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Journal ArticleDOI

Mutagenicity of constituents identified in pulp and paper mill effluents using the Salmonella/mammalian-microsome assay.

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TLDR
Modifications of the Salmonella test for volatile mutagens enabled the detection of the mutagenicity of 3 additional chlorinated aliphatic hydrocarbons dichloromethane, dichloroethane and trichloroETHane.
Abstract
About 300 compounds have been reported in the literature as constituents of pulp-mill effluent. Previously, in our screening program, 10 resin acids identified in effluent were examined for potential mutagenicity in the Salmonella/mammalian-microsome assay. Neoabietic acid was the only resin acid which was found to be mutagenic. Now, a program to screen for mutagenicity of 48 additional compounds, belonging to chemical classes of chlorinated aliphatic and aromatic hydrocarbons, phenols, aldehydes, quinones, and carboxylic acids, has been completed. Only 2 of these compounds, tetrachloropropene and pentachloropropene, were found to be mutagenic, showing dose-related increases in His+ reversion mutations, in the standard Salmonella test. Metabolic activation with a preparation of Aroclor 1254-induced liver homogenate (S9) greatly reduced the mutagenic responses of these 2 compounds. Modifications of the Salmonella test for volatile mutagens enabled the detection of the mutagenicity of 3 additional chlorinated aliphatic hydrocarbons dichloromethane, dichloroethane and trichloroethane.

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Citations
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Journal ArticleDOI

Mutagenicity and genotoxicity of nitroarenes: All nitro-containing chemicals were not created equal

TL;DR: The nitrated polycyclic aromatic hydrocarbons constitute a group of chemicals of environmental concern which display a broad spectrum of mutagenic, genotoxic and carcinogenic properties and are the most potent direct-acting bacterial mutagens.
Journal ArticleDOI

The genotoxicity of industrial wastes and effluents.

TL;DR: The evaluation of hazardous wastes and effluents by genotoxicity assays may provide data useful not only for hazard identification but for comparative risk assessment.

Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) on a request from the Commission, Flavouring Group Evaluation 22: Ring-substituted phenolic substances from chemical groups 21 and 25: Question No EFSA-Q-2003-165

TL;DR: The Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food (the Panel) is asked to advise the Commission on the implications for human health of chemically defined flavouring substances used in or on foodstuffs in the Member States as mentioned in this paper.
References
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Journal ArticleDOI

Methods for detecting carcinogens and mutagens with the salmonella/mammalian-microsome mutagenicity test

TL;DR: The methods described include the standard plate test, the use and storage of the bacterial tester strains, preparation and use of the liver homogenates, and the methods of inducing the rats for elevated microsomal enzyme activity.
Journal ArticleDOI

Detection of carcinogens as mutagens in the Salmonella/microsome test: assay of 300 chemicals

TL;DR: There is a high correlation between carcinogenicity and mutagenicity: 90% (156/174) of carcinogens are mutagenic in the test and despite the severe limitations inherent in defining non-carcinogenicity, few "non-Carcinogens" show any degree of mutageniability.
Journal ArticleDOI

Carcinogens are Mutagens: A Simple Test System Combining Liver Homogenates for Activation and Bacteria for Detection

TL;DR: It is proposed that a ring system sufficiently planar for a stacking interaction with DNA base pairs and a part of the molecule capable of being metabolized to a reactive group are discussed in terms of the theory of frameshift mutagenesis.
Journal ArticleDOI

Human, rat and mouse liver-mediated mutagenicity of vinyl chloride in S. typhimurium strains.

TL;DR: The mutagenic response for TA 1530 strain was enhanced 7‐, 4‐ or 5‐fold when fortified postmitochondrial liver fractions from humans, rats or mice were added and the enzyme‐mediated vinyl chloride mutagenicity was dependent on an NADPH generating system and the enzymes activity was localized in a liver microsomal fraction.
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