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Comparison of the Multiple Reaction Monitoring and Enhanced Product Ion Scan Modes for Confirmation of Stilbenes in Bovine Urine Samples Using LC–MS/MS QTRAP® System

机译:使用LC–MS / MSQTRAP®系统对牛尿样品中的方丁烯进行确认的多重反应监测和增强的产物离子扫描模式的比较

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摘要

In accordance with Commission Decision 2002/657/EC, confirmatory methods for the detection of prohibited substances should comply with specific requirements, including the criteria for confirmation. Two strategies: multiple reaction monitoring (MRM) and enhanced product ion (EPI) scanning functions were compared for confirming the anabolic compounds from synthetic stilbenes group in bovine urine samples. In the research, twenty samples fortified at the Recommended Concentration (RC) of 1 µg L−1 with diethylstilbestrol, dienestrol and hexestrol were analyzed by liquid chromatography-tandem mass spectrometry on a QTRAP 5500 instrument. The analytical procedure, validated in accordance with the Commission Decision 2002/657/EC, used in the official control of hormones in Poland was applied. The validation parameters were in agreement with 2002/657/EC performance criteria. The effectiveness of MRM and EPI scanning modes for confirmation purposes was evaluated based on the percentage of the results confirmed. In all urine samples recorded in the MRM mode, the confirmation criteria (retention time, relative intensities between transitions) have been fulfilled. The presence of stilbenes in all urine samples using EPI scan mode was confirmed too as evidenced by a good matching of stilbenes spectra in the samples to the reference spectra with critical match factor above 0.7. The results of the research show that EPI scanning function provides the same effectiveness for confirmation of banned compounds as the mostly used MRM scan mode and can be an additional tool to confirm the doubtful case results in the analysis of hormones residues, even at such low concentration levels.
机译:根据委员会决定2002/657 / EC,用于检测违禁物质的确认方法应符合特定要求,包括确认标准。比较了两种策略:多重反应监测(MRM)和增强的产物离子(EPI)扫描功能,以确认牛尿液样品中合成的斯蒂苯类药物的合成代谢化合物。在研究中,在QTRAP 5500仪器上通过液相色谱-串联质谱法分析了二十种样品,其中推荐浓度(RC)为1 µg L -1 并带有己烯雌酚,己烯雌酚和己烯雌酚。采用了根据委员会决定2002/657 / EC验证的分析程序,该程序用于波兰的激素官方管制。验证参数与2002/657 / EC性能标准一致。基于确认结果的百分比,评估了MRM和EPI扫描模式用于确认目的的有效性。在以MRM模式记录的所有尿液样本中,都符合确认标准(保留时间,转换之间的相对强度)。还通过EPI扫描模式确认了所有尿液样品中均存在斯蒂尔苯,这可以通过临界匹配因子大于0.7的样品中斯蒂尔苯谱与参考谱的良好匹配来证明。研究结果表明,EPI扫描功能可提供与最常用的MRM扫描模式相同的确认禁用化合物的功效,并且即使在如此低的浓度下,也可以用作确认激素残留分析中可疑病例结果的另一种工具水平。

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