Evidence map›Paper›PMID 41837159›Full record

ArticleRSC advances2026

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

Romain Chevigny, Henna Rahkola, Efstratios D Sitsanidis, Tatu Kumpulainen, Lisa J White, Lotta-Riina Sundberg, Jennifer R Hiscock, Mika Pettersson, Maija Nissinen

Abstract read
In one paragraph

Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Romain ChevignyDepartment of Chemistry, Nanoscience Center, University of Jyväskylä FI-40014 Jyväskylä Finland maija.nissinen@jyu.fi.ORCID https://orcid.org/0000-0002-5463-9745
Henna RahkolaDepartment of Chemistry, Nanoscience Center, University of Jyväskylä FI-40014 Jyväskylä Finland maija.nissinen@jyu.fi.ORCID https://orcid.org/0009-0006-8667-3944
Efstratios D SitsanidisDepartment of Chemistry, Nanoscience Center, University of Jyväskylä FI-40014 Jyväskylä Finland maija.nissinen@jyu.fi.ORCID https://orcid.org/0000-0001-5727-1336
Tatu KumpulainenDepartment of Chemistry, Nanoscience Center, University of Jyväskylä FI-40014 Jyväskylä Finland maija.nissinen@jyu.fi.ORCID https://orcid.org/0000-0001-9469-9294
Lisa J WhiteSchool of Natural Sciences, University of Kent Canterbury Kent CT2 7NH UK.
Lotta-Riina SundbergDepartment of Biological and Environmental Science, Nanoscience Center, University of Jyväskylä FI-40014 Jyväskylä Finland.ORCID https://orcid.org/0000-0003-3510-4398
Jennifer R HiscockSchool of Natural Sciences, University of Kent Canterbury Kent CT2 7NH UK.ORCID https://orcid.org/0000-0002-1406-8802
Mika PetterssonDepartment of Chemistry, Nanoscience Center, University of Jyväskylä FI-40014 Jyväskylä Finland maija.nissinen@jyu.fi.ORCID https://orcid.org/0000-0002-6880-2283
Maija NissinenDepartment of Chemistry, Nanoscience Center, University of Jyväskylä FI-40014 Jyväskylä Finland maija.nissinen@jyu.fi.ORCID https://orcid.org/0000-0001-7560-4632

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Identifiers

PMID41837159
PMCPMC12980527

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.