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Subchronic Inhalation Toxicity of Silver Nanoparticles

Authors
Sung, Jae HyuckJi, Jun HoPark, Jung DuckYoon, Jin UkKim, Dae SungJeon, Ki SooSong, Moon YongJeong, JayoungHan, Beom SeokHan, Jeong HeeChung, Yong HyunChang, Hee KyungLee, Ji HyunCho, Myung HaingKelman, Bruce J.Yu, Il Je
Issue Date
Apr-2009
Publisher
OXFORD UNIV PRESS
Keywords
lung; nanoparticles
Citation
TOXICOLOGICAL SCIENCES, v.108, no.2, pp 452 - 461
Pages
10
Journal Title
TOXICOLOGICAL SCIENCES
Volume
108
Number
2
Start Page
452
End Page
461
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/23231
DOI
10.1093/toxsci/kfn246
ISSN
1096-6080
1096-0929
Abstract
The subchronic inhalation toxicity of silver nanoparticles was studied in Sprague-Dawley rats. Eight-week- old rats, weighing approximately 253.2 g (males) and 162.6 g (females), were divided into four groups (10 rats in each group): fresh-air control, low dose (0.6 x 10(6) particle/cm(3), 49 mu g/m(3)), middle dose (1.4 x 10(6) particle/cm(3), 133 mu g/m(3)), and high dose (3.0 x 10(6) particle/cm(3), 515 mu g/m(3)). The animals were exposed to silver nanoparticles (average diameter 18-19 nm) for 6 h/day, 5 days/week, for 13 weeks in a whole-body inhalation chamber. In addition to mortality and clinical observations, body weight, food consumption, and pulmonary function tests were recorded weekly. At the end of the study, the rats were subjected to a full necropsy, blood samples were collected for hematology and clinical chemistry tests, and the organ weights were measured. Bile-duct hyperplasia in the liver increased dose dependently in both the male and female rats. Histopathological examinations indicated dose-dependent increases in lesions related to silver nanoparticle exposure, including mixed inflammatory cell infiltrate, chronic alveolar inflammation, and small granulomatous lesions. Target organs for silver nanoparticles were considered to be the lungs and liver in the male and female rats. No observable adverse effect level of 100 mu g/m(3) is suggested from the experiments.
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