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[利用液相色谱-串联质谱法测定畜禽水产品中硝基咪唑类及其主要代谢物的分析方法]

[Analytical Method for Nitroimidazoles and Their Major Metabolites in Livestock and Fishery Products Using LC-MS/MS].

作者信息

Sakai Takatoshi, Nemoto Satoru, Teshima Reiko, Akiyama Hiroshi

机构信息

National Institute of Health Sciences.

出版信息

Shokuhin Eiseigaku Zasshi. 2017;58(4):180-187. doi: 10.3358/shokueishi.58.180.

DOI:10.3358/shokueishi.58.180
PMID:28855472
Abstract

A sensitive and reliable method for the simultaneous determination of four nitroimidazoles (ipronidazole (IPZ), dimetridazole (DMZ), metronidazole (MNZ) and ronidazole (RNZ)) and three metabolites (IPZ-OH, MNZ-OH and 2-hydroxymethyl-1-methyl-5-nitroimidazole (HMMNI)) in livestock and fishery products was developed. The analytes were extracted from samples with acetone containing acetic acid. The crude extracts were defatted by liquid-liquid partition using acetonitrile and n-hexane followed by solid-phase extraction using a cartridge column packed with divinylbenzene-N-vinylpyrolidone copolymer bearing sulfo groups. The analytes in the eluate from the cartridge column were extracted with ethyl acetate after addition of ammonium sulfate. The solvent was removed from the extract, and the residue was dissolved in 0.1 vol% formic acid. The HPLC separation was performed on a C18 column with a gradient formed from water containing 0.1 vol% formic acid and acetonitrile containing 0.1 vol% formic acid. For detection of the analytes, tandem mass spectrometry with positive ion electrospray ionization was used. The recovery tests were performed on 10 livestock and fishery products. The truenesse ranged from 74.6 to 111.1%, with repeatability of 0.5-8.3 RSD% for the entire procedure. The limit of quantification was 0.0001 mg/kg for IPZ, IPZ-OH, MNZ and MNZ-OH, and 0.0002 mg/mg for DMZ, RNZ and HMMNI.

摘要

建立了一种灵敏可靠的方法,用于同时测定畜禽和水产品中的四种硝基咪唑(异丙硝唑(IPZ)、二甲硝唑(DMZ)、甲硝唑(MNZ)和洛硝哒唑(RNZ))及三种代谢物(IPZ-OH、MNZ-OH和2-羟甲基-1-甲基-5-硝基咪唑(HMMNI))。用含乙酸的丙酮从样品中提取分析物。粗提物先通过乙腈和正己烷液-液分配脱脂,然后使用装有含磺酸基团的二乙烯基苯-N-乙烯基吡咯烷酮共聚物的柱式固相萃取小柱进行净化。在柱式小柱洗脱液中加入硫酸铵后,用乙酸乙酯萃取分析物。将提取物中的溶剂去除,残留物溶解于0.1%(体积分数)甲酸中。采用含0.1%(体积分数)甲酸的水和含0.1%(体积分数)甲酸的乙腈形成的梯度,在C18柱上进行高效液相色谱分离。采用正离子电喷雾电离串联质谱法检测分析物。对10种畜禽和水产品进行了回收率测试。整个过程的真实度范围为74.6%至111.1%,相对标准偏差(RSD%)的重复性为0.5-8.3%。IPZ、IPZ-OH、MNZ和MNZ-OH的定量限为0.0001 mg/kg,DMZ、RNZ和HMMNI的定量限为0.0002 mg/kg。

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