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蓝光介导的粪肠球菌体外失活。

Blue light-mediated inactivation of Enterococcus faecalis in vitro.

机构信息

Endodontics Unit, Section of Dental Medicine, University of Geneva, Geneva, Switzerland.

出版信息

Photodiagnosis Photodyn Ther. 2013 May;10(2):134-40. doi: 10.1016/j.pdpdt.2012.11.002. Epub 2012 Dec 5.

DOI:10.1016/j.pdpdt.2012.11.002
PMID:23769279
Abstract

In dentistry, residual infection remains a major cause of failure after endodontic treatment; many of these infections involve Enterococcus faecalis. In the current study, we explored the possibility that blue light activated photosensitizers could be used, in principle, to inactivate this microbe as an adjunct disinfection strategy for endodontic therapy. Three blue light absorbing photosensitizers, eosin-Y, rose bengal, and curcumin, were tested on E. faecalis grown in planktonic suspensions or biofilms. Photosensitizers were incubated for 30 min with bacteria then exposed to blue light (450-500 nm) for 240 s. Sodium hypochlorite (3%) was used as a control. After 48 h, the viability of E. faecalis was estimated by measuring colony-forming units post-exposure vs. untreated controls (CFU/mL). Blue light irradiation alone did not alter E. faecalis viability. For planktonic cultures, blue light activated eosin-Y (5 μM), rose bengal (1 μM), or curcumin (5 μM) significantly (p<0.05) reduced E. faecalis viability compared to exposure to the unirradiated photochemicals. For biofilm cultures, concentrations of light-activated eosin-Y, rose bengal, and curcumin of 100, 10, and 10 μM respectively, completely suppressed E. faecalis viability (p<0.05). Although the current results are limited to an in vitro model, they support further exploration of blue light activated antimicrobials as an adjunct therapy in endodontic treatment.

摘要

在牙科领域,根管治疗后残留感染仍然是治疗失败的主要原因;这些感染中有许多涉及粪肠球菌。在本研究中,我们探索了使用蓝光激活光敏剂作为根管治疗辅助消毒策略来灭活这种微生物的可能性。在浮游悬液或生物膜中培养粪肠球菌,然后测试了三种蓝光吸收光敏剂:曙红 Y、玫瑰红苯并和姜黄素。将光敏剂与细菌孵育 30 分钟,然后用蓝光(450-500nm)照射 240 秒。次氯酸钠(3%)用作对照。暴露后 48 小时,通过暴露后与未经处理的对照(CFU/mL)相比测量粪肠球菌的菌落形成单位来估计粪肠球菌的活力。单独的蓝光照射不会改变粪肠球菌的活力。对于浮游培养物,蓝光激活的曙红 Y(5μM)、玫瑰红苯并(1μM)或姜黄素(5μM)与未辐照光化学物质相比,显著(p<0.05)降低了粪肠球菌的活力。对于生物膜培养物,浓度分别为 100、10 和 10μM 的光激活曙红 Y、玫瑰红苯并和姜黄素完全抑制了粪肠球菌的活力(p<0.05)。尽管目前的结果仅限于体外模型,但它们支持进一步探索蓝光激活的抗菌剂作为根管治疗辅助治疗的可能性。

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