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Hydrolytic Degradation Profile and RP-HPLC Estimation of Cilostazol in Tablet Dosage Form

A simple, selective, precise and stability-indicating high-performance liquid-chromatographic method of analysis of cilostazol in pharmaceutical dosage form was developed and validated. The solvent system consisted of 10 mM phosphate buffer (pH 6.0):acetonitrile:methanol (20:40:40). Retention time o...

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Bibliografske podrobnosti
Main Authors: Basniwal, P. K., Shrivastava, P. K., Jain, Deepti
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications 2008
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2792494/
https://ncbi.nlm.nih.gov/pubmed/20046716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0250-474X.41459
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