Development and validation of stability indicating the RP-HPLC method for the estimation of related compounds of guaifenesin in pharmaceutical dosage forms

AIM AND BACKGROUND: A stability-indicating gradient reverse phase liquid chromatographic (RP-LC) method was developed for the quantitative determination of related substances of guaifenesin in pharmaceutical formulations. MATERIALS AND METHODS: The baseline separation for guaifenesin and all impurit...

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Detalles Bibliográficos
Autores principales: Reddy, Sunil Pingili, Babu, K. Sudhakar, Kumar, Navneet, Sekhar, Y. V. V. Sasi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Symposium - HPLC
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658082/
https://www.ncbi.nlm.nih.gov/pubmed/23781462
http://dx.doi.org/10.4103/2229-4708.93391

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658082/
https://www.ncbi.nlm.nih.gov/pubmed/23781462
http://dx.doi.org/10.4103/2229-4708.93391

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