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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...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792494/ https://www.ncbi.nlm.nih.gov/pubmed/20046716 http://dx.doi.org/10.4103/0250-474X.41459 |