The Effect of Immobilization Methods of P9‐4 Antimicrobial Peptide Onto Gelatin Methacrylate on Multidrug‐Resistant Bacteria: A Comparative Study

Abstract: Wound dressings play a crucial role in wound management by providing a protective barrier and creating an optimal environment for healing. Photocrosslinkable hydrogels, such as gelatin methacrylate (GelMA), have gained attention for their unique properties but often lack antimicrobial activity. To enhance their effectiveness, researchers are exploring methods to incorporate antimicrobial agents into photocrosslinkable hydrogel dressings. Immobilization of antimicrobial peptides (AMPs) onto hydrogel matrices may be achieved through physical or chemical methods. Although, chemical immobilization, using techniques like EDC/NHS chemistry, has shown promise in enhancing antimicrobial properties of hydrogels, the capacity for immobilization may be limited by the structure of hydrogel. Physical methods, such as immersing, offer alternatives but may have different efficacy and biocompatibility. The study aims to chemically immobilize GelMA with P9‐4 AMP by photoinduced conjugation and EDC/NHS chemistry and compare its antimicrobial efficacy with a physical immobilization method. Chemical immobilization by EDC/NHS chemistry significantly enhances the antimicrobial effect of GelMA hydrogels against multi‐drug resistant Psuedomonas aeruginosa (MDR P. aeruginosa) and methicillin‐resistant Staphylococcus aureus (MRSA) while maintaining favorable biocompatibility. Study highlights the potential of AMP‐functionalized GelMA as advanced wound dressings for reducing infections caused by antibiotic‐resistant bacteria and offers a promising approach for future research in wound management.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
The Effect of Immobilization Methods of P9‐4 Antimicrobial Peptide Onto Gelatin Methacrylate on Multidrug‐Resistant Bacteria: A Comparative Study ; day:04 ; month:09 ; year:2024 ; extent:14
Macromolecular bioscience ; (04.09.2024) (gesamt 14)

Creator
Pulat, Günnur
Çelebi, Nisa Nilsu
Bilgiç, Eda

DOI
10.1002/mabi.202400324
URN
urn:nbn:de:101:1-2409051405518.910669096180
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:33 AM CEST

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Associated

  • Pulat, Günnur
  • Çelebi, Nisa Nilsu
  • Bilgiç, Eda

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