Fluorous oligoarginines as supra-enhancers for intracellular and transdermal peptide delivery

Research output: Contribution to journalArticlepeer-review

Abstract

Peptides are increasingly recognized as important therapeutics due to their specificity and potency. However, their clinical application is often hindered by numerous barriers, including low bioavailability, poor cell membrane and tissue penetration. To address these limitations, we developed a library of fluorous penetrating peptides and identified fluorinated hexa-arginine (FR6) as a super-enhancer for cell and tissue penetration. FR6 markedly enhances the intracellular delivery of a variety of peptides by improving membrane permeability, facilitating their uptake across diverse cell types. It greatly improves the penetration of bioactive peptides in 3D tumor spheroids, allowing for improved therapeutic efficacy. More importantly, FR6 demonstrates remarkable potential for transdermal delivery of peptide drugs, effectively enhancing the penetration of peptides like acetyl hexapeptide-8 for treating UVB-induced skin photoaging. Our findings underscore the use of FR6 as a super-enhancer in overcoming multiple physiological barriers during cell, tissue and transdermal delivery.

Original languageEnglish
Pages (from-to)305-316
Number of pages12
JournalBioactive Materials
Volume59
DOIs
StatePublished - May 2026

Keywords

  • Fluorous cationic peptides
  • Intracellular peptide delivery
  • Photodamage therapy
  • Transdermal peptide delivery
  • Tumor penetration

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