摘要

Background: A rapid and highly sensitive assay method has been developed and validated for the estimation of memantine (MEM) in rat plasma using liquid chromatography coupled to tandem mass spectrometry with electro spray ionization in the positive-ion mode. Method validation was performed as per United States Food and Drug Administration (US FDA) guidelines. Methods: The assay procedure involves a simple liquid-liquid extraction of MEM and phenacetin (internal standard, IS) from rat plasma using methyl tert-butyl methyl ether. Chromatographic separation was achieved with 0.2% formic acid: acetonitrile (40:60, v/v) at a flow rate of 0.50 ml/min on an Atlantis dC18 column with a total run time 3.0 min. The MS/MS ion transitions monitored were 180.10 (R) 163.30 for MEM and 180.10 (R) 110.10 for IS. Results: The results met the acceptance criteria mentioned in the guidelines. The lower limit of quantitation achieved was 0.025 ng/ml and the linearity was observed from 0.025 to 220 ng/ml. The intra-and inter-day precision was in the range of 0.88-6.84 and 2.57-6.79%, respectively. Conclusions: An LC-ESI-MS/MS for the determination of MEM in rat plasma employing simple liquid extraction was developed and validated with high sensitivity and selectivity. This novel method has been applied to a pharmacokinetic study in rats.

  • 出版日期2014-12

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