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.
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页数:8
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