D'Amico Emira, Di Lodovico Silvia, Pierfelice Tania Vanessa, Tripodi Domenico, Piattelli Adriano, Iezzi Giovanna, Petrini Morena, D'Ercole Simonetta
Department of Medical, Oral and Biotechnological Sciences, University G. d'Annunzio of Chieti-Pescara, 66100 Chieti, Italy.
Department of Pharmacy, University G. d'Annunzio of Chieti-Pescara, 66100 Chieti, Italy.
Gels. 2024 Jan 29;10(2):110. doi: 10.3390/gels10020110.
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.
本研究旨在评估基于使用含5%δ-氨基乙酰丙酸(ALAD)的凝胶45分钟,随后用630 nm发光二极管(LED)照射7分钟的光动力疗法(PDT)在不损伤牙龈的情况下根除菌株的能力。使用口腔菌株和牙龈成纤维细胞(hGFs)来实现这些目标。从生物膜生物量、菌落形成单位(CFU/mL)计数、通过活/死分析的细胞活力以及细胞膜流动性变化方面评估对临床耐药菌株的潜在抗真菌作用。关于hGFs,进行了活力测定、形态分析(光学显微镜、扫描电子显微镜(SEM)和共聚焦激光扫描显微镜(CLSM))以及活性氧(ROS)和胶原蛋白产生的测定。ALAD介导的光动力疗法(ALAD-aPDT)治疗对……显示出显著的抗生物膜活性,生物膜生物量和CFU/mL的减少证实了这一点。细胞活力受到该治疗的强烈影响,而相反,细胞膜的流动性保持不变。hGFs的结果显示无细胞毒性,并且接受ALAD-aPDT处理的细胞在形态上没有差异,预期CLSM结果显示肌动蛋白丝增粗增加。仅在0小时和3小时时ROS产生增加,而治疗7天后胶原蛋白出现增加。