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Int J Biol Macromol ; 277(Pt 4): 134250, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39089541

ABSTRACT

The current treatments for wounds often fail to induce adequate healing, leaving wounds vulnerable to persistent infections and development of drug-resistant microbial biofilms. New natural-derived nanoparticles were studied to impair bacteria colonization and hinder the formation of biofilms in wounds. The nanoparticles were fabricated through polyelectrolyte complexation of chitosan (CS, polycation) and hyaluronic acid (HA, polyanion). UV-induced photo-crosslinking was used to enhance the stability of the nanoparticles. To achieve this, HA was methacrylated (HAMA, degree of modification of 20 %). Photo-crosslinked nanoparticles obtained from HAMA and CS had a diameter of 478 nm and a more homogeneous size distribution than nanoparticles assembled solely through complexation (742 nm). The nanoparticles were loaded with the antimicrobial agent bacitracin (BC), resulting in nanoparticles with a diameter of 332 nm. The encapsulation of BC was highly efficient (97 %). The BC-loaded nanoparticles showed significant antibacterial activity against gram-positive bacteria Staphylococcus aureus, Methicillin-resistant S. aureus and S. epidermidis. Photo-crosslinked HAMA/CS nanoparticles loaded with BC demonstrated inhibition of biofilm formation and a positive effect on the proliferation of mammalian cells (L929). These crosslinked nanoparticles have potential for the long-term treatment of wounds and controlled antibiotic delivery at the location of a lesion.


Subject(s)
Anti-Bacterial Agents , Bacitracin , Biofilms , Chitosan , Hyaluronic Acid , Nanoparticles , Chitosan/chemistry , Chitosan/pharmacology , Hyaluronic Acid/chemistry , Hyaluronic Acid/pharmacology , Nanoparticles/chemistry , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Bacitracin/pharmacology , Bacitracin/chemistry , Biofilms/drug effects , Drug Carriers/chemistry , Methacrylates/chemistry , Methacrylates/pharmacology , Animals , Microbial Sensitivity Tests , Staphylococcus aureus/drug effects , Cross-Linking Reagents/chemistry , Mice
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