measurements were excluded from the data set, because very high concentrations were detected in the blank filter control samples. As we only included one blank sample in the analysis, it was not possible to conclude whether the Zn and Mg came from the particles or were the result of background contamination. In turn, several of the constituents of lubrication oil and diesel particles were not measured, including P and Ca, although the mass percentages of these would be expected to be low.
The combustion of all three fuels resulted in significant particulate PAH emissions. The PAH emissions in this study were primarily combustion-derived, since HVO and RME have essentially no aromatic components in the fuel. The PAH fraction of the total particle mass was substantially higher for HVO13 than for DEP13. This may partly be explained by higher PM1 emission levels from DEP13 compared to HVO13. RME13, the emissions from combustion with the oxygenated biofuel RME, contained lower amounts of PAHs compared to both DEP13 and HVO13. Oxygen containing biodiesel, such as RME, has previously been found to reduce PAH emissions [57, 58]. The cause of this relation is not clear, but the oxygen available in the fuel may influence both the soot formation and its precursors (of which PAHs are major components) as well as the oxidation (i.e., in combustion removal) of soot and PAHs. As combustion temperatures were reduced with the addition of EGR (decreased intake O2), the PAHs/PM1 and PAHs/EC ratios increased strongly. It is interesting to note that the ratio of BaPeq compared to the total PAHs are higher for DEP9.7 compared to the other samples. This can indicate that the low temperature combustion favors the formation of larger and more genotoxic PAHs. Nonetheless, the main parameter driving the sum of benzo(a)pyrene equivalents (BaPeq) was the total sum of emitted PAHs (see Table 3 and Additional file L), and not differences in the PAH composition.
Inhalation is the golden standard for testing pulmonary toxicity, whereas pulmonary intratracheal instillation allows control of the deposited dose, and is thus suitable for comparison of hazard potential between different particles. We used 0.1% Tween as vehicle [35, 59], since all five diesel exhaust particle samples could be dispersed using this vehicle. Furthermore, two different control groups were included, vehicle controls and blank filter extraction controls.
Histopathology and particle retention
Black particles compatible with DEP were readily observed in lungs 28 days post-exposure to DEP13 and HVO13. In RME13-exposed lungs, some large aggregates of particles were observed, but overall there seemed to be less particles present at day 28 in RME13, DEP9.7 and DEP17 exposed lungs than in DEP13 and HVO13. As the amount of particles appeared to be greatest for the two DEP types with the most pronounced inflammatory response, differences in biopersistence of the particles could potentially explain the observed differences in pulmonary responses at day 28. Unfortunately, we do not have data to address this further in the current study, but DEP13 and HVO13 were the two diesel exhaust particles with highest content of EC, reflecting the insoluble carbon core. However, RME13 was similar in OC/EC ratio to DEP13 and HVO13, and if the response was dependent on the EC content, we would expect a similar response. There could be a difference in the EC nanostructure for RME particles, considering the content of 10% O2 in the fuel itself. This might change the combustion characteristics and the soot oxidation, and previous studies have reported different nanostructures depending of renewable diesel fuels compared to diesel [60, 61].
Inflammation and acute phase response
The total deposited surface area is an important predictor of neutrophil influx into the lung for insoluble particles . We found dose-dependent inflammation for most of the studied particles at day 1. Interestingly, RME13 did not induce inflammation in terms of neutrophil or lymphocyte influx at the assessed dose levels despite having similar SSA as the other particles. In addition, DEP13 appeared to be more inflammogenic than the other diesel exhaust particles, as increased influx of neutrophils and lymphocytes was still observed 90 days post-exposure. At day 28, no dose-response relationship was observed. This could be due to the low level of inflammation caused by the relatively low dose levels used in the current study. The standard diesel exhaust particles NIST2975 and NIST1650b did not induce neutrophil influx at 54 μg/mouse 28 days post-exposure in similar experimental set-ups [12, 62].
Acute phase response is the systemic response to various types of insults including bacterial infections, virus, infarction and all types of chronic inflammatory conditions , and acute phase response is a risk factor for cardiovascular disease in prospective epidemiological studies . The acute phase protein serum amyloid A is causally related to atherosclerosis by promoting formation of atherosclerotic plaques . We have previously shown that inhalation and pulmonary exposure to particles induce a dose dependent acute phase response [10, 20, 66], and we use Saa3 mRNA levels as a biomarker of pulmonary acute phase response . All the diesel exhaust particles except RME13 induced increased Saa3 mRNA levels in the lung at day 1, and DEP13 even induced increased Saa3 mRNA levels at day 28 alongside CB. Saa3 mRNA levels have been shown to correlate closely with neutrophil influx and deposited surface area for insoluble particles such as CB and TiO2 nanoparticles and carbon nanotubes [10, 20, 44, 46]. We have previously shown that pulmonary exposure to NIST2975 induced pulmonary Saa3 expression as well as increased plasma levels of SAA3  and that pulmonary Saa3 expression correlate with plasma SAA3 protein levels . In the current study, Saa3 mRNA levels correlated closely with neutrophil influx and deposited EC, but poorly with estimated deposited surface area on day 1 post-exposure. This could suggest that other particle components affecting the nanostructure in relation to the organic carbon content, in addition to SSA, are important contributors to the acute phase response of diesel exhaust particles. The acute phase response is an important cardiovascular disease risk factor , and inflammation may be linked to other pathologies including fibrosis  and secondary genotoxicity [69, 70].
DNA damage and ROS generation
The comet assay detects single strand breaks in DNA, and these can be caused by bulky PAH-DNA adducts and by particle-induced oxidative DNA damage. DNA damage in BAL and lung tissue may be caused by particles, metal ions, or PAHs released from the particles. DNA damage in the liver may be caused by primary genotoxicity caused by translocated particles  and by PAHs released into systemic circulation [71, 72]. In the current study, particle-induced DNA strand break levels in the liver on day 90 and in lung on day 28 correlated with particle-induced ROS, whereas PAH levels did not correlate with DNA strand break levels. The correlation between ROS and DNA damage observed for liver tissue was good (R2 = 0.8348), whereas the correlation for lung tissue depends heavily on a single data point for CB. However, both the ROS forming potential and the genotoxic effects of CB in vivo have been reported many times [5, 22, 37, 73]. Carbon black nanoparticles did not induce DNA strand breaks in the current study, but we have previously found CB-induced DNA strand breaks in BAL, lung and liver following inhalation and instillation [5, 22, 36, 44, 62, 74, 75]. We used 0.1%Tween80 as vehicle, since not all the DEPs could be dispersed satisfactory in pure water or 2% serum, which are the preferred vehicles [12, 40,41,42,43,44,45]. We have previously compared the effect of vehicle on CB-, TiO2- and CNT-induced toxicity . CB-induced inflammation and genotoxicity in terms of DNA strand breaks in BAL cells were assessed for CB dispersed in pure water, 2% serum, 0.05% serum albumin, 10% BAL in saline, 10% BAL in water and 0.1%Tween80. The inflammatory response of CB was vehicle-dependent, but was numerically similar when CB was dispersed in pure water or in 0.1% tween. CB-induced DNA strand breaks in BAL cells were detected when CB was dispersed in pure water, 2% serum, 10% BAL in saline and 10% BAL in water, but not when CB was dispersed in 0.1%Tween80. It is therefore possible, that DEP-induced DNA strand breaks were underestimated in the current study.
When blank filter extraction control was used as reference, DEP13, DEP17, HVO13 and RME13 induced DNA strand breaks in lung and liver tissues. Particles with a diameter < 100 nm are able to translocate from the lung to the systemic circulation  and thus all DEP should be able to translocate from lung to systemic circulation. Subsequent accumulation in liver has previously been shown to occur for particles of similar size as the particles in the current study (approx. 20 nm), and particle-dependent ROS generation was suggested as the likely cause of the observed DNA strand breaks in liver following pulmonary exposure to carbon nanoparticles . This suggests that carbon nanoparticles induce primary genotoxicity likely caused by ROS.
Carbon black nanoparticles are very efficient ROS generators  and induce oxidative DNA damage [37, 73] in vivo and in vitro. Carbon black nanoparticles and diesel exhaust particles have similar mutagenic potential in cell studies [16, 73] and diesel exhaust and carbon nanoparticles had similar carcinogenic potency in chronic inhalation studies in rats [78, 79]. This suggests that insoluble carbon nanoparticles such as the carbon core of diesel exhaust particles has the same mutagenic and carcinogenic potency as intact diesel exhaust. The present study supports the notion that particle-generated ROS contributes to the particle-induced genotoxicity.
Particle mass concentration and importance of fuel
The main effect of fuel type was that the PM emission rate in the undiluted exhaust was reduced by 65% for the two renewable diesels (HVO13 and RME13), compared to DEP13. RME13 clearly had less toxicological potential per mass for the endpoints included in this study, in terms of less inflammation and acute phase response, which are risk factors for cardiovascular disease. When taking into account the reduced PM1 emission factor, HVO also had a reduced toxicological response for most endpoints compared to MK1 diesel. Our results are in disagreement with the results by Brito et al.  and Shvedova et al. , who found that inhalation of soybean biodiesel exhaust increased inflammatory responses/cytokine secretion per mass compared to diesel in mice. Shvedova et al.  hypothesized that this is caused by increased oxidative stress caused by the organic matter, while we did not find any correlation with OC content.
Multiple animal studies (reviewed in ) have reported no difference in respiratory, cardiovascular and systemic response between biodiesel and petroleum diesel. Recently, Møller et al.  reviewed the available literature on cell and animal studies, and concluded that the evidence of biodiesel-induced inflammatory, oxidative stress and genotoxicity response is weak and inconsistent between studies. Furthermore, engine type, combustion conditions and after-treatment have been identified as major determinants of the chemical composition of the diesel exhaust particles [47, 81]. Thus, a major strength of the current study is that five different DEP were assessed in the same experimental setup, and that the three different fuel types were evaluated using the same engine, combustion conditions and after-treatment, thus ensuring comparability.
The mass emission should be considered when assessing the toxicity potential of the engine “output”, where reduced mass emission from the engine may lead to reduced toxicity potential of the engine output, even if the absolute toxicity per ng of particles is higher. In this study, the mice exposure dose levels varied by a factor of three. The PM emission factor for DEP13 was the same three-fold higher compared to RME13 and HVO13. Taking the PM emission factor into account, a comparison of engine emissions corresponds to comparing neutrophil influx following exposure to DEP13 at 54 μg and RME13 and HVO13 at 18 μg (Fig. 3 a), and this comparison shows that DEP13 induces more inflammation than RME13 and HVO13, which did not induce significantly increased neutrophil influx at 18 μg. However, a similar comparison for Saa3 mRNA levels does not show as clear a picture.
In summary, exposure to particles from RME fuel with 13% intake O2 concentration resulted in the least inflammation and acute phase response, whereas the physicochemically similar HVO13 and DEP13 induced more inflammation and acute phase response. The small differences in the assessed physicochemical properties of RME13 compared to HVO13 and DEP13 cannot explain the lower inflammatory response. However, RME fuel contains oxygen that can alter the soot formation and oxidation processes, leading to different particle properties, which influence the particle toxicity. A change in particle toxicity may derive from either altered surface structure of the carbon core, for example in terms of the frequency of edge sites and the composition of strongly bound surface oxides, or by changes in the chemical composition of the organic components. A major part of the organic components is lubrication oil derived , but organic compounds derived from the combustion of the fuel are also emitted and may partition to the particle phase. Future studies can include direct measurements of the surface properties of collected samples, for example by X-Ray Photo Electron Spectroscopy. Future studies should also focus on understanding if the lower toxic effect of RME is valid under other driving conditions, such as with varied load and during real-world driving cycles. The extraction and re-dispersion procedure may also influence particle composition and future studies can investigate this further. DEP17 and HVO13 had the highest ROS production and 90 days post-exposure DNA strand breaks were increased in both lung and liver compared to blank filter extraction controls. The particle-induced ROS production correlated with DNA strand break levels in lung tissue on day 28 and liver tissue on day 90.
We conclude that fuel type and combustion conditions are important factors for the physicochemical particle properties measured in this study, and that combustion conditions were more important than the fuel type. Among the tested fuels (Diesel, HVO, and RME), RME induced the least toxic response. We aimed at clarifying the relationship between physicochemical properties and toxicity. Estimated deposited surface area, elemental carbon, organic carbon, and PAHs correlated well with neutrophil influx, and ROS correlated with genotoxicity in lung tissue on day 28 and in liver on day 90. PAH content did not correlate with genotoxicity. Our study highlights specific surface area, elemental carbon content and ROS-generating potential as physicochemical predictors of diesel particle toxicity. Engine conditions that favor high combustion temperatures were found associated with higher ROS formation and more DNA strand breaks. These results may guide safe-by-design decisions for combustion engines.
Material and methods
Particle generation, collection and extraction
The particles were generated, collected and extracted as described in detail in Gren et al. , where the same particles are studied with other endpoints (in Gren et al. the particles are named slightly differently). Briefly, particles were generated with a modern heavy-duty diesel engine, operating on petroleum diesel (Swedish ultra low sulfur MK1) and two types of renewable diesels, hydrotreated vegetable oil (HVO; no aromatic and no oxygen content) and rapeseed methyl ester (RME, no aromatic but 10.6% oxygen) with no external exhaust after-treatment system. The engine was operated at a constant low load, and particle properties adjusted by varying the amount of exhaust gas recirculation (EGR). The amount of EGR changes the intake O2 concentration to the combustion cylinder, which in turn changes combustion temperature and thus the combustion conditions. An increase in EGR results in a decrease in intake O2 concentration and combustion temperature. In comparison to studies that generate particles from simulating realistic driving conditions, the advantage of our study design is the high control of combustion parameters that enable strong repeatability, and the possibility to link toxicological responses and particle physicochemical properties directly to combustion conditions.
The particles were collected on PTFE filters (Whatman PTFE, 150 mm, pore size 5 μm) using the final filter stage of a high volume cascade impactor (HVCI, BGI Inc.). The last impactor stage provided a cut-off size of 1 μm (PM1) for the filter sampling. The filters were soaked in 50 ml analytical grade methanol and sonicated (30 min, < 25 °C) three times. The extracts were pooled and dried with low-pressure evaporation (150 mbar, < 35 °C) in 10 mL glass vials . A non-exposed PTFE filter was extracted with the same procedure and used as a “filter blank” reference sample. The gravimetric mass extraction efficiency was for all samples ≥85%. There was no clear trend in extraction efficiency for samples high in organic or elemental carbon (OC, EC) respectively. Furthermore, measured OC and EC mass fraction (%) were similar for air samples collected on quartz filters  and the PM extracted using methanol from the PTFE samples. This difference were within ±15% for all samples except DEP17 (± 25%). These minor differences might be due to uncertainties with gas phase OC adsorption onto quartz filters in the air sampling. The small variations ensures that the two main classes of constituents (OC and EC) were both efficiently extracted.
Carbon black Printex90 was provided by Evonik Degussa GmbH (Frankfurt, Germany) [5, 73, 83]. Diesel particle SRM 2975 (referred to as NIST2975) was obtained from the National Institute of Standards and Technology (Gaithersburg, MD, USA). The certificate of analysis is avaiable at http://www.nist.gov.
Transmission electron microscopy (TEM) and analysis of organic (OC) and elemental (EC) carbon
The organic carbon (OC) and elemental carbon (EC) of the extracted particles were measured with a thermal-optical carbon analyzer (Sunset Laboratory Inc.), using the EUSAAR_2 protocol. To analyze the soot particles microstructure, samples were collected with electrostatic precipitation (Nanometer Aerosol Sampler, model 3089, TSI Inc.) on Cu-grids with lacey carbon coating (Whatman PTFE, 150 mm, pore size 5 μm) as well as the extracted particles were deposited in instillation vehicle on Cu-grids with lacey carbon coating (data not shown) and imaged by transmission electron microscopy (JEOL 3000F) operating at 300 kV. The primary particle determination and estimation of specific surface area (SSA) is described in Gren et al. . In brief, the primary particle diameter was manually measured with ImageJ software . The specific surface area (SSA) of each primary particle was estimated by using the primary particle size (d_pp) and diesel soot density (ρ_pp) of 1.8 μg/m3  with the formula SSA =6/(ρ_pp · d_pp) . By assuming point contact between the primary particles in the agglomerates, the geometric mean of the lognormal distribution of SSA of all measured primary particles within a sample was used as the mean SSA. The particle mobility size distribution in the diluted exhaust was measured from the dilution tunnel with a fast particulate analyzer (model DMS500, Cambustion Ltd.). The fast particulate analyzer measures the number size distribution of 5–1000 nm by classification of particles by their electrical mobility.
PAHs and metal analysis
Particle samples, blank control filters and standard reference material NIST2975 were solvent-extracted using dichloromethane, as previously described in detail . Extracts were analyzed for 20 native PAHs, 13 alkylated PAHs, 14 nitrated PAHs, 10 oxygenated PAHs and 6 dibenzothiophenes (DBT), using an Agilent 5975C mass spectrometer (MS) coupled to a 7890A gas chromatograph (GC, Agilent Technologies). Names, nominal masses, retention times and the associated deuterium labeled internal standards (IS) and recovery standards (RS) for all investigated compounds are shown in Additional file K.
Only one PAH analysis was performed for each combustion condition, however, at least two separate filter collections were pooled to account for engine variability.
The metal analysis was carried out as previously described in Bendtsen et al. , but with slightly modified extraction times. Briefly, as it was not possible to transfer the amount of ≤1 mg particle matter from the received vials to containers suitable for microwave-assisted acid digestion, a volume of 1 mL of 25% (v/v) nitric acid was directly added to the vials. For the preparation of reference material NIST2975 and CB (n = 2), 1 mg of material were weighed into 13 mL polypropylene tubes (Sarstedt, Nümbrecht, Germany) and 1 mL of 25% (v/v) nitric acid added. Samples were first agitated at 600 oscillations per min overnight (Stuart Scientific SF1 shaker), then incubated for approximately 7 h at room temperature without agitation and then shaken for another 72 h and transferred with 6 mL of ultrapure water into polypropylene tubes. Before analysis, the samples were centrifuged for 5 min at 4500 x g (Heraeus Multifuge X3 FR, Thermo Scientific), because no complete digestion of the particles was achieved. A volume of 5 mL of the supernatant was transferred to a new polypropylene tube and diluted 5-fold with 5% nitric acid. A triple quadrupole inductive coupled plasma mass spectrometer (ICP-MS) (Agilent 8900 ICP-QQQ, Santa Clara, USA) equipped with a MicroMist borosilicate glass concentric nebulizer and a Scott type double-pass water-cooled spray chamber was run in no gas (Cd, Hg, Pb, Bi, U) or helium (remaining elements) mode with 0.1–3 s integration time per mass. Quantification was performed based on external calibration.
Reactive oxygen species (ROS) assay
The level of ROS generated by the DEPs and CB were determined using the acellular 2′,7′ dichlorodihydrofluorescein diacetate (DCFH2-DA) assay. We used the protocol previously described in detail [77, 86] with the addition, that all materials were tested for auto-fluorescence as this may interfere with the assay. CB Printex 90 was tested alongside the DEPs as benchmark particle. Briefly, the DCFH2-DA (#D399, Invitrogen) was chemically hydrolyzed in the dark with NaOH to generate 2′,7′ dichlorodihydrofluorescein (DCFH2), which was further diluted with phosphate buffer (pH 7.4) to 0.04 mM. The PM suspensions were prepared using 16 min sonication (Branson S-450D) in Hank’s balanced saline solution (HBSS, without phenol, #H6648, Sigma Aldrich). The PM suspensions were further diluted in HBSS and tested at 0 μg/ml and eight doubling PM concentrations from 1.05 up to 101.25 μg/ml. The final concentration of DCFH2 at assay start was 0.01 mM. Generated ROS caused formation of 2′,7′ dichlorofluorescein (DCF) from DCFH2 that was spectrofluorimetrically measured following 3 h of incubation in the dark (37 °C and 5% CO2). Excitation and emission wavelengths were λex = 490 nm and λem = 520 nm, respectively (Victor Wallac-21,420; PerkinElmer, Skovlunde, Denmark). Auto-fluorescence was measured by replacing the ROS probe by Hank’s balanced saline solution (HBSS) at the highest tested PM concentrations.
Dynamic light scattering
Dynamic Light Scattering (DLS) was used to analyze hydrodynamic size distributions of particles in suspension (Malvern Zetasizer Nano ZS, Malvern Instruments Ltd., UK). Determinations were carried out directly in the solutions used for instillation in 1 ml polystyrene cuvettes at 25 °C. Six repeated same sample measurements were analyzed and average was calculated. For the calculation of hydrodynamic size, values from reference particle carbon black Printex90 was used (refractive (Ri) = 2.020, absorption indices (Rs) = 2000) for all particles, with standard optical and viscosity properties for H2O.
The study was in agreement with Directive 2010/63/EU of the European Parliament and of the Council of 22 September 2010 on the protection of mice used for scientific purposes, and the Danish Animal Experimentation Act (LBK 474 15/05/2014). The study was approved by The Animal Experiments Inspectorate under The Ministry of Environment and Food of Denmark (License: 2015-15-0201-00465) and the local Animal Welfare Committee responsible for ensuring implementation of 3R policy at the National Research Center for the Working Environment.
For this study, 492 female C57BL/6Tac mice were used. They were 7 weeks old at arrival and group-housed in standard cages with 6–8 mice with ad libitum access to tap water and Altromin 1324 rodent diet. All mice were housed in 1290D euro standard Type 3 cages on saw dust bedding with mouse house, wooden chew blocks and Enviro Dri nesting material as enrichment. The mice were kept at 21 ± 1 °C and 50 ± 10% humidity in a 12 h light-dark circle.
After one week of acclimatization, mice were exposed to a single dose of collected particles of either 6 μg, 18 μg or 54 μg per mouse by intratracheal instillation (6–8 mice per dose per exposure).
As it is only possible to expose a certain number of mice per day, the study was spread out on several days. First cohort was exposed to RME13 and CB, second cohort was exposed to DEP13, third cohort was exposed to DEP9.7, fourth cohort was exposed to DEP17, and fifth cohort was exposed to HVO13. For each exposure cohort there were four vehicle control mice, which were pooled together as one final control group for each post-exposure day for data evaluation. All cohorts were euthanized on day 1, day 28 and day 90 post-exposure. On day 28 and day 90, five additional mice per exposure were dedicated for histology (except for CB). In groups subjected to 1-day exposure to DEP13, DEP9.7, DEP17 and HVO13, some animals were initially not correctly dosed or cell recovery procedures failed upon euthanization. Therefore, a new cohort of mice was exposed, comprising two animals per dose for 1-day exposures, supplementing the groups from the original study.
Particles were suspended in Nanopure Diamond Water with 0.1% Tween80 and sonicated for 16 min using a Branson Sonifier S-450D (Branson Ultrasonics Corp, Danbury, CT, USA) (see description in ). The suspensions were diluted and re-sonicated for 2 min. Nanopure Diamond Water with 0.1% Tween80 was prepared similarly as vehicle. All solutions were prepared fresh for each instillation day and instilled within 1 h.
Instillation procedure was carried out as previously described [12, 87]. In brief, mice were exposed during isoflurane anesthesia to the suspended particles in vertical position with back support. A diode light was placed at the larynx visualizing the breathing pattern, to ensure correct delivery. 200 μl air was placed in the syringe after the instillation volume (50 μl) and administered post-exposure, to ensure maximum delivery into the lung. The mice were then returned to the home cage, placed on a heating plate, to ensure optimal recovery from anesthesia. Following the procedure and until euthanization, the mice were under observation for signs of discomfort. In case of weight loss (maximum 20%) and/or clear signs of discomfort (ruffled fur, isolation, facial pain expression, changed respiration, reduced activity), the mouse was taken out of the study and euthanized.
Organ harvest and preparation
Sedation, bronchoalveolar lavage (BAL), euthanization, organ harvest and procedures for analysis of mRNA, protein, and DNA strand breaks in the Comet assay were carried out as previously described .
Statistical analysis of in vivo data
Data was analyzed with GraphPad Prism (GraphPad Prism, version 7.03 for Windows, GraphPad Software, La Jolla California USA, www.graphpad.com). BAL fluid data was log10 transformed to achieve normal distribution. If no cells were counted across all cell types for one mouse, for instance due to high number of erythrocytes, it was considered as a cell processing error and the mouse was removed from the particular dataset. Values of zero within one cell type were replaced by the value of 0.25, generating an arbitrary low value of < 500 cells, considered as the detection limit of the differential count. Parametric data were analyzed by one-way ANOVA followed by Dunnett’s (comparison to control group). Nonparametric data was analyzed by Kruskal-Wallis followed by Dunn’s multiple comparisons test. Linear regressions were performed on log-transformed data, after testing the normality of the residuals.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
International Agency for Research on Cancer Monographs database, 2010. https://monographs.iarc.fr/agents-classified-by-the-iarc/. Accessed 27 July 2018.
Salvi S, Blomberg A, Rudell B, Kelly F, Sandström T, Holgate S, et al. Acute inflammatory responses in the airways and peripheral blood after short-term exposure to diesel exhaust in healthy human volunteers. Am J Respir Crit Care Med. 1999;159(3):702–9. https://doi.org/10.1164/ajrccm.159.3.9709083 https://www.atsjournals.org/doi/abs/10.1164/ajrccm.159.3.9709083.
Vermeulen R, Portengen L, Silverman DT, Garshick E, Steenland K. Meta-analysis of lung cancer risk from exposure to diesel exhaust: vermeulen et Al. Respond Environ Health Perspect. 2014;122(9):A230–1. https://doi.org/10.1289/ehp.1408428R.
Andersen MHG, Frederiksen M, Saber AT, Wils RS, Fonseca AS, Koponen IK, et al. Health effects of exposure to diesel exhaust in diesel-powered trains. Part Fibre Toxicol. 2019;16(1):21. https://doi.org/10.1186/s12989-019-0306-4.
Saber AT, Bornholdt J, Dybdahl M, Sharma AK, Loft S, Vogel U, et al. Tumor necrosis factor is not required for particle-induced genotoxicity and pulmonary inflammation. Arch Toxicol. 2005;79(3):177–82. https://doi.org/10.1007/s00204-004-0613-9 Epub 2004 Nov 11.
Saber AT, Jacobsen NR, Bornholdt J, Kjaer SL, Dybdahl M, Risom L, et al. Cytokine expression in mice exposed to diesel exhaust particles by inhalation. Role of tumor necrosis factor. Part Fibre Toxicol. 2006;3:4. https://doi.org/10.1186/1743-8977-3-4.
Hougaard KS, Jensen KA, Nordly P, Taxvig C, Vogel U, Saber AT, et al. Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice. Part Fibre Toxicol. 2008;5:3. https://doi.org/10.1186/1743-8977-5-3.
Husain M, Kyjovska ZO, Bourdon-Lacombe J, Saber AT, Jensen KA, Jacobsen NR, et al. Carbon black nanoparticles induce biphasic gene expression changes associated with inflammatory responses in the lungs of C57BL/6 mice following a single intratracheal instillation. Toxicol Appl Pharmacol. 2015;289(3):573–88. https://doi.org/10.1016/j.taap.2015.11.003 Epub 2015 Nov 10.
Saber AT, Jensen KA, Jacobsen NR, Birkedal R, Mikkelsen L, Moller P, et al. Inflammatory and genotoxic effects of nanoparticles designed for inclusion in paints and lacquers. Nanotoxicology. 2012;6(5):453–71. https://doi.org/10.3109/17435390.2011.587900 Epub 2011 Jun 7.
Saber AT, Lamson JS, Jacobsen NR, Ravn-Haren G, Hougaard KS, Nyendi AN, et al. Particle-induced pulmonary acute phase response correlates with neutrophil influx linking inhaled particles and cardiovascular risk. PLoS One. 2013;8(7):e69020. https://doi.org/10.1371/journal.pone.0069020 Print 2013.
Jacobsen NR, Moller P, Jensen KA, Vogel U, Ladefoged O, Loft S, et al. Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE−/− mice. Part Fibre Toxicol. 2009;6:2. https://doi.org/10.1186/1743-8977-6-2.
Bendtsen KM, Brostrøm A, Koivisto AJ, Koponen I, Berthing T, Bertram N, et al. Airport emission particles: exposure characterization and toxicity following intratracheal instillation in mice. Part Fibre Toxicol. 2019;16(1):23. https://doi.org/10.1186/s12989-019-0305-5.
Mills NL, Miller MR, Lucking AJ, Beveridge J, Flint L, Boere AJ, et al. Combustion-derived nanoparticulate induces the adverse vascular effects of diesel exhaust inhalation. Eur Heart J. 2011;32(21):2660–71. https://doi.org/10.1093/eurheartj/ehr195 Epub 2011 Jul 13.
Fiebig M, Wiartalla A, Holderbaum B, Kiesow S. Particulate emissions from diesel engines: correlation between engine technology and emissions. J Occup Med Toxicol. 2014;9(1):6. https://doi.org/10.1186/1745-6673-9-6 https://www.ncbi.nlm.nih.gov/pubmed/24606725.
Sydbom A, Blomberg A, Parnia S, Stenfors N, Sandström T, Dahlén SE. Health effects of diesel exhaust emissions. Eur Respir J. 2001;17(4):733 http://erj.ersjournals.com/content/17/4/733.abstract.
Jacobsen NR, Moller P, Cohn CA, Loft S, Vogel U, Wallin H. Diesel exhaust particles are mutagenic in FE1-MutaMouse lung epithelial cells. Mutat Res. 2008;641(1–2):54–7. https://doi.org/10.1016/j.mrfmmm.2008.03.001 Epub 2008 Mar 18.
Zhao Y, Li M, Wang Z, Xu G, Yuan Y. Effects of exhaust gas recirculation on the functional groups and oxidation characteristics of diesel particulate matter. Powder Technol. 2019;346:265–72. https://doi.org/10.1016/j.powtec.2019.02.016 http://www.sciencedirect.com/science/article/pii/S0032591019301184.
Burtscher H. Physical characterization of particulate emissions from diesel engines: a review. J Aerosol Sci. 2005;36(7):896–932. https://doi.org/10.1016/j.jaerosci.2004.12.001 http://www.sciencedirect.com/science/article/pii/S0021850204004124.
Schmid O, Stoeger T. Surface area is the biologically most effective dose metric for acute nanoparticle toxicity in the lung. J Aerosol Sci. 2016;99:133–43. https://doi.org/10.1016/j.jaerosci.2015.12.006 http://www.sciencedirect.com/science/article/pii/S0021850215301166.
Saber AT, Jacobsen NR, Jackson P, Poulsen SS, Kyjovska ZO, Halappanavar S, et al. Particle-induced pulmonary acute phase response may be the causal link between particle inhalation and cardiovascular disease. Wiley Interdiscip Rev-Nanomed Nanobiotechnol. 2014;6(6):517–31. https://doi.org/10.1002/wnan.1279 <Go to ISI>://WOS:000343823300001.
Saber AT, Halappanavar S, Folkmann JK, Bornholdt J, Boisen AM, Moller P, et al. Lack of acute phase response in the livers of mice exposed to diesel exhaust particles or carbon black by inhalation. Part Fibre Toxicol. 2009;6:12. https://doi.org/10.1186/1743-8977-6-12.
Modrzynska J, Berthing T, Ravn-Haren G, Jacobsen NR, Weydahl IK, Loeschner K, et al. Primary genotoxicity in the liver following pulmonary exposure to carbon black nanoparticles in mice. Part Fibre Toxicol. 2018;15(1):2. https://doi.org/10.1186/s12989-017-0238-9.
Møller P, Scholten RH, Roursgaard M, Krais AM. Inflammation, oxidative stress and genotoxicity responses to biodiesel emissions in cultured mammalian cells and animals. Crit Rev Toxicol. 2020:1–19. https://doi.org/10.1080/10408444.2020.1762541.
International Agency for Research in Cancer, https://monographs.iarc.fr/iarc-monographs-preamble-preamble-to-the-iarc-monographs/. Accessed Oct 2019. 2019.
Savic N, Rahman MM, Miljevic B, Saathoff H, Naumann KH, Leisner T, et al. Influence of biodiesel fuel composition on the morphology and microstructure of particles emitted from diesel engines. Carbon. 2016;104:179–89. https://doi.org/10.1016/j.carbon.2016.03.061 http://www.sciencedirect.com/science/article/pii/S0008622316302500.
Aatola H, Larmi M, Sarjovaara T, Mikkonen S. Hydrotreated vegetable oil (HVO) as a renewable diesel fuel: trade-off between NOx, particulate emission, and fuel consumption of a heavy duty engine. SAE International; 2008.
Tan P-q, J-y Z, Hu Z-y, D-m L, A-m D, D-m D. Effects of fuel properties on exhaust emissions from diesel engines. J Fuel Chem Technol. 2013;41(3):347–55. https://doi.org/10.1016/S1872-5813(13)60021-3 http://www.sciencedirect.com/science/article/pii/S1872581313600213.
Othman MF, Adam A, Najafi G, Mamat R. Green fuel as alternative fuel for diesel engine: A review. Renew Sustain Energy Rev. 2017;80:694–709. https://doi.org/10.1016/j.rser.2017.05.140 http://www.sciencedirect.com/science/article/pii/S1364032117307840.
Bae C, Kim J. Alternative fuels for internal combustion engines. Proc Combust Inst. 2017;36(3):3389–413. https://doi.org/10.1016/j.proci.2016.09.009 http://www.sciencedirect.com/science/article/pii/S1540748916304850.
Geng P, Cao E, Tan Q, Wei L. Effects of alternative fuels on the combustion characteristics and emission products from diesel engines: A review. Renew Sustain Energy Rev. 2017;71:523–34. https://doi.org/10.1016/j.rser.2016.12.080 http://www.sciencedirect.com/science/article/pii/S1364032116311327.
Gren L, Malmborg VB, Jacobsen NR, Shukla PC, Bendtsen KM, Eriksson AC, et al. Effect of renewable fuels and intake O2 concentration on diesel engine emission characteristics and reactive oxygen species (ROS) formation. 2020;11(6):641 https://www.mdpi.com/2073-4433/11/6/641.
Park K, Kittelson DB, Zachariah MR, McMurry PHJJNR. Measurement of inherent material density of nanoparticle agglomerates. 2004;6(2):267–72. https://doi.org/10.1023/B:NANO.0000034657.71309.e6 https://doi.org/10.1023/B:NANO.0000034657.71309.e6.
Ball JC, Straccia AM, Young WC, Aust AE. The formation of reactive oxygen species catalyzed by neutral, aqueous extracts of NIST ambient particulate matter and diesel engine particles. J Air Waste Manag Assoc. 2000;50(11):1897–903.
Carbon black in the form of inhalable dust [MAK Value Documentation, 2002]. The MAK-Collection for Occupational Health and Safety.
Hadrup N, Bengtson S, Jacobsen NR, Jackson P, Nocun M, Saber AT, et al. Influence of dispersion medium on nanomaterial-induced pulmonary inflammation and DNA strand breaks: investigation of carbon black, carbon nanotubes and three titanium dioxide nanoparticles. Mutagenesis. 2017;32(6):581–97. https://doi.org/10.1093/mutage/gex042 <Go to ISI>://WOS:000424976300007.
Bengtson S, Knudsen KB, Kyjovska ZO, Berthing T, Skaug V, Levin M, et al. Differences in inflammation and acute phase response but similar genotoxicity in mice following pulmonary exposure to graphene oxide and reduced graphene oxide. PLoS One. 2017;12(6). https://doi.org/10.1371/journal.pone.0178355 <Go to ISI>://WOS:000402611800040.
Bourdon JA, Saber AT, Jacobsen NR, Jensen KA, Madsen AM, Lamson JS, et al. Carbon black nanoparticle instillation induces sustained inflammation and genotoxicity in mouse lung and liver. Part Fibre Toxicol. 2012;9:5. https://doi.org/10.1186/1743-8977-9-5.
Saber AT, Jacobsen NR, Mortensen A, Szarek J, Jackson P, Madsen AM, et al. Nanotitanium dioxide toxicity in mouse lung is reduced in sanding dust from paint. Part Fibre Toxicol. 2012;9(1):4. https://doi.org/10.1186/1743-8977-9-4.
Billing AM, Knudsen KB, Chetwynd AJ, Ellis LA, Tang SVY, Berthing T, et al. Fast and robust proteome screening platform identifies neutrophil extracellular trap formation in the lung in response to cobalt ferrite nanoparticles. ACS Nano. 2020;14(4):4096–110. https://doi.org/10.1021/acsnano.9b08818.
Hadrup N, Rahmani F, Jacobsen NR, Saber AT, Jackson P, Bengtson S, et al. Acute phase response and inflammation following pulmonary exposure to low doses of zinc oxide nanoparticles in mice. Nanotoxicology. 2019;13(9):1275–92. https://doi.org/10.1080/17435390.2019.1654004.
Hadrup N, Saber AT, Kyjovska ZO, Jacobsen NR, Vippola M, Sarlin E, et al. Pulmonary toxicity of Fe(2)O(3), ZnFe(2)O(4), NiFe(2)O(4) and NiZnFe(4)O(8) nanomaterials: inflammation and DNA strand breaks. Environ Toxicol Pharmacol. 2020;74:103303. https://doi.org/10.1016/j.etap.2019.103303.
Danielsen PH, Knudsen KB, Štrancar J, Umek P, Koklič T, Garvas M, et al. Effects of physicochemical properties of TiO(2) nanomaterials for pulmonary inflammation, acute phase response and alveolar proteinosis in intratracheally exposed mice. Toxicol Appl Pharmacol. 2020;386:114830. https://doi.org/10.1016/j.taap.2019.114830.
Barfod KK, Bendtsen KM, Berthing T, Koivisto AJ, Poulsen SS, Segal E, et al. Increased surface area of halloysite nanotubes due to surface modification predicts lung inflammation and acute phase response after pulmonary exposure in mice. Environ Toxicol Pharmacol. 2020;73:103266. https://doi.org/10.1016/j.etap.2019.103266.
Poulsen SS, Jackson P, Kling K, Knudsen KB, Skaug V, Kyjovska ZO, et al. Multi-walled carbon nanotube physicochemical properties predict pulmonary inflammation and genotoxicity. Nanotoxicology. 2016;10(9):1263–75. https://doi.org/10.1080/17435390.2016.1202351 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5020352/.
Poulsen SS, Saber AT, Williams A, Andersen O, Kobler C, Atluri R, et al. MWCNTs of different physicochemical properties cause similar inflammatory responses, but differences in transcriptional and histological markers of fibrosis in mouse lungs. Toxicol Appl Pharmacol. 2015;284(1):16–32. https://doi.org/10.1016/j.taap.2014.12.011 Epub 2014 Dec 29. https://www.ncbi.nlm.nih.gov/pubmed/25554681.
Poulsen SS, Knudsen KB, Jackson P, Weydahl IEK, Saber AT, Wallin H, et al. Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice. PLoS One. 2017;12(4):26. https://doi.org/10.1371/journal.pone.0174167 <Go to ISI>://WOS:000399353500034.
Hadrup N, Zhernovkov V, Jacobsen NR, Voss C, Strunz M, Ansari M, et al. Acute phase response as a biological mechanism-of-action of (Nano)particle-induced cardiovascular disease. Small (Weinheim an der Bergstrasse, Germany). 2020;16(21):e1907476. https://doi.org/10.1002/smll.201907476.
Jackson P, Kling K, Jensen KA, Clausen PA, Madsen AM, Wallin H, et al. Characterization of genotoxic response to 15 multiwalled carbon nanotubes with variable physicochemical properties including surface functionalizations in the FE1-Muta(TM) mouse lung epithelial cell line. Environ Mol Mutagen. 2015;56(2):183–203. https://doi.org/10.1002/em.21922 Epub 2014 Nov 12.
Kittelson DBW, F. W, Arnold M. Review of diesel particulate matter sampling methods supplemental report # 2 aerosol dymamics, laboratory and on-road studies; 1998.
Desantes JM, Bermúdez V, García JM, Fuentes E. Effects of current engine strategies on the exhaust aerosol particle size distribution from a heavy-duty diesel engine. J Aerosol Sci. 2005;36(10):1251–76. https://doi.org/10.1016/j.jaerosci.2005.01.002 http://www.sciencedirect.com/science/article/pii/S0021850205000182.
Lapuerta M, Martos FJ, Herreros JM. Effect of engine operating conditions on the size of primary particles composing diesel soot agglomerates. J Aerosol Sci. 2007;38(4):455–66. https://doi.org/10.1016/j.jaerosci.2007.02.001 http://www.sciencedirect.com/science/article/pii/S0021850207000249.
Matti MM. Chemical characterization of particulate emissions from diesel engines: A review. J Aerosol Sci. 2007;38(11):1079–118. https://doi.org/10.1016/j.jaerosci.2007.08.001 http://www.sciencedirect.com/science/article/pii/S0021850207001231.
Lapuerta M, Armas O, Ballesteros R, Fernández J. Diesel emissions from biofuels derived from Spanish potential vegetable oils. Fuel. 2005;84(6):773–80. https://doi.org/10.1016/j.fuel.2004.11.010 http://www.sciencedirect.com/science/article/pii/S0016236104003540.
Murtonen T, Aakko-Saksa P, Kuronen M, Mikkonen S, Lehtoranta K. Emissions with heavy-duty diesel engines and vehicles using FAME, HVO and GTL fuels with and without DOC+POC Aftertreatment. SAE Int J Fuels Lubricants. 2010;2(2):147–66 www.jstor.org/stable/26271549.
Zhang L, Yang L, Zhou Q, Zhang X, Xing W, Wei Y, et al. Size distribution of particulate polycyclic aromatic hydrocarbons in fresh combustion smoke and ambient air: A review. J Environ Sci. 2020;88:370–84. https://doi.org/10.1016/j.jes.2019.09.007 http://www.sciencedirect.com/science/article/pii/S1001074219315165.
Shamun S, Novakovic M, B. Malmborg V, Preger C, Shen M, E. Messing M, et al. Detailed characterization of particulate matter in alcohol exhaust emissions. int Symp Diagnostics Modeling Combustion int Combustion Engines. 2017;2017(9):B304. https://doi.org/10.1299/jmsesdm.2017.9.B304.
Brito JM, Belotti L, Toledo AC, Antonangelo L, Silva FS, Alvim DS, et al. Acute cardiovascular and inflammatory toxicity induced by inhalation of diesel and biodiesel exhaust particles. Toxicol Sci. 2010;116(1):67–78. https://doi.org/10.1093/toxsci/kfq107.
Shvedova AA, Yanamala N, Murray AR, Kisin ER, Khaliullin T, Hatfield MK, et al. Oxidative stress, inflammatory biomarkers, and toxicity in mouse lung and liver after inhalation exposure to 100% biodiesel or petroleum diesel emissions. J Toxicol Environ Health A. 2013;76(15):907–21. https://doi.org/10.1080/15287394.2013.825217 https://pubmed.ncbi.nlm.nih.gov/24156694 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671493/.
Christophersen DV, Jacobsen NR, Jensen DM, Kermanizadeh A, Sheykhzade M, Loft S, et al. Inflammation and vascular effects after repeated Intratracheal instillations of carbon black and lipopolysaccharide. PLoS One. 2016;11(8). https://doi.org/10.1371/journal.pone.0160731 <Go to ISI>://WOS:000382876700006.
Strzelec A, Vander Wal RL, Lewis SA, Toops TJ, Daw CS. Nanostructure and burning mode of light-duty diesel particulate with conventional diesel, biodiesel, and intermediate blends. Int J Engine Res. 2017;18(5–6):520–31. https://doi.org/10.1177/1468087416674414.
Strzelec A, Toops TJ, Daw CS. Oxygen reactivity of devolatilized diesel engine particulates from conventional and biodiesel fuels. Energy Fuel. 2013;27(7):3944–51. https://doi.org/10.1021/ef400440a.
Kyjovska ZO, Jacobsen NR, Saber AT, Bengtson S, Jackson P, Wallin H, et al. DNA strand breaks, acute phase response and inflammation following pulmonary exposure by instillation to the diesel exhaust particle NIST1650b in mice. Mutagenesis. 2015;30(4):499–507. https://doi.org/10.1093/mutage/gev009 <Go to ISI>://WOS:000357885900005.
Ye RD, Sun L. Emerging functions of serum amyloid A in inflammation. J Leukoc Biol. 2015;98(6):923–9. https://doi.org/10.1189/jlb.3VMR0315-080R https://www.ncbi.nlm.nih.gov/pubmed/26130702.
Ridker PM, Hennekens CH, Buring JE, Rifai N. C-reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. N Engl J Med. 2000;342(12):836–43. https://doi.org/10.1056/nejm200003233421202.
Thompson JC, Wilson PG, Shridas P, Ji A, de Beer M, de Beer FC, et al. Serum amyloid A3 is pro-atherogenic. Atherosclerosis. 2018;268:32–5. https://doi.org/10.1016/j.atherosclerosis.2017.11.011 http://www.sciencedirect.com/science/article/pii/S0021915017313813.
Halappanavar S, Jackson P, Williams A, Jensen KA, Hougaard KS, Vogel U, et al. 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(6):425–39. https://doi.org/10.1002/em.20639.
Poulsen SS, Saber AT, Mortensen A, Szarek J, Wu DM, Williams A, et al. Changes in cholesterol homeostasis and acute phase response link pulmonary exposure to multi-walled carbon nanotubes to risk of cardiovascular disease. Toxicol Appl Pharmacol. 2015;283(3):210–22. https://doi.org/10.1016/j.taap.2015.01.011 <Go to ISI>://WOS:000352120200006.
Nikota J, Banville A, Goodwin LR, Wu D, Williams A, Yauk CL, et al. Stat-6 signaling pathway and not Interleukin-1 mediates multi-walled carbon nanotube-induced lung fibrosis in mice: insights from an adverse outcome pathway framework. Part Fibre Toxicol. 2017;14(1):37. https://doi.org/10.1186/s12989-017-0218-0.
Donaldson K, Poland CA, Schins RP. Possible genotoxic mechanisms of nanoparticles: criteria for improved test strategies. Nanotoxicology. 2010;4:414–20. https://doi.org/10.3109/17435390.2010.482751.
Halappanavar S, van den Brule S, Nymark P, Gaté L, Seidel C, Valentino S, et al. Adverse outcome pathways as a tool for the design of testing strategies to support the safety assessment of emerging advanced materials at the nanoscale. Part Fibre Toxicol. 2020;17(1):16. https://doi.org/10.1186/s12989-020-00344-4.
Müller AK, Farombi EO, Møller P, Autrup HN, Vogel U, Wallin H, et al. DNA damage in lung after oral exposure to diesel exhaust particles in big blue® rats. Mutation Res/Fundamental Mol Mechanisms Mutagenesis. 2004;550(1):123–32. https://doi.org/10.1016/j.mrfmmm.2004.02.010 http://www.sciencedirect.com/science/article/pii/S0027510704000740.
Dybdahl M, Risom L, Moller P, Autrup H, Wallin H, Vogel U, et al. DNA adduct formation and oxidative stress in colon and liver of big blue rats after dietary exposure to diesel particles. Carcinogenesis. 2003;24(11):1759–66. https://doi.org/10.1093/carcin/bgg147 Epub 2003 Aug 14.
Jacobsen NR, Saber AT, White P, Moller P, Pojana G, Vogel U, et al. Increased mutant frequency by carbon black, but not quartz, in the lacZ and cII transgenes of muta mouse lung epithelial cells. Environ Mol Mutagen. 2007;48(6):451–61. https://doi.org/10.1002/em.20300.
Bourdon JA, Halappanavar S, Saber AT, Jacobsen NR, Williams A, Wallin H, et al. Hepatic and pulmonary Toxicogenomic profiles in mice Intratracheally instilled with carbon black nanoparticles reveal pulmonary inflammation, acute phase response, and alterations in lipid homeostasis. Toxicol Sci. 2012;127(2):474–84. https://doi.org/10.1093/toxsci/kfs119 <Go to ISI>://WOS:000304198400015.
Jackson P, Hougaard KS, Boisen AM, Jacobsen NR, Jensen KA, Møller P, et al. Pulmonary exposure to carbon black by inhalation or instillation in pregnant mice: effects on liver DNA strand breaks in dams and offspring. Nanotoxicology. 2012;6(5):486–500. https://doi.org/10.3109/17435390.2011.587902.
Kreyling WG, Semmler M, Erbe F, Mayer P, Takenaka S, Schulz H, et al. Translocation of ultrafine insoluble iridium particles from lung epithelium to extrapulmonary organs is size dependent but very low. J Toxicol Environ Health A. 2002;65(20):1513–30. https://doi.org/10.1080/00984100290071649.
Jacobsen NR, Pojana G, White P, Moller P, Cohn CA, Korsholm KS, et al. Genotoxicity, cytotoxicity, and reactive oxygen species induced by single-walled carbon nanotubes and C(60) fullerenes in the FE1-Mutatrade markMouse lung epithelial cells. Environ Mol Mutagen. 2008;49(6):476–87. https://doi.org/10.1002/em.20406.
Heinrich U, Fuhst R, Rittinghausen S, Creutzenberg O, Bellmann B, Koch W, et al. 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(4):533–56. https://doi.org/10.3109/08958379509015211.
Saber AT, Poulsen SS, Hadrup N, Jacobsen NR, Vogel U. Commentary: the chronic inhalation study in rats for assessing lung cancer risk may be better than its reputation. Part Fibre Toxicol. 2019;16(1):44. https://doi.org/10.1186/s12989-019-0330-4.
Godri Pollitt KJ, Chhan D, Rais K, Pan K, Wallace JS. Biodiesel fuels: A greener diesel? A review from a health perspective. Sci Total Environ. 2019;688:1036–55. https://doi.org/10.1016/j.scitotenv.2019.06.002 http://www.sciencedirect.com/science/article/pii/S0048969719325550.
Topinka J, Milcova A, Schmuczerova J, Mazac M, Pechout M, Vojtisek-Lom M. Genotoxic potential of organic extracts from particle emissions of diesel and rapeseed oil powered engines. Toxicol Lett. 2012;212(1):11–7. https://doi.org/10.1016/j.toxlet.2012.04.017.
Ruusunen J, Tapanainen M, Sippula O, Jalava PI, Lamberg H, Nuutinen K, et al. A novel particle sampling system for physico-chemical and toxicological characterization of emissions. Anal Bioanal Chem. 2011;401(10):3183–95. https://doi.org/10.1007/s00216-011-5424-2 Epub 2011 Sep 30.
Jackson P, Vogel U, Wallin H, Hougaard KS. Prenatal exposure to carbon black (printex 90): effects on sexual development and neurofunction. Basic Clin Pharmacol Toxicol. 2011;109(6):434–7. https://doi.org/10.1111/j.1742-7843.2011.00745.x Epub 2011 Jul 20.
Schneider CA, Rasband WS, Eliceiri KW. NIH image to ImageJ: 25 years of image analysis. Nat Methods. 2012;9(7):671–5. https://doi.org/10.1038/nmeth.2089 https://www.ncbi.nlm.nih.gov/pubmed/22930834.
Rissler J, Messing ME, Malik AI, Nilsson PT, Nordin EZ, Bohgard M, et al. Effective density characterization of soot agglomerates from various sources and comparison to aggregation theory. Aerosol Sci Tech. 2013;47(7):792–805. https://doi.org/10.1080/02786826.2013.791381.
Hogsberg T, Jacobsen NR, Clausen PA, Serup J. Black tattoo inks induce reactive oxygen species production correlating with aggregation of pigment nanoparticles and product brand but not with the polycyclic aromatic hydrocarbon content. Exp Dermatol. 2013;22(7):464–9. https://doi.org/10.1111/exd.12178.
Jackson P, Lund SP, Kristiansen G, Andersen O, Vogel U, Wallin H, et al. An experimental protocol for maternal pulmonary exposure in developmental toxicology. Basic Clin Pharmacol Toxicol. 2011;108(3):202–7. https://doi.org/10.1111/j.1742-7843.2010.00644.x https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1742-7843.2010.00644.x.
We greatly appreciate technical assistance of Michael Guldbrandsen, Dorte Larsen, Eva Terrida, Anne-Karin Asp, Noor Irmam, and Anne Abildtrup. We thank Bo Strandberg from Division of Occupational and Environmental Medicine, Lund University, Sweden for expert consultancy on PAH analysis. KL thanks Agilent for providing the Agilent 8900 ICP-QQQ instrument.
This work was supported by Danish Centre for Nanosafety II financed on the Financial Law in Denmark. The particle characterisation part of the study was funded by the Swedish Research Council FORMAS and AFA Insurance.
Ethics approval and consent to participate
The study was in agreement with Directive 2010/63/EU of the European Parliament and of the Council of 22 September 2010 on the protection of mice used for scientific purposes, and the Danish Animal Experimentation Act (LBK 474 15/05/2014). The study was approved by The Animal Experiments Inspectorate under The Ministry of Environment and Food of Denmark (License: 2015-15-0201-00465) and the local Animal Welfare Committee responsible for ensuring implementation of 3R policy at the National Research Center for the Working Environment.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Bendtsen, K.M., Gren, L., Malmborg, V.B. et al. Particle characterization and toxicity in C57BL/6 mice following instillation of five different diesel exhaust particles designed to differ in physicochemical properties. Part Fibre Toxicol 17, 38 (2020). https://doi.org/10.1186/s12989-020-00369-9
- Diesel exhaust particles - ultrafine particles
- Intratracheal instillation
- Exhaust gas recirculation
- Renewable diesel fuels