Ph.D. Program in Dental Biomedical Sciences, University of Maryland School of Dentistry, Baltimore, MD 21201, USA.
Department of Restorative Dental Sciences, College of Dentistry, Imam Abdulrahman Bin Faisal University, Dammam 34212, Saudi Arabia.
Int J Mol Sci. 2020 Oct 15;21(20):7612. doi: 10.3390/ijms21207612.
Caries-related biofilms and associated complications are significant threats in dentistry, especially when biofilms grow over dental restorations. The inhibition of cariogenic biofilm associated with the onset of carious lesions is crucial for preventing disease recurrence after treatment. This in vitro study defined optimized parameters for using a photosensitizer, toluidine blue O (TBO), activated via a red light-emitting diode (LED)-based wireless device to control the growth of cariogenic biofilms. The effect of TBO concentrations (50, 100, 150, and 200 μg/mL) exposed to light or incubated in the dark was investigated in successive cytotoxicity assays. Then, a mature biofilm model under sucrose challenge was treated with different TBO concentrations (50, 100, and 150 μg/mL), different light energy doses (36, 108, and 180 J/cm), and different incubation times before irradiation (1, 3, and 5 min). The untreated biofilm, irradiation with no TBO, and TBO incubation with no activation represented the controls. After treatments, biofilms were analyzed via colony-forming units (CFUs) and live/dead assay. The percentage of cell viability was within the normal range compared to the control when 50 and 100 μg/mL of TBO were used. Increasing the TBO concentration and energy dose was associated with biofilm inhibition ( < 0.001), while increasing incubation time did not contribute to bacterial elimination ( > 0.05). Irradiating the biofilm via 100 μg/mL of TBO and ≈180 J/cm energy dose resulted in ≈3-log reduction and a higher amount of dead/compromised colonies in live/dead assay compared to the control ( < 0.001). The light energy dose and TBO concentration optimized the bacterial elimination of biofilms. These results provide a perspective on the determining parameters for highly effective photo-killing of caries-related biofilms and display the limitations imposed by the toxicity of the antibacterial photodynamic therapy's chemical components. Future studies should support investigations on new approaches to improve or overcome the constraints of opportunities offered by photodynamic inactivation of caries-related biofilms.
龋相关生物膜及其相关并发症是口腔医学的重大威胁,尤其是当生物膜在牙修复体上生长时。抑制与龋病病变相关的致龋生物膜对于预防治疗后疾病复发至关重要。本体外研究定义了使用光敏剂甲苯胺蓝 O(TBO)的最佳参数,该光敏剂通过基于红色发光二极管(LED)的无线装置激活,以控制致龋生物膜的生长。研究了 TBO 浓度(50、100、150 和 200μg/mL)在暴露于光或在黑暗中孵育时的作用,然后在连续的细胞毒性测定中进行了研究。然后,用不同浓度的 TBO(50、100 和 150μg/mL)、不同光能量剂量(36、108 和 180J/cm)和不同辐照前孵育时间(1、3 和 5min)处理在蔗糖挑战下成熟的生物膜模型。未处理的生物膜、无 TBO 照射和无激活 TBO 孵育作为对照。处理后,通过菌落形成单位(CFU)和活/死测定分析生物膜。与对照相比,当使用 50 和 100μg/mL 的 TBO 时,细胞活力百分比在正常范围内。增加 TBO 浓度和能量剂量与生物膜抑制相关(<0.001),而增加孵育时间对细菌清除没有贡献(>0.05)。用 100μg/mL 的 TBO 和约 180J/cm 的能量剂量照射生物膜导致与对照相比,活/死测定中≈3 对数减少和更多的死/受损菌落(<0.001)。光能量剂量和 TBO 浓度优化了生物膜的细菌清除。这些结果为确定高效光杀伤与龋病相关生物膜的参数提供了一个视角,并显示了抗菌光动力疗法化学成分的毒性所施加的限制。未来的研究应支持对新方法的研究,以改善或克服光动力灭活与龋病相关生物膜带来的机会的限制。