A new approach to the toxicity testing of carbon-based nanomaterials - The clonogenic assay

被引:178
作者
Herzog, Eva
Casey, Alan
Lyng, Fiona M.
Chambers, Gordon
Byrne, Hugh J.
Davoren, Maria
机构
[1] Dublin Inst Technol, Focas Inst, Radiat & Environm Sci Ctr, Dublin 8, Ireland
[2] Dublin Inst Technol, Focas Inst, Phys Mol Mat Grp, Dublin 8, Ireland
关键词
single-walled carbon nanotubes; carbon black; cytotoxicity; colony size; pulmonary toxicity; dermal toxicity;
D O I
10.1016/j.toxlet.2007.08.009
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The cellular toxicity of three types of carbon nanoparticles, namely HiPco (R) single-walled carbon nanotubes (SWCNT), arc discharge SWCNT and Printex 90 carbon black nanoparticles, was studied on three different cell models including the human alveolar carcinoma epithelial cell line (A549), the normal human bronchial epithelial cell line (BEAS-2B) and the human keratinocyte cell line (HaCaT) using the clonogenic assay. Carbon nanomaterials are known to interact with colorimetric indicator dyes frequently used in cytotoxicity assays. By employing the clonogenic assay, any such interactions could be avoided, allowing a more reliable method for the in vitro toxicity assessment of carbon-based nanoparticles. It could be shown that the toxicity of as produced SWCNT samples differs between cell lines and the SWCNT production method used, with HiPco SWCNT samples being more reactive compared to arc discharge produced SWCNT samples, both eliciting a stronger cytotoxic response than carbon black. Furthermore, it was possible to distinguish between effects on cell viability and cell proliferation by including colony size as an additional endpoint in the clonogenic assay. All three particle types were highly effective in inhibiting cell proliferation in all three cell lines, whereas only HaCaT and BEAS-2B cells also showed decreased cell viability. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:49 / 60
页数:12
相关论文
共 52 条
[1]   Applications of carbon nanotubes in drug delivery [J].
Bianco, A ;
Kostarelos, K ;
Prato, M .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2005, 9 (06) :674-679
[2]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[3]   Opinion - The role of apoptosis in cancer development and treatment response [J].
Brown, JM ;
Attardi, LD .
NATURE REVIEWS CANCER, 2005, 5 (03) :231-237
[4]   Spectroscopic analysis confirms the interactions between single walled carbon nanotubes and various dyes commonly used to assess cytotoxicity [J].
Casey, A. ;
Herzog, E. ;
Davoren, M. ;
Lyng, F. M. ;
Byrne, H. J. ;
Chambers, G. .
CARBON, 2007, 45 (07) :1425-1432
[5]   Probing the interaction of single walled carbon nanotubes within cell culture medium as a precursor to toxicity testing [J].
Casey, A. ;
Davoren, M. ;
Herzog, E. ;
Lyng, F. M. ;
Byrne, H. J. ;
Chambers, G. .
CARBON, 2007, 45 (01) :34-40
[6]   Interaction of carbon nanotubes with sugar complexes [J].
Casey, A ;
Farrell, GF ;
McNamara, M ;
Byrne, HJ ;
Chambers, G .
SYNTHETIC METALS, 2005, 153 (1-3) :357-360
[7]  
DAVEREN M, 2007, TOXICOLOGY, V21, P438
[8]   In vitro toxicity evaluation of single walled carbon nanotubes on human A549 lung cells [J].
Davoren, Maria ;
Herzog, Eva ;
Casey, Alan ;
Cottineau, Benjamin ;
Chambers, Gordon ;
Byrne, Hugh J. ;
Lyng, Fiona M. .
TOXICOLOGY IN VITRO, 2007, 21 (03) :438-448
[9]   Carbon nanotube electron sources and applications [J].
de Jonge, N ;
Bonard, JM .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 2004, 362 (1823) :2239-2266
[10]   Carbon nanotubes: A review of their properties in relation to pulmonary toxicology and workplace safety [J].
Donaldson, Ken ;
Aitken, Robert ;
Tran, Lang ;
Stone, Vicki ;
Duffin, Rodger ;
Forrest, Gavin ;
Alexander, Andrew .
TOXICOLOGICAL SCIENCES, 2006, 92 (01) :5-22