A Novel Validated UHPLC Method for the Estimation of Rosuvastatin and Its Complete Impurity Profile in Tablet Formulations

A key step in the development of medicinal products is the research and validation of selective and sensitive analytical methods for the control of impurities from synthesis and degradation. As most impurities are similar in structure to the drug substance, the achievement of chemo-selective conditi...

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Detalles Bibliográficos
Autores principales: Mammone, Francesca Romana, Zanitti, Leo, Puxeddu, Michela, La Regina, Giuseppe, Silvestri, Romano, Borioni, Anna, Cirilli, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824232/
https://www.ncbi.nlm.nih.gov/pubmed/36615620
http://dx.doi.org/10.3390/molecules28010431

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824232/
https://www.ncbi.nlm.nih.gov/pubmed/36615620
http://dx.doi.org/10.3390/molecules28010431

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