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Quantitative multiresidue analysis of antibiotics in milk and milk powder by ultra-performance liquid chromatography coupled to tandem quadrupole mass spectrometry

机译:超高效液相色谱-串联四极杆质谱联用技术对牛奶和奶粉中的抗生素进行多残留定量分析

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A simple and fast multiresidue extraction and purification method was developed for the determination of 61 veterinary drugs, belonging to seven classes, in milk and milk powder. The extraction depends on the acetonitrile solvent, followed by a single step to remove lipids with fatty acid chains using a new reversed phase SPE without traditional pre-equilibration and washing steps before eluting SPE. The purifying lipid effect of the present preparation method was evaluated by comparing the response changes of ion peak areas of the milk endogenous metabolites before and after SPE treatment using ultra-fast LC coupled to tandem quadrupole and TOF MS. Subsequently, UPLC coupled to tandem quadrupole MS was performed for the quantitative analysis of milk and milk powder samples spiked with 61 veterinary drugs, including beta-lactam, macrolide, amide alcohol, forest amine, sulfanilamide, tetracyclines, and quinolones antibiotics. This method is very simple, fast, sensitive, and selective, and allows the good recoveries of all compounds, with a recovery range of 61.5-118.6%, and coefficients of variation of less than 11.6%. The 61 compounds behave in the dynamic range 0.01-200 mu g kg(-1), with correlation coefficient >0.99. The limits of quantification for the analytes are in the range 0.01-5.18 mu g kg(-1). Finally, this method has been successfully applied to the screening of veterinary drugs in 50 commercial bovine milk and milk powder samples, and ceftiofur and ciprofloxacin were detected in some brand samples. (C) 2016 Elsevier B.V. All rights reserved.
机译:建立了一种简单,快速的多残留物提取和纯化方法,用于测定牛奶和奶粉中的61种兽药,共七类。萃取取决于乙腈溶剂,然后只需一步即可使用新的反相SPE去除具有脂肪酸链的脂质,而无需传统的预平衡和洗脱步骤即可洗脱SPE。通过比较使用串联四极杆和TOF MS的超快液相色谱进行SPE处理之前和之后,牛奶内源性代谢物的离子峰面积的响应变化,评估了本制备方法的纯化脂质效果。随后,将UPLC与串联四极杆质谱联用进行定量分析加标了61种兽药的牛奶和奶粉样品,其中包括β-内酰胺,大环内酯,酰胺醇,森林胺,磺胺,四环素和喹诺酮类抗生素。该方法非常简单,快速,灵敏且选择性强,可实现所有化合物的良好回收率,回收率范围为61.5-118.6%,变异系数小于11.6%。这61种化合物的动态范围为0.01-200μg kg(-1),相关系数> 0.99。分析物的定量限为0.01-5.18μg kg(-1)。最终,该方法已成功应用于50种商品牛乳和奶粉样品中的兽药筛选,并且在某些品牌样品中检测到头孢噻呋和环丙沙星。 (C)2016 Elsevier B.V.保留所有权利。

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