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首页> 外文期刊>Data in Brief >Synacinn?: Bacterial reverse mutation test data in five histidine-requiring strains of Salmonella Typhimurium
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Synacinn?: Bacterial reverse mutation test data in five histidine-requiring strains of Salmonella Typhimurium

机译:Synacinn ?:细菌反向突变试验数据在五种组氨酸的菌株中的沙门氏菌伤寒菌株

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The present data described the analysis of mutagenicity in SynacinnTMby assessing the point mutations occurring due to Synacinn? exposure to five tester strains ofSalmonella typhimurium(TA1537, TA1535, TA98, TA100 and TA102), in the presence or absence of an exogenous mammalian metabolic activation system (S9). It was conducted in two Phases - Phase I (Dose Range Finding experiment-DRF) and Phase II (Mutagenicity Assay 1 and 2). DRF and Mutagenicity Assay 1 was conducted employing plate incorporation method, while Mutagenicity Assay 2 was performed using pre-incubation method. Formulation analysis pertaining to SynacinnTMwas performed for both Mutagenicity Assay 1 and 2. Dose formulations were prepared fresh on each day of the experiment. Adventol 50% v/v in purified water was selected as a suitable vehicle based on the preliminary solubility test. Based on the Phase I analysis, 5 mg/plate was selected as the highest concentration of SynacinnTMfollowed by lower concentrations of 2.5, 1.25, 0.625 and 0.313 mg/plate for the Mutagenicity Assays. Genetic integrity of all the tester strains used was confirmed by performing genotyping before their use. All the data acceptability criteria were fulfilled confirming the validity of the test.
机译:本数据描述了Synacinntmby中的致突变性分析评估Synacinn由于Synacinn而发生的点突变?在存在或不存在外源哺乳动物代谢活化系统(S9)的情况下,暴露于五个测试杆菌(TA1537,TA1535,TA98,TA98,TA98,TA102)。它以两相 - I阶段I(剂量范围发现实验-DRF)和II期(诱变性测定1和2)进行。进行使用平板掺入法进行DRF和致突变性测定方法,而使用预孵育方法进行致突变性测定2。与Synacinntmwas进行的制剂分析对突变性测定1和2进行的Synacinntmwas进行了新鲜制剂在实验的每一天中制备了新的制剂。基于初步溶解度试验,选择纯净水中的AdventOx 50%V / V。基于IP相分析,选择5mg /板作为突变性测定的较低浓度为2.5,1.25,0.625和0.313mg /板的较低浓度的Sysacinntm的最高浓度。通过在使用前进行基因分型来证实所使用的所有测试菌株的遗传完整性。所有数据可接受性标准都符合确认测试的有效性。

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