Determination of repaglinide in human plasma by high-performance liquid chromatography-tandem mass spectrometry

被引:17
作者
Zhang, Jie [1 ]
Gao, Feng [1 ]
Guan, Xin [1 ]
Sun, Yan-tong [1 ,2 ]
Gu, Jing-kai [1 ]
Fawcett, J. Paul [3 ]
机构
[1] Jilin Univ, Coll Life Sci, Res Ctr Drug Metab, Changchun 130012, Jilin, Peoples R China
[2] Jilin Univ, Sch Pharmaceut Sci, Changchun 130012, Jilin, Peoples R China
[3] Univ Otago, Sch Pharm, Dunedin, New Zealand
关键词
Repaglinide; Pharmacokines; LC-MS/MS; Human plasma;
D O I
10.1016/j.apsb.2011.04.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A rapid and sensitive method based on high-performance liquid chromatography tandem mass spectrometry (LC MS/MS) has been developed for the determination of repaglinide in human plasma. The analyte and internal standard (I.S.), diazepam, were extracted from plasma (25 mu L) by liquid liquid extraction with diethyl ether dichloromethane (60:40, v/v) and separated on a XDB-C-18 column using acetonitrile ammonium acetate buffer (pH 6.8, 0.01 mol/L) as mobile phase. The retention times of repaglinide and I.S. were 1.95 and 2.35 min, respectively. Detection was carried out using API 4000 mass spectrometer with an ESI interface operating in the multiple reaction monitoring (MRM) mode. The assay was linear over the concentration range 0.050-50 ng/mL with a limit of detection (LOD) of 0.010 ng/mL. Intra- and inter -day precisions (as relative standard deviation, R.S.D.) were <= 5.07 A and <= 11.2%, respectively, and accuracy (as relative error, R.E.) was from 0.593% to 1.26%. The assay was successfully applied to a pharmacokinetic study involving a single oral administration of a tablet containing 2 mg repaglinide to each of 10 healthy volunteers. (C) 2011 Institute of Materia Medica, Chinese Academy of Medical Sciences and Chinese Pharmaceutical Association. Production and hosting by Elsevier B.V. All rights reserved.
引用
收藏
页码:40 / 45
页数:6
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