Simultaneous determination of mercapturic acids derived from ethylene oxide (HEMA), propylene oxide (2‐HPMA), acrolein (3‐HPMA), acrylamide (AAMA) and N,N ‐dimethylformamide (AMCC) in human urine using liquid chromatography/tandem mass spectrometry

化学 色谱法 丙烯酰胺 丙烯醛 尿 环氧乙烷 巯基尿酸 人口 固相萃取 检出限 谷胱甘肽 有机化学 生物化学 酶 催化作用 聚合物 人口学 社会学 共聚物
作者
Thomas Schettgen,A. Musiol,Thomas Kraus
出处
期刊:Rapid Communications in Mass Spectrometry [Wiley]
卷期号:22 (17): 2629-2638 被引量:84
标识
DOI:10.1002/rcm.3659
摘要

Mercapturic acids are highly important and specific biomarkers of exposure to carcinogenic substances in occupational and environmental medicine. We have developed and validated a reliable, specific and very sensitive method for the simultaneous determination of five mercapturic acids derived from several high-production chemicals used in industry, namely ethylene oxide, propylene oxide, acrylamide, acrolein and N,N-dimethylformamide. Analytes are enriched and cleaned up from urinary matrix by offline solid-phase extraction. The mercapturic acids are subsequently separated by means of high-performance liquid chromatography on a Luna C8 (2) column and specifically quantified by tandem mass spectrometric detection using isotopically labelled analytes as internal standards. The limits of detection (LODs) for N-acetyl-S-2-carbamoylethylcysteine (AAMA) and N-acetyl-S-2-hydroxyethylcysteine (HEMA) were 2.5 microg/L and 0.5 microg/L urine, while for N-acetyl-S-3-hydroxypropylcysteine (3-HPMA), N-acetyl-S-2-hydroxypropylcysteine (2-HPMA) and N-acetyl-S-(N-methylcarbamoyl)cysteine (AMCC) it was 5 microg/L. These LODs were sufficient to detect the background exposure of the general population. We applied the method on spot urine samples of 28 subjects of the general population with no known occupational exposure to these substances. Median levels for AAMA, HEMA, 3-HPMA, 2-HPMA and AMCC in non-smokers (n = 14) were 52.6, 2.0, 155, 7.1 and 113.6 microg/L, respectively. In smokers (n = 14), median levels for AAMA, HEMA, 3-HPMA, 2-HPMA and AMCC were 243, 5.3, 1681, 41.7 and 822 microg/L, respectively. Due to the simultaneous quantification of these mercapturic acids, our method is well suited for the screening of workers with multiple chemical exposures as well as the determination of the background excretion of the general population.

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