Silica coating influences the corona and biokinetics of cerium oxide nanoparticles

Background The physicochemical properties of nanoparticles (NPs) influence their biological outcomes. Methods We assessed the effects of an amorphous silica coating on the pharmacokinetics and pulmonary effects of CeO2 NPs following intratracheal (IT) instillation, gavage and intravenous injection in rats. Uncoated and silica-coated CeO2 NPs were generated by flame spray pyrolysis and later neutron-activated. These radioactive NPs were IT-instilled, gavaged, or intravenously (IV) injected in rats. Animals were analyzed over 28 days post-IT, 7 days post-gavage and 2 days post-injection. Results Our data indicate that silica coating caused more but transient lung inflammation compared to uncoated CeO2. The transient inflammation of silica-coated CeO2 was accompanied by its enhanced clearance. Then, from 7 to 28 days, clearance was similar although significantly more 141Ce from silica-coated (35 %) was cleared than from uncoated (19 %) 141CeO2 in 28 days. The protein coronas of the two NPs were significantly different when they were incubated with alveolar lining fluid. Despite more rapid clearance from the lungs, the extrapulmonary 141Ce from silica-coated 141CeO2 was still minimal (<1 %) although lower than from uncoated 141CeO2 NPs. Post-gavage, nearly 100 % of both NPs were excreted in the feces consistent with very low gut absorption. Both IV-injected 141CeO2 NP types were primarily retained in the liver and spleen. The silica coating significantly altered the plasma protein corona composition and enhanced retention of 141Ce in other organs except the liver. Conclusion We conclude that silica coating of nanoceria alters the biodistribution of cerium likely due to modifications in protein corona formation after IT and IV administration.


Background
With rapid growth in nanotechnology-enabled consumer products, engineered nanomaterials (ENMs) are increasingly common. At the same time, there are rising public concerns about adverse effects of ENMs on human health and the environment. Among the ENMs introduced into the global nanotechnology market, nanoceria (CeO 2 ) has moved to the fore with a wide array of applications. The ability of cerium to switch oxidation states between Ce (III) and Ce (IV) is crucial for many nanobiomedical applications [1][2][3][4]. Further, parameters such as the method employed to synthesize CeO 2 , its particle size, and the extent of doping with other agents may alter the cerium oxidation state [3,5].
The toxicity data on CeO 2 from studies undertaken during the last decade are mixed and report a range of biological effects [6]. A number of in vivo and in vitro studies evaluating the biological effects of CeO 2 have reported toxicity and oxidative stress [7][8][9][10]. However, recently there are also reports highlighting putative antioxidant activity of CeO 2 and its ability to protect against oxidative stress-driven disorders [11][12][13]. Baer et al. have shed light on the influence of synthesis method, particle size and aging of CeO 2 on biological outcomes [5]. Many studies have underscored the need for defining nanoparticle characteristics employed in biological studies. There are conflicting data on CeO 2 toxicity and the consequences of different concentrations [14,15].
It is important to consider the extent of particle agglomeration in air and liquid media as a crucial factor contributing to discrepancies between in vivo inhalation versus instillation studies. Nanoparticle agglomeration is primarily influenced by NP intrinsic properties such as surface chemistry, charge, and primary particle size, but also from properties of suspending medium such as ionic strength [16][17][18][19].
Nanoparticle recognition by alveolar macrophages is a determinant of effective lung clearance. There is evidence that particle agglomeration aids in promotion of effective phagocytosis in alveolar macrophages; smaller (<100 nm) and more abundant structures may make macrophage mediated "surveillance" less effective [20]. Scientists are creating nanoparticles with functional surfaces designed to reduce inflammogenicity and lower toxicity while improving useful physicochemical properties. Developing strategies to mitigate toxicity of NPs without altering their core properties (a safer-by-design approach) is a vigorously pursued area of research [21][22][23]. In some cases, surface encapsulation of nanomaterials with a thin layer of amorphous silica renders them less cytotoxic and reduces DNA damage. Coating nanoparticles with amorphous silica can enhance nanoparticle stability in colloidal suspensions and facilitate effective uptake by professional phagocytes, stem cells, and other cell types with reduced toxicity [24][25][26]. Unlike crystalline silica that induces sustained inflammation and resultant fibrosis, amorphous silica evokes a transient and reversible inflammatory response [27].
We recently investigated the pulmonary clearance and extrapulmonary translocation of radiolabled Ce after intratracheal instillation of CeO 2 [15]. Our study showed that only 12 % of the instilled Ce dose was cleared from the rat lung during 28 days post-exposure. In another investigation, we found that inhalation of CeO 2 caused more lung injury and inflammation than CeO 2 coated with amorphous silica after one day post-exposure [28]. Previous reports have proposed that the protein corona formed on particles can influence biological effects [29]. To our knowledge this is the first study investigating the influence of surface properties of cerium oxide nanoparticles on protein corona formation, pulmonary effects, and the translocation and distribution of nanoceria after pulmonary and intravenous administration. We employed amorphous silica coating as a model to test the hypothesis that surface coating of CeO 2 would alter its protein corona and thus influence the biokinetics of the core nanoceria. We chose nanoceria due to its slow lung clearance and relatively low solubility [15,[30][31][32]. The aim of our study was to compare the clearance kinetics and bioavailability of cerium after intratracheal, intragastric, and intravenous administration of silica-coated versus uncoated CeO 2 in rats.

Synthesis and characterization of CeO 2 and silica-coated CeO 2
Uncoated and silica-coated CeO 2 were made by flame spray pyrolysis using the Versatile Engineered Nanomaterial Generation System (VENGES) at Harvard University [33]. Detailed physicochemical and morphological characterization of these NPs was reported earlier [21,28]. In summary, the uncoated and silica-coated CeO 2 had a cubic fluorite-like structure (Fig. 1). A nanothin (2-4 nm) amorphous silica layer hermetically encapsulated the CeO 2 core in a coating reactor after their initial synthesis in an aerosol reactor [21] (Fig. 1b). The silica coating on the surface was revealed as fine optically transparent film surrounding the dark and opaque CeO 2 , as verified by Xray diffraction (XRD) and electron microscopy analyses. The average crystal size of the primary uncoated and silica-coated NPs was 32.9 and 32.6 nm, respectively. Their specific surface areas (SSA) were 28 m 2 /g (uncoated) and 27.8 m 2 /g (silica-coated) ( Table 1). The extent of the silica coating was assessed by X-ray photoelectron spectroscopy and by photocatalytic methods. The persistence of the silica coating in the lungs of rats was at least 3 days after inhalation [34].
Assessments by dynamic light scattering (DLS) showed that as an aqueous dispersion the particles essentially behaved as "nanoagglomerates" of 136 ± 1.1 nm (uncoated) and 208 ± 2.9 nm (silica-coated). The hydrodynamic diameters of the two CeO 2 types are shown in Table 1. The zeta potential of NP suspensions was also evaluated in distilled water. Uncoated CeO 2 exhibited a positive zeta potential (34.5 ± 3.1 mV) and the silica coating changed the zeta potential to negative −26.8 ± 0.3 mV (Table 1). DLS analysis was also performed on both nanoceria after in vitro incubation with harvested rat bronchoalveolar lining (BAL) fluid to determine if the lipoprotein corona alters agglomeration size and zeta potential. We found that this corona significantly increased the hydrodynamic diameter (136 to 1463 nm) and changed the zeta potential (34.5 to −20.8 mV) of uncoated CeO 2 . The effects of the lipoprotein corona on silica-coated CeO 2 were more modest (Table 1). After incubation in rat plasma and the formation of the protein corona, the hydrodynamic diameters of both CeO 2 NP types were significantly increased and the surface charge of uncoated CeO 2 was also altered from positive to negative zeta potential (Table 1). Similar to protein corona formed with BAL incubation, the increase in D H with plasma protein corona formation was more pronounced with uncoated CeO 2 NPs.
Pulmonary responses to intratracheally instilled CeO 2 and silica-coated CeO 2 We compared the pulmonary responses of rats to uncoated versus silica-coated CeO 2 at 1 and 5 days after IT instillation in rats as described previously [35]. This experiment was performed to also determine the safe dose for intratracheal instillation of CeO 2 and silicacoated CeO 2 NPs where inflammation or injury was minimal. Groups of 6 rats (272 ± 13 g body weight) were instilled with 0.2, 1 or 5 mg/kg of each type of CeO 2 . Control animals were instilled with an equivalent volume of distilled water. We found that coated and uncoated CeO 2 NPs induced a dose-dependent injury and inflammation as indicated by increased neutrophils (Fig. 2a) in the BAL fluid at 24 h post-instillation. Both NPs also increased the levels of myeloperoxidase (MPO), albumin and lactate dehydrogenase (LDH) (Fig. 2b). Interestingly, the numbers of lavaged macrophages increased for uncoated and decreased for silica-coated CeO 2 with increasing dose (Fig. 2c). At 0.2 and 1 mg/kg doses, only the silica-coated CeO 2 instilled rats showed elevated LDH, MPO, and albumin levels. However, five days post-dosing with 1 mg/ kg of silica-coated CeO 2 there were decreased PMN counts ( Fig. 2d). At this time, there were also reductions in other inflammatory biomarkers such as MPO, albumin and LDH (Fig. 2e). However, significant increase in macrophage numbers was observed in silicacoated CeO 2 groups (Fig. 2f ).
In vivo clearance and translocation of 141 CeO 2 and silica-coated 141 CeO 2 after IT instillation in rats The lung levels of 141 Ce after a single IT instillation of either radioactive uncoated CeO 2 or silica-coated CeO 2 were evaluated in rats for 28 days. Animals were sacrificed at 5 min, and 2, 7 and 28 days post-instillation and various organs were collected to determine the retained cerium concentration. The lung clearance profiles for both nanoparticle types showed no differences during the first two days post-IT instillation. Interestingly, the lung clearance was markedly different between day 2 and day 7 for the two NPs (Fig. 3a). We observed that~22 % of the 141 Ce from the silica-coated CeO 2 and only~8 % of the 141 Ce from the uncoated CeO 2 dose disappeared from the lungs during this period. Between day 7 and day 28 post-IT instillation, the difference in the fraction of cleared NPs was statistically significant but relatively small (8.1 % for uncoated 141 CeO 2 vs. 10.4 % for silica-coated CeO 2 ). By 28 days postinstillation,~81 % of uncoated CeO 2 still remained in the lungs. Coating of CeO 2 with amorphous silica enhanced the overall clearance of CeO 2 by an additional 16 %.
Translocation of radioactive cerium from the lungs to other organs was evaluated by measuring 141 Ce in the different collected tissues. Low detectable fractions of radioactivity for Ce from both NP types were found in the liver,  SSA -specific surface area D xrd -primary particle size based on X-ray diffraction D H -hydrodynamic diameter ζ -zeta potential N.A. -not applicable bone/bone marrow, spleen and kidneys (<1 %) (Fig. 3b). Estimated tissue cerium concentration in these organs were higher for uncoated CeO 2 ( Table 2). The elimination of 141 Ce from both particle types was mostly via the feces (Fig. 4b) and to a much lesser extent via the urine (Fig. 4a). Furthermore, we found that the total recovered 141 Ce in examined tissues, feces, and urine was significantly higher in uncoated than silica-coated CeO 2 (Figs. 3 and 4). In the case of silica-coated CeO 2 , we speculate that the missing radioactivity may have been in organs not examined such as lymph nodes, adipose tissue, pancreas, adrenals, teeth, nails, tendons, nasal tissues, and the rest of the head.

Biodistribution of CeO 2 within the lungs and protein corona formation
Since the protein corona on NP surfaces may modulate their cell interaction and overall biological effects, we examined the composition of adsorbed proteins on the NP surface when incubated with collected cell-free BAL fluid. First, we found that incubation of NPs in concentrated BAL fluid significantly altered their aggregate sizes (Table 1). Compared with the suspension in deionized water, both nanoceria types exhibited larger and more variable hydrodynamic diameter. Uncoated nanoceria also formed larger agglomerates than the coated NPs. In addition, we found that the total amount of adsorbed protein was significantly higher in silica-coated than uncoated CeO 2 especially albumin, C3, and transferrin ( Fig. 5a, b). However, we found no differences in the quantitative distribution of the two NP types 24 h post-IT instillation among the three measured compartments (Fig. 5c). The majority of 141 Ce activity was associated with the lavaged lungs. Additionally, hyperspectral imaging analysis, to determine the extent of NP uptake in BAL cells after 5 days post-IT instillation, revealed a higher number of particle-containing cells in the silica-coated than uncoated group (Fig. 6).

Biodistribution of uncoated and silica-coated CeO 2 after gavage administration in rats
At 5 min and 7 days post-gavage of uncoated CeO 2 or silica-coated CeO 2 we measured absorption of 141 Ce from the gut. As expected, nearly 100 % of the dose was recovered at 5 min in the stomach for both types of NPs (Fig. 7a). The 141 Ce levels in tissues other than the gastrointestinal (GI) tract were extremely low (0.004 % for uncoated, 0.002 % for silica-coated CeO 2 ) by day 7 (Fig. 7b). Very low levels of 141 Ce were excreted in the urine (Fig. 7c) and nearly 99 % of both CeO 2 NPs was excreted in feces by day 7 (Fig. 7d). As there was very low radioactivity detected in any of the collected organs and in urine samples over a period of 7 days, we conclude that both uncoated and silica-coated CeO 2 do not significantly translocate through the intestinal barrier.
Tissue concentration of cerium at 7 days post-gavage is shown in Table 3.

Tissue distribution of 141 CeO 2 and silica-coated 141 CeO 2 NPs after intravenous injection
The distribution of intravenously injected NPs at 2 h and 2 days post-injection is shown in Fig. 8a and b, respectively. Radioactive 141 Ce from both NP types was predominantly retained in the liver, spleen, and bone, organs that typically take up circulating particles by macrophages with access to the blood. The silica coating led to a redistribution of 141 Ce over a period of 2 days from the liver to the spleen and other organs (Fig. 8b). The silica coating also enhanced the tissue concentration of 141 Ce in several organs but decreased in the liver (Tables 4 and 5).
To determine the influence of silica coating on NP-plasma protein interactions, we analyzed the hydrodynamic diameters of NPs and characterized the protein corona formed after incubation of NPs in rat plasma in vitro. We found significant increases in agglomerate sizes of both NP types compared to when suspended in protein-free deionized water (Table 1). We also found differences in the protein corona composition between the 2 NP types (Fig. 9a, b). The fecal excretion of 141 Ce post-injection of NPs during the first 24 h was far  Data are mean ± SE ng/g cerium concentration, n = 5/group Ce concentration was estimated (ng/μCi NPs x μCi/g tissue ) *P < 0.05, CeO 2 vs. silica-coated CeO 2 lower than after IT instillation (0.05 % v. 3 %), suggesting that some CeO 2 NPs in the lungs may be removed by mucociliary transport. It also suggests that absorbed cerium is eliminated slowly from the body.

Discussion
Progress in nanotechnology has produced a variety of nanoparticle generation systems which synthesize nanoparticles of desired size and properties. The in-house VENGES system employed in this study enabled us to control primary particle size and aerosol size distribution. This platform also allowed for in-flight coating of CeO 2 with a nanothin layer of amorphous silica [21]. This flame-based silica-coating process has recently been explored as a means of high yield scalable manufacturing of silica-coated nanosized ENMs with cores of TiO 2 , Fe 2 O 3 , or Ag [36].
In this study, we sought to examine the effect of surface modification of CeO 2 with amorphous silica on acute pulmonary responses as well as on CeO 2 pharmacokinetics after IT instillation, gavage, and IV injection. We observed that exposure of rats to silica-coated CeO 2 caused higher dose-dependent inflammatory responses compared to uncoated particles and a vehicle-only control group, as evidenced by increases in BAL parameters. However, the inflammatory effects induced by silicacoated CeO 2 were transient and subsided by day 5 (Fig. 2d and e). This is consistent with our recent study in which 1 mg/kg dose of silica-coated CeO 2 NPs also caused higher but transient inflammation [34]. We note that these findings are in contrast to our previously published report on the toxic and inflammatory effects of the same particles after inhalation exposure, where we showed that inhaled silica-coated CeO 2 induced less toxicity and inflammation after exposure for 2 h per day for 4 consecutive days [28]. This discordance may be explained based on the higher doses used here and the different exposure method (bolus IT instillation vs. inspired aerosols over 8 h). Although IT instillation is a reliable method for administering a precise dose to the lungs, it differs from inhalation exposure in terms of particle distribution, dose rate, the extent of NP agglomeration and ressulting patterns of injury and clearance. Baisch et al. observed that inflammatory responses following intratracheal instillation were higher than those seen following whole body inhalation for single and repeated exposures of titanium dioxide NPs when deposited doses were comparable [37].

Fate of intratracheally-instilled nanoceria
The lung clearance of uncoated CeO 2 observed in this study was similar to our recent report on CeO 2 NM-212. NM-212 was synthesized by a precipitation method unlike the CeO 2 NPs used here which were flame-generated [38]. Our data are consistent with a study by He et al. where 63.9 ± 8.2 % of the intratracheally instilled dose still remained in the lungs after 28 days [31]. We found that the extent of silica-coated CeO 2 clearance from the lung was significantly higher (~35 %) than uncoated CeO 2 (~19 %). But an important finding was the significant influence of the silica coating on the lung clearance of CeO 2 from days 2 to day 7. This period of more rapid clearance coincided with the initial phase characterized by greater inflammation and increased air-blood barrier permeability.
As the pulmonary surfactant lies at the outermost aspect of the air-blood barrier, inhaled and deposited NPs first encounter the biomolecules of the alveolar lining layer. This fluid consists of an ultra-thin layer of aqueous hypophase and a surface active lipoprotein mixture usually known as the pulmonary surfactant layer [39]. Pulmonary surfactant is composed of 85-90 % w/w phospholipids and Data are mean ± SEM, n = 5/group 10 % w/w proteins [40]. Adsorption of phospholipids and proteins on the NP surface takes place rapidly [41]. Therefore, it is reasonable to assume that interactions of NPs with lung cells occur mostly with the NP-lipoprotein complex and not with bare NP surfaces [42]. Importantly, the adsorption of proteins and phospholipids on NPs may modulate their overall biological effects [43,44].
We examined the protein corona formed on the surface of our test NPs as they encounter the lung lining fluid. The incubation of NPs in BAL fluid significantly increased their hydrodynamic sizes and changed the zeta potential of CeO 2 NPs likely due to their interactions with phospholipids and proteins. Presumably, instilled NPs would immediately acquire protein coronas in vivo changing their surface charge and extent of aggregation unlike those in water suspension and in dry aerosols. The type of proteins comprising the corona may also impact NP translocation [45]. Aggregate size alterations could also influence the pulmonary effects and translocation of the core nanoceria. Notably, we found significantly more protein adsorbed in the "hard corona" of silica-coated compared to uncoated CeO 2 . The amounts of specific proteins comprising the hard corona shown in Fig. 5b were based on NP mass (μg/mg NPs). When expressed as amount of protein per unit surface area (μg/m 2 ) of NPs, silica-coated CeO 2 still bind more BAL proteins than uncoated NPs. Significantly more albumin, SP-A, α-1 antitrypsin, transferrin, and C3 proteins were present in the corona of silica-coated CeO 2 . These belong to the class of proteins that shuttle across the alveolar-epithelial barrier [46]. Receptor-mediated transport processes in the alveolar epithelium have been reported for albumin and transferrin [46]. Translocation of intratracheally instilled 125 I-albumin from air spaces into the blood compartment has been reported previously [47]. Rapid translocation of synthetic organic NPs comprised of human serum albumin and a fluorophore has been demonstrated [48]. Whether this enhanced adsorption of albumin and transferrin onto silica- coated nanoceria contribute to their small but higher translocation through the lungs needs further investigation.
Studies have reported that some of the proteins present in BAL exhibit immunological functions (e.g., C3 and SP-A) [49][50][51]. It has been shown that coating of magnetite and TiO 2 with SP-A improved their uptake in macrophages [52]. Our findings that the lipoprotein corona changes the agglomerate size and zeta potential of CeO 2 also suggest that the corona can affect the manner in which alveolar macrophages interact, recognize, phagocytose, and process CeO 2 NPs. Alveolar macrophages are the primary phagocytic cells for ultrafine particles in the lungs [53]. Particles may adhere to the surfaces of type I and type II epithelial cells as well, but lung parenchymal cells are less capable of phagocytosis [54]. AMs play a critical role in NP-induced inflammation and oxidative stress. Most of the deposited particles in the alveolar region are phagocytosed within a 24 h period after particle deposition, as long as the dose is not beyond the ingestion capacity of AMs [55,56]. Notably, functionalized NPs are more effectively phagocytosed than non-functionalized NPs [57][58][59][60]. Recognition and phagocytosis of nanoparticles by AMs is a key component in nanoparticle dissolution and clearance.
We examined whether silica coating affects the distribution of CeO 2 within the different lung compartments after the first 24 h post-instillation. We found no significant differences in the amount of radioactive CeO 2 in lavaged alveolar cells, in cell-free supernatant, or in lavaged lungs. Furthermore, no significant difference was found in the number of AMs with internalized CeO 2 NPs assessed by hyperspectral imaging of lavaged AMs. However, at 5 days post-instillation, significantly more AMs were found to have internalized silica-coated than uncoated CeO 2 . This enhanced uptake could be due to different corona profile, altered aggregate size or abundant recruitment of AMs observed with silica-coated CeO 2 . It is possible that this enhanced uptake of silica-coated CeO 2 by activated AMs and the higher inflammation could lead to greater translocation of particles or particle-containing cells into the lymphatic system. For the lung parenchyma, clearance involves a slower phase, occurring in the alveoli. It consists of phagocytosis of particles from the lung surface by AMs and to a lesser extent by particles entering the lymphatics and subsequent accumulation in the regional lymph nodes.
We were unable to measure the lymphatic clearance of CeO 2 NPs since lymph nodes were not included in this study. However, we have previously shown that 65 Zn from 65 ZnO NPs was more significantly translocated to tracheobronchial lymph nodes when coated similarly with amorphous silica [22]. Interestingly, despite the greater clearance from the lungs, 141 Ce from silica-coated CeO 2 was slightly lower in all the organs we examined (0.73 vs. 0.93 %). The cerium concentration retained in the liver, bone, kidneys, heart, and testes was lower. Excretion in the feces was also lower (12 vs. 19 %).

Fate of ingested nanoceria
Data from animal and human studies show that inhaled nanoparticles are subject to different site-dependent clearance mechanisms [20]. These mechanisms include a fast clearance phase, which can be observed in the tracheobronchial region and is attributed to the mucociliary elimination with subsequent ingestion into the gastrointestinal tract and excretion via the feces. Thus, the oral exposure to nanoparticles is pertinent from an environmental exposure perspective, such as the ultrafine fraction of air pollution exposures. As a surrogate for entry of particles into the GI tract from the lungs, we also investigated the influence of silica coating on the bioavailability of Fig. 6 Quantitative assessment of uptake of CeO 2 by alveolar macrophages at 24 h post-instillation. BAL cells were analyzed using hyperspectral imaging. a The image shows uncoated and silica-coated CeO 2 mapped as bright pixels (pointed arrows) inside the cells. BAL cells isolated at 24 h and 5 days after IT-instillation were scored. b Numbers of macrophages with or without internalized CeO 2 at 1 and 5 days postinstillation. Significantly more cells with ingested silica-coated CeO 2 were seen at 5 days. Data are mean ± SEM, n = 3 rats/group, n = 3000 cells scored/group. * P < 0.05, Student t test CeO 2 after gavage. Our data showed a rapid clearance of both types of CeO 2 . We found that nearly 100 % of the uncoated CeO 2 and~95 % of silica-coated CeO 2 were eliminated in the feces within 7 days post-gavage. Despite the higher dose we used for gavage, there was negligible radioactivity in any organ or in urine samples collected over a period of 7 days. As has been demonstrated previously, neither CeO 2 NP type cross the intestinal barrier nor is there dissolution followed by absorption [15,32,61].

Fate of intravenously injected nanoceria
Due to increasing interest in CeO 2 for potential nanomedical applications, we also investigated whether silica coating would affect the tissue distributions of IV-injected CeO 2 . Consistent with our earlier study [62], both CeO 2 types were immediately taken up in organs rich in mononuclear phagocytes with direct access to the circulating blood, such as those in the liver (87 %), spleen (4 %), and bone (0.5 %). At 2 h, the total recovered 141 Ce in all organs examined were 92.6 % (uncoated) and 92.2 % (silica-coated CeO 2 ) of the total injected dose. Despite the significantly higher agglomerate size of uncoated nanoceria after interaction with plasma proteins, their liver uptake measured at 2 h was not different from silica-coated NPs. However, the silica coating enhanced the overall amount of cerium in some other organs. We found that binding of plasma proteins to the CeO 2 surface  Data are mean ± SE ng/g cerium concentration, n = 5/group Ce concentration was estimated (ng/μCi NPs x μCi/g tissue ) No significant difference was observed between the two group was altered by the silica coating. Notably, bound albumin and α-2 hs glycoprotein were higher in silica-coated CeO 2 .
A recent study showed that albumin-coated liposomes were taken up more efficiently than uncoated liposomes by murine macrophages [63]. The silica coating in our study also caused a significant reduction (6 %) in the liver retention of 141 Ce with concomitant increases in the spleen and bone two days post-exposure. This likely reflects either enhanced dissolution of Kupffer cell-ingested silica-coated CeO 2 or the release of intact NPs into the blood likely due to their smaller aggregate size (Table 1). Very small amounts of 141 Ce (3.8-5.8 %) were cleared from the body two days post-exposure, indicating that absorbed cerium is biopersistent, as reported in other studies [32,64].

Conclusions
In summary, we found that silica coating of CeO 2 caused a higher but transient lung inflammation and a higher lung clearance. It also altered the biodistribution of cerium when CeO 2 were injected intravenously. These effects correlated with enhanced adsorption of proteins in lung lining fluid and plasma onto the silica coating. As surface chemistry greatly influences the formation of the nanoparticle corona, our future studies will focus on understanding nano-bio interactions with lung and plasma lipoproteins and their influence on toxicity and biokinetics of NPs.

Synthesis of CeO 2 and silica-coated CeO 2 nanoparticles
Detailed procedures of generating these nanoparticles have been reported [21,28,33].

Animals
The protocols used in this study were approved by the Harvard Medical Area Animal Care and Use Committee. Male Wistar Han rats (8 weeks old) were obtained from Charles River Laboratories (Wilmington, MA) and were housed in standard microisolator cages under controlled conditions of temperature, humidity, and light at the Harvard Center for Comparative Medicine. They were fed commercial chow (PicoLab Rodent Diet 5053, Framingham, MA) and were provided with reverse-osmosis purified water ad libitum. The animals were acclimatized in the facility for at least 7 days before the start of experiments.

Preparation of CeO 2 nanoparticle suspensions for animal dosing
Particle suspensions at specified concentrations were prepared in sterile distilled water in conical polyethylene tubes. A critical dispersion sonication energy (DSE cr ) to achieve the smallest particle agglomerate size was used, as previously reported [16]. The suspensions were sonicated at 242 J/ml (20 min/ml at 0.2 watt power output) in a cup sonicator fitted on Sonifier S-450A (Branson Ultrasonics, Danbury, CT, USA). The sample tubes were immersed in running cold water to minimize heating of the particles during sonication. The hydrodynamic diameter (D H ), polydispersity index (PdI), and zeta potential (ζ) of each suspension were measured by dynamic light scattering using a Zetasizer Nano-ZS (Malvern Instruments, Worcestershire, UK).

Assessment of pulmonary effects of CeO 2 nanoparticles -Bronchoalveolar lavage and analyses
This experiment was performed to determine the influence of an amorphous silica coating on CeO 2 pulmonary effects and also to identify a safe dose for pharmacokinetic studies on instilled materials. Thirty five rats (wt. = 267 ± 15 g) were instilled intratracheally with either uncoated or coated CeO 2 NP suspensions at 0.2, 1.0, and 5 mg/kg (n = 5 rats/ group). Another group of rats were instilled with an equivalent volume of distilled water and served as controls.
The particle suspensions were delivered to the lungs through the trachea, as described earlier [35]. Twenty-four hours later, rats were anesthetized and then euthanized via exsanguination, with a cut in the abdominal aorta. The trachea was exposed and cannulated. The lungs were then lavaged 12 times with 3 mL of Ca ++ -and Mg ++ -free 0.9 % sterile PBS. The cells from all washes were separated from the supernatant by centrifugation (350 x g at 4°C for 10 min). Total cell count and hemoglobin measurements were made from the cell pellets. A dilute cell suspension was cytocentrifuged, the cytospin was stained, and differential cell counting was performed. The supernatant from the first two washes was clarified via centrifugation (14,500 x g at 4°C for 30 min), and used for standard spectrophotometric assays for LDH, MPO, and albumin [65].

Pharmacokinetics of intratracheally-instilled, gavaged and intravenously injected 141 CeO 2 nanoparticles
The nanoparticle dose used for both NPs was 1 mg/kg for IT instillation, 1 mg/kg for IV injection, and 5 mg/kg for gavage administration. Neutron-activated 141 CeO 2 NPs were suspended in sterile distilled water at 0.67 mg/ ml for IT instillation (1.5 ml/kg body weight) at 1 mg/ml for IV injection (1 ml/kg) or at 5 mg/ml for gavage administration (1 ml/kg) and sonicated as described above. The radioactivity in multiple aliquots of each suspension was measured in a WIZARD Gamma Counter (Perkin-Elmer, Inc., Waltham, MA). Each rat was anesthetized with isoflurane (Piramal Healthcare, Bethlehem, PA). The 141 CeO 2 NP suspension was delivered to the lungs through the trachea, into the bloodstream via the penile vein, or into the stomach via the esophagus. Each rat was then placed in a metabolic cage with food and water ad libitum for fecal and urine sample collection. Five rats from the IT group were humanely sacrificed at 5 m, 2 d, 7 d and 28 d post-dosing. The same number of rats were analyzed at 5 m and 7 d post-gavage, and at 2 h and 2 d post-IV injection. Analysis of rats at 5 min post-IT instillation and post-gavage was performed to obtain an accurate measure of the initial deposited dose. Since we anticipated that clearance from the gastrointestinal tract would be relatively fast, the gavage experiment spanned only 7 days. Twenty four-hour samples of feces and urine were collected at selected time points (0-24 h, 2-3 days, 6-7 days, 9-10 days, 13-14 days, 20-21 days, and 27-28 days post-IT instillation; 0-24 h, 2-3 days, and 6-7 days post-gavage; and 0-24 h post-IV injection).
At each endpoint, rats were anesthetized and as much blood as possible was collected from the abdominal aorta. Plasma and red blood cells were separated by centrifugation at 3000 x g for 10 min at 4°C. After euthanasia, the whole lungs, brain, heart, spleen, kidney, gastrointestinal tract, testes, liver, two femoral bones, and multiple samples of skeletal muscle, bone marrow, and skin were collected and placed in pre-weighed tubes. Each sample weight was recorded. Radioactivity was measured in a WIZARD Gamma Counter (PerkinElmer, Inc., Waltham, MA). Disintegrations per minute were calculated from the measured counts per minute (minus background) and the counter efficiency. Data were expressed as μCi/g and as a percentage of the administered dose retained in each organ. All radioactivity data were adjusted for physical decay over the entire observation period. The radioactivity in organs and tissues not measured in their entirety was estimated from measured aliquots as a percentage of total body weight as follows: skeletal muscle, 40 %; bone marrow, 3.2 %; peripheral blood, 7 %; skin, 19 %; and bone, 6 % [66,67].

Pulmonary distribution of 141 CeO 2 nanoparticles
To determine the pulmonary distribution of instilled 141 CeO 2 NPs within the lungs at 1 d post-instillation, a separate cohort of rats were IT-instilled with 1 mg/kg of either 141 CeO 2 or silica-coated 141 CeO 2 . Twenty-four hours later, the lungs were lavaged as described above. The BAL fluid was centrifuged at 350 x g for 10 min at 4°C to separate lavaged cells from the supernatant. The cell pellets were resuspended in 0.5 ml PBS. The lavaged lungs, BAL supernatants and cell pellets were analyzed for 141 Ce. The total radioactivity in each of the three lung compartments was expressed as a percentage of the total radioactivity recovered in the whole lungs.
Characterization of protein corona formation on CeO 2 and silica-coated CeO 2 nanoparticles in lung lining fluid and plasma Nanoparticles (1 mg/mL) were incubated in 4 mL rat plasma for 30 min at 37°C. Then, the suspension was centrifuged for 10 min at 14,500 x g. The resulting pellet was washed in DI water three times. After the final washing step, the NP pellet containing 'hard corona' was suspended in 20 μL of DI water to which 10 μL of 4x Laemmli sample buffer was added and vortexed. The sample was then heated to 95°C for 7 min. After cooling to room temperature, 60 μL of mixed solution (57 μL Laemmli and 3 μL βME) was added to 18 μL of the sample. The samples were then loaded onto a gel and proteins were visualized by 1D SDS-PAGE in combination with Coomassie staining. Gel bands were excised and subjected to a modified in-gel trypsin digestion procedure [68]. Peptides were later extracted and then dried in a speed-vac (~1 h). The samples were then stored at 4°C until analysis. On the day of analysis, the samples were reconstituted in 5-10 μL of HPLC solvent A (2.5 % acetonitrile, 0.1 % formic acid). A gradient was formed and peptides were eluted with increasing concentrations of solvent B (97.5 % acetonitrile, 0.1 % formic acid) [69]. Eluted peptides were subjected to electrospray ionization and then analyzed in an LTQ Orbitrap Velos Pro ion-trap mass spectrometer (Thermo Fisher Scientific, San Jose, CA). Peptides were detected, isolated, and fragmented to produce a tandem mass spectrum of specific fragment ions for each peptide. Peptide sequences (and protein identity) were determined by matching protein databases with the acquired fragmentation pattern by the software program, Sequest (ThermoFisher, San Jose, CA).

Assessment of alveolar macrophage uptake of nanoceria in vivo
Non-radioactive CeO 2 and silica-coated CeO 2 NPs were instilled in a separate cohort of rats at the same dose and concentration (1 mg/kg, 0.67 mg/ml). At 1 or 5 days post-instillation, rats were sacrificed and their lungs lavaged as described above. BAL cells were cytocentrifuged and fixed on microscope slides. Uptake of nanoceria by cells was analyzed in an Olympus BX-41 microscope (CytoViva®, Auburn, AL) hyperspectral image analysis software. Each macrophage was scored for the presence of internalized NPs.

Statistical analyses
Data were analyzed using multivariate analysis of variance (MANOVA) followed by Bonferroni (Dunn) post hoc tests using SAS Statistical Analysis Software (SAS Institute, Cary, NC). CytoViva data were analyzed by Student t test.