Quantitative determination of rifampicin in aquatic products by stable isotope-dilution high liquid chromatography-tandem mass spectrometry

被引:6
|
作者
Li, Qin [1 ,2 ,3 ]
Cao, Jingyuan [4 ]
Han, Gang [1 ,3 ]
Liu, Huan [1 ,3 ]
Yan, Jie [1 ,3 ]
Wu, Lidong [1 ,3 ]
Li, Jincheng [1 ,2 ,3 ]
机构
[1] Shanghai Ocean Univ, Coll Fisheries & Life Sci, Shangha, Peoples R China
[2] Chinese Acad Fishery Sci, Beijing 100141, Peoples R China
[3] Minist Agr & Rural Affairs, Key Lab Control Qual & Safety Aquat Prod, Beijing, Peoples R China
[4] Beijing Univ Agr, Beijing, Peoples R China
关键词
aquatic products; determination; high liquid chromatography-tandem mass spectrometry; rifampin;
D O I
10.1002/bmc.4810
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rifampicin is a semi-synthetic broad-spectrum antibiotic obtained from rifamycin B. It is one of the most effective first-line antituberculosis drugs and is widely used in clinical practice. In the present study, we describe a rapid and sensitive method for the determination of rifampin in aquatic products by stable isotope-dilution high liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Samples were extracted with the acetonitrile, degreased by hexane, and then concentrated by nitrogen blowing. After separation using a C-18 column with a mixture of acetonitrile and water as mobile phase, it was determined by HPLC-MS/MS using the stable isotope-dilution calibration method. The performance of our method was validated. The limit of detection was 0.25 mu g kg(-1) and the limit of quantification was 0.5 mu g kg(-1). At the three spiked levels of 0.5, 1.0 and 5.0 mu g kg(-1), the average recoveries of rifampicin in different aquatic products were between 75.28 and 107.6%, and the relative standard deviation ranged from 0.81 to 13.23%. This method was successfully applied for the determination of rifampin in different kinds of aquatic products and rifampicin residue was found in aquatic products obtained from markets in Beijing, China.
引用
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页数:8
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