Acute toxicity and pharmacokinetics of 13 nm-sized PEG-coated gold nanoparticles

被引:502
|
作者
Cho, Wan-Seob [2 ]
Cho, Minjung [2 ]
Jeong, Jinyoung [1 ]
Choi, Mina [2 ]
Cho, Hea-Young [3 ]
Han, Beom Seok [2 ]
Kim, Sheen Hee [2 ]
Kim, Hyoung Ook [2 ]
Lim, Yong Taik [1 ]
Chung, Bong Hyun [1 ]
Jeong, Jayoung [2 ]
机构
[1] Korea Univ Sci & Technol, Korea Res Inst Biosci & Biotechnol, Sch Engn, Nanobiotechnol Bionanotechnol Res Ctr, Taejon 305806, South Korea
[2] Korea Food & Drug Adm, Natl Inst Toxicol Res, Dept Toxicol Res, Div Toxicol Pathol, Seoul 122704, South Korea
[3] Korea Food & Drug Adm, Natl Inst Toxicol Res, Dept Pharmacol Res, Div Safety Pharmacol, Seoul 122704, South Korea
关键词
Gold nanoparticles; Pharmacokinetics; Intravenous injection; Inflammation; Accumulation;
D O I
10.1016/j.taap.2008.12.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In general, gold nanoparticles are recognized as being as nontoxic. Still, there have been some reports on their toxicity, which has been shown to depend on the physical dimension, surface chemistry, and shape of the nanoparticles. in this study, we carry out an in vivo toxicity study using 13 nm-sized gold nanoparticles coated with PEG (MW 5000). In our findings the 13 nm sized PEG-coated gold nanoparticles were seen to induce acute inflammation and apoptosis in the liver. These nanoparticles were found to accumulate in the liver and spleen for up to 7 days after injection and to have long blood circulation times. In addition, transmission electron microscopy showed that numerous cytoplasmic vesicles and lysosomes of liver Kupffer cells and spleen macrophages contained the PEG-coated gold nanoparticles. These findings of toxicity and kinetics of PEG-coated gold nanoparticles may have important clinical implications regarding the safety issue as PEG-coated gold nanoparticles are widely used in biomedical applications. (C) 2009 Elsevier Inc. All rights reserved
引用
收藏
页码:16 / 24
页数:9
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