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The Potential for Genotoxicity, Mutagenicity and Endocrine Disruption in Triclosan and Triclocarban Assessed through a Combination of In Vitro Methods.

Authors :
Chrz, Jan
Dvořáková, Markéta
Kejlová, Kristina
Očadlíková, Danuše
Svobodová, Lada
Malina, Lukáš
Hošíková, Barbora
Jírová, Dagmar
Bendová, Hana
Kolářová, Hana
Source :
Journal of Xenobiotics. Mar2024, Vol. 14 Issue 1, p15-30. 16p.
Publication Year :
2024

Abstract

Triclosan and Triclocarban, preservatives widely used in cosmetics and other consumer products, underwent evaluation using a battery of new-approach methodologies in vitro (NAMs). Specifically, the Microplate Ames Test (MPF™ Test, Xenometrix, Allschwil, Switzerland) was employed to assess mutagenicity, the Comet assay in vitro on the HaCat cell line and the Mammalian Chromosome Aberration Test were utilized to evaluate genotoxicity, and the XenoScreen® YES/YAS assay was applied to investigate endocrine disruption. The chemicals did not exhibit any positive responses for mutagenicity. However, the mammalian chromosome aberration test identified both chemicals as being positive for genotoxicity at 10 µg/mL. In the Comet assay, the percentage of DNA in the tail significantly increased in a concentration-dependent manner (at 5 and 10 µg/mL for Triclosan, at 2.5, 5, and 10 µg/mL for Triclocarban). The positive response depended on the increasing concentration and the duration of exposure. Triclosan, but not Triclocarban in any of the endocrine assays performed, indicated a potential for endocrine activity in the anti-estrogenic and anti-androgenic assays. The positive in vitro results detected were obtained for concentrations relevant to final products. The alarming findings obtained with the use of new-approach methodologies (NAMs) justify the current precautionary regulatory approach, limiting the use of these preservatives. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20394705
Volume :
14
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Xenobiotics
Publication Type :
Academic Journal
Accession number :
176328872
Full Text :
https://doi.org/10.3390/jox14010002