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Stress Degradation Studies on Lisinopril Dihydrate Using Modified Reverse Phase High Performance Liquid Chromatography
Department of Pharmaceutical Chemistry, College of Pharmacy, Salman bin Abdulaziz University, Al-Kharj, KSA
- 1 Department of Pharmaceutical Chemistry, College of Pharmacy, Salman bin Abdulaziz University, Al-Kharj, KSA
American Journal of Analytical Chemistry·Volume 05 (2014)·Pages 316–322·Published 3 April 2014·DOI10.4236/ajac.2014.55039
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Abstract
A simple, precise, accurate and sensitive reverse phase high performance liquid chromatographic method for simultaneous estimation of lisinopril dihydrate and its degradation products occuring under different ICH prescribed stress conditions has been modified. Drug was resolved on a C18 column, utilizing modified mobile phase of tetra butyl ammonium hydroxide solution and acetonitrile. Ultra violet detection was carried out at 210 nm. The method was modified with respect to linearity, precision, accuracy, selectivity, specificity and ruggedness. The results obtained revealed that lisinopril dihydrate was an active product slightly changed under stress conditions.
KeywordsLisinopril DihydrateStabilityUV LightSun LightHigh TemperaturePharmaceutical ExcipientsHigh Performance Liquid Chromatography
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