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在串联液相色谱-电喷雾电离质谱/质谱分析之前,使用分子印迹固相萃取吸附剂从鸡蛋样品中测定四种5-硝基咪唑及其三种代谢物。

Use of molecularly imprinted solid-phase extraction sorbent for the determination of four 5-nitroimidazoles and three of their metabolites from egg-based samples before tandem LC-ESIMS/MS analysis.

作者信息

Mohamed Rayane, Mottier Pascal, Treguier Laureen, Richoz-Payot Janique, Yilmaz Ecevit, Tabet Jean-Claude, Guy Philippe A

机构信息

Nestlé Research Center, Nestec Ltd., P.O. Box 44, Vers-Chez-Les-Blanc, 1000 Lausanne 26, Switzerland.

出版信息

J Agric Food Chem. 2008 May 28;56(10):3500-8. doi: 10.1021/jf072807h. Epub 2008 May 6.

DOI:10.1021/jf072807h
PMID:18457401
Abstract

A nitroimidazole, molecularly imprinted polymer (MIP) was tested to extract four 5-nitroimidazoles (i.e., dimetridazole (DMZ), ipronidazole (IPZ), metronidazole (MNZ), and ronidazole (RNZ)) and three of their metabolites (i.e., DMZOH, IPZOH, and MNZOH) from egg powder samples. Various MIP templates were produced, and their selectivity was assessed on nitroimidazole standard solutions using liquid chromatography coupled with ultraviolet detection. The optimal cleanup was then used for the extraction of nitroimidazole in egg powder samples, and their quantification was achieved by isotope dilution LC-ESIMS/MS. The sample preparation entails a solubilization of the samples with water and acetonitrile followed by a MISPE cleanup step before LC-ESIMS/MS analysis. Data acquisition was achieved using selected reaction monitoring, and quantification was done with five deuterated analogues (i.e., DMZ- d(3), RNZ- d(3), IPZ- d(3), DMZOH- d(3), and IPZOH- d(3)). DMZOH- d(3) was used to quantify MNZ and MNZOH since they do not have their corresponding internal standards. The method was validated according to the European Union criteria by spiking experiments at concentration levels of 1, 2, and 3 microg/kg. At these three levels and for compounds having their own internal standards, acceptable performance data were obtained, with internal standard corrected recoveries ranging from 91 to 111%, and decision limits (CCalpha) and detection capabilities (CCbeta) were below 0.34 and 0.39 microg/kg, respectively.

摘要

对一种硝基咪唑分子印迹聚合物(MIP)进行了测试,以从蛋粉样品中提取4种5-硝基咪唑(即二甲硝唑(DMZ)、异丙硝唑(IPZ)、甲硝唑(MNZ)和洛硝哒唑(RNZ))及其3种代谢物(即DMZOH、IPZOH和MNZOH)。制备了各种MIP模板,并使用液相色谱-紫外检测法在硝基咪唑标准溶液上评估其选择性。然后将最佳净化方法用于蛋粉样品中硝基咪唑的提取,并通过同位素稀释液相色谱-电喷雾离子阱串联质谱法进行定量。样品制备包括用水和乙腈溶解样品,然后在液相色谱-电喷雾离子阱串联质谱分析之前进行分子印迹固相萃取净化步骤。使用选择反应监测进行数据采集,并用5种氘代类似物(即DMZ-d(3)、RNZ-d(3)、IPZ-d(3)、DMZOH-d(3)和IPZOH-d(3))进行定量。由于MNZ和MNZOH没有相应的内标,因此使用DMZOH-d(3)对它们进行定量。该方法根据欧盟标准,通过在1、2和3μg/kg浓度水平下的加标实验进行了验证。在这三个浓度水平下,对于有自身内标的化合物,获得了可接受的性能数据,内标校正回收率在91%至111%之间,决策限(CCα)和检测能力(CCβ)分别低于0.34和0.39μg/kg。

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