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DNA adducts in peripheral blood lymphocytes from aluminum production plant workers determined by 32P-postlabeling and enzyme-linked immunosorbent assay.

机译:通过32P后标记和酶联免疫吸附测定法测定了铝生产厂工人外周血淋巴细胞的DNA加合物。

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摘要

32P-Postlabeling analysis and enzyme-linked immunosorbent assay (ELISA) have been used to detect DNA adducts in peripheral blood lymphocytes from primary aluminum production plant workers who were exposed occupationally to a mixture of polycyclic aromatic hydrocarbons (PAHs). Preliminary results reported here are from a comparative study being performed in two aluminum plants. The levels of aromatic DNA adducts have been determined by the 32P-postlabeling assay in samples collected on two occasions, 1 year apart. PAH-DNA adduct levels have also been determined by competitive ELISA in the second set of DNA samples. The results show the necessity of follow-up biomonitoring studies to detect possible alterations in biological effect induced by changing exposures. The comparison of the results obtained by 32P-postlabeling and ELISA may lead to a better understanding of the power and weaknesses of the two methods applied in these studies.
机译:32P后标记分析和酶联免疫吸附测定(ELISA)已用于检测原铝生产厂工人的外周血淋巴细胞中的DNA加合物,这些工人职业性地接触了多环芳烃(PAH)的混合物。此处报告的初步结果来自在两家铝厂进行的比较研究。芳香族DNA加合物的水平已通过32P后标记测定法确定了两次间隔1年收集的样品中的含量。 PAH-DNA加合物的水平也已经通过竞争性ELISA在第二组DNA样品中确定。结果表明,有必要进行后续的生物监测研究,以检测由暴露量变化引起的生物学效应可能的改变。通过32P后标记和ELISA获得的结果的比较可能会导致对这些研究中使用的两种方法的功效和弱点有更好的了解。

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