Development and Validation of a HPLC and an UV Spectrophotometric Methods for Determination of Dexibuprofen in Pharmaceutical Preparations

A high-performance liquid chromatographic (HPLC) and a ultraviolet (UV) methods were developed and validated for the quantitative determination of Dexibuprofen (DI) in pharmaceutical dosage form. HPLC was carried out by reversed phase technique on a RP-18 column with a mobile phase composed of aceto...

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Detalles Bibliográficos
Autores principales: Muralidharan, Selvadurai, Meyyanathan, Subramania Nainar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263711/
https://www.ncbi.nlm.nih.gov/pubmed/22389866
http://dx.doi.org/10.5402/2011/948314

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263711/
https://www.ncbi.nlm.nih.gov/pubmed/22389866
http://dx.doi.org/10.5402/2011/948314

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