Biodistribution, pharmacokinetics and toxicology of Ag2S near-infrared quantum dots in mice

被引:220
|
作者
Zhang, Yan [1 ,2 ]
Zhang, Yejun [1 ,2 ]
Hong, Guosong [3 ]
He, Wei [1 ,2 ]
Zhou, Kun [1 ,2 ]
Yang, Kai [4 ]
Li, Feng [1 ,2 ]
Chen, Guangcun [1 ,2 ]
Liu, Zhuang [4 ]
Dai, Hongjie [3 ]
Wang, Qiangbin [1 ,2 ]
机构
[1] Chinese Acad Sci, Div Nanobiomed, Suzhou 215123, Peoples R China
[2] Chinese Acad Sci, ILab, Suzhou Inst Nanotech & Nanobion, Suzhou 215123, Peoples R China
[3] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[4] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Peoples R China
关键词
Ag2S quantum dots; Biocompatibility; Pharmacokinetics; Biodistribution; Toxicology; WALLED CARBON NANOTUBES; BILIARY-EXCRETION; FLUORESCENCE; AGENTS; CELLS;
D O I
10.1016/j.biomaterials.2013.01.089
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Ag2S quantum dots (QDs) have been demonstrated as a promising near-infrared II (NIR-II, 1.0-1.4 mu m) emitting nanoprobe for in vivo imaging and detection. In this work, we carefully study the long-term in vivo biodistribution of Ag2S QDs functionalized with polyethylene glycol (PEG) and systematically examine the potential toxicity of Ag2S QDs over time. Our results show that PEGylated-Ag2S QDs are mainly accumulated in the reticuloendothelial system (RES) including liver and spleen after intravenous administration and can be gradually cleared, mostly by fecal excretion. PEGylated-Ag2S QDs do not cause appreciable toxicity at our tested doses (15 and 30 mg/kg) to the treated mice over a period of 2 months as evidenced by blood biochemistry, hematological analysis and histological examinations. Our work lays a solid foundation for further biomedical applications of Ag2S QDs as an important in vivo imaging agent in the NIR-II region. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3639 / 3646
页数:8
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