首页> 外文期刊>Analytica chimica acta >Multi-residue determination of 115 veterinary drugs and pharmaceutical residues in milk powder, butter, fish tissue and eggs using liquid chromatography-tandem mass spectrometry
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Multi-residue determination of 115 veterinary drugs and pharmaceutical residues in milk powder, butter, fish tissue and eggs using liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法测定奶粉,黄油,鱼组织和鸡蛋中的115种兽药和药物残留

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A simple and sensitive multi-residue method for the determination of 115 veterinary drugs and pharmaceuticals, belonging in more than 20 different classes, in butter, milk powder, egg and fish tissue has been developed. The method involves a simple generic solid-liquid extraction step (solvent extraction, SE) with 0.1% formic acid in aqueous solution of EDTA 0.1% (w/v)-acetonitrile (ACN)-methanol (MeOH) (1: 1: 1, v/v) with additional ultrasonic-assisted extraction. Precipitation of lipids and proteins was promoted by subjecting the extracts at very low temperature (-23 degrees C) for 12 h. Further cleanup with hexane ensures fat removal from the matrix. Analysis was performed by liquid chromatography coupled with electrospray ionization and tandem mass spectrometry (LC-ESI-MS/MS). Two separate runs were performed for positive and negative ionization in multiple reaction monitoring mode (MRM). Particular attention was devoted to extraction optimization: different sample-to-extracting volume ratios, different concentrations of formic acid in the extraction solvent and different ultrasonic extraction temperatures were tested in butter, egg and milk powder samples. The method was also applied in fish tissue samples. It was validated, on the basis of international guidelines, for all four matrices. Quantitative analysis was performed by means of standard addition calibration. For over 80% of the analytes, the recoveries were between 50% and 120% in all matrices studied, with RSD values in the range of 1-18%. Limits of detection (LODs) and quantification (LOQs) ranged from 0.008 mu g kg(-1) (oxfendazole in butter) to 3.15 mg kg(-1) (hydrochlorthiazide in egg). The evaluated method provides reliable screening, quantification, and identification of 115 veterinary drug and pharmaceutical residues in foods of animal origin and has been successfully applied in real samples. (C) 2015 Elsevier B.V. All rights reserved.
机译:已经开发了一种简单灵敏的多残留方法,用于测定黄油,奶粉,鸡蛋和鱼肉中的115种兽药和药物,这些兽药和药物属于20多个不同类别。该方法包括一个简单的通用固液萃取步骤(溶剂萃取,SE),该溶液中含0.1%甲酸的EDTA 0.1%(w / v)-乙腈(ACN)-甲醇(MeOH)(1:1:1:1)溶液。 ,v / v),并附加超声辅助提取。通过将提取物置于极低的温度(-23摄氏度)下12小时,可以促进脂质和蛋白质的沉淀。进一步用己烷净化可确保从基质中去除脂肪。通过液相色谱结合电喷雾电离和串联质谱分析(LC-ESI-MS / MS)进行分析。在多个反应监控模式(MRM)中分别进行了两个正离子和负离子电离运行。特别关注提取优化:在黄油,鸡蛋和奶粉样品中测试了不同的样品与提取物的体积比,不同的萃取溶剂中的甲酸浓度和不同的超声波萃取温度。该方法也适用于鱼类组织样品。已根据国际准则对所有四个矩阵进行了验证。通过标准添加校准进行定量分析。对于超过80%的分析物,在所有研究的基质中回收率在50%至120%之间,RSD值在1-18%的范围内。检测限(LOD)和定量限(LOQ)从0.008μg kg(-1)(黄油中的奥芬达唑)到3.15 mg kg(-1)(鸡蛋中的盐酸噻嗪)。经评估的方法可对动物源性食品中的115种兽药和药用残留物进行可靠的筛选,定量和鉴定,并已成功应用于实际样品中。 (C)2015 Elsevier B.V.保留所有权利。

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