Abstract
A rapid and highly sensitive assay method has been developed and validated for the estimation of galantamine (GLM) in rat plasma using liquid chromatography coupled to tandem mass spectrometry with electrospray ionization in the positive-ion mode. The assay procedure involves a simple liquid-liquid extraction of GLM and phenacetin (internal standard, IS) from rat plasma using acetonitrile. Chromatographic separation was achieved with 0.2% formic acid:acetonitrile (50:50, v/v) at a flow rate of 0.60mL/min on an Atlantis dC18 column with a total run time 2.5min. The MS/MS ion transitions monitored were 288.10→213.10 for GLM and 180.10→110.10 for IS. Method validation was performed as per United States Food and Drug Administration guidelines and the results met the acceptance criteria. The lower limit of quantitation achieved was 0.12ng/mL and linearity was observed from 0.12 to 525ng/mL. The intra- and inter-day precision were in the ranges of 4.73-11.7 and 5.83-8.64%, respectively. This novel method has been applied to a pharmacokinetic study in rats.
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Suresh, P. S., Mullangi, R., & Sukumaran, S. K. (2014). Highly sensitive LC-MS/MS method for determination of galantamine in rat plasma: Application to pharmacokinetic studies in rats. Biomedical Chromatography, 28(12), 1633–1640. https://doi.org/10.1002/bmc.3191
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