UPLC-MS/MS for simultaneous quantification of vortioxetine and its metabolite Lu AA34443 in rat plasma and its application to drug interactions

被引:3
作者
Gu, Er-Min [1 ]
Shao, Yuanyuan [2 ]
Xu, Wei-Feng [1 ]
Ye, Lei [2 ]
Xu, Ren-ai [2 ]
机构
[1] First Peoples Hosp Jiashan, Jiaxing 314100, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 1, Wenzhou 325000, Zhejiang, Peoples R China
关键词
Vortioxetine; Lu AA34443; Pharmacokinetic interaction; UPLC-MS/MS; Inhibitory effect; CYTOCHROME-P450; ANTIDEPRESSANT; AMIODARONE;
D O I
10.1016/j.arabjc.2020.09.056
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Vortioxetine is currently used as the first-line therapy drug for major depressive disorder (MDD). In the present study, we aimed to develop and fully validate an ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method for the simultaneous quantification of vortioxetine and its major metabolite Lu AA34443 in plasma and to investigate the effects of dronedarone and amiodarone on vortioxetine metabolism in rats. After protein precipitation with acetonitrile, the separation of vortioxetine, Lu AA34443 and duloxetine (internal standard, IS) were finished on an Acquity BEH C18 (2.1 mm x 50 mm, 1.7 mu m) column and their detections were conducted by a Xevo TQ-S triple quadrupole tandem mass spectrometer in the positive ion mode. The assay displayed excellent linearity in the range of 0.5-50 ng/mL for vortioxetine, and 5-1000 ng/mL for Lu AA34443. The results of this method exhibited that the precision, accuracy, matrix effect, recovery, and stability of vortioxetine and Lu AA34443 met all requirements for the quantitation in plasma samples. The validated assay was further successfully employed to study the effects of dronedarone (80 mg/kg) and amiodarone (60 mg/kg) on vortioxetine metabolism in rats. The results showed that dronedarone and amiodarone could increase the concentration of vortioxetine and have inhibitory effect on vortioxetine metabolism. Thus, vortioxetine dose interruption or reduction may be considered. (C) 2020 The Authors. Published by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:8218 / 8225
页数:8
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