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Acute Pulmonary Toxicity and Body Distribution of Inhaled Metallic Silver Nanoparticles

机译:吸入金属纳米银的急性肺毒性和人体分布

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摘要

The purpose of this study was to determine the acute pulmonary toxicity of metallic silver nanoparticles (MSNPs, 20.30 nm in diameter). Acute pulmonary toxicity and body distribution of inhaled MSNPs in mice were evaluated using a nose-only exposure chamber (NOEC) system. Bronchoalveolar lavage (BAL) fluid analysis, Western blotting, histopathological changes, and silver burdens in various organs were determined in mice. Mice were exposed to MSNPs for 6 hrs. The mean concentration, total surface area, volume and mass concentrations in the NOEC were maintained at 1.93 × 107 particles/cm3, 1.09 × 1010 nm2/cm3, 2.72 × 1011 nm3/cm3, and 2854.62 μg/m3, respectively. Inhalation of MSPNs caused mild pulmonary toxicity with distribution of silver in various organs but the silver burdens decreased rapidly at 24-hrs post-exposure in the lung. Furthermore, inhaled MSNPs induced activation of mitogen-activated protein kinase (MAPK) signaling in the lung. In summary, single inhaled MSNPs caused mild pulmonary toxicity, which was associated with activated MAPK signaling. Taken together, our results suggest that the inhalation toxicity of MSNPs should be carefully considered at the molecular level.
机译:这项研究的目的是确定金属银纳米颗粒(直径为20.30 nm)的急性肺毒性。使用仅鼻暴露室(NOEC)系统评估了小鼠吸入的MSNP的急性肺毒性和身体分布。在小鼠中测定了支气管肺泡灌洗液(BAL),蛋白质印迹,组织病理学变化和各种器官中的银负荷。将小鼠暴露于MSNP 6小时。 NOEC中的平均浓度,总表面积,体积和质量浓度分别保持在1.93×10 7 颗粒/ cm 3 ,1.09×10 10 nm 2 / cm 3 ,2.72×10 11 nm 3 / cm 3 和2854.62μg/ m 3 。吸入MSPNs会引起轻度的肺毒性,并且银会分布在各个器官中,但在肺部暴露后24小时,银的负担会迅速降低。此外,吸入的MSNPs诱导了肺中促分裂原活化蛋白激酶(MAPK)信号的激活。总之,单次吸入MSNPs会引起轻度的肺毒性,这与活化的MAPK信号传导有关。综上所述,我们的结果表明,应在分子水平上仔细考虑MSNP的吸入毒性。

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