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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Multi-class confirmatory method for analyzing trace levels of tetracyline and quinolone antibiotics in pig tissues by ultra-performance liquid chromatography coupled with tandem mass spectrometry
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Multi-class confirmatory method for analyzing trace levels of tetracyline and quinolone antibiotics in pig tissues by ultra-performance liquid chromatography coupled with tandem mass spectrometry

机译:超高效液相色谱-串联质谱法分析猪组织中痕量四环素和喹诺酮类抗生素的多类确证方法

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An ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC/MS/MS) method was developed to screen and confirm multi-class veterinary drug residues in pig tissues including pig kidney, liver and meat. Twenty-one drugs of two different classes including seven tetracyclines and four types of quinolones (quinoline, naphthyridine, pyridopyrimidine and cinoline) were determined simultaneously in a single run. The homogenized sample tissues were extracted with EDTA-McIlvaine buffer solution and further purified using a polymer-based Oasis HLB solid-phase extraction (SPE) cartridge. An ACQUITY UPLC (TM) BEH C-18 column was used to separate the analytes followed by tandem mass spectrometry using an electrospray ionization source. MS data acquisition was performed in the positive ion multiple reaction monitoring mode, selecting two ion transitions for each target compound. Recovery studies were performed at different fortification levels. The overall average recoveries from pig muscle, kidney, and liver fortified with quinolones and tetracyclines at three levels ranged from 80.2 to 117.8% based on the use of matrix-fortified calibration with the coefficients of variation ranging from 2.1 to 17.8% (n=6). The limits of quantitation (LOQs) of quinolones and tetracyclines in different tissues ranged from 0.03-4.50 mu g/kg and 0.16-10.00 mu g/kg, respectively. The effects of the extraction solvent, SPE cartridge, elution solvent and sample matrix on the analyte recovery as well as the effects of the mobile phase composition and column temperature on the chromatographic behavior were also studied. Copyright (C) 2007 John Wiley & Sons, Ltd.
机译:开发了一种超高效液相色谱-串联质谱(UPLC / MS / MS)方法,以筛选和确认猪组织(包括猪肾,肝和肉)中的多类兽药残留。在一次运行中同时测定了21种不同类别的药物,包括7种四环素和4种喹诺酮类药物(喹啉,萘啶,吡啶并嘧啶和茶碱)。匀浆的样品组织用EDTA-McIlvaine缓冲溶液萃取,并使用基于聚合物的Oasis HLB固相萃取(SPE)柱进一步纯化。使用ACQUITY UPLC(TM)BEH C-18色谱柱分离分析物,然后使用电喷雾电离源进行串联质谱分析。 MS数据采集是在阳离子多重反应监测模式下进行的,为每种目标化合物选择两个离子跃迁。在不同的设防水平上进行了恢复研究。根据使用矩阵强化校正方法的变异系数从2.1%至17.8%(n = 6),三种水平的喹诺酮和四环素强化的猪肌肉,肾脏和肝脏的总体平均回收率介于80.2至117.8%之间)。不同组织中喹诺酮和四环素的定量限(LOQ)分别为0.03-4.50μg / kg和0.16-10.00μg / kg。还研究了萃取溶剂,SPE柱,洗脱溶剂和样品基质对分析物回收率的影响,以及流动相组成和柱温对色谱行为的影响。版权所有(C)2007 John Wiley&Sons,Ltd.

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