Américo Bortolazzo Correr

Effect of the increase of energy density on knoop hardness of dental composites light-cured by conventional QTH, LED and xenon plasma arc

The aim of this study was to evaluate the effect of the increase of energy density on Knoop hardness of Z250 and Esthet-X composite resins. Cylindrical cavities (3 mm in diameter X 3 mm in depth) were prepared on the buccal surface of 144 bovine incisors. The composite resins were bulk-inserted and polymerized using different light-curing units and times: conventional QTH (quartz-tungsten-halogen; 700 mW/cm(2); 20 s, 30 s and 40 s); LED (light-emitting diode; 440 mW/cm(2); 20 s, 30 s and 40 s); PAC (xenon plasma arc; 1700 mW/cm(2); 3 s, 4.5 s and 6 s). The specimens were stored at 37 degrees C for 24 h prior to sectioning for Knoop hardness assessment. Three measurements were obtained for each depth: top surface, 1 mm and 2 mm. Data were analyzed statistically by ANOVA and Tukeys test (p<0.05). Regardless of the light source or energy density, Knoop hardness of Z250 was statistically significant higher than that of Esthet-X (p<0.05). Specimens cured with PAC had lower hardness than those cured with QTH and LED (p<0.05). Higher Knoop hardness was obtained when the energy density was increased for LED and PAC (p<0.05). No statistically significant differences (p>0.05) were found for QTH. Knoop hardness values decreased with the increase of depth. The increase of energy density produced composites with higher Knoop hardness means using LED and PAC.

Effects of surface treatments, thermocycling, and cyclic loading on the bond strength of a resin cement bonded to a lithium disilicate glass ceramic.

SUMMARY Objectives : The aim of this present study was to investigate the effect of two surface treatments, fatigue and thermocycling, on the microtensile bond strength of a newly introduced lithium disilicate glass ceramic (IPS e.max Press, Ivoclar Vivadent) and a dual-cured resin cement. Methods : A total of 18 ceramic blocks (10 mm long × 7 mm wide × 3.0 mm thick) were fabricated and divided into six groups (n=3): groups 1, 2, and 3-air particle abraded for five seconds with 50-μm aluminum oxide particles; groups 4, 5, and 6-acid etched with 10% hydrofluoric acid for 20 seconds. A silane coupling agent was applied onto all specimens and allowed to dry for five seconds, and the ceramic blocks were bonded to a block of composite Tetric N-Ceram (Ivoclar Vivadent) with RelyX ARC (3M ESPE) resin cement and placed under a 500-g static load for two minutes. The cement excess was removed with a disposable microbrush, and four periods of light activation for 40 seconds each were performed at right angles using an LED curing unit (UltraLume LED 5, Ultradent) with a final 40 second light exposure from the top surface. All of the specimens were stored in distilled water at 37°C for 24 hours. Groups 2 and 5 were submitted to 3,000 thermal cycles between 5°C and 55°C, and groups 3 and 6 were submitted to a fatigue test of 100,000 cycles at 2 Hz. Specimens were sectioned perpendicular to the bonding area to obtain beams with a cross-sectional area of 1 mm(2) (30 beams per group) and submitted to a microtensile bond strength test in a testing machine (EZ Test) at a crosshead speed of 0.5 mm/min. Data were submitted to analysis of variance and Tukey post hoc test (p≤0.05). Results : The microtensile bond strength values (MPa) were 26.9 ± 6.9, 22.2 ± 7.8, and 21.2 ± 9.1 for groups 1-3 and 35.0 ± 9.6, 24.3 ± 8.9, and 23.9 ± 6.3 for groups 4-6. For the control group, fatigue testing and thermocycling produced a predominance of adhesive failures. Fatigue and thermocycling significantly decreased the microtensile bond strength for both ceramic surface treatments when compared with the control groups. Etching with 10% hydrofluoric acid significantly increased the microtensile bond strength for the control group.

Can the Hydrophilicity of Functional Monomers Affect Chemical Interaction

The number of carbon atoms and/or ester/polyether groups in spacer chains may influence the interaction of functional monomers with calcium and dentin. The present study assessed the chemical interaction and bond strength of 5 standard-synthesized phosphoric-acid ester functional monomers with different spacer chain characteristics, by atomic absorption spectroscopy (AAS), ATR-FTIR, thin-film x-ray diffraction (TF-XRD), scanning electron microscopy (SEM), and microtensile bond strength (μTBS). The tested functional monomers were 2-MEP (two-carbon spacer chain), 10-MDP (10-carbon), 12-MDDP (12-carbon), MTEP (more hydrophilic polyether spacer chain), and CAP-P (intermediate hydrophilicity ester spacer). The intensity of monomer-calcium salt formation measured by AAS differed in the order of 12-MDDP=10-MDP>CAP-P>MTEP>2-MEP. FTIR and SEM analyses of monomer-treated dentin surfaces showed resistance to rinsing for all monomer-dentin bonds, except with 2-MEP. TF-XRD confirmed the weaker interaction of 2-MEP. Highest µTBS was observed for 12-MDDP and 10-MDP. A shorter spacer chain (2-MEP) of phosphate functional monomers induced formation of unstable monomer-calcium salts, and lower chemical interaction and dentin bond strength. The presence of ester or ether groups within longer spacer carbon chains (CAP-P and MTEP) may affect the hydrophilicity, μTBS, and also the formation of monomer-calcium salts.

Halogen and LED light curing of composite: temperature increase and Knoop hardness

This study assessed the Knoop hardness and temperature increase provided by three light curing units when using (1) the manufacturers’ recommended times of photo-activation and (2) standardizing total energy density. One halogen – XL2500 (3M/ESPE) – and two light-emitting diode (LED) curing units – Freelight (3M/ESPE) and Ultrablue IS (DMC) – were used. A type-K thermocouple registered the temperature change produced by the composite photo-activation in a mold. Twenty-four hours after the photo-activation procedures, the composite specimens were submitted to a hardness test. Both temperature increase and hardness data were submitted to ANOVA and Tukey’s test (5% significance). Using the first set of photo-activation conditions, the halogen unit produced a statistically higher temperature increase than did both LED units, and the Freelight LED resulted in a lower hardness than did the other curing units. When applying the second set of photo-activation conditions, the two LED units produced statistically greater temperature increase than did the halogen unit, whereas there were no statistical differences in hardness among the curing units.

Effect of different photoinitiators and reducing agents on cure efficiency and color stability of resin-based composites using different LED wavelengths

OBJECTIVES To evaluate the effect of photoinitiators and reducing agents on cure efficiency and color stability of resin-based composites using different LED wavelengths. METHODS Model resin-based composites were associated with diphenyl(2,4,6-trimethylbenzoyl) phosphine oxide (TPO), phenylbis(2,4,6-trimethylbenzoyl) phosphine oxide (BAPO) or camphorquinone (CQ) associated with 2-(dimethylamino) ethyl methacrylate (DMAEMA), ethyl 4-(dimethyamino) benzoate (EDMAB) or 4-(N,N-dimethylamino) phenethyl alcohol (DMPOH). A narrow (Smartlite, Dentisply) and a broad spectrum (Bluephase G2, Ivoclar Vivadent) LEDs were used for photo-activation (20 J/cm(2)). Fourier transform infrared spectroscopy (FT-IR) was used to evaluate the cure efficiency for each composite, and CIELab parameters to evaluated color stability (ΔE00) after aging. The UV-vis absorption spectrophotometric analysis of each photoinitiator and reducing agent was determined. Data were analyzed using two-way ANOVA and Tukeys test for multiple comparisons (α=0.05). RESULTS Higher cure efficiency was found for type-I photoinitiators photo-activated with a broad spectrum light, and for CQ-systems with a narrow band spectrum light, except when combined with an aliphatic amine (DMAEMA). Also, when combined with aromatic amines (EDMAB and DMPOH), similar cure efficiency with both wavelength LEDs was found. TPO had no cure efficiency when light-cured exclusively with a blue narrowband spectrum. CQ-systems presented higher color stability than type-I photoinitiators, especially when combined with DMPOH. CONCLUSIONS After aging, CQ-based composites became more yellow and BAPO and TPO lighter and less yellow. However, CQ-systems presented higher color stability than type-I photoinitiators, as BAPO- and TPO-, despite their higher cure efficiency when photo-activated with corresponding wavelength range. CLINICAL SIGNIFICANCE Color matching is initially important, but color change over time will be one of the major reasons for replacing esthetic restorations; despite the less yellowing of these alternative photoinitiators, camphorquinone presented higher color stability.

Effects of different photo-polymerization protocols on resin–dentine μTBS, mechanical properties and cross-link density of a nano-filled resin composite

OBJECTIVES To evaluate the effects of four different light-curing protocols on the microtensile bond strength (μTBS), ultimate tensile strength (UTS), Knoop micro-hardness (KH) and cross-link density (CLD) of a nano-filled resin composite. METHODS Filtek Supreme XT (3M-ESPE) was used for the entire experiments following four light-curing approaches: ST, standard irradiance; HI, high irradiance; PD, pulse delay; SS, soft start. The specimens were submitted to different storage periods (24h or 6 months), cut into match-sticks and subsequently submitted to μTBS testing. Hourglass specimens were also prepared for UTS and KH. Cylindrical specimens were prepared for the CLD evaluation after absolute ethanol challenge. The results were statistically analyzed with a two-way ANOVA and Tukeys test (α=0.05). RESULTS For UTS and KH, continuous irradiance (PD and SS) induced statistically higher results (p<0.05) both after 24h and 6 months of water storage compared to ST and HI groups. However, a drop in UTS and KH was obtained after 6 months in all groups. The μTBS was not affected by the different light-curing approaches and, no statistical differences (p>0.05) were observed between 24h and 6 months storage. The CLD evaluation showed a statistical drop in KH after 24h of ethanol storage for PD and SS (step-curing protocols) compared to those attained in continuous mode (ST and HI). CONCLUSION The soft-start mode may improve the UTS and KH of nano-filled resin composites without compromising the resin-dentine μTBS. However, both the step-curing protocols may reduce the cross-link density of the composite polymeric network. CLINICAL SIGNIFICANCE High irradiances photo-polymerization may be adequate for direct aesthetic restorations such as veneers and onlays. Meanwhile, the soft start protocol would seem more appropriate for the photo-polymerization of high c-factors class I and II restorations.

In-depth Polymerization of Dual-cured Resin Cement Assessed by Hardness

This study investigates the in-depth polymerization of dual-cured resin cement (Enforce; Dentsply, shades A2, B1, and opaque). Cylindrical specimens are obtained by photo-activation through ceramic. Control samples are light-cured without using ceramic. Samples are tested after 15 min or 24 h. Knoop hardness readings are made at 100, 300, 500, and 700 μm depth. Hardness is generally dependent on the mode of activation and post-cure time. Shades A2 and B1 show higher hardness values than opaque resin. Hardness at 100 μm is higher than at 700 μm. A linear relationship between hardness and depth is observed.

Effect of light-curing units, post-cured time and shade of resin cement on knoop hardness

The aim of this study was to evaluate the Knoop hardness after 15 min and 24 h of different shades of a dual-cured resin-based cement after indirect photoactivation (ceramic restoration) with 2 light-curing units (LCUs). The resin cement Variolink II (Ivoclar Vivadent) shade XL, A2, A3 and opaque were mixed with the catalyst paste and inserted into a black Teflon mold (5 mm diameter x 1 mm high). A transparent strip was placed over the mold and a ceramic disc (Duceram Plus, shade A3) was positioned over the resin cement. Light-activation was performed through the ceramic for 40 s using quartz-tungsten-halogen (QTH) (XL 2500; 3M ESPE) or light-emitting diode (LED) (Ultrablue Is, DMC) LCUs with power density of 615 and 610 mW/cm(2), respectively. The Koop hardness was measured using a microhardness tester HMV 2 (Shimadzu) after 15 min or 24 h. Four indentations were made in each specimen. Data were subjected to ANOVA and Tukeys test (alpha=0.05). The QTH LCU provided significantly higher (p<0.05) KHN values than the LED LCU. When the post-cure times were compared for the same shade, QTH and LED at 24 h provided significantly higher (p<0.05) KHN values than at 15 min. It may be concluded that the Knoop hardness was generally dependent on the LCU and post-cure time. The opaque shade of the resin cement showed lower Knoop hardness than the other shades for both LCUs and post-cure times.

Effect of Etching Time and Light Source on the Bond Strength of Metallic Brackets to Ceramic

This study evaluated the bond strength of brackets to ceramic testing different etching times and light sources for photo-activation of the bonding agent. Cylinders of feldspathic ceramic were etched with 10% hydrofluoric acid for 20 or 60 s. After application of silane on the ceramic surface, metallic brackets were bonded to the cylinders using Transbond XT (3M Unitek). The specimens for each etching time were assigned to 4 groups (n=15), according to the light source: XL2500 halogen light, UltraLume 5 LED, AccuCure 3000 argon laser, and Apollo 95E plasma arc. Light-activation was carried out with total exposure times of 40, 40, 20 and 12 s, respectively. Shear strength testing was carried out after 24 h. The adhesive remnant index (ARI) was evaluated under magnification. Data were subjected to two-way ANOVA and Tukeys test (α=0.05). Specimens etched for 20 s presented significantly lower bond strength (p<0.05) compared with those etched for 60 s. No significant differences (p>0.05) were detected among the light sources. The ARI showed a predominance of scores 0 in all groups, with an increase in scores 1, 2 and 3 for the 60 s time. In conclusion, only the etching time had significant influence on the bond strength of brackets to ceramic.

The role of spacer carbon chain in acidic functional monomers on the physicochemical properties of self-etch dental adhesives

OBJECTIVES To evaluate the effects of acidic functional monomers with different hydrophilicity and spacer carbon chain length on the degree of conversion (DC), wettability (contact angle), water sorption (WS) and ultimate tensile strength (UTS) of experimental one-step self-etch adhesives (1-SEAs). METHODS A series of standard resin blends was prepared with each formulation containing 15mol% of each acidic monomer. The structural variations of the acidic monomers were MEP (spacer chain with 2 carbons), MDP (10-carbons), MDDP (12-carbons), MTEP (more hydrophilic polyether spacer) and CAP-P (intermediate hydrophilicity ester spacer). Dumbbell-shaped and disc specimens were prepared and tested for UTS and WS, respectively. DC was assessed by FTIR, while the wettability of each 1-SEA was evaluated on glass slides and flat dentine surfaces. Results were analysed with one-way ANOVA and Tukeys test (p<0.05). RESULTS The outcomes showed lower UTS for CAP-P, control blend and MEP than MTEP, MDDP and MDP (p<0.05). The degree of conversion was statistically similar for all resins (p=0.122). On dentine, the wettability was higher (lower contact angle) with the most hydrophilic monomer MTEP. Higher WS was attained using MTEP. Different lengths of the spacer chains did not result in different wettability and WS (p>0.05). CONCLUSION At similar molar percentage, different acidic functional monomers induced similar degree of conversion and different UTS when included in a 1-SEA. However, the inclusion of highly hydrophilic monomer may increase the wettability on dentine and the WS.