Y Koishi’s research while affiliated with Nagasaki University Hospital and other places

The purpose of this study was to evaluate 2 thione primers and 3 resin adhesives for enhancement of bonding strength to a silver-palladium-copper-gold alloy. Two different sized disk specimens (10- and 8-mm diameter by 2.5-mm thick) were prepared from a silver-palladium-copper-gold alloy (Castwell M.C. 12, GC). The specimens were airborne-particle abraded with 50-microm-grain alumina, conditioned either with a thiouracil primer (Metaltite, Tokuyama Dental) or with a triazine dithione primer (V-Primer, Sun Medical), and then bonded with 1 of 3 acrylic resins: a benzoyl peroxide-amine redox-initiated resin adhesive (Multi-Bond, Tokuyama Dental) or a tri-nbutylborane-initiated resin adhesive (Super-Bond C&B and Super-Bond Quick, Sun Medical). For each adhesive, unprimed specimens were prepared as experimental controls. Shear bond strength was determined after thermocycling (100,000 cycles). Use of primers significantly (P < .05) enhanced the bond strength of specimens in all adhesives. Irrespective of the type of primer, the strength of Multi-Bond adhesive was significantly (P < .05) lower than that of Super-Bond C&B and Super-Bond Quick adhesives. The strength of the 2 tri-n-butylborane-initiated adhesives did not differ significantly (P > .05). The mean strength of the Super-Bond C&B adhesive was 40.4 MPa with Metaltite and 37.8 MPa with V-Primer; that of Super-Bond Quick adhesive was 40.9 MPa with Metaltite and 36.5 MPa with V-Primer. Use of thione primers effectively enhanced the strength of the bond to the silver-palladium-copper-gold alloy. Furthermore, the combinations of primers and tri-n-butylborane-initiated adhesives were found to be more efficient for bonding.

The purpose of this study was to evaluate the color stability of two acrylic resin adhesives with different activation systems: a benzoyl peroxide (BPO)-amine redox system and a tri-n-butylborane (TBB) derivative system. The colorimetric values of the two resins in different shades (Clear and Ivory) were determined (n=5) 24 hours after polymerization as a baseline using the L*a*b* system of the Commission Internationale de l'Eclairage (CIE). The specimens were thereafter immersed in distilled water, and the color difference (deltaE*) values were calculated. After 24 weeks, the TBB-initiated material showed a significantly (p<0.05) lower color change than the BPO-amine-initiated material. The deltaE* values for the BPO-amine-initiated materials were 6.9 for Clear and 15.8 for Ivory, whereas those for the TBB-initiated materials were 1.3 and 1.8 respectively. Thus, it was concluded that the TBB-initiated material had superior color stability to that of the BPO-amine-initiated material.

The purpose of the current study was to evaluate the effect of functional monomers with phosphorus on bonding durability to titanium. Three metal conditioners (Alloy Primer, AP; Metal Link, ML; Eyesight Opaque Primer, EP) were assessed. The functional monomers for base metal are 10-methacryloyloxydecyl dihydrogenphosphate (MDP) for the AP, 6-methacryloxyhexyl phosphonoacetate (MHPA) for the ML, and methacrylatephosphate (MP) for the EP. Cast disk specimens made of high-purity titanium (T-Alloy H) were air-abraded with 70μm alumina, primed with three conditioners, and then bonded with an acrylic resin adhesive (Super-Bond C&B). Shear bond strengths were determined both before and after thermocycling (20, 000 cycles). Before thermocycling, the shear bond strengths for the AP and ML groups were significantly higher than those for the EP and unprimed (defined as control) groups (p<0.05). The AP group exhibited significantly higher bond strength than the ML group after thermocycling (p<0.05). Significant difference was not found between the EP and the unprimed groups regardless of thermocycling application (p>0.05).

The purpose of this study was to evaluate the influence of visible-light exposure on water absorption, solubility and colour stability of dual-curable luting composites. Using eight dual-curable luting composites (2bond2, Bistite II, G-CERA Cosmotech II, Imperva Dual, Linkmax, Lute-It, Panavia Fluoro Cement and Variolink II), disk specimens were prepared by the following two methods: (i) dual-cured specimens; exposed with visible-light from a light-curing unit, and (ii) chemical-cured specimens; chemically polymerized without exposure. Five specimens were produced for each material and curing mode. Water absorption and solubility were determined according to standardized testing methods, and the data were compared using analysis of variance (ANOVA) and contrasts. With regard to colour stability, the colour difference (DeltaE*) values between 24 h and the other immersion periods (1, 2, 3, 4, 8, 12, 16, 20 and 24 weeks) were calculated and then analysed by repeated measure ANOVA. The dual-cured specimens exhibited significantly lower solubility values than the chemical-cured specimens except for the Lute-It material. The dual-cured Linkmax material exhibited the lowest solubility (0.51 +/- 0.01 microg mm(-3)) and the lowest DeltaE* value after 24 weeks (2.64 +/- 0.39). The dual-curable luting composites should be light-exposed after seating of restorations in order to reduce water absorption and solubility, and to improve colour stability.

This study was conducted to evaluate influence of visible-light exposure on colour stability of dual-curable luting composite. Using six dual-curable luting composites [Bistite II (BI), Clapearl DC (CL), Dicor Light Activated Cement (DI), G-Cera Cosmotech II (GC), Lute-It (LU) and Variolink II (VA), disk specimens were prepared with the following two methods: (i) dual-cured specimens, exposure with visible-light from a photo-curing unit for 120 s and (ii) chemical-cured specimens, chemically cured without exposure. Five specimens were produced for each material and curing mode. After 24 h, all specimens were immersed in distilled water at 37 degrees C for 24 weeks, during which colour accuracy was measured with a dental colorimeter. The colours characterized in the Commission Internationale d'Eclairage (CIE) L*a*b* colour space were first determined 24 h after preparation (baseline colour evaluation), and again after 1, 2, 3, 4, 8, 12, 16 and 24 weeks. The colour difference (Delta E*) values between 24 h and the other immersion periods were calculated, and then analysed by repeated measure analysis of variance (ANOVA). In addition, the Delta E* values after 24 weeks for dual-cured specimens were compared with those for chemical-cured specimens by one-way ANOVA and by contrasts for each composite (P < 0.05). The Delta E* values were influenced by the material and curing mode as well as immersion period (P=0.0001). After 24 weeks the dual-cured specimens showed significantly lower Delta E* values than the chemical-cured specimens, except for the VA material. The CL material exhibited the least colour change (1.9 +/- 0.2) among the dual-cured specimens, and the VA material showed the least (4.5 +/- 0.9) among the chemical-cured specimens after 24 weeks. Dual-curable luting composites should be polymerized with the dual modes to ensure colour stability.

This study determined the colour accuracy of a photo-activated prosthetic composite with various thicknesses and shades for the purpose of evaluating the relationship between material thickness variation and colour reproducibility. Four light shades (A1, B1, C1 and D2) and four dark shades (A4, B4, C4 and D4) of a representative photo-activated prosthetic composite (Artglass) for body paste were assessed. The specimens were prepared with thicknesses of 0.5, 1.0, 1.5, 2.0, 2.5 and 3.0 mm. The L*a*b* colour parameter of each shade was measured using a dental colorimeter (ShadeEye) connected to a computer. The overall colour accuracy of groups of five specimens was compared by means of analysis of variance (ANOVA) and Scheffe's S multiple range test (P=0;05). In addition, L*a*b* colour difference (Delta E*) values between the 3.0 mm thickness and the other thicknesses were calculated. Three-factor ANOVA revealed that all colour parameters were influenced by the thickness as well as by the shade letter and shade tab (P < 0.05). The L* value consistently decreased for all shades as thickness increased, although there was no obvious correlation between the thickness of the material and either the a* or b* values. Among the Delta E* values, the values between the 2.5 and 3.0 mm thicknesses were the lowest, and values were found to be lower than 2.0 for all shades. The colour accuracy of the photo-activated prosthetic composite was related to the thickness of the material regardless of the shade. For acceptable colour reproducibility, a composite material thickness of at least 2.5 mm was found to be required.

This study determined the depth of cure of different shades of a prosthetic composite material with the aim of evaluating the influence of shade variation on post-curing material properties. Four light shades having small tabs (A1, B1, C1 and D2) and four dark shades having higher tabs (A4, B4, C4 and D4) of a prosthetic composite (Artglass) for body paste based on the Vita Lumin Shade guide were selected. Specimens of each shade were exposed with the proprietary photo-curing unit (UniXS) for periods 20, 30, 60 and 90 s. The curing depth of the material for each shade was determined with a scraping technique described by the International Organization for Standardization (ISO 4049), and average values of groups of five specimens were compared using analysis of variance (ANOVA) and Scheffe's S intervals (P < 0.05). The L*a*b* colour parameters of five specimens after 90 s exposure were measured using a small-area dental colorimeter (ShadeEye) in order to determine the colorimetric differences. Three-factor ANOVA revealed that the depth of cure was influenced by shade letter (A, B, C or D) and shade tab (1 and 2, or 4) as well as by the exposure period (P=0.05). Curing depth of the light shades was consistently greater than that of the dark shades. Among the eight shades selected, B1 shade demonstrated the greatest curing depth, while A4 shade exhibited the lowest curing depth. For all shades, longer exposure increased the depth of cure. All of the light shades exhibited higher L* values than any of the four dark shades. Curing depth of the composite material was found to be related to the Vita shade variation and the exposure period.