Pan Ryh-Nan, Kuo Benjamin Pei-Chung, Pao Li-Heng
Department of Disaster Management, Taiwan Police College, Taipei, Taiwan, Republic of China.
J Chromatogr Sci. 2012 Mar;50(3):277-82. doi: 10.1093/chromsci/bms001.
A sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS-MS) method for the determination of quetiapine was developed and validated over the linearity range 1-1500 ng/mL with 0.1 mL of plasma using clozapine as the internal standard. Detection was performed on a triple-quadrupole tandem mass spectrometer using positive electrospray ionization and quantification was performed by selected reaction monitoring mode. The MS-MS ion transitions monitored were m/z 384.1 → 253.1 and 327.0 → 270.0 for quetiapine and clozapine, respectively. The between- and within-run precision was less than 7.44% and accuracy was less than 10.2%. The lower limit of quantification was 1 ng/mL. The extraction recoveries of quetiapine were over 90%. The method is proved to be accurate and specific, and was applied to the pharmacokinetic study in healthy Chinese volunteers.
建立了一种灵敏且具选择性的液相色谱-串联质谱(LC-MS-MS)法测定喹硫平,以氯氮平为内标,在1 - 1500 ng/mL线性范围内,使用0.1 mL血浆进行方法验证。在三重四极杆串联质谱仪上采用正电喷雾电离进行检测,并通过选择反应监测模式进行定量。监测的MS-MS离子跃迁分别为喹硫平的m/z 384.1 → 253.1和氯氮平的m/z 327.0 → 270.0。批间和批内精密度均小于7.44%,准确度小于10.2%。定量下限为1 ng/mL。喹硫平的提取回收率超过90%。该方法被证明准确且特异,并应用于健康中国志愿者的药代动力学研究。