A validated ultra high-pressure liquid chromatography method for separation of candesartan cilexetil impurities and its degradents in drug product

INTRODUCTION: A selective, specific, and sensitive “Ultra High-Pressure Liquid Chromatography” (UPLC) method was developed for determination of candesartan cilexetil impurities as well asits degradent in tablet formulation. MATERIALS AND METHODS: The chromatographic separation was performed on Water...

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Detalles Bibliográficos
Autores principales: Kumar, Namala Durga Atchuta, Babu, K. Sudhakar, Gosada, Ullas, Sharma, Nitish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658068/
https://www.ncbi.nlm.nih.gov/pubmed/23781475
http://dx.doi.org/10.4103/2229-4708.97718

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658068/
https://www.ncbi.nlm.nih.gov/pubmed/23781475
http://dx.doi.org/10.4103/2229-4708.97718

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