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Determination of nitrofurans metabolites residues in aquatic products by ultra-performance liquid chromatography-tandem mass spectrometry

机译:超高效液相色谱-串联质谱法测定水产品中硝基呋喃代谢物残留

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摘要

A method was described for monitoring four nitrofuran metabolites including 5-methylmorpholino-3amino-2-oxazolidinone (AMOZ), 3-amino-2-oxazolidone (ADZ), 1-amino-hydantoin (AHD) and semicarbazide (SEM) in aquatic products. The analytes were quantified by ultra-performance liquid chromatography-tandem mass spectrometry operating in positive ion multiple monitoring mode (MRM) after 2-nitrobenzaldehyde derivatization. The matrix calibration curve was established with correlation coefficient (R-2 >0.99) in the range of 1-100 ng ml(-1). Limit of detection and limit of quantification for all analytes were 0.5 and 1.5 pg kg-1, respectively. Recovery rates and relative standard deviations ranged from 88% to 112% and 2% to 4%, respectively. The validated method was successfully applied to detect nitrofuran metabolites in 120 fish samples. The analytes were detected in 6/16 species of fish samples, with a total detection rate of 6.5%. AOZ was most frequently detected (8.3%), followed by AMOZ (7.5%), AHD (5.0%) and SEM (5.0%). The method is proposed for monitoring nitrofuran metabolites in aquatic products. (C) 2015 Elsevier Ltd. All rights reserved.
机译:描述了一种监测水产品中四种硝基呋喃代谢物的方法,包括5-甲基吗啉代-3氨基-2-恶唑烷酮(AMOZ),3-氨基-2-恶唑烷酮(ADZ),1-氨基乙内酰脲(AHD)和氨基脲(SEM) 。在2-硝基苯甲醛衍生化后,通过在阳离子多重监测模式(MRM)下运行的超高效液相色谱-串联质谱法对分析物进行定量。建立相关系数(R-2> 0.99)在1-100 ng ml(-1)范围内的基质校准曲线。所有分析物的检出限和定量限分别为0.5和1.5 pg kg-1。回收率和相对标准偏差分别为88%至112%和2%至4%。验证的方法已成功应用于120个鱼样品中的呋喃代谢物检测。在6/16种鱼类样品中检测到分析物,总检测率为6.5%。最常见的是AOZ(8.3%),其次是AMOZ(7.5%),AHD(5.0%)和SEM(5.0%)。提出了监测水产品中硝基呋喃代谢物的方法。 (C)2015 Elsevier Ltd.保留所有权利。

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