Development and validation of an LC-UV method for the determination of sulfonamides in animal feeds

被引:10
|
作者
Kumar, P. [1 ]
Companyo, R. [1 ]
机构
[1] Univ Barcelona, Dept Quim Analit, E-08028 Barcelona, Spain
关键词
sulphonamides; feed analysis; SPE; LC-UV; PHASE LIQUID-CHROMATOGRAPHY; SULFAMETHAZINE; SWINE;
D O I
10.1002/dta.296
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple LC-UV method was developed for the determination of residues of eight sulfonamides (sulfachloropyridazine, sulfadiazine, sulfadimidine, sulfadoxine, sulfamethoxypyridazine, sulfaquinoxaline, sulfamethoxazole, and sulfadimethoxine) in six types of animal feed. C18, Oasis HLB, Plexa and Plexa PCX stationary phases were assessed for the clean-up step and the latter was chosen as it showed greater efficiency in the clean-up of interferences. Feed samples spiked with sulfonamides at 2 mg/kg were used to assess the trueness (recovery %) and precision of the method. Mean recovery values ranged from 47% to 66%, intra-day precision (RSD %) from 4% to 15% and inter-day precision (RSD %) from 7% to 18% in pig feed. Recoveries and intra-day precisions were also evaluated in rabbit, hen, cow, chicken and piglet feed matrices. Calibration curves with standards prepared in mobile phase and matrix-matched calibration curves were compared and the matrix effects were ascertained. The limits of detection and quantification in the feeds ranged from 74 to 265 mu g/kg and from 265 to 868 mu g/kg, respectively. Copyright (c) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:368 / 375
页数:8
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