Simultaneous determination of flupirtine and its major active metabolite in human plasma by liquid chromatography-tandem mass spectrometry

被引:12
作者
Chen, XY
Zhong, DF
Xu, HY
Schug, B
Blume, H
机构
[1] Shenyang Pharmaceut Univ, Lab Drug Metab & Pharmacokinet, Shenyang 110016, Peoples R China
[2] SocraTec R&D GmbH, D-61440 Oberursel, Germany
来源
JOURNAL OF CHROMATOGRAPHY B | 2001年 / 755卷 / 1-2期
基金
中国国家自然科学基金;
关键词
flupirtine; D-13223;
D O I
10.1016/S0378-4347(01)00076-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid, selective and sensitive HPLC-tandem mass spectrometry method was developed and validated for simultaneous determination of flupirtine and its active metabolite D-13223 in human plasma. The analytes and internal standard diphenhydramine were extracted from plasma samples by liquid-liquid extraction, and chromatographed on a C-18 column. The mobile phase consisted of acetonitrile-water-formic acid (60:40:1, v/v/v), at a flow rate of 0.5 ml/min. Detection was performed on a triple quadrupole tandem mass spectrometer by selected reaction monitoring (SRM) mode via atmospheric pressure chemical ionization (APCI). The method has a limit of quantitation of 10 ng/ml for flupirtine and 2 ng/ml for D-13223, using 0.5-ml plasma sample. The linear calibration curves were obtained in the concentration range of 10.0-1500.0 ng/ml for flupirtine and 2.0-300.0 ng/ml for D-13223. The intra- and inter-run precision (RSD), calculated from quality control (QC) samples was less than 7.2% for flupirtine and D-13223. The accuracy as determined from QC samples was less than 5% for the analytes. The overall extraction recoveries of flupirtine and D-13223 were determined to be about 66% and 78% on average, respectively. The method was applied for the evaluation of the pharmacokinetics of flupirtine and active metabolite D-13223 in volunteers following peroral administration. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:195 / 202
页数:8
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