Zou Jianjun, Dai Li, Wang Guang Ji, Zhu Yubing, Fan Hongwei, Xiao Da Wei
Department of Clinical Pharmacology, Nanjing First Hospital Affiliated to Nanjin Medical University, Nanjing, The People's Republic of China.
Arzneimittelforschung. 2008;58(9):429-34. doi: 10.1055/s-0031-1296534.
A sensitive liquid chromatography-tandem mass spectrometry (LC/MS/MS) method was developed and validated for the determination of trimetazidine (CAS 13171-25-0) in human plasma, using pseudoephedrine as internal standard (IS). Plasma samples were simply pretreated with methanol for deproteinization. The chromatographic separation was performed on a C18 column with a mobile phase of 3 mmol/L ammonium acetate solution-methanol (15:85, v/v) at a flow rate of 0.3 mL/min. The chromatographic separation was achieved in less than 3.2 min. The linearity was established over the concentration range of 1-100 ng/mL. Both intra- and inter-batch standard deviations were less than 9.5%. The method was successfully applied to study the relative bioavailability of trimetazidine hydrochloride tablets in healthy Chinese volunteers and the pharmacokinetic parameters of the reference and test tablets were compared.
建立了一种灵敏的液相色谱-串联质谱(LC/MS/MS)法,以伪麻黄碱为内标(IS),用于测定人血浆中的曲美他嗪(CAS 13171-25-0)。血浆样品只需用甲醇进行简单的蛋白沉淀预处理。采用C18柱,以3 mmol/L醋酸铵溶液-甲醇(15:85,v/v)为流动相,流速为0.3 mL/min进行色谱分离。在不到3.2分钟内实现了色谱分离。在1-100 ng/mL的浓度范围内建立了线性关系。批内和批间标准偏差均小于9.5%。该方法成功应用于研究健康中国志愿者中盐酸曲美他嗪片的相对生物利用度,并比较了参比片和受试片的药代动力学参数。