Der Pharma Chemica
Journal for Medicinal Chemistry, Pharmaceutical Chemistry and Computational Chemistry


RP-HPLC method for the determination of Valacyclovir in bulk and Pharmaceutical formulation

Author(s): M Sugumaran, V Bharathi, R Hemachander and M Lakshmi

A reverse phase high performance liquid chromatography (RP-HPLC) has been developed for the estimation of valacyclovir in bulk drug and pharmaceutical dosage form. The quantification was carried out using C18 column and mobile phase consisting of 0.067 M phosphate buffer at pH 6.5: acetonitrile : methanol (70:20:10 % v/v), at flow rate of 0.5 mL/min. The separation was performed at ambient temperature. Eluents were monitored by UV detector set at 244 nm. The method was statistically validated for the linearity, precision, accuracy, LOD and LOQ. The linearity was found to be in the range of 5-30 μg/mL. The proposed method was found to be simple, precise, accurate, rapid, economic and reproducible for the estimation of valacyclovir in bulk drug and tablet.

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