Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 646 Songtao Road, Shanghai 201203, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 May 1;878(15-16):1181-4. doi: 10.1016/j.jchromb.2010.03.013. Epub 2010 Mar 16.
A rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for the determination of picamilon concentration in human plasma. Picamilon was extracted from human plasma by protein precipitation. High performance liquid chromatography separation was performed on a Venusil ASB C(18) column with a mobile phase consisting of methanol -10mM ammonium acetate-formic acid (55:45:01, v/v/v) at a flow rate of 0.65ml/min. Acquisition of mass spectrometric data was performed in selected reaction monitoring mode, using the transitions of m/z 209.0-->m/z (78.0+106.0) for picamilon and m/z 152.0-->m/z (93.0+110.0) for paracetamol (internal standard). The method was linear in the concentration range of 1.00-5000ng/ml for the analyte. The lower limit of quantification was 1.00ng/ml. The intra- and inter-assay precision were below 13.5%, and the accuracy was between 99.6% and 101.6%. The method was successfully applied to characterize the pharmacokinetic profiles of picamilon in healthy volunteers. This validated LC-MS/MS method was selective and rapid, and is suitable for the pharmacokinetic study of picamilon in humans.
建立并验证了一种用于测定人血浆中吡卡尼隆浓度的快速液相色谱-串联质谱(LC-MS/MS)法。吡卡尼隆经蛋白沉淀法从人血浆中提取。采用甲醇-10mM 乙酸铵-甲酸(55:45:01,v/v/v)作为流动相,在 Venusil ASB C18 柱上以 0.65ml/min 的流速进行高效液相色谱分离。以 m/z 209.0-->m/z(78.0+106.0)(分析物)和 m/z 152.0-->m/z(93.0+110.0)(内标物)进行选择反应监测模式下的质谱数据采集。该方法在分析物浓度为 1.00-5000ng/ml 范围内呈线性。定量下限为 1.00ng/ml。日内和日间精密度均低于 13.5%,准确度在 99.6%至 101.6%之间。该方法成功应用于描述健康志愿者中吡卡尼隆的药代动力学特征。该验证后的 LC-MS/MS 方法具有选择性和快速性,适用于人体吡卡尼隆的药代动力学研究。