Koo Tae-Sung, Kim Soo-Jin, Lee Jongjoo, Ha Dong-Jin, Baek Myoungki, Moon Hongsik
Life Science R&D Park, SK Holdings Co. Ltd, Daejeon, 305-712, Korea.
Biomed Chromatogr. 2011 Dec;25(12):1389-94. doi: 10.1002/bmc.1625. Epub 2011 Mar 9.
A liquid chromatography-tandem mass spectrometric (LC/MS/MS) method was developed for the determination of an atypical antipsychotic drug, lurasidone, in rat plasma. The method involves the addition of acetonitrile and ziprasidone (internal standard) solution to plasma samples, followed by centrifugation. An aliquot of the supernatant was diluted with water and directly injected into the LC/MS/MS system. The separations were performed on a column packed with octadecylsilica (5 μm, 2.0 × 50 mm) with 0.1% formic acid and 0.1% formic acid in acetonitrile as mobile phase and the detection was performed using tandem mass spectrometry by multiple-reaction monitoring via an electrospray ionization source. The standard curve was linear (r = 0.9982) over the concentration range 0.002-1 μg/mL. The intra- and inter-assay precisions were 1.7 and 8.6%, respectively. The accuracy range was from 90.3 to 101.8%. The lower limit of quantification was 2.0 ng/mL using 50 μL of rat plasma sample. The developed analytical method was successfully applied to the pharmacokinetic study of lurasidone in rats.
建立了一种液相色谱-串联质谱(LC/MS/MS)法,用于测定大鼠血浆中一种非典型抗精神病药物鲁拉西酮。该方法包括向血浆样品中加入乙腈和齐拉西酮(内标)溶液,然后离心。取上清液的一份用水分稀释后直接注入LC/MS/MS系统。分离在填充有十八烷基硅胶(5μm,2.0×50mm)的色谱柱上进行,以0.1%甲酸和乙腈中的0.1%甲酸为流动相,采用串联质谱通过电喷雾电离源进行多反应监测检测。标准曲线在0.002-1μg/mL浓度范围内呈线性(r = 0.9982)。批内和批间精密度分别为1.7%和8.6%。准确度范围为90.3%至101.8%。使用50μL大鼠血浆样品时,定量下限为2.0ng/mL。所建立的分析方法成功应用于鲁拉西酮在大鼠体内的药代动力学研究。