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Methodologies for bulky DNA adduct analysis and biomonitoring of environmental and occupational exposures

机译:庞大的DNA加合物分析和环境和职业曝光生物的方法

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摘要

It is undisputed that DNA adduct formation is one of the key processes in early carcinogenesis. Therefore, analysis of DNA adduct levels may be one of the best tools available to characterize exposure to complex mixtures of genotoxic chemicals as occurring in different environmental and occupational exposure settings. However, from an analytical point of view the detection and quantification of DNA adducts is a challenging enterprise as extremely high sensitivity and selectivity are required. The entire spectrum of chromatographic techniques, including thin-layer chromatography (TLC), gas and liquid chromatography as well as capillary electrophoresis has been used in combination with different detection systems, all with their own specific characteristics. Among the various combinations of techniques, the TLC-~(32)P-postlabeling combination appears to meet best with criteria of sensitivity and requirements of minimal amounts of material. Recent developments in the application of capillary electrophoresis in combination with either immunochemical or mass spectrometric detection techniques may offer new and promising approaches, with higher selectivity as compared to TLC-~(32)P postlabeling. The applicability of these new techniques in biomonitoring studies aiming at the exposure and risk assessment of low and chronic exposures remains to be determined. In this paper we compare and discuss the advantages and limitations of different techniques used in DNA adduct analysis, with specific emphasis on those adducts formed by the polycyclic aromatic hydrocarbons and heterocyclic aromatic amines.
机译:无可争议的是,DNA加合物形成是早期致癌物中的关键过程之一。因此,DNA加合水平的分析可以是可用于在不同环境和职业暴露环境中发生的遗传毒性化学品的复杂混合物的性质的最佳工具之一。然而,从分析的角度来看,DNA加合物的检测和定量是一个具有挑战性的企业,因为需要极高的灵敏度和选择性。包括薄层色谱(TLC),气体和液相色谱以及毛细管电泳的整个色谱技术,以及不同的检测系统,所有这些都与其自身的特定特征一起使用。在各种技术组合中,TLC-〜(32)P-Postlabeling组合似乎最佳地满足敏感性标准和最小量的材料要求。毛细管电泳与免疫化学或质谱检测技术相结合的近期发展可能提供新的和有前途的方法,与TLC-〜(32)P后标签相比具有更高的选择性。这些新技术在旨在暴露和风险评估的生物监测研究中的适用性仍有待确定。在本文中,我们比较和探讨DNA加合物分析中使用的不同技术的优缺点,具有特异性强调由多环芳烃和杂环芳族胺形成的那些加合物。

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