首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development and validation of an ultra performance liquid chromatography-quadrupole time of flight-mass spectrometry (in MSE mode) method for the quantitative determination of 20 antimicrobial residues in edible muscle tissue of European sea bass
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Development and validation of an ultra performance liquid chromatography-quadrupole time of flight-mass spectrometry (in MSE mode) method for the quantitative determination of 20 antimicrobial residues in edible muscle tissue of European sea bass

机译:欧洲鲈鱼可食用肌肉组织中20例抗菌残留量的超高效液相色谱 - 四极其时间的开发与验证

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A UPLC-QTOF-MS method for the simultaneous determination of 20 veterinary drug residues and metabolites (tetracyclines, quinolones, sulfonamides and diaminopyrimidines) in edible muscle plus skin tissue of European sea bass (Dicentrarchus Labrax) was developed. For the identification of analytes a positive electrospray ionization quadropole time-of flight mass spectrometer operating in MSE mode (UPLC-QTOF-MSE) was used. MSE mode provides high chromatographic resolution and accurate mass measurements in both MS and MS/MS modes simultaneously in a single run. Separation was achieved on a UPLC BEH C18 (50 mm X 2.1 mm, 1.7 mu m) column in a gradient elution program of 10 min. Examined antibiotics were isolated easily after a simple solid-liquid extraction procedure with acidic acetonitrile (0.1% v/v formic acid) and Na-2 EDTA 0.1 M. Recovery rates from muscle plus skin tissue ranged from 93.8% to 107.5% for all targeted compounds. The detection limits and the limits of quantification ranged from 2.22 to 15.00 mu g/kg, and from 6.67 to 45.46 mu g/kg, respectively. The developed method was validated in terms of selectivity, matrix effect, linearity, accuracy, precision, stability and sensitivity, CC alpha and CC beta according to European Union Decision 2002/657/EC. The proposed method was applied for the analysis of contaminated fish samples after in feed administration of danofloxacin mesylate. (C) 2018 Elsevier B.V. All rights reserved.
机译:对于在可食用肌肉加欧洲海鲈(粗养)的皮肤组织20个兽药残留和代谢物(四环素类,喹诺酮类,磺胺类和二氨基嘧啶)的同时测定UPLC-QTOF-MS方法的开发。对于分析物的鉴定,使用了MSE模式(UPLC-QTOF-MSE)的正飞行电喷雾离子化四极时的质谱仪操作。 MSE模式提供高色谱分辨率和在MS和MS / MS模式在单次运行同时精确质量测量。分离在10分钟的梯度洗脱程序上的UPLC BEH C18实现英寸(50毫米×2.1毫米,1.7微米)柱。检查抗生素与酸性乙腈(0.1%体积/体积的甲酸)和Na-2 EDTA一个简单的固 - 液萃取过程0.1从肌肉加上皮肤组织M.回收率从93.8%至107.5%为所有目标后容易分离化合物。的检测限和定量限从2.22至15.00微米克/千克范围,和从6.67至45.46微米克/公斤,分别。所提出的方法是根据欧洲联盟决策657分之2002/ EC中选择性,基体效应,线性度,准确度,精密度,稳定性和敏感度,CCα和CC的β方面验证。在达氟沙星甲磺酸盐的施用进料施加于受污染的鱼样品的分析后所提出的方法。 (c)2018年elestvier b.v.保留所有权利。

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