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跨物种微生物的甲苯胺蓝 O 和碘化钾的抗菌光动力效应。

Antimicrobial Photodynamic Effect of Cross-Kingdom Microorganisms with Toluidine Blue O and Potassium Iodide.

机构信息

Fujian Key Laboratory of Oral Diseases & Fujian Provincial Engineering Research Center of Oral Biomaterial & Stomatological Key Lab of Fujian College and University, School of Stomatology, Fujian Medical University, Fuzhou 350002, China.

Restorative Dental Sciences (Endodontics), Faculty of Dentistry, The University of Hong Kong, Hong Kong 999077, China.

出版信息

Int J Mol Sci. 2022 Sep 27;23(19):11373. doi: 10.3390/ijms231911373.

Abstract

() and () are prominent microbes associated with rapid and aggressive caries. In the present study, we investigated the antimicrobial efficacy, cytotoxicity, and mechanism of toluidine blue O (TBO)-mediated antimicrobial photodynamic therapy (aPDT) and potassium iodide (KI). The dependence of KI concentration, TBO concentration and light dose on the antimicrobial effect of aPDT plus KI was determined. The cytotoxicity of TBO-mediated aPDT plus KI was analyzed by cell counting kit-8 (CCK-8) assay. A singlet oxygen (O) probe test, time-resolved O detection, and a O quencher experiment were performed to evaluate the role of O during aPDT plus KI. The generation of iodine and hydrogen peroxide (HO) were analyzed by an iodine starch test and Amplex red assay. The anti-biofilm effect of TBO-mediated aPDT plus KI was also evaluated by counting forming unit (CFU) assay. KI could potentiate TBO-mediated aPDT against and in planktonic and biofilm states, which was safe for human dental pulp cells. O measurement showed that KI could quench O signals, implicating that O may act as a principal mediator to oxidize excess iodide ions to form iodine and HO. KI could highly potentiate TBO-mediated aPDT in eradicating and due to the synergistic effect of molecular iodine and HO.

摘要

()和()是与快速和侵袭性龋病相关的主要微生物。在本研究中,我们研究了甲苯胺蓝 O(TBO)介导的抗菌光动力疗法(aPDT)和碘化钾(KI)的抗菌功效、细胞毒性和作用机制。确定了 KI 浓度、TBO 浓度和光剂量对 aPDT 加 KI 抗菌效果的依赖性。通过细胞计数试剂盒-8(CCK-8)测定分析 TBO 介导的 aPDT 加 KI 的细胞毒性。通过单线态氧(O)探针试验、时间分辨 O 检测和 O 淬灭剂实验评估了 O 在 aPDT 加 KI 过程中的作用。通过碘淀粉试验和 Amplex red 测定分析了碘和过氧化氢(HO)的生成。还通过计数形成单位(CFU)测定评估了 TBO 介导的 aPDT 加 KI 的抗生物膜作用。KI 可以增强 TBO 介导的 aPDT 对浮游和生物膜状态下的()和()的作用,对人牙髓细胞是安全的。O 测量表明,KI 可以猝灭 O 信号,这意味着 O 可能作为主要介导物将过量的碘离子氧化成碘和 HO。由于分子碘和 HO 的协同作用,KI 可以高度增强 TBO 介导的 aPDT 以根除()和()。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60a8/9569606/5b1097867649/ijms-23-11373-g001.jpg

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