Development and Validation of a Stability-Indicating RP-UPLC Method for Determination of Rosuvastatin and Related Substances in Pharmaceutical Dosage Form

A stability-indicating reversed phase ultra performance liquid chromatographic (RP-UPLC) method was developed for the determination of related substances in rosuvastatin calcium (ROSV) tablet dosage form. The chromatographic separation was achieved on an Acquity BEH C18 (100 mm × 2.1 mm, 1.7 μm) col...

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Detalles Bibliográficos
Autores principales: Trivedi, Harshal Kanubhai, Patel, Mukesh C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383219/
https://www.ncbi.nlm.nih.gov/pubmed/22896825
http://dx.doi.org/10.3797/scipharm.1201-09

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383219/
https://www.ncbi.nlm.nih.gov/pubmed/22896825
http://dx.doi.org/10.3797/scipharm.1201-09

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