RESUMO
The aim of this study was to investigate the antibacterial effects of 445 nm blue diode lasers and erbium chromium lasers on the biofilm of Enterococcus faecalis in root canal dentin with different thicknesses. Dentin slices with thicknesses of 300, 500, and 1,000 microns were prepared; and after the biofilm formation, they were randomly divided into four groups: group A : Er, Cr:YSGG laser radiation; group B: 445 nm diode laser radiation; group C : laser radiation in three cycles; and control group D: 5 samples of each thickness were selected as a positive control group. Er, Cr:YSGG and diode lasers alone did not significantly reduce the number of bacteria in any of the thicknesses. Only in 1 mm thick sections, the group exposed with the both Er, Cr:YSGG laser and 445 nm diode laser (66%) significantly reduced the number of bacteria. There was a significant difference in a thickness of 0.3 mm compared to a thickness of 1 mm, indicating that these lasers had a better effect at a thickness of 0.3 mm than at 1 mm parts (P-value < 0.008). It seems that these lasers can be used as an adjunct to conventional chemical methods in cleaning infected canals.
RESUMO
BACKGROUND: This study assessed the effect of Biodentine coated with Emdogain (Biodentine/Emdogain) on proliferation and differentiation of human stem cells from the apical papilla (SCAPs). METHODS AND RESULTS: In this in vitro, experimental study, SCAPs were isolated from two immature impacted third molars and cultured. After ensuring the stemness of the cells by assessing the cell surface markers, they were exposed to Biodentine, Emdogain, and Biodentine/Emdogain for 24 and 72 h. The control cells did not receive any intervention. Cell viability was evaluated by the methyl thiazolyl tetrazolium assay. Expression of odontogenic differentiation genes was analyzed by the quantitative reverse transcription polymerase chain reaction. Alkaline phosphatase (ALP) activity was quantified by the respective kit. Data were analyzed by one-way ANOVA, t-test, and Mann-Whitney test (α = 0.05). Cell viability did not change after 24 h of exposure to biomaterials. At 72 h, the viability of the cells exposed to Biodentine and Biodentine/Emdogain decreased compared with the control group. The expression of dentin sialophosphoprotein, dentin matrix protein 1, and bone sialoprotein genes, and ALP activity significantly increased in all three experimental groups, compared with the control group at both 24 and 72 h; this increase was significantly greater in Biodentine/Emdogain group. The number of mineralized nodules significantly increased in all groups after 72 h with a greater rate in Biodentine/Emdogain group. CONCLUSIONS: All biomaterials increased the differentiation of SCAPs, expression of odontogenic genes, and ALP activity, but Biodentine/Emdogain was significantly more effective for this purpose.
