An improved high-throughput liquid chromatographic/tandem mass spectrometric method for terbinafine quantification in human plasma, using automated liquid-liquid extraction based on 96-well format plates

被引:21
作者
Dotsikas, Yannis [1 ]
Apostolou, Constantinos [1 ]
Kousoulos, Constantinos [1 ]
Tsatsou, Georgia [1 ]
Loukas, Yannis L. [1 ]
机构
[1] Univ Athens, Lab Pharmaceut Anal & Bioequivalence Serv GLP Com, Dept Pharmaceut Chem, Sch Pharm, GR-15771 Athens, Greece
关键词
terbinafine; bioequivalence; 96-well format plates; electrospray tandem mass spectrometry;
D O I
10.1002/bmc.738
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fully automated high-throughput liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed for terbinafine quantification in human plasma. The plasma samples were treated by liquid-liquid extraction (LLE) in 2.2mL 96-deepwell plates. Terbinafine and the internal standard (IS) N-methyl-1-naphthalenemethylamine were extracted from human plasma by LLE, using a mixture of methyl t-butyl ether (MTBE)-hexane (70:30, v/v) as the organic solvent. All liquid transfer steps, including preparation of calibration standards and quality control samples, as well as the addition of the IS, were performed automatically by using robotic liquid handling workstations. After vortexing, centrifugation and freezing, the supernatant organic solvent was evaporated and reconstituted in a small volume of a reconstitution solution. Sample analysis was performed by reversed-phase LC-MS/MS, with positive ion electrospray ionization, using multiple reaction monitoring (MRM). The method had a very short sample preparation time and a chromatographic run time of 2.2 min. It was proved to have excellent sensitivity, specificity, accuracy as well as inter- and intraday precision for the quantification of terbinafine in human plasma. The calibration curve was linear for the range of concentrations 5.0-2000.0 ng/mL. The proposed method was applied to the rapid and reliable determination of terbinatine in a bioequivalence study after per os administration of 250mg tablet formulations of terbinatine. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:201 / 208
页数:8
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