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

被引:9
|
作者
Yu, Lixiu [1 ]
Zhou, Ying [1 ]
He, Xiaomeng [1 ]
Li, Huqun [1 ]
Chen, Hui [2 ]
Li, Weiyong [1 ]
机构
[1] Huazhong Univ Sci & Technol, Inst Clin Pharm, Union Hosp, Tongji Med Coll, Wuhan 430022, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Infect Dis, Wuhan 430022, Peoples R China
关键词
Macitentan; Metabolite; HPLC-MS/MS; Human plasma; Pharmacokinetic; ENDOTHELIN RECEPTOR ANTAGONIST; PULMONARY ARTERIAL-HYPERTENSION; HEALTHY-SUBJECTS; PHARMACOKINETICS; PHARMACOLOGY; SAFETY;
D O I
10.1016/j.jchromb.2015.07.053
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Macitentan is a newly approved endothelin receptor antagonist (ERA) for the long-term treatment of PAH with superior receptor-binding properties and a longer duration of action compared to other available ERAs. However, analytical methods for simultaneous determination of macitentan and its active metabolite, ACT-132577, in human plasma have not been fully reported in the literature. In this work, a fast, sensitive, and reliable high-performance liquid chromatography-tandem mass spectrometry method (HPLC-MS/MS) was firstly developed and completely validated for simultaneous determination of macitentan and its active metabolite in human plasma. Plasma samples were processed with a protein precipitation using acetonitrile, followed by chromatographic separation using an Inertsil ODS-SP column (100 x 2.1 mm, 3.5 mu m) under isocratic elution with a mobile phase consisting of acetonitrile and 0.2% formic acid at a flow rate of 0.3 mL/min. Quantification was operated in multiple reaction monitoring (MRM) mode using the transitions m/z 547.1 -> 201.0 for macitentan, m/z 589.0 -> 203.0 for ACT-132577, and m/z 380.5 -> 243.3 for the IS (donepezil). The assay exhibited a linear range of 1-500 ng/mL for both macitentan and ACT-132577. The accuracy and the intra- and inter-precisions were within acceptable ranges and no significant matrix effect was observed during the method validation. The developed method was successfully utilized to a human pharmacokinetic study of macitentan as well as ACT-132577 after oral administration of 10 mg macitentan tablet in healthy Chinese volunteers. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:358 / 363
页数:6
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