Bohm Detlef A, Stachel Carolin S, Gowik Petra
Federal Office of Consumer Protection and Food Safety (BVL), National Reference Laboratories for Contaminants and Residues, Mauerstr. 39-42, D-10117 Berlin, Germany.
J AOAC Int. 2011 Mar-Apr;94(2):407-19.
The described multimethod is suited for the determination of 53 substances of eight antibiotic groups-tetracyclines, quinolones, macrolides, sulfonamides, diphenylsulfones, diamino-pyrimidine derivatives, pleuromutilines, and lincosamides-in cattle and pig muscle. All substances were analyzed simultaneously with the same sample preparation and in one HPLC/MS/MS run. The validation of the multimethod was successfully accomplished with the help of an alternative in-house validation concept requiring only 48 experiments. The substances were validated at concentrations of 0.25, 0.5, 1.0, 1.5, and 2.0 x MRL (maximum residue limit) or 5, 10, 20, 30, and 40 microg/kg for substances without an MRL. The calculated relevant validation parameters were based on and comply with the requirements of Commission Decision 2002/657/EC, i.e., the decision limit, detection capability, repeatability, within-laboratory reproducibility, and recovery. The robustness of the method was demonstrated by varying seven factors of the analytical procedure. Several proficiency tests were carried out successfully to provide evidence for the applicability of the method.
所描述的多方法适用于测定牛和猪肌肉中八类抗生素的53种物质,包括四环素类、喹诺酮类、大环内酯类、磺胺类、二苯砜类、二氨基嘧啶衍生物、截短侧耳素类和林可酰胺类。所有物质在相同的样品制备条件下同时进行分析,并在一次HPLC/MS/MS运行中完成。借助仅需48次实验的替代内部验证概念,该多方法的验证得以成功完成。这些物质在浓度为0.25、0.5、1.0、1.5和2.0倍MRL(最大残留限量)时进行了验证,对于没有MRL的物质则在5、10、20、30和40μg/kg的浓度下进行验证。计算得出的相关验证参数基于并符合委员会第2002/657/EC号决定的要求,即决策限、检测能力、重复性、实验室内再现性和回收率。通过改变分析程序的七个因素证明了该方法的稳健性。成功进行了多次能力验证试验,以证明该方法的适用性。