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Comparative evaluation of three methylene dianiline isomers in the bacterial reverse mutation assay, the in vitro gene mutation test, and the in vitro chromosomal aberration test
被引:4
|作者:
Unterberger-Henig, Elif
[1
]
机构:
[1] BASF SE, Carl Bosch Str 38, D-67056 Ludwigshafen, Germany
关键词:
Methylene dianiline;
4,4 '-MDA;
2,2 '-MDA;
2,4 '-MDA;
in vitro genotoxicity;
reverse bacterial mutation (Ames) test;
chromosomal aberration test;
HPRT locus assay;
risk assessment;
COLLABORATIVE STUDY-GROUP;
MUTAGEN SOCIETY JEMS;
REPEATED-DOSE LIVER;
MICRONUCLEUS TEST;
RATS;
4,4'-METHYLENEDIANILINE;
GENOTOXICITY;
HEPATOCYTES;
DERIVATIVES;
CELLS;
D O I:
10.1177/0748233221091018
中图分类号:
R1 [预防医学、卫生学];
学科分类号:
1004 ;
120402 ;
摘要:
4,4'-MDA is classified as a genotoxic carcinogen based on numerous in vitro and animal data. The consequential assumption that a safe threshold does not exist is not only applied to 4,4'-MDA but also to its structural isomers and impurities 2,2'- and 2,4'-MDA in the absence of substance-specific data. This constitutes a problem in human risk assessments for all three substances as the inherent risks of 2,2'- and 2,4'-MDA and their contribution as impurities to that of 4,4'-MDA are essentially unknown. A comparative in vitro genotoxicity dataset consisting of the bacterial reverse mutation (Ames) test and the chromosomal aberration test in human lymphocytes (both performed according to the current OECD Guidelines) was generated for all three isomers. Furthermore, an in vitro gene mutation test in Chinese hamster ovary (CHO) cells (HPRT locus assay) was conducted with 2,4'-MDA. The results indicate differences regarding the genotoxic mechanism and potential, respectively, between the three structures and suggest that the no-threshold assumption for 4,4'-MDA may not be appropriate for 2,2'- and 2,4'-MDA.
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页码:529 / 543
页数:15
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