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姜黄素介导的抗菌光动力疗法降低了感染牙本质龋微宇宙的活力和生存能力。

Curcumin-mediated antimicrobial photodynamic therapy reduces the viability and vitality of infected dentin caries microcosms.

机构信息

Department of Pediatric Dentistry, Orthodontics and Public Health, Bauru School of Dentistry, University of São Paulo, Brazil.

Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.

出版信息

Photodiagnosis Photodyn Ther. 2018 Dec;24:102-108. doi: 10.1016/j.pdpdt.2018.09.007. Epub 2018 Sep 18.

Abstract

BACKGROUND

To our knowledge, there is a lack of evidence on the effect of Antimicrobial Photodynamic Therapy (aPDT) by the application of curcumin against complex biofilms of dental caries lesions. This study aimed to evaluate the viability, vitality, and acid metabolism of infected dentin caries microcosms treated with curcumin-mediated aPDT.

METHODS

After microcosm biofilms growing anaerobically on bovine dentin disks immersed in McBain medium with 1% sucrose at 37 °C for 5 days, the biofilms were treated by the association of DMSO water solution or 600 μmol L curcumin with 0, 37.5 or 75 J cm blue LED (455 nm). Then, the colony-forming units (CFU) counts of total microorganisms, total streptococci, mutans streptococci, and total lactobacilli were determined by plating. The lactic acid concentration was analyzed by enzymatic spectrophotometry method, while the vitality of intact biofilms was evaluated by confocal laser scanning microscope (CLSM). Statistical analysis was performed by Kruskal Wallis and post-hoc Dunn's tests (P < 0.05).

RESULTS

Curcumin alone did not affect the viability of microorganisms and the vitality of intact biofilms. However, 75 J cm LED alone decreased the total microorganisms and total lactobacilli counts. The combination of curcumin and LED reduced significantly the counts of all microorganism groups and the vitality of intact biofilms. Differences were not observed between the lactic acid concentrations of distinct groups.

CONCLUSIONS

Therefore, curcumin-mediated aPDT was effective in reducing the viability and the vitality of infected dentin caries microcosms, without interfering in their acidogenicity.

摘要

背景

据我们所知,缺乏关于姜黄素介导的光动力疗法(aPDT)对龋齿病变复杂生物膜的影响的证据。本研究旨在评估姜黄素介导的 aPDT 处理感染牙本质龋微宇宙的活力、活力和酸代谢。

方法

在 37°C 下,将 McBain 培养基中的 1%蔗糖溶液中的牛牙本质圆盘浸入培养基中,在无氧条件下培养微宇宙生物膜 5 天后,用 DMSO 水溶液或 600μmol·L 的姜黄素与 0、37.5 或 75 J·cm 的蓝光 LED(455nm)联合处理生物膜。然后,通过平板计数法测定总微生物、总链球菌、变形链球菌和总乳杆菌的菌落形成单位(CFU)计数。通过酶分光光度法分析乳酸浓度,并用共聚焦激光扫描显微镜(CLSM)评估完整生物膜的活力。通过 Kruskal Wallis 和事后 Dunn 检验(P<0.05)进行统计分析。

结果

姜黄素单独使用不会影响微生物的活力和完整生物膜的活力。然而,单独使用 75 J·cm 的 LED 会降低总微生物和总乳杆菌的数量。姜黄素和 LED 的组合显著降低了所有微生物组的数量和完整生物膜的活力。不同组之间的乳酸浓度没有差异。

结论

因此,姜黄素介导的 aPDT 可有效降低感染牙本质龋微宇宙的活力和活力,而不会干扰其产酸能力。

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