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In vitro study of DNA Adduct 8-OHdG Formation by using Bisphenol A in Calf Thymus DNA and 2'-Deoxyguanosine

机译:使用双酚A在小酚胸腺DNA和2'-脱氧核苷中使用双酚A对DNA加合物的体外研究

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The in vitro study of DNA Adduct 8-OHdG Formation due to BisphenolA (BPA) as xenobiotics has been conducted by using calf thymus DNA and 2'deoxyguanosine. The method of study was conducted by incubating calf thymus DNA and 2'dG with compounds trigger to radicals in the variation of pH (7.4 and 8.4), temperature (37°C and 60°C), and BPA concentrations (2 ppm and 10 ppm). To represent the work of CYP 450 enzyme in metabolic process of xenobiotics in the body and the effect of metal presence to the formation of radicals that can lead to 8-OHdG formation, we used iron(II) solution and also fenton reagent (Fe(II) and H2O2). The DNA used has 1.8 purity ratio (checked at λ260/λ280 by using Spectrophotometry UV-Vis). The results by using HPLC method showed that BPA could interact with DNA and DNA base (represent as calf thymus and 2'dG) and potentially induced 8-OHdG formation. The presence of iron(II) metal and Fenton reagent also induced the higher 8-OHdG formation. The higher of pH, temperature and concentrations also lead to 8-OHdG formation (ranger between 4-70 ppb).
机译:通过使用CALF胸腺DNA和2'Deoxyguaosine进行了由于双酚(BPA)引起的DNA加合物8-OHDG形成的体外研究。通过将CALF胸腺DNA和2'DG用化合物触发到PH(7.4和8.4)的变化中的自由基进行研究,进行研究方法,温度(37℃和60℃)和BPA浓度(2ppm和10 ppm)。代表CYP 450酶在体内代谢过程中的作用和金属存在对形成的自由基的影响,可以导致8-OHDG的形成,我们使用铁(II)溶液和Fenton试剂(Fe( II)和H2O2)。使用的DNA具有1.8纯度(通过使用分光光度法UV-VI)在λ260/λ280处检查)。通过使用HPLC方法的结果表明,BPA可以与DNA和DNA碱(表示为CALF胸腺和2'DG)相互作用,并且可能诱导8-OHDG形成。铁(II)金属和Fenton试剂的存在也诱导了较高的8-OHDG形成。 pH值,温度和浓度的越高也导致8-OHDG形成(4-70ppb之间的游池)。

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