Cytotoxicity of single-wall carbon nanotubes on human fibroblasts

被引:312
作者
Tian, Furong
Cui, Daxiang
Schwarz, Heinz
Estrada, Giovani Gomez
Kobayashi, Hisatashi
机构
[1] Max Planck Inst Met Res, D-70569 Stuttgart, Germany
[2] Max Planck Inst Dev Biol, D-72076 Tubingen, Germany
[3] Natl Inst Mat Sci, Tsukuba, Ibaraki 3050044, Japan
关键词
cytotoxicity; carbon nanotubes; fibroblasts;
D O I
10.1016/j.tiv.2006.03.008
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
We present a toxicological assessment of five carbon nanomaterials on human fibroblast cells in vitro. We correlate the physico-chemical characteristics of these nanomaterials to their toxic effect per se, i.e. excluding catalytic transition metals. Cell survival and attachment assays were evaluated with different concentrations of refined: (i) single-wall carbon nanotubes (SWCNTs), (ii) active carbon, (iii) carbon black, (iv) multi-wall carbon nanotubes, and (v) carbon graphite. The refined nanomaterial that introduced the strongest toxic effect was subsequently compared to its unrefined version. We therefore covered a wide range of variables, such as: physical dimensions, surface areas, dosages, aspect ratios and surface chemistry. Our results are twofold. Firstly, we found that surface area is the variable that best predicts the potential toxicity of these refined carbon nanomaterials, in which SWCNTs induced the strongest cellular apoptosis/necrosis. Secondly, we found that refined SWCNTs are more toxic than its unrefined counterpart. For comparable small surface areas, dispersed carbon nanomaterials due to a change in surface chemistry, are seen to pose morphological changes and cell detachment, and thereupon apoptosis/necrosis. Finally, we propose a mechanism of action that elucidates the higher toxicity of dispersed, hydrophobic nanomaterials of small surface area. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1202 / 1212
页数:11
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