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尿液中2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)及其致癌代谢物的生物监测。

Biomonitoring of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and its carcinogenic metabolites in urine.

作者信息

Fede Jean-Marie, Thakur Anup P, Gooderham Nigel J, Turesky Robert J

机构信息

Division of Environmental Health Sciences, Wadsworth Center, New York State Department of Health, Albany, New York 12201, USA.

出版信息

Chem Res Toxicol. 2009 Jun;22(6):1096-105. doi: 10.1021/tx900052c.

Abstract

2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) is a carcinogenic heterocyclic aromatic amine that is produced in cooked meats. The simultaneous analysis of PhIP and its metabolites in human urine is a challenge, because these biomarkers only occur in urine at parts per billion or lower concentrations and must be selectively purifed from thousands of other urinary constituents. We have developed a facile solid-phase extraction method, employing a mixed-mode reverse-phase cation exchange resin, to simultaneously isolate PhIP, its glucuronide conjugates, and the glucuronide conjugates of the genotoxic metabolite 2-hydroxyamino-1-methyl-6-phenylimidazo[4,5-b]pyridine from the urine of meat eaters. PhIP and its metabolites were quantified by liquid chromatography-electrospray ionization/tandem mass spectrometry (LC-ESI/MS/MS), using a triple stage quadrupole mass spectrometer in the selected reaction monitoring scan mode. The lower limit of quantification (LOQ) of PhIP is 5 parts per trillion (ppt), and the LOQ values for the glucuronide conjugates are 50 ppt, when 25 microL of urine is employed for assay. The extraction scheme is versatile and has been employed to isolate other ring-hydroxylated and glucuronidated metabolites of PhIP, for characterization by LC-ESI/MS/MS.

摘要

2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)是一种在熟肉中产生的致癌杂环芳香胺。同时分析人体尿液中的PhIP及其代谢物具有挑战性,因为这些生物标志物在尿液中的浓度仅为十亿分之一或更低,并且必须从数千种其他尿液成分中进行选择性纯化。我们开发了一种简便的固相萃取方法,采用混合模式反相阳离子交换树脂,从肉食者的尿液中同时分离PhIP、其葡萄糖醛酸共轭物以及遗传毒性代谢物2-羟基氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶的葡萄糖醛酸共轭物。使用三重四极杆质谱仪在选择反应监测扫描模式下,通过液相色谱-电喷雾电离/串联质谱法(LC-ESI/MS/MS)对PhIP及其代谢物进行定量。当采用25微升尿液进行分析时,PhIP的定量下限(LOQ)为万亿分之五(ppt),葡萄糖醛酸共轭物的LOQ值为50 ppt。该萃取方案具有通用性,已被用于分离PhIP的其他环羟基化和葡萄糖醛酸化代谢物,以便通过LC-ESI/MS/MS进行表征。

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