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Introduction. The test for the induction of reverse gene mutations (Ames test, OECD* guideline No. 471) is one of the most popular methods for assessing mutagenicity due to its ease of execution and the ability to detect up to 70-80% of substances with carcinogenic activity. The experimental protocol requires a minimum amount of test substance and standard microbiological laboratory equipment. To obtain the primary data, several days from the start of the experiment are required. Despite the existence of publications devoted to the detailed description of the standard Ames test protocol, there is a gap affecting a number of aspects of the procedure for confirming the competence of a testing center using this method in its practice. Materials and methods. When preparing this article, we used the literature data published in domestic and foreign literature over the past 20 years concerning experimental approaches to the implementation of the Ames test. The literature search was carried out in the Scopus, Medline, Google Scholar, RSCI databases. Results. In the FBES “Federal Scientific Center of Hygiene named after F.F. Erisman” of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing the method for assessing the bacterial reverse mutation has found application in assessing the safety of technical products of pesticides, their mixtures and preparative forms, as well as in the examination of equivalence. Testing laboratory center on the basis of the FBES “Federal Scientific Center of Hygiene named after F.F. Erisman” of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing is accredited for compliance with the state standard GOST ISO / IEC 17025-2019 ”General requirements for the competence of testing and calibration laboratories.“ In this article, based on new published data and our own practical experience, a number of necessary conditions are considered for demonstrating the competence of a testing laboratory using the test for the induction of reverse gene mutations in its practice, its ability to obtain reliable results and take actions to manage the risks of laboratory activities. The main attention is paid to ensuring such parameters of the test quality as indicator cultures, metabolic activation system, control of the background of spontaneous mutation, etc. Conclusion. The discussed practical issues can be useful for specialists from research laboratories planning to introduce this method into practice.
Introduction. The test for the induction of reverse gene mutations (Ames test, OECD* guideline No. 471) is one of the most popular methods for assessing mutagenicity due to its ease of execution and the ability to detect up to 70-80% of substances with carcinogenic activity. The experimental protocol requires a minimum amount of test substance and standard microbiological laboratory equipment. To obtain the primary data, several days from the start of the experiment are required. Despite the existence of publications devoted to the detailed description of the standard Ames test protocol, there is a gap affecting a number of aspects of the procedure for confirming the competence of a testing center using this method in its practice. Materials and methods. When preparing this article, we used the literature data published in domestic and foreign literature over the past 20 years concerning experimental approaches to the implementation of the Ames test. The literature search was carried out in the Scopus, Medline, Google Scholar, RSCI databases. Results. In the FBES “Federal Scientific Center of Hygiene named after F.F. Erisman” of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing the method for assessing the bacterial reverse mutation has found application in assessing the safety of technical products of pesticides, their mixtures and preparative forms, as well as in the examination of equivalence. Testing laboratory center on the basis of the FBES “Federal Scientific Center of Hygiene named after F.F. Erisman” of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing is accredited for compliance with the state standard GOST ISO / IEC 17025-2019 ”General requirements for the competence of testing and calibration laboratories.“ In this article, based on new published data and our own practical experience, a number of necessary conditions are considered for demonstrating the competence of a testing laboratory using the test for the induction of reverse gene mutations in its practice, its ability to obtain reliable results and take actions to manage the risks of laboratory activities. The main attention is paid to ensuring such parameters of the test quality as indicator cultures, metabolic activation system, control of the background of spontaneous mutation, etc. Conclusion. The discussed practical issues can be useful for specialists from research laboratories planning to introduce this method into practice.
Introduction. The Ames test is the one of the most popular methods for mutagenicity evaluation of environmental factors. In some cases, this method is suggested to be the only and sufficient assay for the first stage of the equivalence assessment of pesticide technical grade active ingredients (TGAI) to the original products. A limitation of the Ames test is related to the impossibility of an objective equivalence assessment of some cytotoxic TGAIs, in particular, sulfonylureas, and triazolpyrimidines. Based on the mode of action of the pesticides belongs to these chemical classes, we suggested a modification of the plate incorporation method protocol of the Ames test to the increase of maximal non-cytotoxic concentration up to the 5 mg/plate recommended by regulatory documents. Materials and methods. The five strains of Salmonella typhimurium TA98, TA100, TA1535, TA97, TA102 were used. The modification of the protocol included a supplementation of the top agar with isoleucine (1-5 mM). Results. The maximum non-cytotoxic concentrations of thifensulfuron-methyl and florasulam using the standard top agar did not exceed 0.05-0.125 mg/plate. The enrichment of the top agar with isoleucine allowed evaluating the mutagenicity of the substances up to the maximal recommended concentration of 5.0 mg/plate. The number of spontaneous revertants was within the historical limits of the laboratory control obtained under standard conditions. Positive controls showed pronounced mutagenic effects in case of all strains with and without metabolic activation (p≤0.05). Limitations. Mutagenicity was evaluated only for TGAIs, which are acetohydroxyacid synthase inhibitors. Conclusion. The application of the modified Ames test protocol for mutagenicity assessment of TGAIs from the classes of sulfonylureas and triazolpyrimidines under supplementation of the top agar with isoleucine is a more objective way to evaluate their mutagenicity. The proposed protocol expands the possibilities of revealing dangerous mutagenic impurities that may occur in TGAIs in the small quantities, and after entering the environment can cause the gain in the mutation level in living organisms.
Introduction. Titanium dioxide in the Russian Federation is approved for use in the food industry, in the production of medicines and hygiene products. The food additive E171 is a mixture of micro- and nanoparticles of TiO2. In 2010, IARC classified TiO2 in nanoform as a probably carcinogenic to humans (Group 2B). In vitro and in vivo studies of the genotoxicity of titanium dioxide revealed contradictory results, indicating both the presence and absence of TiO2 mutagenicity. The aim of the work is to evaluate the mutagenicity of the food additive E171 in the Ames test using standard and modified protocols. Materials and methods. The ability of food additive E171 (China) to induce reverse gene mutations in 5 strains of Salmonella typhimurium was studied under standard and modified conditions (cultivation of bacteria in the presence of methylated b-cyclodextrin (MCD) and/or pre-incubation for 1 hour in potassium phosphate buffer, pH 5.5 containing 10 mM NaCl and/or 3M MCD). Results. A sample of food additive E171 based on rutile titanium dioxide does not induce gene mutations in S. typhimurium in standard experiments. Modification of the Ames test protocol (decrease of the incubation mixture pH, addition of 10 mM NaCl) revealed statistically significant dose-dependent effects in TA100, TA98, and TA97 strains under metabolic incubation conditions. However, the fold increase of the number of revertants in the experimental plates compared to the negative control was < 2. Limitations. The research is limited to the mutagenicity assessment of food additive E171 (titanium dioxide) in the Ames test. Conclusion. The evaluation of the mutagenicity of titanium dioxide in other in vitro and in vivo tests taking into account the size and shape of the particles, is necessary to resolve the issue of its genetic safety as a food dye. A full range of studies will be performed on other samples of titanium dioxide presented in the market of the Russian Federation.
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