Rapid ultraperformance liquid chromatography-tandem mass spectrometry method for quantification of oxcarbazepine and its metabolite in human plasma

被引:21
作者
Bhatt, Mitesh [1 ,2 ]
Shaha, Sanjay [2 ]
Shivprakash [1 ]
机构
[1] Synchron Res Serv Private Ltd, Chambers, Ahmadabad 380054, Gujarat, India
[2] Shree UP Arts Smt MG Panchal Sci & VL Shah Commer, Dept Chem, Vijapur, Gujarat, India
关键词
oxcarbazepine; 10,11-dihydro-10-hydroxycarbamazepine; imipramine; LC-MS/MS; human plasma; Acquity; UPLC; SOLID-PHASE EXTRACTION; MAIN METABOLITES; LC-MS/MS; ANTIEPILEPTIC DRUGS; EPILEPTIC PATIENTS; PHARMACOKINETICS; MONOHYDROXY; VALIDATION;
D O I
10.1002/bmc.1510
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid and sensitive ultraperformance liquid chromatography tandem mass spectrometry assay was developed for the simultaneous analysis of oxcarbazepine and its main metabolite in human plasma. The assay involves a simple solid-phase extraction procedure of 0.3 mL of human plasma and analysis was performed on a triple-quadrupole tandem mass spectrometer in multiple reaction monitoring mode via electrospray ionization. Separation was achieved on an Acquity UPLC (TM) BEH C(18) column (50 x 2.1 mm, i.d., 1.7 mu m) with isocratic elution at a flow-rate of 0.25 mL/min and imipramine was used as the internal standard. The standard calibration curve was linear over the range 9.580-5070.205 ng/mL for oxcarbazepine (OXC) and 19.444-10290.800 ng/mL for 10,11-dihydro-10-hydroxycarbamazepine (MHD), expressed by the linear correlation coefficient r(2), which was better than 0.995 for OXC and MHD. The intra-and inter-day precision and accuracy of the quality control samples were within 10.0%. The recoveries were 81.0, 89.6 and 66.6% for OXC, MHD and imipramine, respectively. The total run time was 1.5 min only for each sample, which makes it possible to analyze more than 350 samples per day. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:751 / 759
页数:9
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