Analytical method development and validation for the estimation of Dipyridamole in pharmaceutical dosage form by HPLC
Journal Title: Indian Journal of Research in Pharmacy and Biotechnology - Year 2017, Vol 5, Issue 5
Abstract
A simple, rapid, accurate and reproducible reverse phase high performance liquid chromatography method for the quantitative determination of Dipyridamole in tablet dosage form was studied in this experiment. With the optimized chromatographic conditions, the drugs were linear in the concentration range of 10 µg/ml to 30 of µg/ml Dipyridamole, methyl paraben and propyl paraben. The correlation co – efficient was found to be above 0.999 for all three drugs. The percentage purity was found to be 99.9 and 100.1 for Dipyridamole.
Authors and Affiliations
Madhuri Nuvvula, M. Jyothsna, D. Jeevan Mani Babu
Keywords
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- EP ID EP33483
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