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Potassium iodide enhances inactivation of Streptococcus mutans biofilm in antimicrobial photodynamic therapy with red laser
Affiliation:1. Department of Restorative Dental Science – Operative Division, College of Dentistry, King Saud University, Riyadh 11545, Saudi Arabia;2. Department of Restorative Dental Science – Endodontic Division, College of Dentistry, King Saud University, Riyadh 11545, Saudi Arabia;1. Department of Restorative and Prosthetic Dentistry, College of Dentistry, Dar Al Uloom University, Riyadh, Saudi Arabia;2. Department of OMFS and Diagnostic Sciences, Riyadh Elm University, Riyadh, Saudi Arabia;3. Department of Oral Biology, Liaquat College of Medicine and Dentistry, Karachi, Pakistan;4. Visiting Researcher center of Immunobiology, Blizard Institute, Barts and London School of medicine and dentistry London United Kingdom;5. Dept of Restorative and Prosthetic Dentistry, College of Dentistry, Dar Al Uloom University, Riyadh, Saudi Arabia;1. Diagnostic Sciences and Oral Biology, College of Dentistry, King Khalid University, Abha, Saudi Arabia;2. Pediatric Dentistry and Orthodontic Sciences, College of Dentistry, King Khalid University, Abha, Saudi Arabia
Abstract:ObjectiveTo evaluate the effect of potassium iodide (KI) addition on antimicrobial photodynamic therapy (aPDT) mediated by red laser (λ = 660 nm) and methylene blue in Streptococcus mutans biofilm model.MethodsS. mutans biofilms were cultured in 96-well plates containing BHI broth with 1% sucrose for 18 h, 10% CO2 and 37 °C and divided in groups (n = 3, in triplicate): C (NaCl 0.9%); CX (0.2% chlorhexidine); P (photosensitizer); KI (10, 25 and 50 mM); PKI (10, 25 and 50 mM); L (L1: 100 J/cm2, 9 J; L2: 200 J/cm2, 18 J); PL (photosensitizer + L1 or L2); KIL (KI at 10, 25 and 50 mM + L1 or L2); and PKIL (photosensitizer + 10, 25 and 50 mM KI + L1 or L2). Biofilms were submitted to three pre-irradiation (PI) times (5, 10, and 15 min). After the treatments, microbial counting's reduction was analyzed by Kruskal-Wallis and post-hoc Dunn's tests, respectively, and the interaction between light parameters and the PI times by two-way ANOVA (p < 0.05).ResultsThe S. mutans viability significantly reduced in all aPDT groups, in the presence or absence of KI (p < 0.05). For all PI times, PKIL groups (10, 25, and 50 mM) significantly differed from PL groups (p < 0.05) with a reduction of 9.0 logs reached at 50 mM of KI with 15 min of PI, irradiated at 18 J. We found no significant interaction between PI time and irradiation (p > 0.05).ConclusionThe addition of KI to PDT mediated by methylene blue and red laser promoted an additional effect in reducing the microbial viability of S. mutans biofilm.
Keywords:Methylene Blue
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