Evolution of roughness and optical properties of resin composites submitted to whitening toothpastes-cigarette smoking cycling.

PURPOSE: To evaluate the effect of cycling whitening toothpaste with cigarette smoking (WTCS) on the evolution of roughness, color, translucency, and gloss of microfilled, microhybrid, and nanofilled resin composites. METHODS: 15 specimens of Durafill - DVS, Empress Direct - ED, and Z350 - FZ were divided into three groups according to the toothpastes:: conventional, control group, (Colgate - C) and Whitening (Colgate Luminous White - CW and Oral B 3D White - OW) and roughness, color, translucency, and gloss were evaluated before and after the specimens were submitted to WTCS for 8 weeks. Data were analyzed by two-way ANOVA, 3-way repeated measures ANOVA, and Tukey HSD post hoc test (α= 0.05). RESULTS: Only ED and FZ brushed with CW and FZ brushed with C presented an increase in roughness after WTCS. The three composites suffered a significant color alteration after WTCS. Excepting DVS brushed with CW, all the other groups presented a significant reduction in translucency after WTCS. DVS was the only resin composite that maintained its gloss stability after WTCS. Whitening toothpastes behaved similarly to conventional (control) toothpaste regarding the evolution of roughness and optical stability of the three resin composites. CLINICAL SIGNIFICANCE: Whitening toothpastes were not capable of maintaining the color stability of the three resin composites after 8 weeks of toothpastes-cigarette smoking cycling.

Microhardness evaluation of in situ vital bleaching and thickening agents on human dental enamel.

Bleaching systems and thickening agents lead to changes in the tooth enamel matrix as a result of an unspecific oxidation of the bleaching gel in the enamel. This reaction may result in a loss of mineral content and a decrease in microhardness. The aim of this study was to evaluate the effects of different bleaching systems and their thickening agents on the microhardness of human enamel in situ. Two dental slabs (3 x 3 x 2 mm) obtained from third molars were fixed on the buccal facial aspects of the maxillary first molars in a group of 45 volunteers. The volunteers were treated with 10% carbamide peroxide gel with carbopol as the thickening agent (group 1), 2% carbopol gel (group 2), 10% carbamide peroxide paste with poloxamer as the thickening agent (group 3), poloxamer (group 4), or 6.5% hydrogen peroxide strips for 21 days (group 5) (experimental treatment factor). The effects of the experimental treatment were evaluated by microhardness tests performed both before and after treatment (time factor). Data were submitted to split-plot analysis of variance and Tukey tests. Only time showed a statistically significant difference (P < .0001). All treatments reduced the enamel microhardness during treatment. Clinically, a reduction in microhardness can be expected after dental bleaching.

Effect of long-term water storage on etch-and-rinse and self-etching resin-dentin bond strengths.

This study sought to evaluate the long-term bond strength of etch-and-rinse and self-etch adhesive systems to dentin after one year of water storage. Crown fragments from the buccal surface of extracted bovine incisors were ground flat to expose dentin surfaces. Four etch-and-rinse and two self-etch bonding agents were used according to manufacturers' instructions. Bonded specimens were stored in water for either 24 hours or one year at 37 delete C. After elapsed storage times, specimens were tested for shear bond strength (SBS) at 0.5 mm/min. Data were analyzed by ANOVA and Tukey's tests (p < 0.05). Both evaluated factors (adhesive system and storage time) and their interactions were statistically significant. Single Bond produced the highest SBS regardless of the water degradation period. One-year water storage reduced the SBS of Prime & Bond NT and One-Up Bond F significantly; the other adhesives performed similarly. Long-term bond strengths of etch-and-rinse and self-etch adhesive systems are susceptible to hygroscopic and hydrolytic effects to varying extents, depending on their chemistry and structure. The presence of monomers with different properties might induce preferential degradation of specific adhesive polymer systems.