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Simultaneous determination of trimethoprim and diaveridine in tissues of chicken, porcine, and fish by hydrophilic interaction liquid chromatography-tandem mass spectrometry.

机译:亲水相互作用液相色谱-串联质谱法同时测定鸡肉,猪和鱼组织中的甲氧苄啶和地丁定。

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A sensitive liquid chromatography-tandem mass spectrometry method for simultaneous determination of trimethoprim and diaveridine in edible tissue samples (chicken and porcine muscle; liver, kidney, and fat tissues as well as fish muscle) was developed and validated in this study. Trimethoprim, diaveridine, and the internal standard trimethoprim-D3 were extracted from samples using acetonitrile. The Oasis MCX Solid-Phase Extraction Cartridge was selected for cleaning up the extracts. Chromatographic separation was performed on a hydrophilic interaction liquid chromatography column with gradient elution. The analytes were determined using triple-quadrupole mass spectrometry in positive electrospray ionization and multiple reaction monitoring mode. The relative recoveries from spiked samples ranged from 82.5 to 117.2 %, with the relative standard deviations generally being below 15.4 %. Limits of detection and quantification for analytes were within 0.3-1 and 1-2 mug kg-1, respectively. The proposed method was successfully applied to detect trimethoprim and diaveridine in real samples. copyright Springer Science+Business Media New York 2013.
机译:建立了同时测定可食用组织样品(鸡和猪肌肉,肝,肾,脂肪组织以及鱼肉)中甲氧苄啶和丁二胺定的灵敏液相色谱-串联质谱方法。使用乙腈从样品中提取甲氧苄氨嘧啶,乙胺嘧啶和内标甲氧苄啶-D 3 。选择了Oasis MCX固相萃取柱来清洁萃取物。在具有梯度洗脱的亲水相互作用液相色谱柱上进行色谱分离。使用三重四极杆质谱在正电喷雾电离和多反应监测模式下测定分析物。加标样品的相对回收率介于82.5%至117.2%之间,相对标准偏差通常低于15.4%。分析物的检出限和定量限分别在0.3-1和1-2杯子kg -1 之内。该方法成功地用于实际样品中甲氧苄啶和丁二啶的检测。版权所有Springer Science + Business Media纽约,2013年。

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