Xia Xi, Li Xiaowei, Zhang Suxia, Ding Shuangyang, Jiang Haiyang, Li Jiancheng, Shen Jianzhong
Department of Pharmacology and Toxicology, College of Veterinary Medicine, China Agricultural University, National Reference Laboratory for Residues of Veterinary Drugs, Beijing 100094, China.
J Chromatogr A. 2008 Oct 24;1208(1-2):101-8. doi: 10.1016/j.chroma.2008.08.055. Epub 2008 Aug 20.
A simple and specific method has been developed for the simultaneous determination of four 5-nitroimidazoles and their two corresponding metabolites and four nitrofurans in pork. The sample preparation procedure was based on a simple solvent extraction/derivatization combined with solid-phase extraction (SPE) cleanup. The target compounds were identified and quantitatively determined by high-performance liquid chromatography (HPLC) coupled with electrospray ionization tandem mass spectrometry (ESI/MS/MS) operated in multiple reaction monitoring mode. The overall corrected recoveries ranged between 93 and 106%, with relative standard deviations (RSDs) of 7-13% for the entire procedure. The detection limits of the method for the 10 compounds under study ranged from 0.01 to 0.2microg/kg.
已开发出一种简单且特异的方法,用于同时测定猪肉中四种5-硝基咪唑及其两种相应代谢物和四种硝基呋喃。样品制备程序基于简单的溶剂萃取/衍生化结合固相萃取(SPE)净化。目标化合物通过高效液相色谱(HPLC)与在多反应监测模式下运行的电喷雾电离串联质谱(ESI/MS/MS)联用进行鉴定和定量测定。整个方法的总体校正回收率在93%至106%之间,整个过程的相对标准偏差(RSD)为7%-13%。该方法对所研究的10种化合物的检测限为0.01至0.2μg/kg。