ABSTRACT
The aim of this study was to evaluate the differences in setting times based on the methods for dental root canal sealers and calcium silicate cement used in root-end filling. Five kinds of dental root canal sealers and four kinds of calcium silicate cement for root-end filling were selected for the experiments. All materials were mixed according to the manufacturers’ instructions and stored at 37 ℃ with a relative humidity of 95%. Setting time was measured using a 1/4 pound Gillmore needle and a 1 pound Gillmore needle to determine the time until indentation was no longer visible or the time until 2 mm penetration was no longer possible. The determination of indentation was based on the absence of visible impressions on the material surface when Gillmore needle was placed vertically. When comparing indentation time and penetration time using same type of Gillmore needle, only ProRoot MTA using 1 pound Gillmore needle showed significant difference between measuring methods (P0.05). By this study, we could expect to measure a setting time relatively similar to real clinical conditions through indentation method.
ABSTRACT
The purpose of this study was to evaluate the remineralization effect of experimental fluoride varnish mixed with nano-tricalcium phosphate (TCP) and nano-hydroxyapatite (HA) on bovine teeth under demineralization and remineralization cycling by Vickers hardness. After fabrication of rosin-based experimental fluoride varnish with 5 wt% of NaF (EX) in the laboratory, 10 wt% of nano-hydroxyapatite (HA+EX) and nano-TCP (TC+EX) were mixed, respectively. Casein phosphopeptide-amorphous calcium phosphate (Tooth mousse) (CP) was used for comparison. Bovine incisors were impregnated by acrylic resin and exposed to caries inducing solution for 72 hours. EX, HA+EX, TC+EX, and CP were applied on the surface of bovine teeth. The specimens were immersed in a demineralization solution for 1 hour and in a re-mineralization solution for 23 hours and the cycle was repeated for 20 days. Vickers hardness was measured at baseline and after each treatment. CP group showed the highest hardness value at 24 hours after application of each material (p0.05).On the 10th day of de-/re-mineralization cycling, the TC+EX group showed the highest hardness value (p0.05). On the 20th day, the TC+EX group kept the highest hardness value, followed by HA+EX and EX groups (p<0.05). In conclusion, experimental fluoride varnish with 10 wt% of nano-TCP showed higher remineralization effect on the enamel of bovine teeth during the de/re-mineralization cycling.
ABSTRACT
The purpose of this study was to evaluate the sustainability of antibacterial effect against Streptococcus mutans of experimental fluoride varnish mixed with 2-hydroxyethyl methacrylate (HEMA) and/or glutaraldehyde. Experimental fluoride varnish (EX1) was fabricated. To make fluoride varnish with adhesive materials, EX1 was mixed with 5 wt% of glutaraldehyde (EX2), 35 wt% of HEMA (EX3) or both 5 wt% of glutaraldehyde and 35 wt% of HEMA (EX4). 5 μL of each experimental group was applied to 6 mm diameter polyethylene terephthalate film discs. Disks were stored in distilled water in a shaking incubator at 37℃ for 1 hour, 3 hours, 8 hours, 12 hours, 24 hours, 5 days and 10 days. The antibacterial activities against S. mutans were evaluated by agar diffusion test with the discs at each time. The antibacterial activities were sustained up to 10 days in all groups. The antibacterial activities of EX3 and EX4 were significantly higher than other groups from 8 hours to 10 days and there were no significant differences from EX2 at 10 days. HEMA with and without glutaraldehyde can be applied to fluoride varnish to increase the sustainability of antibacterial activities.
ABSTRACT
We evaluated the antibacterial, anti-inflammatory, and inhibitory effect of osteoclast differentiation of Brachypodium sylvaticum (BS) to find out the possibility of preventing periodontal disease. The inhibition of Porphyromonas gingivalis (P. gingivalis) growth by BS and the sustainability of the antibacterial activity was assessed. The production of pro-inflammatory cytokines from lipopolysaccharide (LPS)-induced RAW 264.7 cells were measured using enzyme-linked immunosorbent assays (ELISA), and the production of nitric oxide (NO) and cell viability were measured. Osteoclast differentiation was evaluated by Tartrate-resistant acid phosphatase (TRAP) staining, and TRAP activity. BS showed significant antibacterial activity and sustainable antibacterial activity in P. gingivalis. We also found out that the BS significantly decreased secretion of pro-inflammatory cytokines [tumor necrosis factor (TNF-α) and interleukin-6 (IL-6)] and NO production without cytotoxicity. Furthermore, BS inhibited the differentiation of bone marrow macrophages (BMMs) obtained from mouse bone marrow cells into osteoclasts without cytotoxicity. Taken together, BS can be a promising candidate for a preventive and improving agent of periodontal disease having antibacterial, anti-inflammatory, and inhibitory effects of osteoclast differentiation.
ABSTRACT
The purpose of this study was to evaluate the remineralization effect of experimental fluoride varnish mixed with nano-tricalcium phosphate (TCP) and nano-hydroxyapatite (HA) on bovine teeth under demineralization and remineralization cycling by Vickers hardness. After fabrication of rosin-based experimental fluoride varnish with 5 wt% of NaF (EX) in the laboratory, 10 wt% of nano-hydroxyapatite (HA+EX) and nano-TCP (TC+EX) were mixed, respectively. Casein phosphopeptide-amorphous calcium phosphate (Tooth mousse) (CP) was used for comparison. Bovine incisors were impregnated by acrylic resin and exposed to caries inducing solution for 72 hours. EX, HA+EX, TC+EX, and CP were applied on the surface of bovine teeth. The specimens were immersed in a demineralization solution for 1 hour and in a re-mineralization solution for 23 hours and the cycle was repeated for 20 days. Vickers hardness was measured at baseline and after each treatment. CP group showed the highest hardness value at 24 hours after application of each material (p0.05).On the 10th day of de-/re-mineralization cycling, the TC+EX group showed the highest hardness value (p0.05). On the 20th day, the TC+EX group kept the highest hardness value, followed by HA+EX and EX groups (p<0.05). In conclusion, experimental fluoride varnish with 10 wt% of nano-TCP showed higher remineralization effect on the enamel of bovine teeth during the de/re-mineralization cycling.
ABSTRACT
The purpose of this study was to evaluate the sustainability of antibacterial effect against Streptococcus mutans of experimental fluoride varnish mixed with 2-hydroxyethyl methacrylate (HEMA) and/or glutaraldehyde. Experimental fluoride varnish (EX1) was fabricated. To make fluoride varnish with adhesive materials, EX1 was mixed with 5 wt% of glutaraldehyde (EX2), 35 wt% of HEMA (EX3) or both 5 wt% of glutaraldehyde and 35 wt% of HEMA (EX4). 5 μL of each experimental group was applied to 6 mm diameter polyethylene terephthalate film discs. Disks were stored in distilled water in a shaking incubator at 37℃ for 1 hour, 3 hours, 8 hours, 12 hours, 24 hours, 5 days and 10 days. The antibacterial activities against S. mutans were evaluated by agar diffusion test with the discs at each time. The antibacterial activities were sustained up to 10 days in all groups. The antibacterial activities of EX3 and EX4 were significantly higher than other groups from 8 hours to 10 days and there were no significant differences from EX2 at 10 days. HEMA with and without glutaraldehyde can be applied to fluoride varnish to increase the sustainability of antibacterial activities.
ABSTRACT
We evaluated the antibacterial, anti-inflammatory, and inhibitory effect of osteoclast differentiation of Brachypodium sylvaticum (BS) to find out the possibility of preventing periodontal disease. The inhibition of Porphyromonas gingivalis (P. gingivalis) growth by BS and the sustainability of the antibacterial activity was assessed. The production of pro-inflammatory cytokines from lipopolysaccharide (LPS)-induced RAW 264.7 cells were measured using enzyme-linked immunosorbent assays (ELISA), and the production of nitric oxide (NO) and cell viability were measured. Osteoclast differentiation was evaluated by Tartrate-resistant acid phosphatase (TRAP) staining, and TRAP activity. BS showed significant antibacterial activity and sustainable antibacterial activity in P. gingivalis. We also found out that the BS significantly decreased secretion of pro-inflammatory cytokines [tumor necrosis factor (TNF-α) and interleukin-6 (IL-6)] and NO production without cytotoxicity. Furthermore, BS inhibited the differentiation of bone marrow macrophages (BMMs) obtained from mouse bone marrow cells into osteoclasts without cytotoxicity. Taken together, BS can be a promising candidate for a preventive and improving agent of periodontal disease having antibacterial, anti-inflammatory, and inhibitory effects of osteoclast differentiation.