Related Experiment Video
Updated: Aug 6, 2026

A Standardized Ex Vivo Porcine Oromucosal Model for Evaluating Peptide Fluxes
Published on: June 9, 2026
A self-unfolding polymer foil loaded with a permeation enhancer Ionogel for superior oral peptide delivery
Konstantinos Raptis1,2, Reece McCabe3, Marta Rubio-Huertas3
1Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, Copenhagen, 2100, Denmark.
Abstract:
Peptide drugs have gained considerable attention as new molecular entities, due to their high target specificity. However, oral delivery of peptides remains a major challenge, and current formulation approaches typically achieve only low single-digit bioavailability, prompting exploration of synergistic strategies to improve absorption. In this work, a self-unfolding foil device, designed for unidirectional drug release in close proximity to the intestinal mucosa, is combined with a potent permeation enhancer-based ionogel formulation for exploitation of synergies from two different oral delivery approaches. The choline decanoate ionogel is loaded into the foil, and insulin release optimized through hydrophilic surface modification and tailored cavity design. In vivo evaluation in rats demonstrate a bioavailability of 12.5% and a biopotency of 20% relative to subcutaneous administration representing approximately three- and four-fold increases, respectively, compared with the formulation control group. These findings demonstrate that unidirectional release from an advanced drug delivery system can markedly enhance formulation performance and pave the way for further development of similar combinatorial delivery strategies. Overall, this study reports the highest insulin bioavailability achieved with the self-unfolding foil platform to date, and among the highest reported in literature, highlighting its promise for advancing oral peptide delivery in future preclinical studies.
Related Concept Videos
Bioavailability Enhancement: Drug Permeability Enhancement
Site-Targeted Drug Delivery Systems: Polymeric Carriers
Oral Drug Delivery Systems: Delayed-Release Systems
Modified-Release Drug Delivery Systems: Rate-Programmed II
Modified-Release Drug Delivery Systems: Stimuli-Activated
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention

