Soukos N S, Wilson M, Burns T, Speight P M
Department of Oral Pathology, Eastman Dental Institute, London, United Kingdom.
Lasers Surg Med. 1996;18(3):253-9. doi: 10.1002/(SICI)1096-9101(1996)18:3<253::AID-LSM6>3.0.CO;2-R.
Some oral bacteria are susceptible to killing by red light after their sensitization with toluidine blue O (TBO). The photochemotherapy of periodontal disease in vivo would require a therapeutic window where bacteria could be killed without adjacent normal tissue damage.
STUDY DESIGN/MATERIALS AND METHODS: The laser-induced effects of TBO on normal human gingival keratinocytes and fibroblasts have been studied in vitro. For the assessment of viability, the CellTiter 96TM AQueous Non-Radioactive Cell Proliferation Assay was used.
TBO was cytotoxic at low concentrations (5.0 micrograms/ml). Sensitization of keratinocytes and fibroblasts with 2 and 5.0 micrograms/ml TBO, respectively, for 5 min and exposure to light from a 7.3 mW Helium/Neon (HeNe) laser for up to 2 min (0.876J) did not reduce cell viability. However, killing of Streptococcus sanguis was achieved following exposure to HeNe light for 75 sec (0.547J) in the presence of TBO at a concentration of 2.5 micrograms/ml.
The development of a system for the lethal photosensitization of bacteria responsible for periodontal disease may be possible.
一些口腔细菌在用甲苯胺蓝O(TBO)致敏后对红光敏感,可被杀死。牙周病的体内光化学疗法需要一个治疗窗口,在此窗口内可杀死细菌而不损伤相邻正常组织。
研究设计/材料与方法:已在体外研究了TBO对正常人牙龈角质形成细胞和成纤维细胞的激光诱导效应。为评估细胞活力,使用了CellTiter 96TM AQueous非放射性细胞增殖检测法。
低浓度(5.0微克/毫升)的TBO具有细胞毒性。分别用2微克/毫升和5.0微克/毫升的TBO对角质形成细胞和成纤维细胞致敏5分钟,并用7.3毫瓦氦氖(HeNe)激光照射长达2分钟(0.876焦耳),并未降低细胞活力。然而,在浓度为2.5微克/毫升的TBO存在下,用HeNe激光照射75秒(0.547焦耳)后,血链球菌被杀死。
开发一种对引起牙周病的细菌进行致死性光致敏的系统可能是可行的。