Evidence map›Paper›PMID 39530205›Full record

ArticleMacromolecular rapid communications2024

Antimicrobial Peptide SAAP-148-Functionalized Hydrogels from Photocrosslinkable Polymers with Broad Antibacterial Activity.

Muhammad Atif, Gizem Babuççu, Martijn Riool, Sebastian Zaat, Ulrich Jonas

Abstract read
In one paragraph

Article in Macromolecular rapid communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Membrane-Focused Strategies AgainstAntibiotics (Basel, Switzerland) · 2026
    Review
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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

5 authors.

Muhammad AtifMacromolecular Chemistry, Department of Chemistry and Biology, University of Siegen, Adolf-Reichwein-Strasse 2, 57076, Siegen, Germany.
Gizem BabuççuDepartment of Medical Microbiology and Infection Prevention, Amsterdam UMC, Amsterdam institute for Immunology and Infectious Diseases, University of Amsterdam, Meibergdreef 9, Amsterdam, 1105 AZ, The Netherlands.
Martijn RioolDepartment of Medical Microbiology and Infection Prevention, Amsterdam UMC, Amsterdam institute for Immunology and Infectious Diseases, University of Amsterdam, Meibergdreef 9, Amsterdam, 1105 AZ, The Netherlands.
Sebastian ZaatDepartment of Medical Microbiology and Infection Prevention, Amsterdam UMC, Amsterdam institute for Immunology and Infectious Diseases, University of Amsterdam, Meibergdreef 9, Amsterdam, 1105 AZ, The Netherlands.
Ulrich JonasMacromolecular Chemistry, Department of Chemistry and Biology, University of Siegen, Adolf-Reichwein-Strasse 2, 57076, Siegen, Germany.ORCID https://orcid.org/0000-0002-2161-4541

Funding

H2020 Marie Skłodowska-Curie Actions 955664
6 · The paper itself

Abstract

Antimicrobial peptides (AMPs) are promising alternatives to traditional antibiotics for treating skin wound infections. Nonetheless, their short half-life in biological environments restricts clinical applicability. Covalent immobilization of AMPs onto suitable substrates offers a comprehensive solution, creating contact-killing surfaces with long-term functionality. Here, a copolymer of poly[(hydroxy ethyl acrylamide)-co-(4-benzophenone acrylamide)-co-(pentafluorophenyl acrylate)-co-(ECOSURF EH-3 acrylate)], in short poly(HEAAm-co-BPAAm-co-PFPA-co-EH3A), is synthesized by free radical polymerization. Subsequent modification of active ester groups with the amine groups of SAAP-148, results in a copolymer, that is non-cytotoxic to human lung fibroblasts. UV photocrosslinking of the benzophenone units yields a polymer network that forms a hydrogel after swelling with aqueous medium. Both the SAAP-148-modified polymer in solution and the photocrosslinked hydrogels show good antimicrobial activity against strains of Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Acinetobacter baumannii, including multidrug-resistant strains, frequently found in wound infections. The covalent attachment of SAAP-148 prevents leaching, ensuring sustained antimicrobial activity for at least 48 h in diluted human blood plasma and 14 days in PBS. This prolonged retention of antimicrobial activity in human blood plasma significantly enhances its clinical potential. Overall, this study shows the potential of the AMP-functionalized photocrosslinkable polymer as antimicrobial wound dressings, providing an effective alternative to antibiotics.

Indexed as

Anti-Bacterial AgentsEscherichia coliHydrogelsMicrobial Sensitivity TestsPolymersPseudomonas aeruginosaStaphylococcus aureusAcinetobacter baumanniiAntimicrobial PeptidesCross-Linking ReagentsHumansMolecular StructurePhotochemical ProcessesAnti-Bacterial AgentsAntimicrobial PeptidesCross-Linking ReagentsHydrogelsPolymersantimicrobial peptidesphotocrosslinkable hydrogelpolymer modificationSAAP‐148wound infection

Identifiers

PMID39530205
PMCPMC11661662

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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.