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.

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

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.

Este trabalho avaliou o impacto de tempos aumentados de condicionamento ácido e da estratégia adesiva na resistência de união por microcisalhamento de três materiais utilizados como selantes de fóssulas e fissuras. Dois tradicionais selantes, [FluroShield, Dentsply (fotoativado) e AlphaSeal, DFL (quimicamente ativado)] e uma resina composta de baixa viscosidade (Permaflo, Ultradent) foram utilizados de acordo com diferentes tempos de condicionamento ácido (15 s e 30 s) e diferentes estratégias de união (sem aplicação de sistema adesivo, aplicação de um primer + resina hidrófoba, e aplicação apenas de uma resina hidrófoba). Fragmentos de esmalte intacto foram obtidos de incisivos bovinos e os materiais foram aplicados respeitando-se os protocolos anteriormente descritos. Após 24 h, o teste de microcisalhamento foi executado utilizando-se uma máquina de ensaio universal, com velocidade de 0,5 mm/min. O padrão de fratura foi classificado com auxílio de lupa estereoscópica. Os dados foram submetidos aos testes ANOVA a três critérios e de Tukey (α=0.05). Não houve diferenças estatisticamente significantes entre os materiais. Permaflo apresentou maior resistência de união quando o esmalte foi condicionado por 30 s apenas. O sobrecondicionamento do esmalte diminuiu a resistência de união do selante fotopolimerizável. O tratamento prévio do esmalte com primer + resina hidrófoba melhorou a performance adesiva para o AlphaSeal. Todos os materiais apresentaram valores de resistência de união estatisticamente similares em relação ao protocolo adesivo e ao tempo de condicionamento ácido. A resina composta de baixa viscosidade poderá ser utilizada como selante de fóssulas e fissuras. A aplicação de um sistema adesivo de três passos é essencial durante o selamento com selante quimicamente ativado.

This study evaluated the impact of extended etching and bonding strategies on the microshear bond strength of three sealant materials. Two pit-and-fissure sealants [FluroShield, Dentsply (light-cured) and AlphaSeal, DFL (self-cured)] and one light-cured flowable composite resin (Permaflo, Ultradent) were evaluated according to different enamel etching times (15 s or 30 s) and bonding procedures (no adhesive application, application of primer/hydrophobic resin or hydrophobic resin only). Intact enamel blocks were obtained from bovine teeth and sealed via the tested protocols. After 24 h, the microshear bond strength test was performed in a universal testing machine at a crosshead speed of 0.5 mm/min. Failure modes were classified by stereomicroscopy. Data were submitted to a three-way ANOVA and to Tukey's test (α=0.05). There was no statistically significant difference (p>0.05) among the materials. Permaflo showed higher bond strength when etched for 30 s alone. Enamel overetching decreased the bond strength of the light-cured sealant. Primer/bond previous treatment improved bond performance for AlphaSeal. In conclusion, from the tested conditions, all sealant materials presented similar bond strength values in relation to bonding protocol and etching time. The flowable composite can be used as a pit-and-fissure sealant. The use of a three-step adhesive system was essential for the self-cured sealant application.

The aim of this study was to evaluate the effect of different curing methods on the stress generated by the polymerization shrinkage of a restorative composite in two moments: immediately after light exposure and after 5 min. Photoactivation was performed using two different light sources: (1) xenon plasma arc (PAC) light (1,500 mW/cm2 - 3s) and (2) a quartz-tungsten-halogen (QTH) light with three light-curing regimens: continuous exposure (40 s at 800 mW/cm2 - CL); soft-start (10 s at 150 mW/cm2 and 30 s at 800 mW/cm2 - SS) and intermittent light [cycles of 4 s (2 s with light on at 600 mW/cm2 and 2 s of light off), for 80s - IL]. The composite resin was applied between two 5-mm diameter metallic rods, mounted in a servohydraulic machine. The maximum stress was recorded immediately after light exposure (FF) and after 5 min (5F). The results were submitted to ANOVA and Tukey's test (5%). For each method, the results obtained in FF and 5F were, respectively: CL (3.58 and 4.46 MPa); SS (2.99 and 4.36 MPa); IL (3.11 and 4.32 MPa) and PAC (0.72 and 3.27 MPa). The stress generated by the polymerization shrinkage during light exposure can be associated with the photoactivation method used. A significant increase in the stress level was observed during the post-curing period up to 5 min, for all evaluated methods.