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通过柱切换液相色谱-串联质谱法快速测定尿中S-苯巯基尿酸(S-PMA)和S-苄基巯基尿酸(S-BMA)

Fast determination of urinary S-phenylmercapturic acid (S-PMA) and S-benzylmercapturic acid (S-BMA) by column-switching liquid chromatography-tandem mass spectrometry.

作者信息

Schettgen T, Musiol A, Alt A, Kraus T

机构信息

Institute and Outpatient Clinic of Occupational and Social Medicine, University Hospital, Aachen University of Technology, Pauwelsstrasse 30, D-52074 Aachen, Germany.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Mar 1;863(2):283-92. doi: 10.1016/j.jchromb.2008.01.024. Epub 2008 Jan 20.

DOI:10.1016/j.jchromb.2008.01.024
PMID:18258494
Abstract

Benzene and toluene are important industrial chemicals and ubiquitous environmental pollutants. The urinary mercapturic acids of benzene and toluene, S-phenylmercapturic acid (S-PMA) and S-benzylmercapturic acids (S-BMA) are specific biomarkers for the determination of low-level exposures. We have developed and validated a fast, specific and very sensitive method for the simultaneous determination of S-PMA and S-BMA in human urine using an automated multidimensional LC-MS-MS-method that requires no additional sample preparation. Analytes are stripped from urinary matrix by online extraction on a restricted access material, transferred to the analytical column and subsequently determined by tandem mass spectrometry using isotopically labelled S-PMA as internal standard. The lower limit of quantification (LLOQ) for both analytes was 0.05 microg/L urine and sufficient to quantify the background exposure of the general population. Precision within series and between series for S-PMA and S-BMA ranged from 1.0% to 12.2%, accuracy was 108% and 100%, respectively. We applied the method on spot urine samples of 30 subjects of the general population with no known exposure to benzene or toluene. Median levels (range) for S-PMA and S-BMA in non-smokers (n=15) were 0.14 microg/L (<0.05-0.26 microg/L) and 8.2 (1.6-77.4 microg/L), respectively. In smokers (n=15), median levels for S-PMA and S-BMA were 1.22 microg/L (0.17-5.75 microg/L) and 11.5 microg/L (0.9-51.2 microg/L), respectively. Due to its automation, our method is well suited for application in large environmental studies.

摘要

苯和甲苯是重要的工业化学品,也是普遍存在的环境污染物。苯和甲苯的尿中硫醚氨酸,即S - 苯基硫醚氨酸(S - PMA)和S - 苄基硫醚氨酸(S - BMA),是测定低水平暴露的特异性生物标志物。我们开发并验证了一种快速、特异且非常灵敏的方法,使用无需额外样品制备的自动多维液相色谱 - 串联质谱法同时测定人尿中的S - PMA和S - BMA。分析物通过在限进材料上的在线萃取从尿液基质中剥离,转移至分析柱,随后以同位素标记的S - PMA作为内标通过串联质谱法进行测定。两种分析物的定量下限(LLOQ)均为0.05μg/L尿液,足以对普通人群的背景暴露进行定量。S - PMA和S - BMA在系列内和系列间的精密度范围为1.0%至12.2%,准确度分别为108%和100%。我们将该方法应用于30名无已知苯或甲苯暴露史的普通人群的即时尿样。非吸烟者(n = 15)中S - PMA和S - BMA的中位数水平(范围)分别为0.14μg/L(<0.05 - 0.26μg/L)和8.2(1.6 - 77.4μg/L)。吸烟者(n = 15)中S - PMA和S - BMA的中位数水平分别为1.22μg/L(0.17 - 5.75μg/L)和11.5μg/L(0.9 - 51.2μg/L)。由于其自动化特性,我们的方法非常适合用于大型环境研究。

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