Biodistribution and toxicity of intravenously administered silica nanoparticles in mice

被引:261
作者
Xie, Guangping [1 ]
Sun, Jiao [1 ]
Zhong, Gaoren [2 ]
Shi, Liyi [3 ]
Zhang, Dawei [3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 9, Shanghai Biomat Res & Testing Ctr, Shanghai 200030, Peoples R China
[2] Fudan Univ, Sch Pharm, Shanghai 200433, Peoples R China
[3] Shanghai Univ, Nanosci & Technol Res Ctr, Shanghai, Peoples R China
关键词
Tissue distribution; Nanotoxicity; Silica nanoparticles; Quantitative; Endocytosis; GENE DELIVERY; SURFACE MODIFICATION; GOLD NANOPARTICLES; DRUG; SIZE; NANOTECHNOLOGY; AGGREGATION; ENDOCYTOSIS; PARTICLES; CARRIERS;
D O I
10.1007/s00204-009-0488-x
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
As the biosafety of nanotechnology becomes a growing concern, the in vivo nanotoxicity of NPs has drawn a lot of attention. Silica nanoparticles (SiNPs) have been widely developed for biomedical use, but their biodistribution and toxicology have not been investigated extensively in vivo. Although investigations of in vivo qualitative distribution of SiNPs have been reported, the time-dependent and quantitative informations about the distribution of SiNPs are still lacking. Here we investigated the long-term (30 days) quantitative tissue distribution, and subcellular distribution, as well as potential toxicity of two sizes of intravenously administered SiNPs in mice using radiolabeling, radioactive counting, transmission electron microscopy and histological analysis. The results indicated that SiNPs accumulate mainly in lungs, liver and spleen and are retained for over 30 days in the tissues because of the endocytosis by macrophages, and could potentially cause liver injury when intravenously injected.
引用
收藏
页码:183 / 190
页数:8
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