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Determination and characterization of quinolones in foodstuffs of animal origin by CE-UV,  LC-UV, LC-Fl, LC-MS and LC-MS/MS

机译:通过CE-UV,LC-UV,LC-Fl,LC-MS和LC-MS / MS测定和表征动物源食品中的喹诺酮

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摘要

In this work methods for the multiresidue determination of the series of quinolones include in the European regulation in food of animal origin are de veloped and validated in line with Commission Decision 2002/657/EC in terms of linearity, decision limit, capability detection, precision and stability. Mult iresidue methods were established to allow the determination of quinolones covered by EU legislation in 2377/90/EC in muscle of chicken, turkey, pig and cow, plasma of cow and pig, liver of pig and milk of cow. First an extraction step was optimized and a SPE step was applied to clean!up and preconcentrate quinolones prior to their separation by CE or LC and determination by CE!UV, LC!UV, LC!Fl, LC!MS with different ion sources (ESI ,ApCI) and different mass analyser (Q, ToF) and LC!E SI!QqQ tandem mass spectrometry. The limits of quantification obtained are always lower than Maxim um Residue Limit (MRL) established by EU for quinolones in animal products and they can be applied to the control of quinolones in foodstuffs of animal origin . Finally the proposed methods were applied to determine quinolones in samples of turkey and pig muscle, pig plasma and milk of cow. Excellent quality parameters and reduced time of analysis were obtained when LC!ESI!MS/MS is used, although the others techniques presented too satisfactory results.
机译:在这项工作中,根据线性,决策极限,能力检测,精密度方面的要求,根据委员会决定2002/657 / EC,开发并验证了欧洲法规中对动物源食品中多类喹诺酮的多残留测定方法。和稳定性。建立了多种残留方法,可测定2377/90 / EC中欧盟法规涵盖的鸡,火鸡,猪和牛的肌肉,牛和猪的血浆,猪的肝脏和牛的牛奶中的喹诺酮类药物。首先对萃取步骤进行优化,然后将SPE步骤用于纯化和预浓缩喹诺酮,然后通过CE或LC分离喹诺酮并通过CE!UV,LC!UV,LC!F1,LC!MS用不同的离子源进行测定( ESI,ApCI)和不同的质量分析仪(Q,ToF)和LC!E SI!QqQ串联质谱所获得的定量限始终低于欧盟针对动物产品中喹诺酮制定的最大残留限量(MRL),可将其应用于动物源食品中喹诺酮的控制。最后,将所提出的方法用于测定火鸡和猪肌肉,猪血浆和牛乳中的喹诺酮类药物。当使用LC!ESI!MS / MS时,可获得出色的质量参数并减少了分析时间,尽管其他技术也提供了令人满意的结果。

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