Skip to main navigation Skip to search Skip to main content

Oromucosal films for peptide delivery: formulation strategies using permeation enhancers and polymers

  • Sandeep Karki
  • , Sahil Malhotra
  • , Muhammad Ijaz
  • , Eoin D. O’Cearbhaill
  • , Line Hagner Nielsen
  • , David J. Brayden*
  • *Corresponding author for this work
  • University College Dublin

Research output: Contribution to journal › Journal article › Research › peer-review

Abstract

Buccal and sublingual mucosae offer highly vascularized, patient-acceptable routes for systemic peptide delivery, providing a promising alternative to peptide injections and conventional oral peptide dosage forms that suffer from enzymatic degradation, limited permeability, and hepatic first-pass metabolism. Despite these advantages, achieving consistent peptide bioavailability from oromucosal dosage forms remain challenging due to salivary washout, enzymatic instability, and the compact, lipid-rich epithelial structure. This review provides a comprehensive overview of formulation strategies developed to overcome these barriers, with an emphasis on the use of permeation enhancers (PEs), mucoadhesive polymers, and multilayer film architectures. Advances in nanoparticle-integrated films are highlighted for their potential to improve peptide stability and mucosal permeation. The review concludes by addressing patient compliance, translational potential, and regulatory perspectives that shape the clinical advancement of peptide-loaded oromucosal films.

Original languageEnglish
JournalDrug Delivery and Translational Research
Volume16
Pages (from-to)2382–2419
ISSN2190-393X
DOIs
Publication statusPublished - 2026

Keywords

  • Bile salts
  • Mucoadhesive polymers
  • Multilayer films
  • Non-invasive peptide delivery
  • Oromucosal films
  • Translational drug delivery

Fingerprint

Dive into the research topics of 'Oromucosal films for peptide delivery: formulation strategies using permeation enhancers and polymers'. Together they form a unique fingerprint.

Cite this