AI Article Synopsis

  • This study investigates the effectiveness of photodynamic therapy using a gel with 5% delta aminolaevulinic acid (ALAD) and LED light to eliminate oral strains without harming gingival fibroblasts.
  • Results showed significant reduction in biofilm biomass and colony forming units (CFUs/mL), indicating strong antifungal activity against resistant strains, while also confirming cell viability was affected yet membrane fluidity remained intact.
  • The treatment did not harm gingival fibroblasts, showing no cytotoxic effects or major morphological changes, but increased actin filament thickness, while reactive oxygen species (ROS) were elevated shortly after treatment and collagen production improved after one week.

Article Abstract

This study aimed to evaluate the ability of photodynamic therapy, based on the use of a gel containing 5% delta aminolaevulinic acid (ALAD) for 45' followed by irradiation with 630 nm LED (PDT) for 7', to eradicate strains without damaging the gingiva. oral strains and gingival fibroblasts (hGFs) were used to achieve these goals. The potential antifungal effects on a clinical resistant strain were evaluated in terms of biofilm biomass, colony forming units (CFU/mL) count, cell viability by live/dead analysis, and fluidity membrane changes. Concerning the hGFs, viability assays, morphological analysis (optical, scanning electronic (SEM), and confocal laser scanning (CLSM) microscopes), and assays for reactive oxygen species (ROS) and collagen production were performed. ALAD-mediated aPDT (ALAD-aPDT) treatment showed significant anti-biofilm activity against , as confirmed by a reduction in both the biofilm biomass and CFUs/mL. The cell viability was strongly affected by the treatment, while on the contrary, the fluidity of the membrane remained unchanged. The results for the hGFs showed an absence of cytotoxicity and no morphological differences in cells subjected to ALAD-aPDT expected for CLSM results that exhibited an increase in the thickening of actin filaments. ROS production was augmented only at 0 h and 3 h, while the collagen appeared enhanced 7 days after the treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10887768PMC
http://dx.doi.org/10.3390/gels10020110DOI Listing

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