Search

Objectives : To assess the behavior of dual-cure and conventional bulk-fill composite materials on real-time linear shrinkage, shrinkage stress, and degree of conversion. Materials and methods: Two dual-cure bulk-fill materials (Cention, Ivoclar Vivadent (with ion-releasing properties) and Fill-Up!, Coltene) and two conventional bulk-fill composites (Tetric PowerFill, Ivoclar Vivadent; SDR flow + , Dentsply Sirona) were compared to conventional reference materials (Ceram.x Spectra ST (HV), Dentsply Sirona; X-flow; Dentsply Sirona). Light curing was performed for 20 s, or specimens were left to self-cure only. Linear shrinkage, shrinkage stress, and degree of conversion were measured in real time for 4 h (n = 8 per group), and kinetic parameters were determined for shrinkage stress and degree of conversion. Data were statistically analyzed by ANOVA followed by post hoc tests (α = 0.05). Pearson's analysis was used for correlating linear shrinkage and shrinkage force. Results: Significantly higher linear shrinkage and shrinkage stress were found for the low-viscosity materials compared to the high-viscosity materials. No significant difference in degree of conversion was revealed between the polymerization modes of the dual-cure bulk-fill composite Fill-Up!, but the time to achieve maximum polymerization rate was significantly longer for the self-cure mode. Significant differences in degree of conversion were however found between the polymerization modes of the ion-releasing bulk-fill material Cention, which also exhibited the significantly slowest polymerization rate of all materials when chemically cured. Conclusions: While some of the parameters tested were found to be consistent across all materials studied, heterogeneity increased for others. Clinical relevance: With the introduction of new classes of composite materials, predicting the effects of individual parameters on final clinically relevant properties becomes more difficult. [ABSTRACT FROM AUTHOR]

This study investigated polymerization kinetics, linear shrinkage, and shrinkage stress development for six contemporary composite materials of different viscosities cured using radiant exitances of 1100–2850 mW/cm2. Real-time measurements of degree of conversion, linear shrinkage, and shrinkage stress were performed over 5 min using Fourier-transform infrared spectrometry, a custom-made linometer, and a custom-made stress analyzer, respectively. For most tested variables, the factor "material" had a higher effect size than the factor "curing protocol". Maximum polymerization rate and maximum shrinkage stress rate were the most affected by changes in curing conditions. In contrast, no significant effects of curing conditions were identified within each material for shrinkage stress values measured at the end of the 5 min observation period. Linear shrinkage and shrinkage stress values measured after 5 min were closely correlated (R = 0.905–0.982). The analysis of polymerization kinetics suggested that the two composites specifically designed for rapid light-curing responded to higher radiant exitances differently than other composites. Polymerization kinetics and shrinkage stress behavior of contemporary restorative composite materials of different viscosities were overall more affected by material type than differences in curing conditions. Subtle differences in polymerization kinetics behavior shown by the two composites specifically designed for rapid high-intensity light-curing did not translate into significant differences in the development of polymerization shrinkage stress. [ABSTRACT FROM AUTHOR]

We embedded copper-doped mesoporous bioactive glass nanospheres (Cu-MBGN) with antibacterial and ion-releasing properties into experimental dental composites and investigated the effect of Cu-MBGN on the polymerisation properties. We prepared seven composites with a BisGMA/TEGDMA (60/40) matrix and 65 wt.% total filler content, added Cu-MBGN or a combination of Cu-MBGN and silanised silica to the silanised barium glass base, and examined nine parameters: light transmittance, degree of conversion (DC), maximum polymerisation rate (Rmax), time to reach Rmax, linear shrinkage, shrinkage stress (PSS), maximum PSS rate, time to reach maximum PSS rate, and depth of cure. Cu-MBGN without silica accelerated polymerisation, reduced light transmission, and had the highest DC (58.8 ± 0.9%) and Rmax (9.8 ± 0.2%/s), but lower shrinkage (3 ± 0.05%) and similar PSS (0.89 ± 0.07 MPa) versus the inert reference (0.83 ± 0.13 MPa). Combined Cu-MBGN and silica slowed the Rmax and achieved a similar DC but resulted in higher shrinkage. However, using a combined 5 wt.% Cu-MBGN and silica, the PSS resembled that of the inert reference. The synergistic action of 5 wt.% Cu-MBGN and silanised silica in combination with silanised barium glass resulted in a material with the highest likelihood for dental applications in future. [ABSTRACT FROM AUTHOR]

This study aimed to investigate polymerization kinetics and curing light transmittance of two series of experimental dental resin composites filled with 0–40 wt% of either 45S5 bioactive glass (BG) or a customized low-Na F-containing BG. Polymerization kinetics in 0.1-mm and 2-mm thick layers were investigated through real-time degree of conversion measurements using a Fourier transform infrared (FTIR) spectrometer. FTIR spectra were continuously collected at a rate of 2 s−1 during light-curing (1340 mW/cm2). Light transmittance through 2-mm thick composite specimens was measured using a UV–Vis spectrometer at a rate of 20 s−1. Unlike BG 45S5, which led to a dose-dependent reduction in the rate and extent of polymerization, the customized low-Na F-containing BG showed a negligible influence on polymerization. The reduction in light transmittance of experimental composites due to the addition of the low-Na F-containing BG did not translate into impaired polymerization kinetics. Additionally, the comparison of polymerization kinetics between 0.1-mm and 2-mm thick layers revealed that polymerization inhibition identified for BG 45S5 was not mediated by an impaired light transmittance, indicating a direct effect of BG 45S5 on polymerization reaction. A customized low-Na F-containing BG showed favourable behaviour for being used as a functional filler in light-curing dental resin composites. [ABSTRACT FROM AUTHOR]

This study investigated the effect of adding bioactive glass 45S5 (BG) of different particle sizes to dental composite on resin polymerization and shrinkage stress formation. Commercial flowable composite was mixed with either 15 wt% BG fillers (nanometric, micrometric, or hybrid BG) or inert barium glass. Real-time linear polymerization shrinkage and shrinkage stress were recorded, and the degree of conversion was measured using FTIR spectroscopy. The commercial (unmodified) composite developed significantly higher linear shrinkage and shrinkage stress than the groups with 15 wt% added inert or BG fillers. After adding inert barium glass, the composite showed significantly higher linear shrinkage than when micrometric BG was added. The addition of bioactive or inert glass fillers did not affect the degree of conversion. Shrinkage stress can be reduced by adding inert or bioactive fillers (nano- and/or microparticulate BG) without affecting monomer conversion. [ABSTRACT FROM AUTHOR]

The aim of the present study was to investigate polymerization shrinkage, shrinkage force development, and degree of monomer conversion of high- and low-viscosity dimethacrylate- and ormocer-based bulk-fill resin composites. Two flowable bulk-fill composites (SDR, x-tra base), two high-viscosity bulk-fill composites (Bulk Ormocer, SonicFill), and two conventional composite materials (Esthet X flow, Esthet X HD) were photoactivated for 20 s at 1275 mW/cm2. Linear polymerization shrinkage and shrinkage force were recorded in real time using custom-made devices, and the force rate and time to achieve maximum force rate were determined. Degree of conversion was measured using Fourier-transform infrared spectroscopy. Data were analyzed with one-way ANOVA and Tukey's HSD post-hoc test, and bivariate correlations were computed (α = 0.05). The category of high-viscosity bulk-fill resin composites showed the significantly lowest polymerization shrinkage and force development. Within the tested flowable composite materials, SDR bulk-fill generated the significantly lowest shrinkage forces during polymerization and attained the significantly highest degree of conversion. Strong positive correlations were revealed between shrinkage force and both linear polymerization shrinkage (r = 0.902) and maximum force rate (r = 0.701). Linear shrinkage and shrinkage force both showed a negative correlation with filler volume content (r = − 0.832 and r = − 0.704, respectively). Bulk-fill resin composites develop lower shrinkage forces than their conventional flowable and high-viscosity counterparts, respectively, which supports their use for restoring high C-factor posterior cavities. Overall, bulk-fill composites with high filler amount and low force rate showed the most favorable shrinkage force characteristics. [ABSTRACT FROM AUTHOR]

Objective. To investigate the subsurface degree of conversion (DC) and shrinkage force formation of low-viscosity (flowable) bulk-fill composite materials. Materials and methods. Three flowable bulk-fill resin composites [SureFil SDR flow (SDR; Dentsply DeTrey), Venus Bulk Fill (VB; Heraeus Kulzer) and x-tra base (XB; VOCO)] and one conventional flowable control composite material [EsthetX flow (EX; Dentsply DeTrey)] were tested. The materials were photoactivated for 20 s at an irradiance of 1170 mW/cm2 and the DC ( n = 5) was recorded at 0.1-, 1.5- and 4-mm depth using Fourier transform infrared spectroscopy. Shrinkage forces ( n = 5) of 1.5-mm-thick specimens were continuously recorded for 15 min using a custom-made stress analyzer. Data were statistically analyzed by ANOVA, Tukey's HSD and Bonferroni's post-hoc tests ( α = 0.05). Results. SDR generated the significantly lowest shrinkage forces (22.9 ± 1.4 N), but also attained the significantly lowest DC at 1.5-mm depth (67.5 ± 0.8%). The conventional flowable composite EX generated the significantly highest shrinkage forces (40.7 ± 0.7 N) and reached a significantly higher DC (74.4 ± 1.3%) compared to SDR and XB at 1.5-mm depth. The shrinkage force values of VB (29.4 ± 1.1 N) and XB (28.3 ± 0.6 N) were similar ( p > 0.05). All materials attained significantly higher DC at 4-mm depth than at the near-surface. Conclusion. The tested low-viscosity bulk-fill materials show lower shrinkage force formation than a conventional flowable resin composite at high levels of degree of conversion up to 4-mm incremental thickness. [ABSTRACT FROM AUTHOR]

Tauböck TT, Bortolotto T, Buchalla W, Attin T, Krejci I. Influence of light-curing protocols on polymerization shrinkage and shrinkage force of a dual-cured core build-up resin composite. Eur J Oral Sci 2010; 118: 423–429. © 2010 The Authors. Journal compilation © 2010 Eur J Oral Sci This study investigated the influence of time delay and duration of photo-activation on linear polymerization shrinkage, shrinkage force, and hardening of a dual-cured core build-up resin composite. The test material (Rebilda DC) was light-cured for 20 or 60 s either early (2 min) or late (7 min) after the start of mixing. Non-irradiated self-cured specimens served as controls. Linear shrinkage and shrinkage force were measured for 60 min using custom-made devices. Knoop hardness was determined at the end of the observation period. Self-cured controls, showing a linear shrinkage similar to that of specimens early light-cured for 20 s generated the lowest shrinkage force and hardness. A shorter light exposure time (20 s vs. 60 s) reduced linear shrinkage, shrinkage force, and hardness when early light-curing was performed, but did not affect the three properties in specimens light-cured late after the start of mixing. Late photo-activation increased linear shrinkage, irrespective of irradiation time, and resulted in a higher shrinkage force and hardness for short light exposure time. A moderate correlation was found between the two shrinkage properties studied ( r2 = 0.65). In conclusion, improvements in shrinkage behavior of the tested core build-up material were associated with inferior hardening, making it important to adapt curing protocols to the clinical situation. [ABSTRACT FROM AUTHOR]

Previous work has shown that partial replacement of reinforcing fillers with unsilanized silica particles can diminish polymerization shrinkage stress of dental resin composites. The aim of the present study was to investigate whether such an effect can be attained by using unsilanized bioactive glass (BG). Incorporating BG fillers into resin composites is interesting due to their potential for exerting caries-preventive effects. Experimental light-curable composites with a total filler load of 77 wt% were prepared. Reinforcing fillers were partially replaced with 0–60 wt% of BG 45S5 and an experimental low-sodium fluoride-containing BG. The following properties were investigated: linear shrinkage, degree of conversion, shrinkage stress, maximum shrinkage stress rate, and time to achieve maximum shrinkage stress rate. The diminishing effect of BG 45S5 on shrinkage stress was mediated by a decrease in degree of conversion caused by this BG type. In contrast, as the degree of conversion remained unaffected by the experimental BG, the resulting shrinkage behaviour was governed by the effect of varying amounts of silanized and unsilanized fillers on material's viscoelastic properties. The replacement of silanized reinforcing fillers with unsilanized BG did not reduce polymerization shrinkage stress unless the reduction was attained indirectly through a diminished degree of conversion. [ABSTRACT FROM AUTHOR]

This study investigated the effect of bioactive micro-fillers on the light transmittance and polymerization of three commercially available bulk-fill resin composites. These were mixed with 20 wt% bioactive glass 45S5, Portland cement, inert dental barium glass, or nothing (controls). Composites were photo-activated and light transmittance through 4 mm thick specimens was measured in real time. Moreover, degree of conversion (DC) and Knoop hardness (KHN) were assessed. Light transmittance of all bulk-fill composites significantly decreased (p < 0.05) with addition of 20 wt% bioactive glass 45S5 but not when inert barium glass was added. For bulk-fill composites modified with Portland cement, light irradiance dropped below the detection limit at 4 mm depth. The DC at the top surface of the specimens was not affected by addition of bioactive or inert micro-fillers. The bottom-to-top ratio of both DC and KHN surpassed 80% for bulk-fill composites modified with 20 wt% bioactive or inert glass fillers but fell below 20% when the composites were modified with Portland cement. In contrast to Portland cement, the addition of 20 wt% bioactive glass maintains adequate polymerization of bulk-fill composites placed at 4 mm thickness, despite a decrease in light transmittance compared to the unmodified materials. [ABSTRACT FROM AUTHOR]

To investigate the effect of methacrylate polyhedral oligomeric silsesquioxane (POSS-8) particles on the polymerization process, dentin bond strength, and mineral precipitation of universal dental adhesives. Five universal adhesives (Adhese Universal, CLEARFIL Universal Bond, Futurabond U, iBOND Universal, Scotchbond Universal) were filled with POSS-8 particles (10 wt%, additionally 2 wt% and 5 wt% in Scotchbond Universal). The particle size and dispersion in ethanol and acetone were examined by dynamic light scattering. Degree of conversion, linear shrinkage, and shear bond strength to dentin treated with the filled and pure adhesives (controls) were measured. Growth of calcium phosphate (Ca/P) precipitates on the adhesive specimens immersed in artificial saliva for up to 28 days was analyzed by energy-dispersive X-ray spectroscopy and scanning electron microscopy. Statistical analyses were performed using ANOVA and Tukey's post-hoc tests (p < 0.05). The hydrodynamic radius of the particles in acetone (1.4 ± 0.4 nm) and ethanol (1.1 ± 0.4 nm) revealed their good dispersion. POSS-8 did not change the degree of conversion and dentin bond strength of any adhesive. Ca/P precipitates formed on iBOND Universal specimens doped with POSS-8 after 4 weeks of immersion, but were not detected on the unfilled adhesive. The mineral precipitation of all other adhesives was not improved by POSS-8. POSS-8 particles did not compromise polymerization and bonding of universal adhesives. Ca/P precipitation was stimulated by POSS-8 only in iBOND Universal. [ABSTRACT FROM AUTHOR]