Park Een Jeong, Lee Hye Won, Ji Hye Young, Kim Hoe Yoon, Lee Mann Hyung, Park Eun-Seok, Lee Kang Choon, Lee Hye Suk
Drug Metabolism and Bioanalysis Laboratory, College of Pharmacy, Wonkwang University, Iksan, 570-749, Korea.
Arch Pharm Res. 2008 Sep;31(9):1205-11. doi: 10.1007/s12272-001-1290-6. Epub 2008 Sep 20.
A selective, sensitive and rapid hydrophilic interaction liquid chromatography with electrospray ionization tandem mass spectrometry was developed for the determination of donepezil in human plasma. Donepezil was twice extracted from human plasma using methyl tert-butyl ether at basic pH. The analytes were separated on an Atlantis HILIC Silica column with the mobile phase of acetonitrile: ammonium formate (50 mM, pH 4.0) (85:15, v/v) and detected by tandem mass spectrometry in the selective reaction monitoring mode. The calibration curve was linear (r = 0.9994) over the concentration range of 0.10-50.0 ng/mL and the lower limit of quantification was 0.1 ng/mL using 200 muL plasma sample. The coefficient of variation and relative error for intra-and inter-assay at four QC levels were 2.7 to 10.5% and -10.0 to 0.0%, respectively. There was no matrix effect for donepezil and cisapride. The present method was successfully applied to the pharmacokinetic study of donepezil after oral dose of donepezil hydrochloride (10 mg tablet) to male healthy volunteers.
建立了一种选择性、灵敏且快速的亲水作用液相色谱-电喷雾电离串联质谱法,用于测定人血浆中的多奈哌齐。在碱性pH条件下,使用甲基叔丁基醚从人血浆中对多奈哌齐进行两次萃取。分析物在Atlantis HILIC硅胶柱上进行分离,流动相为乙腈:甲酸铵(50 mM,pH 4.0)(85:15,v/v),并采用串联质谱在选择性反应监测模式下进行检测。使用200 μL血浆样品时,校准曲线在0.10 - 50.0 ng/mL浓度范围内呈线性(r = 0.9994),定量下限为每份样品0.1 ng/mL。四个质量控制水平下的批内和批间变异系数及相对误差分别为2.7%至10.5%和 -10%至0%。多奈哌齐和顺阿曲库铵不存在基质效应。本方法成功应用于男性健康志愿者口服盐酸多奈哌齐(10 mg片剂)后的药代动力学研究。