Abstract
Background
Although the surface area metric has been proposed as a possible dose-metric for nanoparticles (NPs), it is limited to low-solubility NPs and the dose-metric for high-solubility NPs is poorly understood. In this study, we aimed to assess the appropriate dose-metric or response-metric for NPs using two cobalt (Co)-based NPs, cobalt monoxide (CoO) and cobalt oxide (Co3O4), which both show distinctive solubility, and determine the role of their soluble Co ions in inflammation.
Methods
We evaluated the physicochemical properties of NPs, including solubility in artificial lysosomal fluid (ALF, pH 5.5). Acute lung inflammogenicity was evaluated by bronchoalveolar lavage fluid analysis using the rat intratracheal instillation model. The appropriate response-metric was then determined by plotting several dose-metrics against parameters for lung inflammation. To investigate the effect of the soluble fraction of CoO NPs, the equivalent doses of Co ions from CoCl2 were instilled.
Results
The Co3O4 and CoO NPs showed about 11.46 % and 92.65 % solubility in ALF, respectively. Instillation of Co3O4 NPs produced neutrophilic inflammation, but CoO NPs induced eosinophilic inflammation. The number of eosinophils showed good correlation with the soluble Co ions dose from NPs (r2 = 0.987, p <0.001), while the number of neutrophils showed good correlation with the surface area dose of the biopersistent NPs (r2 = 0.876, p <0.001). Instillation of CoCl2 showed a similar type and magnitude of inflammation as CoO NPs.
Conclusions
In the Co-based NPs, the eosinophilic inflammation was produced by Co ions based on the ion metric, while the neutrophilic inflammation was developed based on the surface area metric of the biopersistent NPs.
Keywords: Dose-metric, High solubility nanoparticles, Ion metric, Co3O4, CoO, Intratracheal instillation
Background
The selection of an appropriate dose-metric for nanomaterials (NMs) is important for evaluating their toxicity and assessing their risk [1]. Mass, surface area (SA), and number are the possible candidates for dose-metrics for the particulate form of NMs, while the number of fibers of a specific length is an additional candidate for the dose-metric of high aspect ratio NMs (HARNs) [2, 3]. Most studies used lung inflammation models (generally by intratracheal instillation), because the lung is very sensitive to both acute and chronic inflammation and is essentially a closed chamber with very few fraction of the instilled NPs that translocate into the systemic circulation [4]. For example, instillation of gold NPs larger than 5 nm diameter showed less than 1 % extrapulmonary translocation [4]. In an intratracheal instillation model, the SA metric for low-solubility NPs has been proposed as a better metric than either mass or number [5–7]. Under a SA metric, the number of neutrophils of low-solubility low-toxicity NPs showed an overlapped dose–response curve, while intrinsic factors such as surface reactivity contribute to the slope of the curves for low-solubility high-toxicity NPs [5, 7].
Although NPs are rarely soluble in normal physiological environments such as in the interstitial fluid, some NPs such as zinc oxide (ZnO), copper oxide (CuO), and silver (Ag) have considerable solubility in acidic environments such as lysosomal and gastric fluid [8–10]. High-solubility NPs composed of toxic elements generally show higher toxicity than low-solubility NPs of the same compositional elements via the Trojan-horse type mechanism of toxicity [11]. In recent studies, high-solubility ZnO, CuO, and Ag NPs showed acute eosinophilic inflammation with increased cytotoxicity due to their solubilized compositional ions in the rat intratracheal instillation model, while medium-solubility nickel oxide (NiO) and cobalt oxide (Co3O4) NPs caused acute neutrophilic inflammation with immunological responses in the chronic phase, such as delayed type hypersensitivity [8, 12, 13]. Therefore, the evaluation of the differential effects of soluble fraction and biopersistent NPs, using NPs with the same compositional elements but different solubility, might provide important information on the role of solubility in NP toxicology.
Unlike low-solubility NPs, the dose-metric for high-solubility NPs is poorly understood. The first in evaluating the dose-metrics for high-solubility NPs could be the comparison of acute lung inflammogenicity using two NPs with the same compositional elements but different solubility. The next step would then be to compare the dose–response relationship between the high solubility NPs (e.g., Ag, CuO, and ZnO) by normalizing the observed values with the weighed toxicity value of the solubilized ions (e.g., AgCl2, CuCl2, and ZnCl2). In this study, we obtained two cobalt-based NPs, cobalt monoxide (CoO) and cobalt oxide (Co3O4), having a distinct difference in solubility in artificial lysosomal fluid. We then evaluated the role of soluble fraction and biopersistent NPs in acute lung inflammation, using an intratracheal instillation model, to investigate the appropriate response-metric for acute lung inflammation by cobalt-based NPs.
Results
Characterization of NPs
The physicochemical properties of NPs are presented in Table 1. The average size of Co3O4 and CoO NPs measured by transmission electron microscopy (TEM) were 20.2 and 65.4 nm, respectively. TEM images showed that both NPs were spherical without porous structure (Fig. 1). The hydrodynamic size of NPs showed that both NPs showed a “hard agglomerates” in both distilled water (DW) and phosphate-buffered saline (PBS). Co3O4 NPs were less agglomerated than CoO NPs when dispersed in DW, while both NPs showed similar size range about 450 nm when dispersed in PBS (Table 1). Polydispersity showed that Co3O4 NPs were more homogenous than CoO NPs. The zeta potentials of both NPs were positive in DW but negative in PBS, which may be due to the neutral pH of PBS. Incubation of Co3O4 and CoO NPs in artificial lysosomal fluid (ALF) showed 11.46 % and 92.65 % solubility, respectively. Solubility of NPs in PBS was minimal at 0.02 % and 4.12 % for Co3O4 and CoO NPs, respectively. Both NPs showed no endotoxin contamination.
Table 1.
Physicochemical characterization of nanoparticles
| Measure | Co3O4 | CoO |
|---|---|---|
| Primary size (nm) | 20.2 ± 0.4 | 65.4 ± 2.8 |
| Hydrodynamic size (nm) | ||
| in DW | 93.4 ± 1.8 | 380.3 ± 14.4 |
| in PBS | 468.9 ± 24.3 | 449.1 ± 8.9 |
| Polydispersity | ||
| in DW | 0.18 ± 0.03 | 0.72 ± 0.02 |
| in PBS | 0.26 ± 0.02 | 0.69 ± 0.05 |
| Surface area (m2/g) | 35.8 | 8.5 |
| Zeta potential (mV) | ||
| in DW | 39.53 ± 0.72 | 6.99 ± 1.18 |
| in PBS (pH 7.4) | −26.40 ± 0.90 | −21.80 ± 0.45 |
| Solubility (%) in ALF | 11.46 | 92.65 |
| Solubility (%) in PBS | 0.02 | 4.12 |
| Endotoxin | ND | ND |
Data were presented as mean ± SEM
ND, not detected
Fig. 1.
Transmission electron microscopy (TEM) image of (A) cobalt oxide (Co3O4) and (B) cobalt monoxide (CoO) nanoparticles (NPs). Both Co3O4 and CoO NPs showed spherical shape without porous structure
Cytological evaluation of lung inflammogenicity
Instillation of Co3O4 NPs at the high dose produced significant increases in the total number of cells (45.60 ± 7.71, × 105) and neutrophils (25.65 ± 4.80, ×105) compared to the vehicle control, but the number of macrophages, eosinophils, and lymphocytes were comparable to vehicle control (Table 2). Treatment of CoO NPs significantly increased the number of macrophages at the mid dose and eosinophils (3.37 ± 1.23, ×105) at the high dose (Table 2).
Table 2.
Summary of inflammatory cell counts, LDH, total protein, and inflammatory mediators at 24 h after intratracheal instillation of NPs
| BALF measure | VEHPBS | Co3O4 dose (μg/rat) | CoO dose (μg/rat) | ||||
|---|---|---|---|---|---|---|---|
| 40 | 100 | 400 | 40 | 100 | 400 | ||
| Total cells (× 105) | 10.95 ± 1.42 | 23.60 ± 3.64 | 20.48 ± 5.59 | 45.60 ± 7.71*** | 18.90 ± 2.40 | 30.53 ± 0.39 | 23.25 ± 4.10 |
| Macrophages (× 105) | 10.34 ± 1.19 | 23.21 ± 3.55 | 16.67 ± 4.63 | 19.82 ± 3.27 | 17.58 ± 1.81 | 24.46 ± 2.64* | 11.83 ± 3.03 |
| Neutrophils (× 105) | 0.49 ± 0.39 | 0.38 ± 0.10 | 3.79 ± 3.13 | 25.65 ± 4.80*** | 1.18 ± 1.06 | 4.91 ± 2.02 | 8.02 ± 1.85 |
| Eosinophils (× 105) | 0.07 ± 0.02 | 0.00 ± 0.00 | 0.01 ± 0.01 | 0.09 ± 0.05 | 0.10 ± 0.10 | 1.16 ± 0.76 | 3.37 ± 1.23** |
| Lymphocytes (× 105) | 0.05 ± 0.05 | 0.02 ± 0.02 | 0.00 ± 0.00 | 0.05 ± 0.05 | 0.03 ± 0.03 | 0.00 ± 0.00 | 0.04 ± 0.04 |
| LDH (fold vs control) | 1.00 ± 0.05 | 1.23 ± 0.10 | 1.62 ± 0.17 | 3.47 ± 0.15*** | 2.35 ± 0.08*** | 5.41 ± 0.22*** | 9.21 ± 0.30*** |
| Total protein (μg/mL) | 301 ± 5 | 118 ± 14 | 335 ± 116 | 253 ± 18 | 99 ± 5 | 1104 ± 77* | 3767 ± 667*** |
| CINC-3 (pg/mL) | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 | 110.4 ± 39.4** | 0.00 ± 0.00 | 27.3 ± 27.3 | 0.00 ± 0.00 |
| IL-6 (pg/mL) | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 | 123.4 ± 43.6 | 982.0 ± 349.4*** |
| Eotaxin (pg/mL) | 5.7 ± 1.2 | 4.5 ± 1.5 | 67.4 ± 57.4 | 22.5 ± 10.6 | 4.5 ± 1.8 | 265.7 ± 68.9 | 2963.9 ± 870.7*** |
| IL-13 (pg/mL) | 17.7 ± 1.9 | 22.6 ± 4.2 | 28.9 ± 4.5 | 16.9 ± 6.0 | 35.8 ± 4.9 | 49.0 ± 9.7 | 108.5 ± 15.6*** |
Data were presented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001, statistically different from vehicle control (VEHPBS)
VEHPBS, Ca2+-and Mg2+-free PBS was used as VEH for NPs; LDH, lactate dehydrogenase; CINC-3, cytokine-induced neutrophil chemoattractant-3
Lactate dehydrogenase (LDH) and total protein
The levels of LDH by Co3O4 NPs were significantly increased only at high dose (400 μg/rat). However, the levels of LDH in CoO NPs were significantly increased in all treatment groups in a dose-dependent manner (Table 2). The fold increase of LDH in CoO NPs (9.21 ± 0.30) at 400 μg/rat showed much higher level than Co3O4 NPs (3.47 ± 0.15) at the same dose (Table 2). The concentrations of total protein were significantly increased by the mid- and high-dose group of CoO NPs, while Co3O4 NPs showed no significant increases (Table 2).
Expression of pro-inflammatory cytokines in bronchoalveolar lavage fluid (BALF)
Among the 6 pro-inflammatory cytokines measured in BALF, treatment with Co3O4 NPs significantly increased cytokine-induced neutrophil chemoattractant-3 (CINC-3) levels only, while CoO NPs significantly increased the levels of interleukin-6 (IL-6), eotaxin, and IL-13 in a dose-dependent manner (Table 2). IL-1β and tumor necrosis factor-α (TNF-α) showed no significant changes in either treatment groups (data not shown).
Effects of dissolved Co ions on eosinophil recruitment by CoO NPs
To evaluate the effect of dissolved Co ions, we instilled cobalt chloride (CoCl2) dissolved in sterile saline into the lungs of rats at an equivalent Co ion dose for CoO NPs. Treatment of CoCl2 showed significant increases in the number of neutrophils and eosinophils, the levels of LDH and total protein, and the levels of IL-6 and eotaxin in BALF compared to the vehicle control (Table 3). Based on the equivalent dose of Co ions (31, 79, and 315 μg/rat), the data from CoCl2 produced similar dose–response curves compared to the CoO NPs in various inflammatory markers including the inflammatory cells, LDH, total protein, IL-6, and eotaxin (Fig. 2).
Table 3.
Summary of inflammatory cell counts, LDH, total protein, and inflammatory mediators at 24 h after intratracheal instillation of CoCl2
| BALF measure | VEHsaline | CoCl2 (μg/rat)a | ||
|---|---|---|---|---|
| 69 (31)b | 173 (79) | 693 (315) | ||
| Total cells (× 105) | 13.65 ± 2.63 | 24.68 ± 5.12 | 28.35 ± 3.96 | 18.30 ± 1.54 |
| Macrophages (× 105) | 11.84 ± 1.36 | 14.12 ± 1.81 | 13.66 ± 0.80 | 2.92 ± 0.746** |
| Neutrophils (× 105) | 1.76 ± 1.38 | 10.48 ± 3.72* | 13.74 ± 3.77** | 11.70 ± 2.75*** |
| Eosinophils (× 105) | 0.02 ± 0.02 | 0.06 ± 0.04 | 0.95 ± 0.56 | 3.63 ± 0.81** |
| Lymphocytes (× 105) | 0.05 ± 0.01 | 0.10 ± 0.04 | 0.04 ± 0.02 | 0.02 ± 0.02 |
| LDH (fold vs control) | 1.00 ± 0.12 | 3.08 ± 0.53* | 6.65 ± 0.78*** | 15.05 ± 0.18*** |
| Total protein (μg/mL) | 270 ± 47 | 341 ± 67 | 700 ± 165 | 5051 ± 917*** |
| CINC-3 (pg/mL) | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 |
| IL-6 (pg/mL) | 0.00 ± 0.00 | 0.00 ± 0.00 | 39.2 ± 39.2 | 734.6 ± 152.3*** |
| Eotaxin (pg/mL) | 10.76 ± 3.27 | 30.94 ± 16.60 | 133.1 ± 49.2 | 699.8 ± 38.1*** |
| IL-13 (pg/mL) | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.00 ± 0.00 |
aCo ions were prepared by dissolving CoCl2 in saline and treated at equivalent dose for Co of CoO NPs (40, 100, and 400 μg/rat)
bParenthesis represents the Co ions mass for CoCl2 which is equivalent Co ions doses of CoO NPs
Data were presented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001, statistically different from vehicle control (VEHsaline)
VEHsaline, sterile 0.9 % saline was used as a vehicle control for CoCl2; LDH, lactate dehydrogenase; CINC-3, cytokine-induced neutrophil chemoattractant-3
Fig. 2.
Comparison of inflammatory parameters for cobalt monoxide (CoO) nanoparticles (NPs) and cobalt chloride (CoCl2). Number of (A) total cells, (B) macrophages, (C) neutrophils, (D) eosinophils, and levels of (E) LDH, (F) total protein, (G) IL-6, and (H) eotaxin. Both treatment groups had same doses for cobalt ions (31, 79, and 315 μg/rat). Note that the inflammatory parameters of CoO NPs were similar with the CoCl2 which implies that the toxicity of CoO NPs was derived from their solubilized cobalt ions. Values are mean ± SEM (n = 4) for each treatment group. The data from CoO NPs were compared with the vehicle control (Ca2+- and Mg2+-free phosphate buffered saline) to determine statistical significance. * p < 0.05, ** p < 0.01, *** p < 0.001. The data from CoCl2 were compared with the vehicle control (0.9 % saline). $ p < 0.05, $$ p < 0.01, $$$ p < 0.001
Correlation between dose-metrics and inflammatory parameters
To evaluate the best-fit dose–response curve, various dose-metrics, including mass, SA, fraction of soluble Co ions, and SA of biopersistent NPs, were plotted against the acute lung inflammatory parameters produced by Co3O4 and CoO treatment. When the number of eosinophils from each NP was plotted against mass, SA, or SA of biopersistent NPs, each NP showed a separate dose–response curve, while the dose–response curves from two NPs overlapped when they were plotted against soluble Co ions (r2 = 0.987, p < 0.001) (Fig. 3A-D). When the number of neutrophils from each NP was plotted against various dose-metrics, only the SA dose of biopersistent NPs showed good correlation (r2 = 0.876, p < 0.001), while other dose-metrics showed separate curves (Fig. 3E-H). In line with the dose–response curves of eosinophils, the dose–response curves of LDH and total protein from NPs overlapped when they were plotted against the soluble Co ion dose, while other dose-metrics showed separate curves (Fig. 4).
Fig. 3.
Correlation between the inflammatory parameters of nanoparticles (NPs) and dose-metrics including soluble Co ions, mass, surface area (SA), and SA dose of biopersistent NPs. Correlation between the number of eosinophils and (A) Co ions, (B) mass dose of NPs, (C) SA dose of NPs, or (D) SA dose of biopersistent NPs. Correlation between the number of neutrophils and (E) Co ions, (F) mass dose of NPs, (G) SA dose of NPs, or (H) SA dose of biopersistent NPs. When the dose–response curves of cobalt oxide (Co3O4) and cobalt monoxide (CoO) NPs were significantly different, separate curves were drawn with either linear regression or non-linear regression, while when the dose–response curves of each NP overlapped, the combined curves were prepared with best-fit regression models and the Pearson correlation test was applied. Values are mean ± SEM (n = 4) for each treatment group
Fig. 4.
Correlation between the toxic parameters [the levels of lactate dehydrogenase (LDH) and total protein] of nanoparticles (NPs) and dose-metrics, including soluble cobalt (Co) ions, mass, surface area (SA), and SA dose of biopersistent NPs. Correlation between the levels of LDH and (A) Co ions, (B) mass dose of NPs, (C) SA dose of NPs, or (D) SA dose of biopersistent NPs. Correlation between the levels of total protein and (E) Co ions, (F) mass dose of NPs, (G) SA dose of NPs, or (H) SA dose of biopersistent NPs. When the dose–response curves of cobalt oxide (Co3O4) and cobalt monoxide (CoO) NPs were significantly different, separate curves were drawn with either linear regression or non-linear regression, while when the dose–response curves of each NP overlapped, the combined curves were prepared with best-fit regression models, and the Pearson correlation test was applied. Values are mean ± SEM (n = 4) for each treatment group
Discussion
Selection of an appropriate dose-metric for NMs is critical for the evaluation of toxicity and risk assessment. The dose-metric for NMs is intricately related to the factors that produce the response. Therefore, the dose-metric of NMs can be variable depending on the biologically effective dose (BED), which is the component of the total dose that produces adverse effects [2]. The BED is influenced not only by the intrinsic characteristics of NMs, including size, shape, soluble fraction, and biopersistence, but also by the extrinsic factors including route of exposure. Among them, the inhalation route is well studied, and SA and number of fibers with specific length were proposed as a proper dose-metric for NPs and fibers, respectively [2]. Although the SA metric has been proposed as a dose-metric for NPs, it is limited to low-solubility NPs such as titanium dioxide and carbon black [5, 6]. Based on the SA dose-metric, the slope of the dose–response curve of low-solubility NPs is dependent on the surface reactivity, such as zeta potential and reactive oxygen species generation potential [7, 8]. However, the dose-metric for high-solubility NPs was poorly understood, although the soluble fraction was known as one of the main factors that influence the BED [14, 15].
Most NPs are rarely soluble at normal physiological conditions, but solubility can be accelerated in acidic conditions, such as in the lysosomal fluid inside cells [16, 17]. Therefore, the significant solubility of NPs in ALF shown in this study is solely due to the chemical reaction. However, further study is needed for the development of a biopersistence assay using a cell-based model or in vivo condition because the biodegradation of NPs can also be accelerated by the enzyme-catalyzed reaction [18, 19]. The dissolution of NPs results in the loss of their surface reactivity, and thus the factors inducing toxicity may depend on the toxicity of their composition ions. Therefore, the SA metric cannot be applied to high-solubility NPs and another proper dose-metric should be considered. Moreover, because the toxicity of high-solubility NPs such as zinc oxide (ZnO) and copper oxide (CuO) were known to cause higher inflammogenicity and cytotoxicity in the acute phase with severe eosinophilic inflammation, a proper dose-metric is very important for risk assessment [20]. Here, we used Co3O4 and CoO, two types of cobalt-based NPs, which have similar types of soluble fractions but different solubility, to evaluate the dose-metric or response-metric for acute lung inflammogenicity.
The Occupational Safety and Health Administration (OSHA) regulated the 8-h permissible exposure limit (PEL) for cobalt metal, dust, and fumes as 0.1 mg/m3 [21]. The retained mass of 100 μg in the lung, the mid dose in this study, would be reached from 28 days (6 h/day) of nasal exposure to a 0.1 mg/m3 cloud of NPs with aerodynamic diameter of 50 nm (typical primary size of NPs used in this study) according to the Multiple-Path Particle Dosimetry (MPPD) deposition model [22]. In our previous study, we found that high solubility NPs can produce acute eosinophilic inflammation but the dose was critical for determining the type of inflammation [8]. Acute eosinophilic inflammation was also reported in the case of an accidental exposure of ZnO to human [23]. Although the bolus deliveries of NPs at a high dose which can be reached after a repeated inhalation scenario do not reflect physiological condition, the high dose used in this study (400 μg/rat) can be a realistic dose for occupational exposure.
In this study, medium-solubility Co3O4 NPs produced a dose-dependent neutrophilic influx, while high-solubility CoO NPs induced an eosinophilic influx into the lung 24 h after treatment. In our previous studies, intratracheal instillation of high-solubility NPs such as ZnO and CuO NPs produced an acute eosinophilia in the lung without any previous sensitization [16, 20, 24]. In this study, the inflammatory potentials of CoO NPs, evaluated by counting cells or measuring cytokines in the BALF, were comparable to ones evaluated after treatment with an identical Co ion mass of CoCl2, although there was some variation in the number of macrophages and the levels of LDH, IL-6, and eotaxin. Therefore, the eosinophilic inflammation produced by CoO NPs was originated from the dissolution of Co ions present inside lysosomes, which is the same mechanism of action as ZnO NPs [16, 25]. This eosinophilic inflammation was mediated by direct induction of eotaxin but the underlying mechanisms were poorly understood. One possible mechanism for non-IgE mediated allergic response is the activation of anaphylatoxins such as C3a and C5a which was reported in some liposomal NPs (e.g., Doxil) and micellar NPs (e.g., Taxol) [26]. However, that mechanism was not known for the acute eosinophilic inflammation by metal oxide NPs which warrants further investigation.
In previous studies, SA has been proposed as a dose-metric for low-solubility NPs in the acute pulmonary inflammation model [5, 27, 28]. For nanofibers, the number of fibers with a specific length has been proposed as one of the main factors contributing to lung inflammation [29–31]. However, the dose-metric for high-solubility NPs has not been reported yet. According to the results from this study, the ion dose-metric can be used for eosinophilic inflammation, cell death, and vascular permeability, because the number of eosinophils and levels of LDH or total protein produced by Co3O4 and CoO NPs had an overlapping dose–response curve when it was plotted against the dose of Co ions. In addition, the SA dose-metric of biopersistent NPs can be used for neutrophilic inflammation because the number of neutrophils produced by Co3O4 and CoO NPs showed a significant correlation when plotted against the SA of biopersistent NPs, while other dose-metrics showed distinctive graphs. These results also imply that the soluble fraction of NPs is the main contributor of eosinophilic inflammation, cell death, and vascular permeability, while the SA of biopersistent NPs is the main contributor of neutrophilic inflammation.
Conclusions
Instillation of two types of Co-based NPs produced different types of inflammation, neutrophilic or eosinophilic inflammation for Co3O4 and CoO NPs, respectively. The eosinophilic inflammation was produced by the dissolved Co ions inside of cells, and thus the appropriate dose-metric for eosinophil influx, cell death, and vascular permeability is the ion metric. On the other hand, neutrophilic inflammation was developed due to the role of biopersistent NPs, and the appropriate dose-metric for neutrophil influx should be the SA metric of biopersistent NPs.
Methods
NPs and physicochemical characterization
Co3O4 and CoO NPs were selected as cobalt-based NPs to evaluate both the role of solubility for NPs and dose-metric for high-solubility NPs. Both NPs were purchased from Nanostructured & Amorphous Materials Inc., (NanoAmor; Houston, TX, USA). The primary size of the NPs was measured by TEM (JEM-1200EX II, JEOL, Tokyo, Japan). The SA of Co3O4 NPs was measured by ParticlesCIC Ltd. (Leeds, UK) using a Micromeritics Tristar 3000 analyzer (Micromeritics Ltd., Bedfordshire, UK) and the SA of CoO NPs was measured by Center for Collaborative Instruments at Ulsan National Institute of Science and Technology (Ulsan, Korea) using a ASAP 2420 (Micromertics Ltd.). The average size was obtained by measuring at least 100 particles using a built-in image analyzer program (JEOL). The hydrodynamic size, polydispersity, and zeta potential of NPs in DW or PBS was measured using a Zetasizer-Nano ZS (Malvern, Malvern Hills, UK). The levels of endotoxin were measured in NPs dispersed in sterile PBS at 800 μg/mL, which is equivalent to 400 μg/rat, the highest dose for an animal study, using an endpoint chromogenic Limulus Amebocyte lysate (LAL) assay kit (Cambrex, Walkersville, MD, USA). The detection limit of the LAL kit was 0.1 EU/mL.
NP solubility test
Evaluation of solubility is essential to understand the role of soluble fractions in NP toxicity. The solubility is variable depending on their environment. Therefore, in our study we incubated NPs with either ALF (55 mM NaCl, 150 mM NaOH, 108 mM citric acid, 0.87 mM CaCl2, 0.67 mM Na2HPO4 · 7H2O, 0.27 mM Na2SO4, 0.52 mM MgCl2 · 6H2O, 0.64 mM glycerin, 0.26 mM sodium citrate dihydrate, 0.39 mM sodium tartrate dihydrate, 0.76 mM sodium lactate, 0.78 mM sodium pyruvate, 1 mL of formaldehyde, pH 5.5) [19] or PBS, pH 7.4 at 100 μg/mL for 24 h at room temperature. After incubation, NP-free supernatant was collected using three rounds of centrifugation at 15,000 g for 30 min. The concentration of soluble cobalt ions was measured by the Center for Collaborative Instruments at Dong-A University (Busan, Korea) using inductively coupled mass spectrometry (ICP-MS) (Hewlett-Packard 4500; Yokogawa, Japan). The fraction of solubilized cobalt ions was calculated and expressed as a percentage by dividing the mass of cobalt ions by the initial mass of cobalt in Co3O4 or CoO NPs.
Intratracheal instillation of NPs
The intratracheal instillation model was selected instead of an inhalation study because the former is an easy and reliable method to identify NP toxicity and compare responses to different particle types [32]. NP suspensions at 80, 200, and 800 μg/mL were prepared by dispersing NPs in sterile Ca2+- and Mg2+-free PBS (Life Technologies, Gaithersburg, MD, USA) and sonicated for 10 min using a bath sonicator (Saehan-Sonic, Seoul, Korea) to break up agglomerates. NP suspensions were prepared and sonicated immediately before use as recommend in a previous study [33]. Six-week-old specific-pathogen-free female rats were purchased from Samtako (Gyeonggi-do, Korea), maintained, and handled according to the policies approved by the Institutional Animal Care and Use Committee of Dong-A University. The instillation (n = 4 per group) was performed according to a previously described method [24]. NP suspensions were instilled at doses of 40, 100, and 400 μg/rat by instilling 0.5 mL of the suspensions.
Preparation of BALF
Twenty-four hour post-instillation, the rats were euthanized via an intraperitoneal injection of tiletamine-zolazepam (Zoletil®, 50 mg/kg) and xylazine (5 mg/kg). The trachea was cannulated with a blunt 14 gauge needle, and the lungs were lavaged in situ four times with cold sterile Ca2+- and Mg2+-free PBS (Life Technologies) at a volume of 8 mL. The first lavage was kept for analysis of LDH, total protein, and pro-inflammatory cytokines. Cell pellets from four lavages were pooled for cell counts. The total number of cells in the BALF was quantified by a nucleocounter (Chemometec, Allerod, Denmark), and 4 × 104 cells were attached to glass slides by cytospin at 27 g for 5 min. The cells were then fixed for 5 min with methanol and stained with Diff-Quik (Thermo Fisher Scientific, Waltham, MA, USA) for the differential cell count.
Analysis of BALF
To evaluate the inflammogenicity using cytological analysis, differential cell counts were performed by counting a minimum of 300 cells under a light microscope (Nikon, Tokyo, Japan). The levels of LDH, a marker for cytotoxicity, were measured in the BALF using an LDH assay kit (Roche Diagnostics, Mannheim, Germany). The concentrations of total protein, a maker for vascular permeability, were measured in the BALF using a bicinchoninic acid (BCA) assay kit (Thermo Fisher Scientific). To evaluate the role of pro-inflammatory cytokines in NP-induced inflammation, CINC-3, eotaxin, IL-1β, IL-6, IL-13, and TNF-α, all from the Duoset ELISA kit (R&D Systems, Minneapolis, MN, USA), were measured in the BALF according to the manufacturer’s protocol.
Instillation of Co ions into the lungs of rats
In our previous study, we found that the eosinophilic inflammation by ZnO NPs was attributed to its high solubility in lysosomal fluid [16]. Because CoO NPs showed a high solubility in ALF and significantly recruited eosinophils, CoCl2 was used to further investigate the role of the dissolved Co ions from CoO NPs. CoCl2 (Sigma-Aldrich, St. Louis, MO, USA) was solubilized in a sterile solution of 0.9 % saline, because Co ions can easily precipitate in a phosphate solution by forming cobalt phosphate, Co3(PO4)2, which is insoluble in DW. The concentrations of CoCl2 for instillation were 69, 173, and 693 μg/rat, which were the equivalent Co ion doses for 40, 100, and 400 μg/rat of CoO NPs, respectively. As a vehicle control, 500 μL of saline was instilled.
Evaluation of appropriate dose-metric
There are many metrics should be regarded for dose–response curves. To our knowledge, dose can be divided into treatment-related dose (mass, number, or SA) and particle-derived dose (surface charge, oxidative potential, solubility, or soluble toxins). In this study, we used Co3O4 and CoO, two types of cobalt-based NPs, which have similar types of soluble fractions but different solubility to evaluate the dose-metric or response metric for acute lung inflammation pattern. Regarding the treatment-related dose, number of particles was excluded because particle number is the worst to describe NP-induced pulmonary inflammatory effects [6]. Regarding the particle-derived dose, surface charge and oxidative potential was excluded not only because we focused on the solubility issue but also the surface charge or oxidative potential is a moving target for high solubility NPs. For this reason, we treated two-cobalt based NPs with a mass metric and converted to several possible dose metrics such as mass of NPs, SA of NPs, soluble fraction of Co ions, or SA of biopersistent NPs. The SA of biopersistent NPs was mathematically calculated by multiplying the ratio of dissolution by the SA of instilled NPs. The appropriate dose-metrics were then plotted against the parameters for lung inflammogenicity, including total cells, differential cell counts, LDH, total protein, and pro-inflammatory cytokines. When the dose–response curves of Co3O4 and CoO NPs were significantly different, separate curves were drawn with either linear regression or non-linear regression using GraphPad Prism Software (GraphPad Prism version 6 for Windows; GraphPad Software, Inc., San Diego, CA, USA). However, when the dose–response curve of each NP was overlapped, combined curves were prepared with best-fit regression models, and the Pearson correlation test was applied.
Statistical analysis
Data were expressed as mean ± SEM (n = 4). We analyzed statistical differences using one-way analysis of variance (ANOVA) followed by post-hoc Tukey’s pairwise comparisons using GraphPad Prism Software (GraphPad Prism version 6 for Windows). The value of p < 0.05 considered statistically significant.
Acknowledgments
This research was supported by the Korean Ministry of Food and Drug Safety (15182MFDS462) and the National Research Foundation of Korea (NRF-2013R1A1A1011330).
Footnotes
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
WSC provided key intellectual input in the concept and design of these studies, performed experiment. JJ and YH performed experiment and aided in the writing of this manuscript. CAP provided expertise for analysis of data and contributed to the writing of the manuscript. All authors read and approved the final manuscript.
Contributor Information
Jiyoung Jeong, Email: dudwlwjd@naver.com.
Youngju Han, Email: aren0416@naver.com.
Craig A. Poland, Email: Craig.Poland@iom-world.org
Wan-Seob Cho, Email: wcho@dau.ac.kr.
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