Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines

被引:357
作者
Lanone, Sophie [1 ,2 ,3 ,4 ]
Rogerieux, Francoise [5 ]
Geys, Jorina [6 ]
Dupont, Aurelie [1 ,2 ,3 ,4 ]
Maillot-Marechal, Emmanuelle [5 ]
Boczkowski, Jorge [1 ,2 ,3 ,4 ,7 ]
Lacroix, Ghislaine [5 ]
Hoet, Peter [6 ]
机构
[1] INSERM, U700, Paris, France
[2] Univ Paris 07, Fac Med, Paris, France
[3] INSERM, Unite U955, F-94010 Creteil, France
[4] Univ Paris 12, Fac Med, F-94010 Creteil, France
[5] INERIS, Verneuil En Halatte, France
[6] Katholieke Univ Leuven, Lab Pneumol, Unit Lung Toxicol, B-3000 Louvain, Belgium
[7] Hop Bichat Claude Bernard, AP HP, CIC 007, F-75877 Paris, France
来源
PARTICLE AND FIBRE TOXICOLOGY | 2009年 / 6卷
关键词
IN-VITRO; CARBON NANOTUBES; LUNG INFLAMMATION; OXIDATIVE STRESS; SURFACE-AREA; PARTICLES; NANOMATERIALS; CYTOTOXICITY; INSTILLATION; EXPOSURE;
D O I
10.1186/1743-8977-6-14
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Background: A critical issue with nanomaterials is the clear understanding of their potential toxicity. We evaluated the toxic effect of 24 nanoparticles of similar equivalent spherical diameter and various elemental compositions on 2 human pulmonary cell lines: A549 and THP-1. A secondary aim was to elaborate a generic experimental set-up that would allow the rapid screening of cytotoxic effect of nanoparticles. We therefore compared 2 cytotoxicity assays (MTT and Neutral Red) and analyzed 2 time points ( 3 and 24 hours) for each cell type and nanoparticle. When possible, TC50 ( Toxic Concentration 50 i.e. nanoparticle concentration inducing 50% cell mortality) was calculated. Results: The use of MTT assay on THP-1 cells exposed for 24 hours appears to be the most sensitive experimental design to assess the cytotoxic effect of one nanoparticle. With this experimental set-up, Copper- and Zinc-based nanoparticles appear to be the most toxic. Titania, Alumina, Ceria and Zirconia-based nanoparticles show moderate toxicity, and no toxicity was observed for Tungsten Carbide. No correlation between cytotoxicity and equivalent spherical diameter or specific surface area was found. Conclusion: Our study clearly highlights the difference of sensitivity between cell types and cytotoxicity assays that has to be carefully taken into account when assessing nanoparticles toxicity.
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页数:12
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共 28 条
[1]   The potential risks of nanomaterials: a review carried out for ECETOC [J].
Borm, Paul J. A. ;
Robbins, David ;
Haubold, Stephan ;
Kuhlbusch, Thomas ;
Fissan, Heinz ;
Donaldson, Ken ;
Schins, Roel ;
Stone, Vicki ;
Kreyling, Wolfgang ;
Lademann, Jurgen ;
Krutmann, Jean ;
Warheit, David ;
Oberdorster, Eva .
PARTICLE AND FIBRE TOXICOLOGY, 2006, 3 (01)
[2]   Size-dependent proinflammatory effects of ultrafine polystyrene particles: A role for surface area and oxidative stress in the enhanced activity of ultrafines [J].
Brown, DM ;
Wilson, MR ;
MacNee, W ;
Stone, V ;
Donaldson, K .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2001, 175 (03) :191-199
[3]   In vitro cytotoxicitiy of silica nanoparticles at high concentrations strongly depends on the metabolic activity type of the cell line [J].
Chang, Jenq-Sheng ;
Chang, Ke Liang B. ;
Hwang, Deng-Fwu ;
Kong, Zwe-Ling .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (06) :2064-2068
[4]   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
[5]   Effects of subchronically inhaled carbon black in three species.: I.: Retention kinetics, lung inflammation, and histopathology [J].
Elder, A ;
Gelein, R ;
Finkelstein, JN ;
Driscoll, KE ;
Harkema, J ;
Oberdörster, G .
TOXICOLOGICAL SCIENCES, 2005, 88 (02) :614-629
[6]   Biomedical applications and potential health risks of nanomaterials: Molecular mechanisms [J].
Lanone, Sophie ;
Boczkowski, Jorge .
CURRENT MOLECULAR MEDICINE, 2006, 6 (06) :651-663
[7]   Exposure of engineered nanoparticles to human lung epithelial cells: Influence of chemical composition and catalytic activity on oxidative stress [J].
Limbach, Ludwig K. ;
Wick, Peter ;
Manser, Pius ;
Grass, Robert N. ;
Bruinink, Arie ;
Stark, Wendelin J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (11) :4158-4163
[8]   General strategies for nanoparticle dispersion [J].
Mackay, ME ;
Tuteja, A ;
Duxbury, PM ;
Hawker, CJ ;
Van Horn, B ;
Guan, ZB ;
Chen, GH ;
Krishnan, RS .
SCIENCE, 2006, 311 (5768) :1740-1743
[9]   Mechanism of lung injury caused by PM10 and ultrafine particles with special referance to COPD [J].
MacNee, W ;
Donaldson, K .
EUROPEAN RESPIRATORY JOURNAL, 2003, 21 :47S-51S
[10]   Surfactant effects on carbon nanotube interactions with human keratinocytes [J].
Monteiro-Riviere, Nancy A. ;
Inman, Alfred O. ;
Wang, Yunyu Y. ;
Nemanich, Robert J. .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2005, 1 (04) :293-299