期刊
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY
卷 94, 期 1, 页码 65-70出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotobiol.2008.07.013
关键词
Photodynamic inactivation; Light emitting diode; Toluidine blue O; Candida spp.; Photosensitizers
资金
- CAPES
- CNPq
- FAPEMIG
In this Study, photodynamic inactivation (PDI) was used to inhibit in vitro growth and adhesion of different Candida isolates to buccal epithelia] cells (BEC). Experimental conditions were optimized and 25 mu M toluidine blue 0 (TBO) and 15 min of irradiation time by light emitting diode (LED) (energy density of 180J/cm(2)) were selected due to higher reductions in cellular viability obtained after treatment. Reduction media of Log(10) 3.41 in viable cellular growth and media of 55% in the inhibition of adhesion to buccal epithelial cells were obtained. Two fluconazole resistant isolates were susceptible to PDI (Log(10) 3.54 in IB05 and Log(10) 1.95 in CG09) and a second session of this treatment for CG09 isolate inhibited cellular viability in 100%, without producing heat. The results permit to Conclude that photodynamic inactivation under these experimental conditions would be a possible alternative approach to inhibit Candida spp. cellular growth and adhesion to buccal epithelia] cells. (C) 2008 Elsevier B.V. All rights reserved.
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