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修订后的气相色谱-质谱法常规测定尿中二烷基磷酸酯的方法。

Revised method for routine determination of urinary dialkyl phosphates using gas chromatography-mass spectrometry.

机构信息

Program in Radiological and Medical Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 May 15;878(17-18):1257-63. doi: 10.1016/j.jchromb.2010.02.005. Epub 2010 Feb 12.

Abstract

Among urinary organophosphorus pesticide (OP) metabolites, dialkyl phosphates (DAPs) have been most often measured as a sensitive biomarker in non-occupational and occupational OP exposure risk assessment. In our conventional method, we have employed a procedure including simple liquid-liquid extraction (diethyl ether/acetonitrile), derivatization (pentafluorobenzylbromide, PFBBr) and clean-up (multi-layer column) for gas chromatography-mass spectrometry (GC-MS) analysis starting from 5-mL urine samples. In this study, we introduce a revised analytical method for urinary DAPs; its main modification was aimed at improving the pre-derivatization dehydration procedure. The limits of detection were approximately 0.15 microg/L for dimethylphosphate (DMP), 0.07 microg/L for diethylphosphate (DEP), and 0.05 microg/L for both dimethylthiophosphate (DMTP) and diethylthiophosphate (DETP) in 2.5-mL human urine samples. Within-run precision (percent of relative standard deviation, %RSD) at the DAP levels varying in the range of 0.5-50 microg/L was 6.0-19.1% for DMP, 3.6-18.3% for DEP, 8.0-25.6% for DMTP and 9.6-27.8% for DETP. Between-run precision at 5 microg/L was below 15.7% for all DAPs. The revised method proved to be feasible to routine biological monitoring not only for occupational OP exposure but also for environmental background levels in the general population. Compared to our previous method, the revised method underscores the importance of adding pre-derivatization anhydration for higher sensitivity and precision.

摘要

在尿有机磷农药(OP)代谢物中,二烷基磷酸酯(DAPs)作为非职业和职业性 OP 暴露风险评估的敏感生物标志物,已被广泛测量。在我们的常规方法中,我们采用了一种包括简单液-液萃取(乙醚/乙腈)、衍生化(五氟苄基溴,PFBBr)和净化(多层柱)的程序,用于从 5 毫升尿样进行气相色谱-质谱(GC-MS)分析。在这项研究中,我们引入了一种改进的尿液 DAP 分析方法;其主要改进旨在改善预衍生化脱水程序。检测限约为 0.15 微克/升的二甲基磷酸酯(DMP)、0.07 微克/升的二乙基磷酸酯(DEP)和 0.05 微克/升的二甲基硫代磷酸酯(DMTP)和二乙基硫代磷酸酯(DETP),在 2.5 毫升人尿样中。在 0.5-50 微克/升范围内的 DAP 水平下,批内精密度(相对标准偏差的百分比,%RSD)为 6.0-19.1%的 DMP、3.6-18.3%的 DEP、8.0-25.6%的 DMTP 和 9.6-27.8%的 DETP。在 5 微克/升时,所有 DAP 的批间精密度均低于 15.7%。该改进方法不仅适用于职业性 OP 暴露的常规生物监测,也适用于一般人群的环境背景水平。与我们之前的方法相比,改进的方法强调了添加预衍生化脱水以提高灵敏度和精密度的重要性。

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