首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Examination of the mutagenicity of RDX and its N-nitroso metabolites using the Salmonella reverse mutation assay.
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Examination of the mutagenicity of RDX and its N-nitroso metabolites using the Salmonella reverse mutation assay.

机译:使用沙门氏菌反向突变测定法检测RDX及其N-亚硝基代谢物的致突变性。

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摘要

The mutagenicity of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and its N-nitroso derivatives hexahydro-1-nitroso-3,5-dinitro-1,3,5-triazine (MNX) and hexahydro-1,3,5-trinitroso-1,3,5-triazine (TNX) were evaluated using the Salmonella tryphimurium reverse mutation assay (Ames assay) with strains TA97a, TA98, TA100, and TA102. Using a preincubation procedure and high S9 activation (9%), RDX was observed to induce weak mutagenesis to strain TA97a with a mutagenicity index (MI) of 1.5-2.0 at a dose range of 32.7-1090microg/plate. MNX induced moderate mutagenesis to strain TA97a with an MI of 1.6-2.8 at a dose range of 21.7-878microg/plate. TNX also induced moderate mutagenesis in strain TA97a with an MI of 2.0-3.5 to TA97a at a dose range of 22.7-1120microg/plate. TNX also caused weak mutagenesis to strain TA100 with S9 activation at the dose of 1200microg/plate. MNX and TNX induced weak to moderate mutagenesis to strain TA102. Strain TA97a was found to be the most sensitive strain among these four strains. No cytotoxicity of RDX, MNX, and TNX was observed at the concentrations used in this study. Doses were verified by HPLC.
机译:六氢-1,3,5-三硝基-1,3,5-三嗪(RDX)及其N-亚硝基衍生物六氢-1-亚硝基-3,5-二硝基-1,3,5-三嗪(MNX )和六氢-1,3,5-三亚硝基-1,3,5-三嗪(TNX)使用沙门氏菌沙门氏菌反向突变试验(Ames试验)和TA97a,TA98,TA100和TA102菌株进行了评估。使用预孵育程序和高S9活化(9%),在32.7-1090microg /板的剂量范围内,观察到RDX对诱变指数(MI)为1.5-2.0的TA97a菌株产生弱诱变作用。 MNX诱导中等诱变,菌株TA97a的MI在1.6-2.8的MI,剂量范围为21.7-878microg /板。 TNX还诱导了TA97a菌株的中等诱变,MI为2.0-3.5至TA97a,剂量范围为22.7-1120microg /板。 TNX还在1200microg /板的剂量下通过S9活化引起TA100菌株的弱诱变。 MNX和TNX诱导了TA102菌株的弱至中等诱变。发现TA97a菌株是这四种菌株中最敏感的菌株。在本研究中使用的浓度下,未观察到RDX,MNX和TNX的细胞毒性。剂量通过HPLC验证。

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