Development of an In Vitro Methodology to Assess the Bioequivalence of Orally Disintegrating Tablets Taken without Water

To assess the probability of bioequivalence (BE) between orally disintegrating tablets (ODTs) taken without water and conventional tablets (CTs) taken with water, an in vitro biorelevant methodology was developed using the BE Checker, which reproduces fluid shifts in the gastrointestinal tract and d...

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Detalles Bibliográficos
Autores principales: Takagi, Toshihide, Masada, Takato, Minami, Keiko, Kataoka, Makoto, Yamashita, Shinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535823/
https://www.ncbi.nlm.nih.gov/pubmed/37765162
http://dx.doi.org/10.3390/pharmaceutics15092192

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535823/
https://www.ncbi.nlm.nih.gov/pubmed/37765162
http://dx.doi.org/10.3390/pharmaceutics15092192

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