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使用液相色谱-串联质谱法对食用动物的组织、牛奶和鸡蛋中的兽用抗菌剂进行定性筛查。

Qualitative screening of veterinary anti-microbial agents in tissues, milk, and eggs of food-producing animals using liquid chromatography coupled with tandem mass spectrometry.

作者信息

Chen Dongmei, Yu Jie, Tao Yanfei, Pan Yuanhu, Xie Shuyu, Huang Lingli, Peng Dapeng, Wang Xu, Wang Yulian, Liu Zhenli, Yuan Zonghui

机构信息

National Reference Laboratory of Veterinary Drug Residues (HZAU) and MAO Key Laboratory for Detection of Veterinary Drug Residues, Huazhong Agricultural University, Wuhan, Hubei 430070, China; MOA Laboratory for Risk Assessment of Quality and Safety of Livestock and Poultry Products, Huazhong Agricultural University, Wuhan, Hubei 430070, China.

National Reference Laboratory of Veterinary Drug Residues (HZAU) and MAO Key Laboratory for Detection of Veterinary Drug Residues, Huazhong Agricultural University, Wuhan, Hubei 430070, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Apr 1;1017-1018:82-88. doi: 10.1016/j.jchromb.2016.02.037. Epub 2016 Mar 3.

Abstract

A method for the analysis of 120 drugs in animal derived food was developed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). These analytes belong to 12 families of veterinary anti-microbial agents (quinolones, macrolides, β-lactams, nitroimidazoles, sulfonamides, lincomycines, chloramphenicols, quinoxalines, tetracyclines, polypeptides, and antibacterial synergists) as well as other compounds not assigned to a particular drug family. The animal derived food samples include muscle and liver of swine, bovine, sheep, and chicken, as well as hen eggs and dairy milk. The sample preparation included ultrasound-assisted extraction (UAE) with acetonitrile-water and a final clean-up with auto solid-phase extraction (SPE) on HLB cartridges. The detection and quantification of 120 anti-microbial agents was performed using LC-MS/MS in positive and negative ion mode. The chromatographic separation was performed on a C18 column using acetonitrile and 0.1% formic acid as the mobile phase. The limit of detection (LOD) and limit of quantification (LOQ) of all drugs in food-producing animals were 0.5-3.0μg/kg and 1.5-10.0μg/kg, respectively. The developed method was successfully utilized to monitor real samples, which demonstrated that it is a simple, fast, and robust method, and could be used as a regulatory to screen for the presence of residues from veterinary anti-microbial drugs in animal-derived foods.

摘要

建立了一种采用液相色谱-串联质谱法(LC-MS/MS)分析动物源性食品中120种药物的方法。这些分析物属于12类兽用抗菌剂(喹诺酮类、大环内酯类、β-内酰胺类、硝基咪唑类、磺胺类、林可霉素类、氯霉素类、喹喔啉类、四环素类、多肽类和抗菌增效剂)以及其他未归入特定药物类别的化合物。动物源性食品样品包括猪、牛、羊和鸡的肌肉和肝脏,以及鸡蛋和牛奶。样品制备包括用乙腈-水进行超声辅助萃取(UAE),最后在HLB柱上通过自动固相萃取(SPE)进行净化。使用LC-MS/MS在正离子和负离子模式下对120种抗菌剂进行检测和定量。色谱分离在C18柱上进行,使用乙腈和0.1%甲酸作为流动相。所有食用动物源性食品中药物的检测限(LOD)和定量限(LOQ)分别为0.5 - 3.0μg/kg和1.5 - 10.0μg/kg。所建立的方法成功用于监测实际样品,表明该方法简单、快速且稳健,可作为监管手段用于筛查动物源性食品中兽用抗菌药物残留的存在情况。

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