Repeated exposures to blue light-activated eosin Y enhance inactivation of E. faecalis biofilms, in vitro

被引:18
作者
Marinic, Karlo [1 ]
Manoil, Daniel [1 ]
Filieri, Anna [1 ]
Wataha, John C. [2 ]
Schrenzel, Jacques [3 ]
Lange, Norbert [4 ]
Bouillaguet, Serge [1 ]
机构
[1] Univ Geneva, Sect Dent Med, Endodont Unit, Geneva, Switzerland
[2] Univ Washington, Dept Restorat Dent, Seattle, WA 98195 USA
[3] Univ Geneva, Univ Hosp Geneva, Infect Dis Serv, Geneva, Switzerland
[4] Univ Geneva, Sch Pharmaceut Sci, Dept Pharmaceut & Biopharmaceut, Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
PHOTODYNAMIC THERAPY; ENTEROCOCCUS-FAECALIS; STREPTOCOCCUS-MUTANS; SINGLET OXYGEN; CELLS; PHOTOINACTIVATION; PHOTOSENSITIZERS; SUSCEPTIBILITY; FRACTIONATION; ERYTHROSINE;
D O I
10.1016/j.pdpdt.2015.06.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: In dentistry, antibacterial photodynamic therapy (a-PDT) has shown promising results for inactivating bacterial biofilms causing carious, endodontic and periodontal diseases. In the current study, we assessed the ability of eosin Y exposed to 3 irradiation protocols at inactivating Enterococcus faecalis biofilms, in vitro. Methods: E. faecalis biofilms formed on hydroxyapatite disks were incubated with eosin Y (10-80 mu M), then activated with blue light using different irradiation protocols. Biofilms exposed to continuous exposure were incubated for 40 min before being light-activated for 960 s. For the intermittent exposure, biofilms were exposed 4 times to the light/photosensitizer combination (960 s total) without renewing the photosensitizer. For repeated a-PDT, the same light dose was delivered in a series of 4 irradiation periods separated by dark periods; fresh photosensitizer was added between each light irradiation. After treatment, bacteria were immediately labeled with LIVE/DEAD BacLight Bacterial Viability kit and viability was assessed by flow cytometry (FCM). Results were statistically analyzed using one-way ANOVA and Tukey multiple comparison intervals (alpha = 0.05). Results: The viability of E. faecalis biofilms exposed to 10 mu M eosin Y, was significantly reduced compared to controls (light only-eosin Y only). After a second exposure to blue light-activated eosin Y, viability significantly decreased from 58% to 12% whereas 6.5% of the bacterial biofilm remained live after a third exposure (p < 0.05). Only 3.5% of the bacterial population survived after the fourth exposure. Conclusions: The results of this study indicate that blue light-activated eosin Y can photoinactivate E. faecalis biofilms grown on hydroxyapatite disks. Also, repeated exposures to blue light-activated eosin Y were shown to significantly improve efficacy. Further studies seem warranted to optimize the antibacterial activity of blue light-activated eosin Y on major oral pathogens. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:393 / 400
页数:8
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