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A LC-MS/MS confirmatory method for determination of chloramphenicol in real samples screened by competitive immunoassay

机译:LC-MS / MS确证方法测定竞争性免疫法筛选的真实样品中的氯霉素

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摘要

A new liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed to confirm chloramphenicol (CAP) residues in foods of animal origin and in urine samples, which were earlier found positive under the screening analysis, performed by competitive enzyme-linked immunoassay (ELISA) technique. The developed LC-MS/MS method was applied to four non-compliant samples from 2008 to 2012; giving concentrations of CAP residues from 1.18 to 3.68 μg kg. All samples, qualified positive by ELISA, were confirmed with the LC-MS/MS technique and found to be non-compliant. The effectiveness of the confirmatory method was proven by participating in a successful proficiency test in year 2010. Both LC-MS/MS and ELISA methods were validated according to the European Union 2002/657/EC decision. The decision limit of the confirmatory method was determined as 0.02 μg kg for CAP in each validated matrix, while the detection capability of the screening test was 0.15 μg kg.
机译:开发了一种新的液相色谱-串联质谱(LC-MS / MS)方法,以确认动物源性食品和尿液样品中的氯霉素(CAP)残留,这些残留物在早期的筛选分析中通过竞争性酶法检测为阳性。连锁免疫分析(ELISA)技术。从2008年到2012年,已开发的LC-MS / MS方法被应用于四个不合格样品。 CAP残留浓度为1.18至3.68μgkg。所有样品(通过ELISA鉴定为阳性)均已通过LC-MS / MS技术确认,发现不合格。通过参加2010年的一次能力验证,证明了该确认方法的有效性。LC-MS / MS和ELISA方法均根据欧盟2002/657 / EC决定进行了验证。在每种经过验证的基质中,CAP的确证方法的判定极限确定为0.02μgkg,而筛选试验的检测能力为0.15μgkg。

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