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Abstract This study investigated the effect of butylated hydroxytoluene (BHT) inhibitor on degree of conversion (DC), flexural strength (FS), flexural modulus (FM), Knoop microhardness (KH), microhardness reduction (HR), and consistency of experimental resin composites at different BHT concentrations: C0 (control-0%); C0.01 (0.01%); C0.025 (0.025%); C0.05 (0.05%); C0.1 (0.1%); and C0.5 (0.5%). For the consistency, the composites were tested immediately after being exposed to a dental chair headlight (0, 20, 40 and 60 s). Data concerning DC, FS, FM, KH, and HR were submitted to one-way ANOVA, while the consistency data was submitted to 2-way ANOVA; mean values were then compared (Tukey's test; α=0.05). The KH, FS and FM analyses showed no significant difference among the composites tested. For DC, C0 showed the highest mean value (74.2%) and differed only from C0.5 (67.2%). For HR, C0.5 showed the lowest mean (13.09%) value and differed from C0 (26.4%) and C0.01 (24.87). The consistency analysis showed no difference among C0.05, C0.1 and C0.5, considering 0 and 20 s of light exposure, while C0 (14.07 mm), C0.01 (13.97 mm), and C0.025 (14.18 mm) showed higher mean values at 0 s when compared to 20 s (12.67, 12.77 and 13.05 mm, respectivelly). Polymerization occurred within 40 s of light exposure for C0, C0.01, C0.025, and C0.05 and within 60 s for C0.1. In conclusion, the BHT concentrations had no significant influence on FS, FM and KH. The higher the BHT concentration, the longer was its handling time under light, with a significant improvement in the HR, but a decrease in DC. Therefore, BHT at 0.1% showed the best outcomes concerning all the BHT concentrations tested.

Resumo O objetivo foi investigar o efeito do inibidor de polimerização BHT no grau de conversão (GC), resistência à flexão (RF), módulo de flexão (MF), microdureza Knoop (KH) e redução da microdureza (RKH), e consistência de um compósito experimental contendo diferentes concentrações de BHT (% em peso): C0 - controle (0%); C0,01 (0,01%); C0,025 (0,025%); C0,05 (0,05%); C0,1 (0,1%); e C0,5 (0,5%). Para o teste de consistência, os compósitos foram testados imediatamente após serem expostos à luz de um refletor odontológico por 0, 20, 40 e 60 s. Os dados relativos a GC, RF, MF, KH e RKH foram submetidos a one-way ANOVA, enquanto os dados de consistência foram submetidos a two-way ANOVA; os valores médios foram comparados (teste de Tukey; α = 0,05). As análises de KH, RF e MF não mostraram diferença significativa entre os compósitos testados. Para GC, C0 apresentou o maior valor médio e diferiu apenas de C0,5. Para a RKH, C0,5 apresentou o menor valor médio e diferiu de C0 e C0,01. A análise de consistência não mostrou diferença entre C0,05, C0,1 e C0,5, considerando-se 0 e 20 s de exposição à luz, enquanto C0, C0,01 e C0,025 apresentaram maiores valores médios a 0 s quando comparados a 20 s. A polimerização ocorreu dentro de 40 s de exposição à luz para C0, C0.01, C0.025 e C0.05 e dentro de 60 s para C0.1. Em conclusão, as concentrações de BHT não tiveram influência significativa sobre RF, MF e KH. Quanto maior a concentração de BHT, maior o tempo de manuseio sob luz, com melhora significativa da RKH, mas diminuição da GC. Portanto, o compósito contendo 0,1 % de BHT apresentou os melhores resultados entre as demais concentrações testadas.

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This study investigated the effect of butylated hydroxytoluene (BHT) inhibitor on degree of conversion (DC), flexural strength (FS), flexural modulus (FM), Knoop microhardness (KH), microhardness reduction (HR), and consistency of experimental resin composites at different BHT concentrations: C0 (control-0%); C0.01 (0.01%); C0.025 (0.025%); C0.05 (0.05%); C0.1 (0.1%); and C0.5 (0.5%). For the consistency, the composites were tested immediately after being exposed to a dental chair headlight (0, 20, 40 and 60 s). Data concerning DC, FS, FM, KH, and HR were submitted to one-way ANOVA, while the consistency data was submitted to 2-way ANOVA; mean values were then compared (Tukey's test; α=0.05). The KH, FS and FM analyses showed no significant difference among the composites tested. For DC, C0 showed the highest mean value (74.2%) and differed only from C0.5 (67.2%). For HR, C0.5 showed the lowest mean (13.09%) value and differed from C0 (26.4%) and C0.01 (24.87). The consistency analysis showed no difference among C0.05, C0.1 and C0.5, considering 0 and 20 s of light exposure, while C0 (14.07 mm), C0.01 (13.97 mm), and C0.025 (14.18 mm) showed higher mean values at 0 s when compared to 20 s (12.67, 12.77 and 13.05 mm, respectivelly). Polymerization occurred within 40 s of light exposure for C0, C0.01, C0.025, and C0.05 and within 60 s for C0.1. In conclusion, the BHT concentrations had no significant influence on FS, FM and KH. The higher the BHT concentration, the longer was its handling time under light, with a significant improvement in the HR, but a decrease in DC. Therefore, BHT at 0.1% showed the best outcomes concerning all the BHT concentrations tested.

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Aim: this study aimed to evaluate the degree of conversion (DC) exhibited by novel formulations of dental adhesive systems including camphorquinone (CQ), phenyl-propanedione (PPD), and bis-alkyl phosphine oxide (BAPO) when cured by mono- or polywave light emitting diodes (LEDs). Methods: an adhesive model was formulated by mixing hydroxyethyl methacrylate (HEMA, 40 wt%) and bisphenol A glycidyl dimethacrylate (BisGMA, 60 wt%) in ethanol (30 wt%). Five materials were then formulated by adding the following photoinitiators: CQ (1 mol%), CQ/PPD (0.5/0.5 mol%), CQ/BAPO (0.5/0.5 mol%), PPD (1 mol%), and BAPO (1 mol%). The DC for each material was measured with Fourier transform infrared spectroscopy. Analysis of variance and Tukey's post-hoc test were used to analyze the data (p < 0.05). Results: Except for CQ, the photoinitiators provided a significantly higher DC in the adhesive systems following photoactivation with a polywave LED. Conclusion: The use of alternative photoinitiators and a polywave LED improved the DC of the adhesive systems examined

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The aim in this study was to evaluate the influence of different ratio of camphorquinone/tertiary amine concentration on the flexural strength (FS), elastic modulus (EM), degree of conversion (DC), yellowing (YL), water sorption (WS) and water solubility (WSL) of experimental composites. Thus, acrylate blends were prepared with different camphorquinone (CQ) and amine (DABE) concentrations and ratios by weight: (CQ/DABE%): 0.4/0.4% (C1), 0.4/0.8% (C2), 0.6/0.6% (C3), 0.6/1.2% (C4), 0.8/0.8% (C5), 0.8/1.6% (C6), 1.0/1.0% (C7), 1.0/2.0% (C8), 1.5/1.5% (C9), 1.5/3.0% (C10). For the FS and EM, rectangular specimens (7x2x1 mm, n=10) were photo-activated by single-peak LED for 20 s and tested at Instron (0.5 mm/min). Then, the same specimens were evaluated by FTIR for DC measurement. For YL, disks (5x2 mm, n=10) were prepared, light-cured for 20 s and evaluated in spectrophotometer using the b aspect of the CIEL*a*b* system. For WS and WSL, the volume of the samples was calculated (mm³). For WS and WSL, composites disks (5x0.5 mm, n=5) were prepared. After desiccation, the specimens were stored in distilled water for 7 days and again desiccated, in order to measure the WS and WSL. Data were submitted to one-way ANOVA and Tukey's test (5%). The groups C8, C9 and C10 showed higher DC, EM and YL means, compared to other composites. Therefore, the FS and WS values were similar among all groups. Also, C1, C2 and C3 presented higher WSL in 7 days, compared to other composites. In general, higher concentrations of camphorquinone promoted higher physical-mechanical properties; however, inducing higher yellowing effect for the experimental composites.

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Abstract The aim in this study was to evaluate the influence of different ratio of camphorquinone/tertiary amine concentration on the flexural strength (FS), elastic modulus (EM), degree of conversion (DC), yellowing (YL), water sorption (WS) and water solubility (WSL) of experimental composites. Thus, acrylate blends were prepared with different camphorquinone (CQ) and amine (DABE) concentrations and ratios by weight: (CQ/DABE%): 0.4/0.4% (C1), 0.4/0.8% (C2), 0.6/0.6% (C3), 0.6/1.2% (C4), 0.8/0.8% (C5), 0.8/1.6% (C6), 1.0/1.0% (C7), 1.0/2.0% (C8), 1.5/1.5% (C9), 1.5/3.0% (C10). For the FS and EM, rectangular specimens (7x2x1 mm, n=10) were photo-activated by single-peak LED for 20 s and tested at Instron (0.5 mm/min). Then, the same specimens were evaluated by FTIR for DC measurement. For YL, disks (5x2 mm, n=10) were prepared, light-cured for 20 s and evaluated in spectrophotometer using the b aspect of the CIEL*a*b* system. For WS and WSL, the volume of the samples was calculated (mm³). For WS and WSL, composites disks (5x0.5 mm, n=5) were prepared. After desiccation, the specimens were stored in distilled water for 7 days and again desiccated, in order to measure the WS and WSL. Data were submitted to one-way ANOVA and Tukey's test (5%). The groups C8, C9 and C10 showed higher DC, EM and YL means, compared to other composites. Therefore, the FS and WS values were similar among all groups. Also, C1, C2 and C3 presented higher WSL in 7 days, compared to other composites. In general, higher concentrations of camphorquinone promoted higher physical-mechanical properties; however, inducing higher yellowing effect for the experimental composites

Resumo O objetivo foi avaliar a influência da concentração e proporção de canforoquinona (CQ)/amina terciária (DABE) na resistência à flexão (RF), módulo flexural (MF), grau de conversão (GC), amarelamento (AM), sorpção (SA) e solubilidade em água (SL) de compósitos experimentais. Blendas acrilatas foram preparadas com diferentes concentrações e proporções de CQ/DABE em peso, como segue: (CQ/DABE%): 0,4/0,4% (C1); 0,4/0,8% (C2); 0,6/0,6% (C3); 0,6/1,2% (C4); 0,8/0,8% (C5); 0,8/1,6% (C6); 1,0/1,0% (C7); 1,0/2,0% (C8); 1,5/1,5% (C9); 1,5/3,0% (C10). Para RF e MF, espécimes retangulares (7x2x1 mm, n=10) foram fotoativados com LED de pico único (Radii Cal) por 20 s e testados em máquina Instron (0,5 mm/min). Após, o GC dos mesmos espécimes (fragmentos) foi mensurado por FTIR. Para AM, discos de compósito (5x2 mm, n=10) foram preparados, fotoativados por 20 s e imediatamente avaliados em espectrofotômetro, considerando o aspecto b do sistema CIEL*a*b*. Para SA e SL, discos de compósito (5x0,5 mm, n=5) foram preparados e seus volumes calculados (mm³). Após desidratação, as amostras foram pesadas e armazenadas em água destilada por 7 dias, pesadas e novamente desidratadas e pesadas, para se calcular o SA e SL. Os dados foram submetidos a one-way ANOVA e teste de Tukey (5%). Os grupos C8, C9 e C10 mostraram maior GC, MF e AM, comparado aos outros grupos. No entanto, RF e SA foram similares entre todos os grupos. Ainda, C1, C2 e C3 apresentaram maior SL em 7 dias comparado aos outros grupos. Em geral, maiores concentrações de CQ promoveram melhores propriedades físico-mecânicas; no entanto, levaram ao maior amarelamento dos compósitos.

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Atualmente, a estética dental tornou-se de grande importância na aparência pessoal, exigindo avanços tecnológicos na área odontológica e, consequentemente, materiais com características ópticas semelhantes aos dentes naturais e que preservam os remanescentes. Os sistemas adesivos tornaram possível a reparação de dentes com alterações na cor, forma ou posições que prejudicavam o equilíbrio estético e funcional. O objetivo deste estudo foi verificar a distribuição de tensões em facetas de cerâmica feldspática e dissilicato de lítio minimamente invasivas, pelo método de elemento finito. foi construído um modelo representativo de um incisivo central superior, com dimensões médias encontradas na literatura. Sobre esse dente, foi simulado um preparo conservador para laminado cerâmico. Sobre o preparo, foi simulado um laminado cerâmico de 0,5mm de espessura, o qual foi discretizado em cerâmica feldspática ou dissilicato de lítio por meio do módulo de elasticidade característico de cada material. Os modelos foram submetidos a cargas de 50 N, sob angulação de 30º em relação ao longo eixo do dente. Os resultados foram apresentados em gráficos de tensão com seus respectivos valores numéricos representados em escala de cores. Por meio da análise de elemento finito foi possível observar que o fragmento cerâmico de dissilicato de lítio apresentou valores numéricos de tensão semelhantes aos de cerâmica feldspática para todos os critérios avaliados, tensão de tração, compressão e cisalhamento. Conclui-se que as cerâmicas de dissilicato de lítio e feldspática foram caracterizadas por um comportamento mecânico semelhante em relação à distribuição das tensões.

Dental aesthetic has currently become of great importance in the appearance, requiring technological advances in the dental area and consequently, materials with optical characteristics similar to the natural teeth and that preserve the remnants. Adhesive systems made possible to repair teeth with changes in color, shape or positions that undermined the aesthetic and functional balance. The aim of this study was to verify the stress distribution in feldspathic ceramics and lithium disilicate minimally invasive through the finite element method. A representative model of a central upper incisor was constructed, with average dimensions found in the literature. On this tooth, a conservative preparation for ceramic laminate was simulated. On the preparations, a 0.5 mm thick ceramic laminate was simulated, which was discretized in feldspathic ceramics or lithium disilicate by means of the elasticity modulus characteristic of each material. The models were submitted to loads of 50 N under an angle of 30º in relation to the tooth long axis. The results were presented in tensile graphs with their respective numerical values represented in color scale. Through the finite element analysis, it was possible to observe that the lithium disilicate ceramic fragment presented tensile numerical values similar to those of feldspathic ceramics for all criteria evaluated, tensile stress, compression and shear. It is concluded that the lithium feldspathic and disilicate ceramics were characterized by a similar mechanical behavior in relation to the stress distribution.

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ABSTRACT Objective To evaluate the influence of phenyl-propanedione on yellowing and chemical-mechanical properties of experimental resin-based materials photoactivated using different light curing units (LCUs). Material and Methods Experimental resin-based materials with the same organic matrix (60:40 wt% BisGMA:TEGDMA) were mechanically blended using a centrifugal mixing device. To this blend, different photoinitiator systems were added in equimolar concentrations with aliphatic amine doubled by wt%: 0.4 wt% CQ; 0.38 wt% PPD; or 0.2 wt% CQ and 0.19 wt% PPD. The degree of conversion (DC), flexural strength (FS), Young’s modulus (YM), Knoop hardness (KNH), crosslinking density (CLD), and yellowing (Y) were evaluated (n=10). All samples were light cured with the following LCUs: a halogen lamp (XL 2500), a monowave LED (Radii), or a polywave LED (Valo) with 16 J/cm2. The results were analysed by two-way ANOVA and Tukey’s test (α=0.05). Results No statistical differences were found between the different photoinitiator systems to KNH, CLS, FS, and YM properties (p≥0.05). PPD/CQ association showed the higher DC values compared with CQ and PPD isolated systems when photoactivated by a polywave LED (p≤0.05). Y values were highest for the CQ compared with the PPD systems (p≤0.05). Conclusion PPD isolated system promoted similar chemical and mechanical properties and less yellowing compared with the CQ isolated system, regardless of the LCU used.

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OBJECTIVE: To evaluate the influence of phenyl-propanedione on yellowing and chemical-mechanical properties of experimental resin-based materials photoactivated using different light curing units (LCUs). MATERIAL AND METHODS: Experimental resin-based materials with the same organic matrix (60:40 wt% BisGMA:TEGDMA) were mechanically blended using a centrifugal mixing device. To this blend, different photoinitiator systems were added in equimolar concentrations with aliphatic amine doubled by wt%: 0.4 wt% CQ; 0.38 wt% PPD; or 0.2 wt% CQ and 0.19 wt% PPD. The degree of conversion (DC), flexural strength (FS), Young's modulus (YM), Knoop hardness (KNH), crosslinking density (CLD), and yellowing (Y) were evaluated (n=10). All samples were light cured with the following LCUs: a halogen lamp (XL 2500), a monowave LED (Radii), or a polywave LED (Valo) with 16 J/cm2. The results were analysed by two-way ANOVA and Tukey's test (α=0.05). RESULTS: No statistical differences were found between the different photoinitiator systems to KNH, CLS, FS, and YM properties (p≥0.05). PPD/CQ association showed the higher DC values compared with CQ and PPD isolated systems when photoactivated by a polywave LED (p≤0.05). Y values were highest for the CQ compared with the PPD systems (p≤0.05). CONCLUSION: PPD isolated system promoted similar chemical and mechanical properties and less yellowing compared with the CQ isolated system, regardless of the LCU used.

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Objective: To evaluate the effect of shade and curing mode on cure efficiency of two dual-cure resin cements. Material and Methods: Two shades (A2 and TRANS) of two different dual-cure resin cements (G-CEM, GC Dental and SET PP, SDI) were submitted to different curing modes: light curing through a 2 mm thick ceramic disc (IPS Empress Esthetic, A2, Ivoclar Vivadent) for 20 s (16 J/cm2), 40 s (32 J/ cm2) or 80 s (64 J/cm2) performed immediately or with 1 or 5 min of delay. Fourier transform infrared spectroscopy (FT-IR) was used to evaluate the degree of conversion (DC) after 48 h. For the statistical analysis, data were submitted to threeway analysis of variance, followed by Tukey’s test for multiple comparisons (p<0.05). Results: Shade influenced DC (%) for the dual-cure resin cements tested (p=0.00001). TRANS shade showed lower DC (%) for both cements when there was no delay before light-curing (p=0.00001). Curing mode also influenced DC (%) for the dual-cure resin cements tested: radiant exposure greater than 32 J/cm2 and delaying light-curing for 1 to 5 min increased the DC (%) for both dual-cure resin cements evaluated. Conclusions: One minute delay prior to light-curing improved the cure efficiency and may be a more clinically acceptable approach to increase the degree of conversion of dual-cure resin cements.

Objetivo: Avaliar a influência da cor e do modo de polimerização no grau de conversão de dois cimentos resinosos duais. Material e Métodos: Duas cores (A2 e TRANS) de dois cimentos resinosos duais (G-CEM, GC Dental e SET PP, SDI) foram submetidos a diferentes modos de cura: fotoativação através de um disco de cerâmica de 2 mm de espessura (IPS Empress Esthetic, A2, Ivoclar Vivadent) por 20 s (16 J/cm2), 40 s (32 J/cm2) ou 80 s (64 J/cm2) realizada imediatamente ou após 1 ou 5 min de espera. Espectrometria com transformada de Fourier (FT-IR) foi utilizada para avaliação do grau de conversão (GC) após 48 h. Para a análise estatística, os dados foram submetidos à análise de variância com três fatores, seguida de teste de Tukey para comparações múltiplas (p=0.05). Resultados: A cor influenciou o GC (%) dos cimentos resinosos duais avaliados (p=0.00001). A cor TRANS resultou menor GC (%) para ambos os cimentos quando não houve espera antes da fotoativação (p=0.00001). O modo de cura também teve influência n o GC (%) dos cimentos resinosos duais avaliados: doses de energia superiores a 32 J/cm2 e espera de 1 ou 5 min antes da fotoativação aumentou o GC (%) dos dois cimentos resinosos duais avaliados. Conclusão: Um min de espera antes da fotoativação melhorou a eficiência de cura e pode ser uma abordagem clinicamente aceitável para aumentar o grau de conversão de cimentos resinosos duais.

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UNLABELLED: The aim of this study was to evaluate the effect of low shrinkage monomers on physicochemical properties of dental resin composites. Two low shrinkage resin composites: one with a crosslink branching monomer (Kalore, GC Corp) and a novel monomer (Venus Diamond, Heraeus Kulzer) were compared to a conventional resin composite formulation (Filtek Z250, 3M/ESPE). The volumetric shrinkage was evaluated by µCT analysis (n=5) and the physicochemical properties by degree of C=C conversion (DC), flexural strength (FS) and Young's modulus (YM) (n=10). All samples were light cured by a LED device (Radii, SDI) with 16 J/cm2. The results were analysed by one-way ANOVA and Tukey test for multiple comparisons (α=0.05). No statistical difference was found between µCT shrinkage values to Kalore (1.8%) and Venus Diamond (1.7%) (p≥0.05); Z250 presented statistical highest shrinkage value (2.0%). Kalore presented higher statistical DC (60.8%) than Venus Diamond (49.5%) and Z250 (49.6%). No statistical difference was found between FS or YM properties to Venus Diamond and Z250; Kalore presented statistical lowest FS and YM properties (p≥0.05). CONCLUSION: Using novel monomers seem to reduce polymerization shrinkage without affecting the physicochemical properties evaluated of resin composites rather than using crosslink branching monomers.

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