Lacosamide is an anti epileptic drug, for which, two simple, sensitive, accurate, precise, and economical methods (method 1 and 2) have been developed for the quantitative estimation of Lacosamide in bulk and pharmaceutical formulation. Method-1 is a simple, accurate and sensitive HPLC method and the chromatographic separation was carried out on C8 column Welchrom (250 × 4.6mm, 5µ.) using a mobile phase composition of potassium dihydrogen phosphate buffer: acetonitrile (850:150 v/v) pumped at flow rate of 1.5 ml/min. The eluent was monitored at 215 nm with a diode array detector. Method-2 was based on condensation reaction between Lacosamide and vanillin in presence of conc. Sulphuric acid involving the formation of violet colored chromogen which showed linearity in the range 100-500µg/ml at a lambda max of 613 nm. The methods were statistically validated for precision, accuracy, robustness and recovery as per ICH guidelines
Cite this article:
Jane J., Dhaval Ladani. Development and Validation of Analytical Methods for Lacosamide. Research J. Pharm. and Tech. 6(5): May 2013; Page 553-555.
Jane J., Dhaval Ladani. Development and Validation of Analytical Methods for Lacosamide. Research J. Pharm. and Tech. 6(5): May 2013; Page 553-555. Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2013-6-5-7