首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of analytical methods for multiresidue determination of quinolones in pig muscle samples by liquid chromatography with ultraviolet detection, liquid chromatography-mass spectrometry and liquid chromagraphy-tandem mass spectrometry
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Development of analytical methods for multiresidue determination of quinolones in pig muscle samples by liquid chromatography with ultraviolet detection, liquid chromatography-mass spectrometry and liquid chromagraphy-tandem mass spectrometry

机译:液相色谱-紫外检测,液相色谱-质谱和液相色谱-串联质谱法测定猪肌肉样品中喹诺酮的多残留分析方法的建立

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摘要

This paper presents a comparison between liquid chromatography with ultraviolet detection (LC-UV), liquid chromatography-mass spectrometry (LC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods developed for the multiresidue determination of 8 quinolones, around their maximum residue levels (MRLs) in pig muscle. The procedure involves common extraction of the quinolones from the tissues by traditional extraction, a step for clean-up and preconcentration of the analytes by solid-phase extraction (SPE) and a subsequent liquid chromatographic analysis. The methods present satisfactory results of linearity, precision and limits of quantification much lower than the MRLs established by the European Union for quinolones in pig tissues. (c) 2005 Elsevier B.V. All rights reserved.
机译:本文介绍了用于多残留测定8种喹诺酮的液相色谱-紫外检测(LC-UV),液相色谱-质谱(LC-MS)和液相色谱-串联质谱(LC-MS / MS)方法之间的比较大约在猪肌肉中的最大残留量(MRL)附近。该程序包括通过传统提取方法从组织中常规提取喹诺酮,通过固相提取(SPE)纯化和预浓缩分析物的步骤以及随后的液相色谱分析。该方法呈现出令人满意的线性,精确度和定量限的结果,远低于欧盟为猪组织中喹诺酮类建立的最大残留限量。 (c)2005 Elsevier B.V.保留所有权利。

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