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Updated: Nov 4, 2025

Models and Methods to Evaluate Transport of Drug Delivery Systems Across Cellular Barriers
Published on: October 17, 2013
Physical methods for enhancing drug absorption from the gastrointestinal tract
Zhi Luo1, Nevena Paunović1, Jean-Christophe Leroux1
1Institute of Pharmaceutical Sciences, Department of Chemistry and Applied Biosciences, ETH Zurich, Zurich, Switzerland.
Oral delivery of peptide and protein drugs faces significant gastrointestinal barriers. Novel physical force-based methods show promise for enhancing drug permeability and bioavailability, despite early-stage development.
Area of Science:
- Pharmacology
- Biotechnology
- Drug Delivery
Background:
- Oral delivery of macromolecules like peptides and proteins is hindered by gastrointestinal barriers.
- Previous strategies (enhancers, nanocarriers, chemical modifications) yielded limited success in improving oral bioavailability.
- Marketed oral peptide drugs generally exhibit very low bioavailability.
Purpose of the Study:
- To provide a critical overview of unconventional physical force-based technologies for oral macromolecule delivery.
- To assess the potential and challenges of these methods for clinical translation.
- To highlight recent advancements in controlling drug permeability across the gastrointestinal mucosa.
Main Methods:
- Review of physical interaction-based approaches: magnetic, acoustic, and mechanical forces.
- Analysis of their impact on drug permeability and spatiotemporal delivery.
- Evaluation of potential and challenges for clinical application.
Main Results:
- Physical force-based methods demonstrate potential for improved oral drug absorption.
- These techniques offer enhanced control over drug permeability and delivery.
- Early-stage research indicates promise for overcoming GI barriers.
Conclusions:
- Physical force-based strategies represent a promising, albeit unconventional, avenue for oral macromolecule delivery.
- Further research is needed to address challenges for successful clinical translation.
- These methods could significantly improve the bioavailability of peptide and protein drugs.
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