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

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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Bibliographic Details
Main Authors: Toshihide Takagi, Takato Masada, Keiko Minami, Makoto Kataoka, Shinji Yamashita
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Pharmaceutics
Subjects:
bioequivalence
orally disintegrating tablets
biorelevant dissolution
gastric emptying
gastrointestinal physiology
drug permeation
Online Access:https://www.mdpi.com/1999-4923/15/9/2192

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https://www.mdpi.com/1999-4923/15/9/2192

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