Bacteria-Derived Cellulose Membranes Modified with Graphene Oxide-Silver Nanoparticles for Accelerating Wound Healing.
Erika Patrícia Chagas Gomes LuzThamyres Freire da SilvaLidyane Souto Maciel MarquesAlexandre AndradeMarcos Vinicius V LoreviceFabia Karine AndradeLiu YangAntonio Gomes de Souza FilhoAndreia F FariaRodrigo Silveira VieiraPublished in: ACS applied bio materials (2024)
This study reports on the modification of bacterial cellulose (BC) membranes produced by static fermentation of Komagataeibacter xylinus bacterial strains with graphene oxide-silver nanoparticles (GO-Ag) to yield skin wound dressings with improved antibacterial properties. The GO-Ag sheets were synthesized through chemical reduction with sodium citrate and were utilized to functionalize the BC membranes (BC/GO-Ag). The BC/GO-Ag composites were characterized to determine their surface charge, morphology, exudate absorption, antimicrobial activity, and cytotoxicity by using fibroblast cells. The antimicrobial activity of the wound dressings was assessed against Staphylococcus aureus , Escherichia coli , and Pseudomonas aeruginosa . The results indicate that the BC/GO-Ag dressings can inhibit ∼70% of E. coli cells. Our findings also revealed that the porous BC/GO-Ag antimicrobial dressings can efficiently retain 94% of exudate absorption after exposure to simulated body fluid (SBF) for 24 h. These results suggest that the dressings could absorb excess exudate from the wound during clinical application, maintaining adequate moisture, and promoting the proliferation of epithelial cells. The BC/GO-Ag hybrid materials exhibited excellent mechanical flexibility and low cytotoxicity to fibroblast cells, making excellent wound dressings able to control bacterial infectious processes and promote the fast healing of dermal lesions.
Keyphrases
- silver nanoparticles
- wound healing
- quantum dots
- induced apoptosis
- escherichia coli
- highly efficient
- staphylococcus aureus
- visible light
- cell cycle arrest
- pseudomonas aeruginosa
- signaling pathway
- endoplasmic reticulum stress
- oxidative stress
- emergency department
- surgical site infection
- cell proliferation
- gold nanoparticles
- drug resistant
- single cell