Acute toxicological effects of copper nanoparticles in vivo

被引:674
作者
Chen, Z
Meng, HA
Xing, GM
Chen, CY
Zhao, YL
Jia, GA
Wang, TC
Yuan, H
Ye, C
Zhao, F
Chai, ZF
Zhu, CF
Fang, XH
Ma, BC
Wan, LJ
机构
[1] Chinese Acad Sci, Lab Bioenvironm Hlth Sci Nanoscale Mat, Beijing 100049, Peoples R China
[2] Peking Univ, Sch Publ Hlth, Dept Occupat & Environm Hlth Sci, Beijing 100083, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100080, Peoples R China
[4] Peking Univ, Hosp 3, Sch Publ Hlth, Dept Clin Lab, Beijing 100083, Peoples R China
[5] Chinese Acad Sci, Grad Sch, Beijing 100864, Peoples R China
基金
中国国家自然科学基金;
关键词
nanotoxicity; LD50; target organs; copper nanoparticles; in vivo;
D O I
10.1016/j.toxlet.2005.10.003
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
To assess the toxicity of copper nanoparticles (23.5 nm) in vivo, LD50, morphological changes, pathological examinations and blood biochemical indexes of experimental mice are studied comparatively with micro-copper particles (17 mu m) and cupric ions (CuCl2 center dot 2H(2)O). The LD50 for the nano-, micro-copper particles and cupric ions exposed to mice via oral gavage are 413, > 5000 and 110 mg/kg body weight, respectively. The toxicity classes of nano and ionic copper particles both are class 3 (moderately toxic), and micro-copper is class 5 (practically non-toxic) of Hodge and Sterner Scale. Kidney, liver and spleen are found to be target organs of nano-copper particles. Nanoparticles induce gravely toxicological effects and heavy injuries on kidney. liver and spleen of experimental mice, but micro-copper particles do not, on mass basis. Results indicate a gender dependent feature of nanotoxicity. Several factors such as huge specific Surface area, ultrahigh reactivity, exceeding consumption of H+, etc. that likely cause the grave nanotoxicity observed in vivo are discussed. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:109 / 120
页数:12
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