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Updated: Jun 10, 2025

Ex Vivo Intestinal Sacs to Assess Mucosal Permeability in Models of Gastrointestinal Disease
Published on: February 9, 2016
Ex vivo permeability study of poorly soluble drugs across gastrointestinal membranes: acceptor compartment media
Andrejs Sitovs1, Valentyn Mohylyuk2
1Leading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, Riga, Latvia; Department of Pharmacology, Faculty of Pharmacy, Rīga Stradiņš University, Riga, Latvia.
Abstract:
Ex vivo drug permeability testing across gastrointestinal (GI) membranes is crucial in drug discovery and oral drug delivery. It is a reliable method for drugs with good solubility, but it poses challenges for poorly soluble drugs, which are common in development pipelines today. Although enabling formulations increase the apparent solubility in the GI compartment (dissolution vessel or permeation chamber's donor compartment), maintaining solubilized drug in the acceptor compartment during ex vivo testing remains largely unresolved. This review compiles and critically evaluates the diverse compositions of acceptor media used in ex vivo permeability studies for poorly soluble drugs, highlighting this significant yet underexplored aspect of pharmaceutical science. An algorithm is proposed for selecting solubility-enhancing additives for the acceptor media in ex vivo permeability studies of poorly soluble drugs.
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