Long-term accumulation and low toxicity of single-walled carbon nanotubes in intravenously exposed mice

被引:322
作者
Yang, Sheng-Tao [1 ]
Wang, Xiang [2 ]
Jia, Guang [2 ]
Gu, Yiqun [3 ]
Wang, Tiancheng [4 ]
Nie, Haiyu [1 ]
Ge, Cuicui [5 ,6 ]
Wang, Haifang [1 ]
Liu, Yuanfang [1 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Dept Biol Chem, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
[2] Peking Univ, Sch Publ Hlth, Dept Occupat & Environm Hlth Sci, Beijing 100083, Peoples R China
[3] Matern Hosp Haidian Dist, Beijing 100080, Peoples R China
[4] Peking Univ, Third Hosp, Dept Clin Lab, Beijing 100083, Peoples R China
[5] Chinese Acad Sci, Inst High Energy Phys, Lab Bioenvironm Hlth Sci Nanoscale Mat & Nanosafe, Beijing 100049, Peoples R China
[6] Chinese Acad Sci, Inst High Energy Phys, Key Lab Nucl Analyt Tech, Beijing 100049, Peoples R China
关键词
Carbon nanotubes; Intravenous administration; Accumulation; Toxicity; Oxidative stress;
D O I
10.1016/j.toxlet.2008.07.020
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The biomedical application of single-walled carbon nanotubes (SWCNTs), such as drug delivery and cancer treatment, requires a clear understanding of their fate and toxicological profile after intravenous administration. In this study, the long-term accumulation and toxicity of intravenously injected SWCNTs in the main Organs (such as liver, lung and spleen) in mice were carefully studied. Although SWCNTs stayed in mice over 3 months, they showed low toxicity to mice. The long-term accumulation of SWCNTs in the main organs was evidenced by using Raman spectroscopy and TEM technique. Statistically significant changes in organ indices and serum biochemical parameters (LDH, ALT and AST) were observed. The histological observations demonstrate that slight inflammation and inflammatory cell infiltration occurred in lung, but the serum immunological indicators (CH 50 level and TNF-alpha level) remained unchanged. No apoptosis was induced in the main organs. The decreasing glutathione (GSH) level and increasing malondialdehyde (MDA) level suggest that the toxicity of SWCNTs might be due to the oxidative stress. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:182 / 189
页数:8
相关论文
共 34 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   An in vitro study of the potential of carbon nanotubes and nanofibres to induce inflammatory mediators and frustrated phagocytosis [J].
Brown, D. M. ;
Kinloch, I. A. ;
Bangert, U. ;
Windle, A. H. ;
Walter, D. M. ;
Walker, G. S. ;
Scotchford, C. A. ;
Donaldson, K. ;
Stone, V. .
CARBON, 2007, 45 (09) :1743-1756
[3]   Effect of single wall carbon nanotubes on human HEK293 cells [J].
Cui, DX ;
Tian, FR ;
Ozkan, CS ;
Wang, M ;
Gao, HJ .
TOXICOLOGY LETTERS, 2005, 155 (01) :73-85
[4]   THIOBARBITURIC ACID REACTION AND AUTOXIDATIONS OF POLYUNSATURATED FATTY ACID METHYL ESTERS [J].
DAHLE, LK ;
HILL, EG ;
HOLMAN, RT .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1962, 98 (02) :253-&
[5]   Translocation and fate of multi-walled carbon nanotubes in vivo [J].
Deng, X. ;
Jia, G. ;
Wang, H. ;
Sun, H. ;
Wang, X. ;
Yang, S. ;
Wang, T. ;
Liu, Y. .
CARBON, 2007, 45 (07) :1419-1424
[6]  
Endo M, 2008, TOP APPL PHYS, V111, P13, DOI 10.1007/978-3-540-72865-8_2
[7]   Carbon nanotube-enhanced thermal destruction of cancer cells in a noninvasive radiofrequency field [J].
Gannon, Christopher J. ;
Cherukuri, Paul ;
Yakobson, Boris I. ;
Cognet, Laurent ;
Kanzius, John S. ;
Kittrell, Carter ;
Weisman, R. Bruce ;
Pasquali, Matteo ;
Schmidt, Howard K. ;
Smalley, Richard E. ;
Curley, Steven A. .
CANCER, 2007, 110 (12) :2654-2665
[8]   Iron bioavailability and redox activity in diverse carbon nanotube samples [J].
Guo, Lin ;
Morris, Daniel G. ;
Liu, Xinyuan ;
Vaslet, Charles ;
Hurt, Robert H. ;
Kane, Agnes B. .
CHEMISTRY OF MATERIALS, 2007, 19 (14) :3472-3478
[9]   Cytotoxicity of carbon nanomaterials: Single-wall nanotube, multi-wall nanotube, and fullerene [J].
Jia, G ;
Wang, HF ;
Yan, L ;
Wang, X ;
Pei, RJ ;
Yan, T ;
Zhao, YL ;
Guo, XB .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (05) :1378-1383
[10]   BROMOBENZENE-INDUCED LIVER NECROSIS - PROTECTIVE ROLE OF GLUTATHIONE AND EVIDENCE FOR 3,4-BROMOBENZENE OXIDE AS HEPATOTOXIC METABOLITE [J].
JOLLOW, DJ ;
MITCHELL, JR ;
ZAMPAGLIONE, N ;
GILLETTE, JR .
PHARMACOLOGY, 1974, 11 (03) :151-169