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

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 t...

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Autores principales: Lanone, Sophie, Rogerieux, Françoise, Geys, Jorina, Dupont, Aurélie, Maillot-Marechal, Emmanuelle, Boczkowski, Jorge, Lacroix, Ghislaine, Hoet, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685765/
https://www.ncbi.nlm.nih.gov/pubmed/19405955
http://dx.doi.org/10.1186/1743-8977-6-14
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author Lanone, Sophie
Rogerieux, Françoise
Geys, Jorina
Dupont, Aurélie
Maillot-Marechal, Emmanuelle
Boczkowski, Jorge
Lacroix, Ghislaine
Hoet, Peter
author_facet Lanone, Sophie
Rogerieux, Françoise
Geys, Jorina
Dupont, Aurélie
Maillot-Marechal, Emmanuelle
Boczkowski, Jorge
Lacroix, Ghislaine
Hoet, Peter
author_sort Lanone, Sophie
collection PubMed
description 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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spelling pubmed-26857652009-05-23 Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines Lanone, Sophie Rogerieux, Françoise Geys, Jorina Dupont, Aurélie Maillot-Marechal, Emmanuelle Boczkowski, Jorge Lacroix, Ghislaine Hoet, Peter Part Fibre Toxicol Research 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. BioMed Central 2009-04-30 /pmc/articles/PMC2685765/ /pubmed/19405955 http://dx.doi.org/10.1186/1743-8977-6-14 Text en Copyright © 2009 Lanone et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lanone, Sophie
Rogerieux, Françoise
Geys, Jorina
Dupont, Aurélie
Maillot-Marechal, Emmanuelle
Boczkowski, Jorge
Lacroix, Ghislaine
Hoet, Peter
Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines
title Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines
title_full Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines
title_fullStr Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines
title_full_unstemmed Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines
title_short Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines
title_sort comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685765/
https://www.ncbi.nlm.nih.gov/pubmed/19405955
http://dx.doi.org/10.1186/1743-8977-6-14
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