Schoket B, Phillips D H, Poirier M C, Vincze I
Department of Biochemistry, Johan Bela National Institute of Public Health, Budapest, Hungary.
Environ Health Perspect. 1993 Mar;99:307-9. doi: 10.1289/ehp.9399307.
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.
32P后标记分析和酶联免疫吸附测定(ELISA)已用于检测职业性接触多环芳烃(PAH)混合物的原铝生产厂工人外周血淋巴细胞中的DNA加合物。此处报告的初步结果来自在两家铝厂进行的一项比较研究。通过32P后标记测定法在相隔1年采集的两次样本中测定了芳香族DNA加合物的水平。在第二组DNA样本中也通过竞争性ELISA测定了PAH-DNA加合物水平。结果表明有必要进行后续生物监测研究,以检测因接触变化引起的生物效应的可能改变。对32P后标记法和ELISA所得结果的比较可能有助于更好地了解这两种方法在这些研究中的优势和不足。