Papers by Author: S.O. Kim

Abstract: he aim of this study was to evaluate the effect of HA on the demineralization resistance and bonding strength of light-curing glass ionomer dental cement. Tests were conducted using (1) pure Fuji II LC GIC, (2) 15% micro HA-Fuji II LC GIC. Physical properties, demineralization resistance and bonding strength to dentin of teeth were determined. The curing depth in all groups were satisfied the requirement of curing depth of ISO 9917-2:2004(minimum curing depth = 1mm). The depth of cure was reduced with addition of HA, presumably due to the light scattering effect of HA particles. Regarding sensitivity to ambient light, there were no detectable changes of the homogeneity in any groups. Also all groups were satisfied the requirement of the flexural strength of ISO 9917-2:2004(minimum flexural strength = 20MPa). 15% HA-Fuji II LC GIC group was found to present a greater flexural strength than pure Fuji II LC GIC, as the addition of HA promotes a chemical reaction between the HA, the glass powder, and the polyacid. Observing under the CLSM after 4 days of demineralization, there were significant differences in the CLSM and SEM images. Pure Fuji II LC GIC group showed greater enamel demineralization layer than in 15% HA-Fuji II LC GIC group. In SEM analysis, there was greater enamel demineralization in the pure Fuji II LC GIC group, and less demineralized under the influence of HA particles, 15% HA-Fuji II LC GIC group had more even surface particles. 15% HA-Fuji II LC GIC group was found to present a greater bonding strength than pure Fuji II LC GIC group. Observing the fractured surfaces under SEM after the bonding strength test, the cohesive failure rate was found to be in increasing order of pure Fuji II LC GIC, 15% HA-Fuji II LC GIC group. There were bone-like apatite particles observed to be formed in 15% HA-Fuji II LC GIC group.

Abstract: Histoacryl® (N-butyl-2-cyanoacrylate) has been widely utilized as a tissue adhesive. The aim of this study was to evaluate the physical and adhesive properties of newly developed cyanoacrylate-based β-TCP composite systems. The β-TCP powder was modified on the surface with citric acid to make this material mixed with cyanoacrylate easily. The setting time of acidtreated β-TCP/ Histoacryl® systems was dramatically prolonged and the polymerization heat was significantly decreased compared to that of untreated β-TCP/Histoacryl® system. The shear bond strength of cyanoacrylate-based β-TCP composites decreased with addition of acid-treated β-TCP filler. The compressive strength of β-TCP/Histoacryl® composites increased strongly with increasing the amount of acid-treated β-TCP filler. The cytotoxicity of the β-TCP/Histoacryl® composites decreased with the increasing of the amount of added β-TCP. These results indicated that our novel β-TCP/Histoacryl® composites had the great potential to serve as adhesives or filling materials in the dental field.

Abstract: Previous studies have shown that hydroxyapatite increases the bonding strength of dental luting cement with human teeth by forming bone-like apatite when it is added to cement. However, due to the low solubility of the hydroxyapatite, its ability to form bone-like apatite decreases in protein-free acellular simulated body fluid with ion concentrations nearly equal to those of the human blood plasma. The purpose of this experiment was to increase the formation of bone-like apatite by mixing hydroxyapatite with β-TCP of high solubility. RelyXTM glass ionomer cement(3M/ESPE, USA) was used as dental luting cement. Film thickness, setting time, and compressive strength was measured for each group of 15% hydroxyapatite, 15% β-TCP, and 15% mixed hydroxyapatite and β-TCP (85:15). Every specimen of each group was immersed in the simulated body fluid for four week before measuring bonding strength, and then their sectional surface was observed under SEM. The most noteworthy result was that the group containing β-TCP produced more amount of bone-like apatite compared with the group composed of only hydroxyapatite.

Abstract: This study aimed to investigate the effects of hydroxyapatite on bonding strength between dental luting cement and human teeth. In the previous study, bonelike forming ability by mixing hydroxyapatite with several bone cements was reported in a protein-free acellular simulated body fluid with ion concentrations nearly equal to those of the human blood plasma. Therefore in this experiment, we assumed that if bonelike apatite layer could form between dental luting cement and human teeth, the bonding strength between the two would improve. In addition, we expected the HA mixed dental luting cement to improve the physical properties. Fuji I glass ionomer and Relyx™ glass ionomer cement were the selected dental luting cements and the film thickness, setting time and compressive strength were measured mixing various concentrations of hydroxyapatite. Glass ionomer cement with the most superior physical properties(Fuji I ; 20% hydroxyapatite, Relyx™ ; 15% hydroxyapatite) was immersed in the simulated body fluid for three weeks and the surface was observed under SEM after measuring the bonding strength. As the concentration of HA increased, the film thickness of hydroxyapatite-glass ionomer cement decreased, the setting time increased, and the compressive strength increased. The most noteworthy results were that bonding strength increased, and that bonelike apatite formed on the tooth surface when observed under SEM.