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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Autori principali:	Toshihide Takagi, Takato Masada, Keiko Minami, Makoto Kataoka, Shinji Yamashita
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	MDPI AG 2023-08-01
Serie:	Pharmaceutics
Soggetti:	bioequivalence orally disintegrating tablets biorelevant dissolution gastric emptying gastrointestinal physiology drug permeation
Accesso online:	https://www.mdpi.com/1999-4923/15/9/2192
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