Simultaneous determination of roflumilast and its metabolite in human plasma by LC-MS/MS: Application for a pharmacokinetic study

被引:7
作者
Cui, Xinge [1 ]
Huang, Jie [2 ]
Zheng, Xin [1 ]
Jiang, Ji [1 ]
Kuang, Yun [2 ]
Hu, Pei [1 ]
机构
[1] Beijing Union Med Coll Hosp, Clin Pharmacol Res Ctr, Beijing, Peoples R China
[2] Cent S Univ, Xiangya Hosp 3, Ctr Clin Pharmacol, Changsha, Hunan, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2016年 / 1029卷
关键词
Roflumilast; Roflumilast N-oxide; LC-MS/MS; Human plasma; Chinese healthy volunteers; OBSTRUCTIVE PULMONARY-DISEASE; RANDOMIZED CLINICAL-TRIALS; N-OXIDE; POLYMORPHISMS; INHIBITOR; COPD;
D O I
10.1016/j.jchromb.2016.06.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Roflumilast had shown good efficacy and safety in Caucasian COPD patients after oral administration of 0.5 mg. The main active metabolite of it is roflumilast N-oxide. A reliable liquid chromatography-tandem mass spectrometry (LC-MS/MS) quantitation method was developed for the simultaneous determination of them in human plasma with rather low limits of quantitation for roflumilast (0.02 ng/mL) and roflumilast N-oxide (0.04 ng/mL). Human plasma samples were prepared by solid phase extraction (SPE), which ensured high recovery and slight matrix effect for the both analytes. This method showed good linearity, accuracy, precision and stability in the range of 0.02-10 ng/mL and 0.04-50 ng/mL for roflumilast and roflumilast N-oxide respectively. The developed method was successfully applied for the pharmacokinetic research in Chinese healthy volunteers after oral administration of 0.25 mg, 0.375 mg and 0.5 mg of roflumilast tablet. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 67
页数:8
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