首页> 外文会议>American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics >Quantification of 1,3-Butadiene-Induced DNA adducts in Human Blood Using Liquid Chromatography-High Resolution Tandem Mass Spectrometry (HPLC-HR MS/MS)
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Quantification of 1,3-Butadiene-Induced DNA adducts in Human Blood Using Liquid Chromatography-High Resolution Tandem Mass Spectrometry (HPLC-HR MS/MS)

机译:使用液相色谱 - 高分辨率串联质谱(HPLC-HR MS / MS)定量1,3-丁二烯诱导的人血液中的DNA加合物

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摘要

Highly sensitive capillary HPLC-ESI~+-HRMS/MS-SRM methods for and nanoHPLC-NSI~+-HR-MS~3 methods for EB-Gua in human DNA have been developed and validated. No significant differences were observed between N7-THBG adduct levels in leukocyte DNA of smokers and nonsmokers (P = 0.60,). Furthermore, smoking cessation did not alter N7-THBG concentrations in human leukocyte DNA, suggesting that BD exposure sources other than smoking contribute to N7-THBG formation in humans. In contrast, N7-THBG adduct concentrations were significantly increased in workers occupationally exposed to BD as compared to controls. Sensitive methodology developed in this work will be used for future studies of BD adduct formation in humans, facilitating human risk assessment from exposure to BD.
机译:已经开发并验证了人体DNA中EB-GUA的高度敏感性毛细管HPLC-ESI〜+ -HRMS / MS-SRM方法,并验证了EB-GUA的eB-GUA方法。 在吸烟者和非吸烟者的白细胞DNA中没有观察到N7-THBG加合水平之间的显着差异(P = 0.60,)。 此外,吸烟停止未改变人白细胞DNA中的N7-THBG浓度,表明除吸烟以外的BD暴露源有助于人类的N7-THBG形成。 相比之下,与对照相比,在职业暴露于BD的工人中,N7-THBG加合物浓度显着增加。 在这项工作中开发的敏感方法将用于对人类的BD加合物形成的未来研究,促进人类风险评估暴露于BD。

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