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dc.contributor.authorMonteiro, Mylene Martins-
dc.contributor.authorSantos, Juliana Amorim dos-
dc.contributor.authorBarbosa, Victor Paiva-
dc.contributor.authorGallo, Camila de Barros-
dc.contributor.authorMarques, Márcia Martins-
dc.contributor.authorGuerra, Eliete Neves Silva-
dc.date.accessioned2022-08-02T14:28:51Z-
dc.date.available2022-08-02T14:28:51Z-
dc.date.issued2022-06-07-
dc.identifier.citationMONTEIRO, Mylene Martins et al. Efects of diferent photobiomodulation therapy doses on cell viability after bacterial and ionizing radiation–induced stress: a pilot in vitro study. Lasers in Dental Science, 07 jun. 2022. DOI: https://doi.org/10.1007/s41547-022-00162-1.pt_BR
dc.identifier.urihttps://repositorio.unb.br/handle/10482/44371-
dc.language.isoInglêspt_BR
dc.publisherSpringerpt_BR
dc.rightsAcesso Restritopt_BR
dc.titleEfects of diferent photobiomodulation therapy doses on cell viability after bacterial and ionizing radiation–induced stress : a pilot in vitro studypt_BR
dc.typeArtigopt_BR
dc.subject.keywordCélulas - cultura e meios de culturapt_BR
dc.subject.keywordLasers em odontologiapt_BR
dc.subject.keywordFibroblastospt_BR
dc.subject.keywordFotobiomodulaçãopt_BR
dc.identifier.doihttps://doi.org/10.1007/s41547-022-00162-1pt_BR
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s41547-022-00162-1pt_BR
dc.description.abstract1Purpose Photobiomodulation therapy has proven to be effective in accelerating cell proliferation, migration, and transcription. The study aimed to analyze the cell viability effects of different parameters of PBMT in a cultured cell line of human gingival fibroblasts after bacterial and ionizing radiation–induced stress. Methods Explant technique was used to produce a primary cell culture. Cells were grown in Dulbecco’s modified Eagle’s medium with 10% fetal bovine serum until stressful condition induction with lipopolysaccharide of Escherichia coli, Porphyromonas gingivalis protein extract, and ionizing radiation. Laser irradiation was carried out in four sessions set with 660 nm wavelength, an output power of 30 mW and 40 mW and energy density of 2, 3, 4, and 5 J/cm2. Results After 24 h from the last laser irradiation session, the groups outputted in 30 mW of power maintained the cell viability while operating with 2, 4, and 5 J/cm2. However, 3 J/cm2 dose significantly decreased cell viability (p < 0.05). When the laser irradiation session was set in a higher power (40 mW), cell viability was reduced using 2, 3, and 5 J/cm2 doses, with statistical significance for 5 J/cm2 (p < 0.001). In addition, operating the same energy using lower power seems to be superior to a higher power, being statically significant for 5 J/cm2 dose (p < 0.001). This pattern followed with all different groups, except by 3 J/cm2. Conclusions The present study showed that delivering 2, 4, and 5 J/ cm2 of density of energy with 30 mW and more time of exposure presented better results on cell viability compared to the same density of energy with output power of 40 mW. Further studies comparing density energy should be conducted.pt_BR
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