Metal ions and graphene-based compounds as alternative treatment options for burn wounds infected by antibiotic-resistant Pseudomonas aeruginosa.
Nathalie KarakyAndrew KirbyAndrew J McBainJonathan A ButlerMohamed El MohtadiCraig E BanksAnthony J SlatePublished in: Archives of microbiology (2020)
Burn infections caused by Pseudomonas aeruginosa pose a major complication in wound healing. This study aimed to determine the antimicrobial effect of metal ions, graphene (Gr), and graphene oxide (GO), individually and in combination, against the planktonic and biofilm states of two antimicrobially resistant clinical strains of P. aeruginosa each with different antibiotic resistance profiles. Minimum inhibitory, minimum bactericidal, and fractional inhibitory concentrations were performed to determine the efficacy of the metal ions and graphene composites individually and their synergy in combination. Crystal violet biofilm and XTT assays measured the biofilm inhibition and metabolic activity, respectively. Molybdenum, platinum, tin, gold, and palladium ions exhibited the greatest antimicrobial activity (MIC = 7.8-26.0 mg/L), whilst GO and Gr demonstrated moderate-to-no effect against the planktonic bacterial cells, irrespective of their antibiograms. Biofilms were inhibited by zinc, palladium, silver, and graphene. In combination, silver-graphene and molybdenum-graphene inhibited both the planktonic and biofilm forms of the bacteria making them potential candidates for development into topical antimicrobials for burns patients infected with antibiotic-resistant P. aeruginosa.
Keyphrases
- pseudomonas aeruginosa
- biofilm formation
- wound healing
- staphylococcus aureus
- cystic fibrosis
- candida albicans
- room temperature
- carbon nanotubes
- acinetobacter baumannii
- quantum dots
- walled carbon nanotubes
- end stage renal disease
- ejection fraction
- aqueous solution
- chronic kidney disease
- escherichia coli
- induced apoptosis
- newly diagnosed
- peritoneal dialysis
- water soluble
- oxidative stress
- silver nanoparticles
- prognostic factors
- cell proliferation
- drug resistant
- single cell
- cell cycle arrest
- signaling pathway
- oxide nanoparticles
- patient reported outcomes