Size-dependent tissue kinetics of PEG-coated gold nanoparticles

被引:219
作者
Cho, Wan-Seob [6 ,7 ]
Cho, Minjung [6 ]
Jeong, Jinyoung [5 ]
Choi, Mina [6 ]
Han, Beom Seok [6 ]
Shin, Hyung-Seon [4 ]
Hong, Jin [1 ]
Chung, Bong Hyun [5 ]
Jeong, Jayoung [1 ]
Cho, Myung-Haing [2 ,3 ]
机构
[1] Korea Food & Drug Adm, Natl Inst Food & Drug Safety Evaluat, Nutr & Funct Food Res Team, Seoul 122704, South Korea
[2] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, Dept Nanofus Technol, Seoul 151742, South Korea
[3] Seoul Natl Univ, Coll Vet Med, Toxicol Lab, Seoul 151742, South Korea
[4] Korea Basic Sci Inst, Environm Tracer Team, Div Earth & Environm Sci, Taejon 305333, South Korea
[5] Korea Univ Sci & Technol, Korea Res Inst Biosci & Biotechnol, Sch Engn, Taejon 305806, South Korea
[6] Korea Food & Drug Adm, Natl Inst Food & Drug Safety Evaluat, Dept Toxicol Res, Seoul 122704, South Korea
[7] Univ Edinburgh, Queens Med Res Inst, Ctr Inflammat Res, ELEGI Colt Lab, Edinburgh EH16 4TJ, Midlothian, Scotland
关键词
Size-dependent kinetics; Metabolism; Gold nanoparticles; Mouse; DIESEL EXHAUST PARTICLES; IN-VIVO; MAGNETIC NANOPARTICLES; DRUG-DELIVERY; SURFACE-AREA; TOXICITY; MICE; BIODISTRIBUTION; ENZYMES; PHARMACOKINETICS;
D O I
10.1016/j.taap.2010.02.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gold nanoparticles (AuNPs) can be used in various biomedical applications, however, very little is known about their size-dependent in vivo kinetics. Here, we performed a kinetic study in mice with different sizes of PEG-coated AuNPs. Small AuNPs (4 or 13 nm) showed high levels in blood for 24 h and were cleared by 7 days, whereas large (100 nm) AuNPs were completely cleared by 24 h. All AuNPs in blood re-increased at 3 months, which correlated with organ levels. Levels of small AuNPs were peaked at 7 days in the liver and spleen and at 1 month in the mesenteric lymph node, and remained high until 6 months, with slow elimination. In contrast, large AuNPs were taken up rapidly (similar to 30 min) into the liver, spleen, and mesenteric lymph nodes with less elimination phase. TEM showed that AuNPs were entrapped in cytoplasmic vesicles and lysosomes of Kupffer cells and macrophages of spleen and mesenteric lymph node. Small AuNPs transiently activated CYP1A1 and 2B, phase I metabolic enzymes, in liver tissues from 24 h to 7 days, which mirrored with elevated gold levels in the liver. Large AuNPs did not affect the metabolic enzymes. Thus, propensity to accumulate in the reticuloendothelial organs and activation of phase I metabolic enzymes, suggest that extensive further studies are needed for practical in vivo applications. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:116 / 123
页数:8
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