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Validation of a liquid chromatography-tandem mass spectrometry screening method to monitor 58 antibiotics in milk: a qualitative approach.

机译:液相色谱-串联质谱筛查方法监测奶中58种抗生素的验证:一种定性方法。

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摘要

A multi-residue method was developed for monitoring antibiotic residues in milk using liquid chromatography coupled to a tandem quadrupole mass spectrometer (LC/MS-MS). Two very short extractions followed by two LC/MS-MS acquisitions allowed the screening of 58 antibiotics belonging to eight different families (penicillins, cephalosporins, sulfonamides, macrolides, lincosamides, aminoglycosides, tetracyclines, and quinolones). This method is currently implemented in the laboratory in a qualitative way, i.e. monitoring the presence or absence of residue in a sample and identification of the analyte before the confirmation step. In order to assess the performance of this method, a validation strategy described in an internal guideline for the validation of screening methods was applied. The aim of the validation was to prove sufficient sensitivity of the method to detect all the targeted antibiotics at the level of interest (maximum residue limit, MRL) at least. According to European Commission Decision 2002/657/EC, the suitable sensitivity of a screening method can be demonstrated when the CCbeta is below or equal to the MRL and so the false-compliant rate below or equal to 5% at the MRL level. The validation scheme was established in order to take into account various variability factors: the apparatus response, the interday repeatability, the matrix effect, etc. The results of the validation clearly demonstrate the suitability of this method for the detection and identification of more than 50 antibiotics and they are in agreement with the results obtained in routine analysis.
机译:开发了一种多残留方法,该方法使用液相色谱与串联四极杆质谱仪(LC / MS-MS)耦合来监测牛奶中的抗生素残留。两次非常短的提取,然后进行两次LC / MS-MS提取,可以筛查属于八个不同家族的58种抗生素(青霉素,头孢菌素,磺酰胺,大环内酯,林可酰胺,氨基糖苷,四环素和喹诺酮)。该方法当前在实验室中以定性方式实施,即在确认步骤之前监视样品中残留物的存在或不存在并鉴定分析物。为了评估该方法的性能,采用了内部指南中描述的用于验证筛选方法的验证策略。验证的目的是证明该方法具有足够的灵敏度,以至少在目标水平(最大残留限量,MRL)下检测所有目标抗生素。根据欧洲委员会第2002/657 / EC号决定,当CCbeta低于或等于MRL并因此在MRL级别下的错误遵守率低于或等于5%时,可以证明筛选方法的适当敏感性。建立验证方案是为了考虑各种可变性因素:设备响应,日间重复性,基质效应等。验证结果清楚地证明了该方法对50多种检测和鉴定的适用性。抗生素,它们与常规分析获得的结果一致。

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