Single and repeated dose toxicity of mesoporous hollow silica nanoparticles in intravenously exposed mice

被引:311
作者
Liu, Tianlong [1 ]
Li, Linlin [1 ]
Teng, Xu [2 ]
Huang, Xinglu [1 ]
Liu, Huiyu [1 ]
Chen, Dong [1 ]
Ren, Jun [1 ]
He, Junqi [2 ]
Tang, Fangqiong [1 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Lab Controllable Preparat & Applicat Nanomat, Beijing 100190, Peoples R China
[2] Capital Med Univ, Sch Basic Med Sci, Dept Biochem & Mol, Beijing 100069, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesoporous hollow silica; Biocompatibility; Biodistribution; Clearance; Repeated dose toxicity; INHALATION TOXICITY; DRUG-DELIVERY; RELEASE; BIOCOMPATIBILITY; NANOTOXICOLOGY; ENDOCYTOSIS; SPHERES; SYSTEM; RATS;
D O I
10.1016/j.biomaterials.2010.10.035
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Mesoporous hollow silica nanoparticles (MHSNs) are emerging as one of the new and promising nanomaterials for biomedical applications, but the biocompatibility of MHSNs in vivo has received little attention. In the present study, the systematic single and repeated dose toxicity, biodistribution and clearance of MHSNs in vivo were demonstrated after intravenous injection in mice. For single dose toxicity, lethal dose 50 (LD50) of 110 nm MHSNs was higher than 1000 mg/kg. Further repeated dose toxicity studies indicated no death was observed when mice were exposed to MHSNs at 20, 40 and 80 mg/kg by continuous intravenous administration for 14 days. These results suggest low toxicity of MHSNs when intravenous injection at single dose or repeated administrations. ICP-OES and TEM results show that the MHSNs mainly accumulate in mononuclear phagocytic cells in liver and spleen. In addition, these particles could be excreted from the body and the entire clearance time of the particles should be over 4 weeks. These findings would be useful for future development of nanotechnology-based drug delivery system and other biomedical applications. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1657 / 1668
页数:12
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