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Hydrophilic interaction chromatography-tandem mass spectrometry of donepezil in human plasma: Application to a pharmacokinetic study of donepezil in volunteers

机译:多奈哌齐在人血浆中的亲水相互作用色谱-串联质谱:在志愿者中多奈哌齐的药代动力学研究中的应用

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摘要

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 μL 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.
机译:建立了选择性,灵敏和快速的亲水相互作用液相色谱-电喷雾电离串联质谱法,用于测定人血浆中的多奈哌齐。使用甲基叔丁基醚在碱性pH值下从人血浆中两次提取多奈哌齐。在乙腈:甲酸铵(50 mM,pH 4.0)(85:15,v / v)的流动相的Atlantis HILIC硅胶柱上分离分析物,并通过串联质谱法在选择性反应监测模式下进行检测。校准曲线在0.10-50.0 ng / mL的浓度范围内是线性的(r = 0.9994),使用200μL血浆样品的定量下限为0.1 ng / mL。在四个QC水平进行的批内和批间分析的变异系数和相对误差分别为2.7%至10.5%和-10.0%至0.0%。多奈哌齐和西沙必利没有基质作用。本方法成功地应用于口服多奈哌齐盐酸盐(10毫克片剂)给男性健康志愿者后的多奈哌齐药代动力学研究。

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