Anti-Biofilm Efficacy of Commonly Used Wound Care Products in In Vitro Settings.
Matthew RegulskiMatthew F MynttiGarth A JamesPublished in: Antibiotics (Basel, Switzerland) (2023)
Considering the prevalence and pathogenicity of biofilms in wounds, this study was designed to evaluate the anti-biofilm capabilities of eight commercially available wound care products using established in vitro assays for biofilms. The products evaluated included dressings with multiple delivery formats for ionic silver including nanocrystalline, gelling fibers, polyurethane (PU) foam, and polymer matrix. Additionally, non-silver-based products including an extracellular polymeric substance (EPS)-dissolving antimicrobial wound gel (BDWG), a collagenase-based debriding ointment and a fish skin-based skin substitute were also evaluated. The products were evaluated on Staphylococcus aureus and Pseudomonas aeruginosa mixed-species biofilms grown using colony drip flow reactor (CDFR) and standard drip flow reactor (DFR) methodologies. Anti-biofilm efficacy was measured by viable plate counts and confocal scanning laser microscopy (CSLM). Four of the eight wound care products tested were efficacious in inhibiting growth of new biofilm when compared with untreated controls. These four products were further evaluated against mature biofilms. BDWG was the only product that achieved greater than 2-log growth reduction (5.88 and 6.58 for S. aureus and P. aeruginosa , respectively) of a mature biofilm. Evaluating both biofilm prevention and mature biofilm disruption capacity is important to a comprehensive understanding of the anti-biofilm efficacy of wound care products.
Keyphrases
- pseudomonas aeruginosa
- staphylococcus aureus
- candida albicans
- biofilm formation
- healthcare
- cystic fibrosis
- wound healing
- palliative care
- methicillin resistant staphylococcus aureus
- quality improvement
- gold nanoparticles
- wastewater treatment
- surgical site infection
- drug delivery
- optical coherence tomography
- single molecule
- pain management
- mass spectrometry
- cancer therapy
- signaling pathway
- soft tissue
- single cell
- label free