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Genotoxicity evaluation of titanium dioxide nanoparticles using the mouse lymphoma assay and the Ames test
•The genotoxicity of Titanium dioxide nanoparticles (TiO2-NPs) was evaluated.•TiO2-NPs did not induce gene mutations in mouse lymphoma L5178Y cells.•TiO2-NPs did not induce reverse mutation in the bacterial strains..•TiO2-NPs cannot be classified as mutagenic and require further confirmatory studies...
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Published in: | Mutation research. Genetic toxicology and environmental mutagenesis 2019-02, Vol.838, p.22-27 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •The genotoxicity of Titanium dioxide nanoparticles (TiO2-NPs) was evaluated.•TiO2-NPs did not induce gene mutations in mouse lymphoma L5178Y cells.•TiO2-NPs did not induce reverse mutation in the bacterial strains..•TiO2-NPs cannot be classified as mutagenic and require further confirmatory studies.
Titanium dioxide nanoparticles (TiO2-NPs) are widely used in the cosmetics, health, and food industries, but their safety and genotoxicity remain a matter of debate. We investigated whether TiO2-NPs could induce gene mutations in mouse lymphoma L5178Y cells and Salmonella typhimurium strains TA97a, TA98, TA100, TA102, and TA1535. Following preliminary tests, 2 mg/mL for the mouse lymphoma gene mutation assay and 1.25 mg/plate for the in vitro bacterial reverse mutation assay (Ames test) were selected as the highest concentrations. Exposure to TiO2-NPs for 4 or 24 h with or without S9 metabolic activation did not increase mutation frequency for any of the concentrations tested in L5178Y cells. In the Ames test, TiO2-NPs did not induce reverse mutation in the bacterial strains. No positive mutagenic responses were observed in either test system, and therefore we cannot classify TiO2-NPs as mutagenic; further testing will be required to determine conclusively whether TiO2-NPs are genotoxic. |
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ISSN: | 1383-5718 1879-3592 |
DOI: | 10.1016/j.mrgentox.2018.11.015 |