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采用液相色谱/电喷雾电离-离子阱质谱法测定2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)及其代谢物2-羟基氨基-PhIP 。

Determination of 2-amino-1-methyl-6-phenylimidazo[4,5- b]pyridine (PhIP) and its metabolite 2-hydroxyamino-PhIP by liquid chromatography/electrospray ionization-ion trap mass spectrometry.

作者信息

Prabhu S, Lee M J, Hu W Y, Winnik B, Yang I, Buckley B, Hong J Y

机构信息

School of Public Health/Environmental and Occupational Health Sciences Institute, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey, USA.

出版信息

Anal Biochem. 2001 Nov 15;298(2):306-13. doi: 10.1006/abio.2001.5392.

Abstract

2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) is the most abundant heterocyclic aromatic amine found in cooked meat. It is metabolically activated by the human cytochrome P450 enzymes to form the carcinogenic metabolite N2-OH-PhIP. PhIP has been found to induce tumors in rats and is a suspected human carcinogen. In the present work, we have developed and validated a liquid chromatography-electrospray ionization/ion trap mass spectrometry (LC-ESI/ITMS) method for the determination of PhIP and N2-OH-PhIP. PhIP was incubated with microsomes prepared from the human liver; the PhIP and N2-OH-PhIP formed were isolated from the biomatrices by solid-phase extraction using C18 cartridges, with recoveries greater than 86%. Subsequently, the products were separated on a microbore reversed-phase C18 liquid chromatograph coupled to an ESI-ITMS. The ESI interface and the ITMS were tuned for various parameters, and data acquisition was performed in selective ion monitoring mode. The detection limit of PhIP and N2-OH-PhIP was 1 and 10 pg, respectively. The method is highly sensitive and selective, has simple sample preparation protocols, and should be applicable to the study of the metabolic activation of PhIP in various human tissues.

摘要

2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)是熟肉中含量最丰富的杂环芳香胺。它通过人细胞色素P450酶进行代谢活化,形成致癌代谢物N2-羟基-PhIP。已发现PhIP可在大鼠体内诱发肿瘤,是一种疑似人类致癌物。在本研究中,我们开发并验证了一种液相色谱-电喷雾电离/离子阱质谱法(LC-ESI/ITMS),用于测定PhIP和N2-羟基-PhIP。将PhIP与人肝制备的微粒体一起孵育;通过使用C18柱进行固相萃取,从生物基质中分离出形成的PhIP和N2-羟基-PhIP,回收率大于86%。随后,将产物在与ESI-ITMS联用的微径反相C18液相色谱仪上进行分离。对ESI接口和ITMS的各种参数进行了优化,并在选择性离子监测模式下进行数据采集。PhIP和N2-羟基-PhIP的检测限分别为1 pg和10 pg。该方法具有高灵敏度和选择性,样品制备方案简单,应适用于研究PhIP在各种人体组织中的代谢活化。

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