Acer tegmentosum extract-mediated silver nanoparticles loaded chitosan/alginic acid scaffolds enhance healing of E. coli-infected wounds

Int J Biol Macromol. 2024 May;267(Pt 2):131389. doi: 10.1016/j.ijbiomac.2024.131389. Epub 2024 Apr 4.

Abstract

This work developed Acer tegmentosum extract-mediated silver nanoparticles (AgNPs) loaded chitosan (CS)/alginic acid (AL) scaffolds (CS/AL-AgNPs) to enhance the healing of E. coli-infected wounds. The SEM-EDS and XRD results revealed the successful formation of the CS/AL-AgNPs. FTIR analysis evidenced that the anionic group of AL (-COO-) and cationic amine groups of CS (-NH3+) were ionically crosslinked to form scaffold (CS/AL). The CS/AL-AgNPs exhibited significant antimicrobial activity against both Gram-positive (G+) and Gram-negative (G-) bacterial pathogens, while being non-toxic to red blood cells (RBCs), the hen's egg chorioallantoic membrane (HET-CAM), and a non-cancerous cell line (NIH3T3). Treatment with CS/AL-AgNPs significantly accelerated the healing of E. coli-infected wounds by regulating the collagen deposition and blood parameters as evidenced by in vivo experiments. Overall, these findings suggest that CS/AL-AgNPs are promising for the treatment of infected wounds.

Keywords: Acer tegmentosum; Antibacterial; Nanoparticles; Scaffolds; Wound healing.

MeSH terms

  • Acer* / chemistry
  • Alginates* / chemistry
  • Alginates* / pharmacology
  • Animals
  • Anti-Bacterial Agents* / chemistry
  • Anti-Bacterial Agents* / pharmacology
  • Chitosan* / chemistry
  • Chitosan* / pharmacology
  • Escherichia coli Infections / drug therapy
  • Escherichia coli* / drug effects
  • Metal Nanoparticles* / chemistry
  • Mice
  • NIH 3T3 Cells
  • Plant Extracts* / chemistry
  • Plant Extracts* / pharmacology
  • Silver* / chemistry
  • Silver* / pharmacology
  • Tissue Scaffolds / chemistry
  • Wound Healing* / drug effects

Substances

  • Chitosan
  • Silver
  • Plant Extracts
  • Anti-Bacterial Agents
  • Alginates