AI Article Synopsis

  • Antimicrobial resistance (AMR) is a major global health threat caused by the overuse of antibiotics, highlighting the need for new antimicrobial solutions.
  • Researchers are exploring porphyrins and metalloporphyrins, which have antimicrobial properties activated by light, as potential agents for battling this issue.
  • This study focuses on embedding these porphyrins into peptide hydrogels, which are biocompatible and effective against both Gram-positive and Gram-negative bacteria, with zinc porphyrins showing the highest efficacy.

Article Abstract

Antimicrobial resistance (AMR) poses a significant global health risk as a consequence of misuse of antibiotics. Owing to the increasing antimicrobial resistance, it became imperative to develop novel molecules and materials with antimicrobial properties. Porphyrins and metalloporphyrins are compounds which present antimicrobial properties especially after irradiation. As a consequence, porphyrinoids have recently been utilized as antimicrobial agents in antimicrobial photodynamic inactivation in bacteria and other microorganisms. Herein, we report the encapsulation of porphyrins into peptide hydrogels which serve as delivery vehicles. We selected the self-assembling Fmoc-Phe-Phe dipeptide, a potent gelator, as a scaffold due to its previously reported biocompatibility and three different water-soluble porphyrins as photosensitizers. We evaluated the structural, mechanical and degradation properties of these hydrogels, their interaction with NIH3T3 mouse skin fibroblasts, and we assessed their antimicrobial efficacy against Gram-positive () and Gram-negative () bacteria. We found out that the hydrogels are cytocompatible and display antimicrobial efficiency against both strains with the zinc porphyrins being more efficient. Therefore, these hydrogels present a promising alternative for combating bacterial infections in the face of growing AMR concerns.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10887087PMC
http://dx.doi.org/10.3390/biom14020226DOI Listing

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