Bharathi D Vijaya, Hotha Kishore Kumar, Jagadeesh B, Mullangi Ramesh, Naidu A
Bioanalytical Department, Integrated Product Development, Dr Reddy's Laboratories Ltd, Bachupalli, Hyderabad, India.
Biomed Chromatogr. 2009 Aug;23(8):804-10. doi: 10.1002/bmc.1189.
A highly sensitive, rapid assay method has been developed and validated for the estimation of montelukast (MTK) in human plasma with liquid chromatography coupled to tandem mass spectrometry with electro spray ionization in the positive-ion mode. Liquid-liquid extraction was used to extract MTK and amlodipine (internal standard, IS) from human plasma. Chromatographic separation was achieved with 10 mM ammonium acetate (pH 6.4): acetonitrile (15:85, v/v) at a flow rate of 0.50 mL/min on a Discovery HS C(18) column with a total run time of 3.5 min. The MS/MS ion transitions monitored were 586.10 --> 422.10 for MTK and 409.20 --> 238.30 for IS. Method validation and clinical sample analysis were performed as per FDA guidelines and the results met the acceptance criteria. The lower limit of quantitation achieved was 0.25 ng/mL and linearity was observed from 0.25 to 800 ng/mL. The intra-day and inter-day precisions were 5.97-8.33 and 7.09-10.13%, respectively. This novel method has been applied to a pharmacokinetic study of MTK in humans.
已开发并验证了一种高灵敏度、快速的检测方法,用于通过液相色谱-串联质谱联用(正离子模式下的电喷雾电离)测定人血浆中的孟鲁司特(MTK)。采用液-液萃取法从人血浆中提取MTK和氨氯地平(内标,IS)。在Discovery HS C(18)柱上,以10 mM醋酸铵(pH 6.4):乙腈(15:85,v/v)为流动相,流速为0.50 mL/min进行色谱分离,总运行时间为3.5分钟。监测的MS/MS离子跃迁为MTK的586.10 --> 422.10和IS的409.20 --> 238.30。按照FDA指南进行方法验证和临床样本分析,结果符合验收标准。实现的定量下限为0.25 ng/mL,在0.25至800 ng/mL范围内观察到线性关系。日内和日间精密度分别为5.97-8.33%和7.09-10.13%。这种新方法已应用于MTK在人体的药代动力学研究。