Wang Xiaolin, Zhang Dan, Liu Man, Zhao Hongna, Du Aihua, Meng Lingjie, Liu Huichen
Department of Clinical Pharmacology, Aerospace Center Hospital, Beijing, 100049, China.
Biomed Chromatogr. 2014 Feb;28(2):218-22. doi: 10.1002/bmc.3008. Epub 2013 Aug 5.
A sensitive and selective LC-MS/MS method for the determination of agomelatine in human plasma was developed and validated. After simple liquid-liquid extraction, the analytes were separated on a Zorbax SB-C18 column (150 × 2.1 mm i.d., 5 µm) with an isocratic mobile phase consisting of 5 mm ammonium acetate solution (containing 0.1% formic acid) and methanol (30:70, v/v) at a flow-rate of 0.3 mL/min. The MS acquisition was performed in multiple reaction monitoring mode with a positive electrospray ionization source. The mass transitions monitored were m/z 244.1 → 185.3 and m/z 285.2 → 193.2 for agomelatine and internal standard, respectively. The methods were validated for selectivity, carry-over, matrix effects, calibration curves, accuracy and precision, extraction recoveries, dilution integrity and stability. The validated method was successfully applied to a pharmacokinetic study of agomelatine in Chinese volunteers following a single oral dose of 25 mg agomelatine tablet.
建立并验证了一种灵敏且具选择性的液相色谱-串联质谱法用于测定人血浆中的阿戈美拉汀。经简单液-液萃取后,分析物在Zorbax SB-C18柱(内径150×2.1 mm,粒径5 µm)上分离,等度流动相由5 mM醋酸铵溶液(含0.1%甲酸)和甲醇(30:70,v/v)组成,流速为0.3 mL/min。质谱采集采用多反应监测模式,电喷雾电离源为正离子模式。监测的阿戈美拉汀和内标的质量跃迁分别为m/z 244.1 → 185.3和m/z 285.2 → 193.2。该方法在选择性、残留、基质效应、校准曲线、准确度和精密度、萃取回收率、稀释完整性及稳定性方面得到验证。经验证的方法成功应用于25 mg阿戈美拉汀片单次口服给药后中国志愿者体内阿戈美拉汀的药代动力学研究。