This study was designed to evaluate the efficacy of resin coating on the regional microtensile bond strength (MTBS) of a resin cement to the dentin walls of Class II cavities. Twenty mesio-occlusal cavities were prepared in human molars. In 10 cavities, a resin coating consisting of a self-etching primer bonding system, Clearfil SE Bond, and a low-viscosity microfilled resin, Protect Liner F, was applied. The other 10 teeth served as a non-coating group. After impression taking and temporization, they were kept in water for one day. Composite inlays were then cemented with a dual-cure resin cement, Panavia F 2.0, and stored in water for one day. Thereafter, MTBSs were measured. Two-way ANOVA (p=0.05) revealed that the MTBS of resin cement to dentin was influenced by resin coating, but not by regional difference. In conclusion, application of a resin coating to the dentin surface significantly improved the MTBS in indirect restorations.
The purpose of this study was to evaluate the microtensile bond strength(MTBS)of a waterless all-in-one adhesive system, Absolute, to dentin. Eighteen human molars were either ground with 600-grit SiC paper or cut with a diamond bur. The following dentin bonding procedures were then performed: dentin surface was kept moist; dentin surface was dried; or dentin surface was dried but equivalent amount of water was added to the adhesive(1:1 by volume) . After adhesive curing, a resin composite was incrementally built up. After the specimens were kept in water for one day, MTBSs were measured at a cross-head speed of 1 mm/min. Two-way ANOVA(p=0.05)indicated that the MTBS of the adhesive system was not influenced by surface texture, but enhanced by the presence of water on tooth surface. It was concluded that water is essential to obtaining good dentin bonding for this adhesive system.
:Objective: Aspects of an Artificial Mouth System (AMS) to model the caries process in bovine enamel biofilm induced white spot enamel lesions (WSEL) were analyzed. Methods: Square shaped and polished bovine enamel slabs were covered with modeling wax and 2.5 mm diameter window was prepared to expose enamel surface at the center of each slab. Artificial biofilms were grown inside an AMS on the slabs using freshly cultured S. muatns (MT8148) in suspended in phosphate buffered saline (PBS), heart infusion (HI) with 1% sucrose and PBS for 20, 30 and 40 hrs at 37°C. The severity of demineralization was quantified by Quantitative Light-induced Fluorescence (QLF, Inspektor, Netherlands). All experiments were repeated three times (n=5 for each group). Results: A circular WSEL could clearly be detected at the center of each slab by naked eyes, which was prominent after dehydration by mild air drying. QLF data showed that severity of demineralization occurred with the increase of time interval, after 40 hours both ∆F (23+/-2.9) and ∆Q (148.75+/-26.78) were significantly more compared to ∆F (10.14+/-2.3) and ∆Q (47.63+/-30.67) of 20 hours Conclusion: An advanced in vitro model of biolfilm induced WSEL was developed that showed promises to be useful in studying enamel demineralization.
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