Publication:
Efficacy of erythrosine and cyanidin-3-glucoside mediated photodynamic therapy on Porphyromonas gingivalis biofilms using green light laser

dc.contributor.authorAroon Teerakapongen_US
dc.contributor.authorTeerasak Damrongrungruangen_US
dc.contributor.authorSajee Sattayuten_US
dc.contributor.authorNoppawan Phumala Moralesen_US
dc.contributor.authorSurada Tantananugoolen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-12-21T06:37:08Z
dc.date.accessioned2019-03-14T08:02:38Z
dc.date.available2018-12-21T06:37:08Z
dc.date.available2019-03-14T08:02:38Z
dc.date.issued2017-12-01en_US
dc.description.abstract© 2017 Elsevier B.V. Background The purpose of this in vitro study was to evaluate the efficacy of erythrosine and cyanidin-3-glucoside as photosensitizers in PDT for the elimination of Porphyromonas gingivalis (P. gingivalis) biofilms. Methods P. gingivalis biofilms were prepared from a chronic periodontitis subject. Erythrosine and cyanidin-3-glucoside were prepared and randomly allocated as follows: 110, 220, 330, and 440 μM erythrosine; 101, 202, 303, and 404 μM anthocyanin; and 440 μM erythrosine + 404 μM cyanidin-3-glucoside. There were 18 PDT experimental groups (non-irradiated/irradiated with a 532-nm green light diode laser at 1.29 J/cm2 for 60 s). The 3 controls were grouped as follows: biofilms exposed to the photosensitizers alone, biofilms exposed to the laser alone, and biofilms exposed to 0.12% chlorhexidine. All sample groups were cultured at 1, 3 and 6 h after PDT and incubated in an anaerobic chamber at 37 °C for 4 days. The surviving fraction was calculated from the log10 CFU/ml. The 330 and 440 μM erythrosine and the 440 μM erythrosine + 404 μM cyanidin-3-glucoside were mixed with spin traps (TEMPO, DMPO), and the electron spin resonance spectra were evaluated. Results The log10 CFU/ml measurements showed that the PDT groups with 330 μM or 440 μM erythrosine and 440 μM erythrosine + 404 μM cyanidin-3-glucoside had statistically significant differences from the other groups (one-way ANOVA and Bonferroni's multiple comparison test, p- value ≤ 0.05). Conclusions PDT using 330 μM erythrosine, 440 μM erythrosine or 440 μM erythrosine + 404 μM cyanidin-3-glucoside irradiated with the laser more effectively inhibited P. gingivalis in biofilms.en_US
dc.identifier.citationPhotodiagnosis and Photodynamic Therapy. Vol.20, (2017), 154-158en_US
dc.identifier.doi10.1016/j.pdpdt.2017.09.001en_US
dc.identifier.issn18731597en_US
dc.identifier.issn15721000en_US
dc.identifier.other2-s2.0-85030717467en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/41660
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85030717467&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleEfficacy of erythrosine and cyanidin-3-glucoside mediated photodynamic therapy on Porphyromonas gingivalis biofilms using green light laseren_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85030717467&origin=inwarden_US

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