The application of quality by design in the development of the liquid chromatography method to determine empagliflozin in the presence of its organic impurities

Analysis of impurities is an important step in the quality control of pharmaceutical ingredients and final products. From drug synthesis or excipients, even in small concentrations, impurities may affect efficacy and safety. The method was developed following Quality by Design (QbD) for the analysis...

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Detalles Bibliográficos
Autores principales: Manoel, Joanna Wittckind, Primieri, Gabriele Bordignon, Bueno, Lívia Maronesi, Wingert, Nathalie Ribeiro, Volpato, Nádia Maria, Garcia, Cássia Virginia, Scherman Schapoval, Elfrides Eva, Steppe, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049826/
https://www.ncbi.nlm.nih.gov/pubmed/35493885
http://dx.doi.org/10.1039/c9ra08442h

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049826/
https://www.ncbi.nlm.nih.gov/pubmed/35493885
http://dx.doi.org/10.1039/c9ra08442h

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