Issue 15, 2026, Issue in Progress

Fmoc-Phe : Fmoc-Leu supramolecular hydrogels with adaptive antibacterial activity

Abstract

The development of adaptive soft materials offers new opportunities to address the effects of antimicrobial resistance. Fmoc-phenylalanine (Fmoc-Phe) and Fmoc-leucine (Fmoc-Leu) based hydrogels are known to demonstrate antibacterial activity. We now show that by combining these two gelators (Fmoc-Phe and Fmoc-Leu) into a multicomponent hydrogel system, we can tune the antibacterial properties of the resultant hydrogel. This tunable antimicrobial behaviour is achieved by varying the Fmoc-Phe : Fmoc-Leu ratio, which also influences self-assembly and, as a result, the physical properties of the material. We show that changing the component ratio can be used to optimise gelation efficiency and modulate viscoelastic, self-healing and thermoresponsive properties. Spectroscopic analyses reveal that while β-sheet organisation is retained independently of the ratio of gelators supplied, system stability (increasing material softness) is observed as a direct result of the proportion of the gelator that remains unassembled in the sol of the resultant hydrogel. Antibacterial assays conducted against clinically relevant Gram-positive and Gram-negative pathogens demonstrate formulation-dependent responses, with Gram-positive strains showing the greatest susceptibility. From these data, we can determine a structure–activity relationship, which demonstrates the importance of compositional tuning as a simple and effective strategy for designing peptide-based hydrogels with tailorable physical, material and antimicrobial properties.

Graphical abstract: Fmoc-Phe : Fmoc-Leu supramolecular hydrogels with adaptive antibacterial activity

Supplementary files

Article information

Article type
Paper
Submitted
14 Nov 2025
Accepted
06 Mar 2026
First published
12 Mar 2026
This article is Open Access
Creative Commons BY license

RSC Adv., 2026,16, 13801-13811

Fmoc-Phe : Fmoc-Leu supramolecular hydrogels with adaptive antibacterial activity

R. Chevigny, H. Rahkola, E. D. Sitsanidis, T. Kumpulainen, L. J. White, L. Sundberg, J. R. Hiscock, M. Pettersson and M. Nissinen, RSC Adv., 2026, 16, 13801 DOI: 10.1039/D5RA08809G

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