Suppr超能文献

采用液相色谱-电喷雾电离串联质谱法分析不同地理来源蜂蜜中的氯霉素。

Analysis of chloramphenicol in honeys of different geographical origin by liquid chromatography coupled to electrospray ionization tandem mass spectrometry.

作者信息

Verzegnassi L, Royer D, Mottier P, Stadler R H

机构信息

Nestlé Research Centre, Nestec Ltd, Vers-Chez-Les-Blanc, CH-1000 Lausanne-26, Switzerland.

出版信息

Food Addit Contam. 2003 Apr;20(4):335-42. doi: 10.1080/0265203031000122003.

Abstract

A sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed to detect trace amounts of the antibiotic chloramphenicol (CAP) in honey. The methodology entailed a solid-phase extraction of aqueous honey solutions followed by liquid-liquid partitioning, filtration and direct injection onto the LC-MS/MS system. Honey extracts were spiked with an isotopically labelled internal standard (d(5)-CAP) to compensate for analyte loss and potential ion suppression during the MS stage. Detection of the analyte was achieved by negative ionization electrospray in the selected reaction monitoring (SAM) mode. For confirmation, four characteristic mass transitions were monitored each for the analyte and the surrogate standard. The method was validated according to the latest European Union criteria for the analyses of veterinary drug residues in food. At all three fortification levels studied (0.1, 0.2, 0.5 microg kg(-1)) the method was accurate to within 15%. The repeatability and within-laboratory reproducibilities were <12 and 18%, respectively. The decision limit (CC alpha) and detection capability (CC beta) were both <0.1 microg kg(-1). The procedure provides a sensitive and reliable method for the determination of residues of chloramphenicol in honey. Numerous raw honeys of various geographical origins were analysed, showing extensive contamination particularly those of Chinese origin.

摘要

建立了一种灵敏的液相色谱串联质谱法(LC-MS/MS)来检测蜂蜜中痕量的抗生素氯霉素(CAP)。该方法包括对蜂蜜水溶液进行固相萃取,然后进行液液分配、过滤,并直接注入LC-MS/MS系统。蜂蜜提取物中加入了同位素标记的内标(d(5)-CAP),以补偿分析物损失和质谱阶段的潜在离子抑制。通过在选择反应监测(SAM)模式下的负离子电喷雾实现对分析物的检测。为进行确证,对分析物和替代标准物分别监测了四个特征性质量跃迁。该方法根据欧盟食品中兽药残留分析的最新标准进行了验证。在所研究的所有三个加标水平(0.1、0.2、0.5微克/千克(-1))下,该方法准确度在15%以内。重复性和实验室内再现性分别<12%和18%。决策限(CCα)和检测能力(CCβ)均<0.1微克/千克(-1)。该方法为测定蜂蜜中氯霉素残留提供了一种灵敏且可靠的方法。对众多不同地理来源的原蜜进行了分析,结果显示污染广泛,尤其是中国产的蜂蜜。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验