The in vitro effect of solutions with or without sugar in dental bleaching.

The interaction of bleaching technique (in-office or at-home) and solutions (deionized distilled water with and without sugar, red wine with and without sugar, coffee with and without sugar) on the effectiveness of in vitro dental bleaching was evaluated. Hydrogen peroxide (HP) 37.5% gel was used for in-office bleaching, 3 applications of 8 min each, 3 sessions with an interval of 7 days. At-home bleaching was performed with 10% Carbamide peroxide (CP), 2 h/day, for 30 days. The enamel vestibular surfaces (n = 72) were subjected daily to test solutions for 45 min, washed with distilled water for 5 min and stored in artificial saliva. The enamel color analysis was performed with a spectrophotometer through color variation (ΔE) and luminosity variation (ΔL). Roughness analysis was performed by atomic force microscopy (AFM) and scanning electron microscopy (SEM). Enamel composition was determined by energy dispersive X-ray spectrometry (EDS). The results were submitted to one-way analysis of variance (ANOVA) for ΔE, ΔL and EDS and two-way for AFM. For ΔE and ΔL there was no statistically significant difference. An increase in roughness was observed on the surface when exposed to a sugar-water solution for at-home bleaching and a lower concentration of Ca and P in the deionized water solution with sugar. Solutions containing or not sugar did not influence the bleaching potential, however the presence of sugar in the water solution increased the surface roughness with CP.

Mechanical properties of bulk-fill composite resin with or without a final layer of conventional composite resin.

The objective of this in vitro study was to evaluate the mechanical properties of different bulk-fill composite resins with or without a final layer of conventional composite resin. The null hypothesis was that the mechanical properties of the material would not change regardless of the addition of a layer of conventional composite. Bar-shaped specimens (25 × 2 × 2 mm) were made from 4 different bulk-fill composites (Filtek One Bulk Fill, Filtek Bulk Fill Flowable, Tetric EvoCeram Bulk Fill, and Tetric EvoCeram Bulk Fill Flow) with or without a final layer of a conventional composite of the same brand (Filtek Supreme for the Filtek materials and Tetric EvoCeram for the Tetric materials). Each specimen was light cured at 2 equidistant points using a multiwave curing light with a power output of 20 J/cm2. All of the specimens were subjected to a 3-point bending test in a universal testing machine at a crosshead speed of 0.75 ± 0.25 mm/min and a load rate of 50 ± 16 N/min, and the flexural strength and elastic modulus were calculated. The mean flexural strength and elastic modulus values were analyzed using 1-way analysis of variance, and then the Tukey test was applied for multiple comparisons between groups (α = 0.05). When a final layer of a conventional composite of the same brand was added, the mean flexural strength of the Tetric groups slightly decreased, while that of the Filtek groups did not change. Application of a final layer of conventional composite resulted in a slight increase in the mean elastic modulus of the Filtek groups and either no change or a slight decrease in the Tetric groups. The addition of a final layer of conventional composite resin did not seem to improve the mechanical properties of any of the tested bulk-fill materials. The addition of a final layer of conventional composite resin can affect the mechanical properties of bulk-fill materials; however, it seems these effects are dependent on the type of conventional composite resin used for the final layer.

In vitro characterization of a biocompatible composite based on poly(3-hydroxybutyrate)/hydroxyapatite nanoparticles as a potential scaffold for tissue engineering.

The use of regeneration scaffolds has been a promising strategy in the bone tissue engineering area. Among the materials available for this purpose the poly(3-hydroxybutyrate) - PHB stands out for its adequate biocompatibility and osteoinduction capacity. Hydroxyapatite, in turn, has as its main characteristics its ability to increase bioactivity and cell proliferation. Thus, the objective of the present study was to obtain PHB composites with nanohydroxyapatite (Hap) (0.05%, 0.20%, and 0.50%) and evaluate the microstructure, thermal and mechanical properties and molecular dynamics. Besides that, in vitro biological properties such as wettability, cell viability and adhesion of L929 fibroblasts cells, enzymatic degradation and radiographic contrast were evaluated. The results indicate a weak interaction between Hap and PHB, however, the dispersion states of the nanoparticles can influence crystallization and thermal stability. Through the evaluation of the mechanical behavior was verified a harder behavior with the Hap addition. The wettability of the systems showed a tendency to increase with the addition of nanoparticles. All systems presented high values of viability and cell adhesion, the latter being more pronounced for systems containing Hap. The nanoparticles acted as a barrier slowing the rate of enzymatic degradation and contributed to the increase in radiographic contrast. The results obtained indicate that the systems are promising for application in tissue engineering.

The use of an elastomeric methacrylate monomer (Exothane 24) to reduce the polymerization shrinkage stress and improve the two-body wear resistance of bulk fill composites.

OBJECTIVES: Characterize the chemical structure of an elastomeric monomer (Exothane 24) and evaluate the degree of conversion (DC), polymerization shrinkage stress (PSS), rate of polymerization (Rp), flexural strength (FStrenght), flexural modulus (FModulus), Vickers hardness (VHardness) and two-body wear resistance of dental bulk fill composites (BFCs) containing Exothane 24. METHODS: The Exothane 24 was characterized using mass spectroscopy, elemental analysis, 13C- and 1H NMR. BFCs were formulated containing Exothane 24 (E10, E25, and E50). Similar BFCs containing regular UDMA (U10, U25, and U50), commercial conventional, and BFCs were used as control groups. ATR-FTIR spectroscopy was used to measure DC and the Rp of the composites. The PSS was measured using the universal testing machine method. Specimen bars were used to assess the FStrenght, FModulus, and VHardness. RBCs were submitted to a two-body wear test using a chewing simulator machine; the rate and volumetric wear loss were evaluated using an optical scanner. Data were analyzed statistically with α = 0.05 and ß = 0.2. RESULTS: Exothane 24 is a urethane isophorone tetramethyl methacrylate monomer with polymerization stress-relieving properties. No differences were found in the DC up to 4 mm in depth for E25. All BFCs had similar FStrenght, except for E50. E25 had the lowest volumetric wear loss and wear rate. E25 had approximately 30% lower PSS and slower Rp than commercial BFCs with similar wear resistance to conventional commercial composites. SIGNIFICANCE: The Exothane 24 reduced the PSS and increased the wear resistance of BFCs; however, the formulation is important to optimize the properties of the BFCs.

Core-shell nanoparticles based on zirconia covered with silver as an advantageous perspective for obtaining antimicrobial nanocomposites with good mechanical properties and less cytotoxicity.

Antimicrobial nanoparticles perform a vast and promising strand of applications, among which, the silver ones stand out due to their broad antimicrobial spectrum. However, their toxicological potential in addition with their not always satisfying mechanical properties limit their wider application. In this sense, the use of core-shell systems can generate materials with improved properties. Thus, the goal of the present work was to obtain zirconia-silver core-shell nanoparticles and, after that, evaluate their properties in systems based on poly(lactide) PLA. Systems containing silver nanoparticles (AgNP), zirconium oxide (ZrNP), a physical mixture of both particles and core-shell nanoparticles (Core-shell NP) were evaluated. The Core-shell NP were characterized by dynamic light scattering (DLS), Energy Dispersive X-Ray (EDX), transmission electronic microscopy (TEM), and antimicrobial activity. The nanocomposite films were evaluated by Fourier transform infrared analysis (FTIR), thermogravimetric analysis (TGA), nano-hardness, tensile strength test, cytotoxicity, and antimicrobial activity. The results obtained from the DLS and EDX analyses confirmed the obtaining of systems covered with silver. Through the TEM analysis, the formation of the core-shell structure with a diameter of about 100 nm was observed. The films containing core-shell NP presented antimicrobial activity with a profile correspondent to the one observed for AgNP. As for cytotoxicity, these particles proved to be less cytotoxic and achieved higher values of hardness (10%), modulus (40%), and toughness (28%) than those observed for AgNP, and these properties were lower than those observed for ZrNP. The core-shell NP also exhibited even greater antimicrobial activities, less cytotoxicity, and largest elastic modulus (17%) than the physical mixture of the particles.

Effect of combining photoinitiators on cure efficiency of dental resin-based composites.

BACKGROUND: Camphorquinone is the most conventionally used photoinitiator in Dentistry. Although different alternative photoinitiators have been proposed, no photoinitiator was capable of completely substituting camphorquinone. The combination of photoinitiators has been considered the best alternative. OBJECTIVES: To evaluate the effect of combining Norrish type I and II photoinitiators on the cure efficiency of dental resin-based composites. METHODOLOGY: Experimental composites were produced containing different photoinitiator systems: Norrish type I-only, mono-alkyl phosphine oxide (TPO); Norrish type II-only, camphorquinone (CQ); or its combination, CQ and TPO, in a 1: 1 molar ratio. UV-vis absorption spectrophotometry was performed to assess the consumption of each photoinitiator after curing (n=3). A multi-wave LED (Bluephase® G2, Ivoclar Vivadent) was pre-characterized and used with a radiant exposure of 24 J/cm2. The degree of conversion was evaluated by Raman spectrometry, and the elution of the monomers by nuclear magnetic resonance analysis (n=3). Data were analyzed using ANOVA and Tukey's test (α=0.05; ß=0.2). RESULTS: The combination of CQ and TPO increased the consumption of the photoinitiator system compared to CQ-only (p=0.001), but presented similar consumption compared to TPO-only (p=0.52). There was no significant difference in the degree of conversion between the composites regardless of the photoinitiator system (p=0.81). However, the elution of the monomers was reduced when both photoinitiators were combined. TPO-based material presented the highest elution of monomers. CONCLUSIONS: The combination of the photoinitiator systems seems to be beneficial for the cure efficiency of dental resin-based composites.

Production and Characterization of Poly (Lactic Acid)/Nanostructured Carboapatite for 3D Printing of Bioactive Scaffolds for Bone Tissue Engineering.

Biocompatible scaffolds are porous matrices that are bone substitutes with great potential in tissue regeneration. For this, these scaffolds need to have bioactivity and biodegradability. From this perspective, 3D printing presents itself as one of the techniques with the greatest potential for scaffold manufacturing with porosity and established structure, based on 3D digital modeling. Thus, the objective of the present work was to produce 3D scaffolds from the poly (lactic acid) (PLA) and the nanostructured hydroxyapatite doped with carbonate ions (CHA). For this purpose, filaments were produced via fusion for the fused-filament 3D printing and used to produce scaffolds with 50% porosity in the cubic shape and 0/90°configuration. The dispersive energy spectroscopy and Fourier transform infrared spectroscopy (FTIR) analysis demonstrated the presence of CHA in the polymeric matrix, confirming the presence and incorporation into the composite. The thermogravimetric analysis made it possible to determine that the filler concentration incorporated in the matrix was very similar to the proposed percentage, indicating that there were no major losses in the process of obtaining the filaments. It can be assumed that the influence of CHA as a filler presents better mechanical properties up to a certain amount. The biological results point to a great potential for the application of PLA/CHA scaffolds in bone tissue engineering with effective cell adhesion, proliferation, biocompatibility, and no cytotoxicity effects.

Effect of combining photoinitiators on cure efficiency of dental resin-based composites

Abstract Camphorquinone is the most conventionally used photoinitiator in Dentistry. Although different alternative photoinitiators have been proposed, no photoinitiator was capable of completely substituting camphorquinone. The combination of photoinitiators has been considered the best alternative. Objectives: To evaluate the effect of combining Norrish type I and II photoinitiators on the cure efficiency of dental resin-based composites. Methodology: Experimental composites were produced containing different photoinitiator systems: Norrish type I-only, mono-alkyl phosphine oxide (TPO); Norrish type II-only, camphorquinone (CQ); or its combination, CQ and TPO, in a 1: 1 molar ratio. UV-vis absorption spectrophotometry was performed to assess the consumption of each photoinitiator after curing (n=3). A multi-wave LED (Bluephase® G2, Ivoclar Vivadent) was pre-characterized and used with a radiant exposure of 24 J/cm2. The degree of conversion was evaluated by Raman spectrometry, and the elution of the monomers by nuclear magnetic resonance analysis (n=3). Data were analyzed using ANOVA and Tukey's test (α=0.05; β=0.2). Results: The combination of CQ and TPO increased the consumption of the photoinitiator system compared to CQ-only (p=0.001), but presented similar consumption compared to TPO-only (p=0.52). There was no significant difference in the degree of conversion between the composites regardless of the photoinitiator system (p=0.81). However, the elution of the monomers was reduced when both photoinitiators were combined. TPO-based material presented the highest elution of monomers. Conclusions: The combination of the photoinitiator systems seems to be beneficial for the cure efficiency of dental resin-based composites.

Effect of alternative solvent evaporation techniques on mechanical properties of primer-adhesive mixtures / Efeito de técnicas alternativas utilizando evaporação de solvente nas propriedades mecânicas da mistura primer-adesivo

ABSTRACT This study evaluated the influence of the mode and time of solvent evaporation on the tensile strength (TS), flexural strength (FS) and elastic modulus (EM) of two adhesive systems: Scotchbond Multipurpose (SBMP) and Clearfil SE (CSEB). For this purpose, rectangular samples (2x1x7 mm) were prepared with 10 μL of primer and the solvents were evaporated with air spray at (23±1) ºC, (40±1) ºC and negative control (without spray). For each temperature, the times of 5, 20, 30, and 60 seconds were investigated. The statistical results showed that evaporation at 40±1ºC resulted in better EM for the two adhesives tested and all the evaporation times evaluated. However, there were no significant differences between the times and modes of evaporation for TS. The results of this study indicate that evaporation at a temperature of (40±1) °C could improve the elastic modulus of both adhesives tested, regardless of the evaporating time.

RESUMO Este estudo avaliou a influência do modo e do tempo de evaporação do solvente na resistência à tração (RT), resistência à flexão (RF) e módulo de elasticidade (MR) de dois sistemas adesivos: Scotchbond Multipurpose (SBMP) e Clearfil SE (CSEB). Para isso, amostras retangulares (2x1x7 mm) foram preparadas com 10 μL de primer e os solventes foram evaporados com aerossol a (23±1) ºC, (40±1) ºC e controle negativo (sem aerossol). Para cada temperatura, foram avaliados os tempos de 5, 20, 30 e 60 segundos. Os resultados estatísticos mostraram que a evaporação a (40±1) ºC resultou em melhor MR para os dois adesivos testados e todos os tempos de evaporação avaliados. No entanto, não houve diferenças significativas entre os tempos e modos de evaporação na RT. Os resultados deste estudo indicam que a evaporação a uma temperatura de (40±1) °C poderia melhorar o módulo de elasticidade de ambos os adesivos testados, independentemente do tempo de evaporação.

In vitro evaluation of physicochemical properties of soft lining resins after incorporation of chlorhexidine.

STATEMENT OF PROBLEM: Incorporating chlorhexidine into soft lining materials has been suggested to reduce biofilm development on the material surface and treat denture stomatitis. However, evaluation of the physicochemical properties of this material is necessary. PURPOSE: The purpose of this in vitro study was to evaluate the physicochemical properties of resin-based denture soft lining materials modified with chlorhexidine diacetate (CDA). MATERIAL AND METHODS: Two soft lining resins were tested, one based on polymethyl methacrylate (PMMA) and the other on polyethyl methacrylate (PEMA), into which 0.5%, 1.0%, or 2.0% of CDA was incorporated; the control group had no CDA. The specimens were stored for 2 hours, 48 hours, 7, 14, 21, and 28 days and then analyzed for polymer crystallinity, Shore A hardness, degree of monomer conversion, residual monomer leaching, and CDA release. Data were analyzed by using a 3-way ANOVA and the Tukey HSD test (α=.05). RESULTS: The polymer crystallinity of PEMA and PMMA did not change after CDA incorporation. Shore A hardness increased over time, but not for any CDA concentrations tested after 28 days (P>.05). Considering the degree of conversion, PMMA-based resin showed no statistically significant difference (P>.05). However, PEMA-based resin showed a significant decrease (P<.05), which was reflected in a significant increase in residual monomer leaching from PEMA-based resin with the incorporation of 0.5% and 1.0% CDA (P<.05), mainly in the first 48 hours. PMMA-based resin showed no change in monomer leaching (P>.05). For both resins, the CDA release kinetics were related to monomer leaching; for PEMA-based resin, the values were significantly higher in the first 48 hours (P<.05), and for PMMA-based resin, the values were more sustained up to the last day of analysis. CONCLUSIONS: The incorporation of CDA did not affect the physicochemical properties of soft resins. The properties of PMMA were better than those of PEMA.

Correction to: The use of clays for chlorhexidine controlled release as a new perspective for longer durability of dentin adhesion.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Evaluation of the physical and antifungal effects of chlorhexidine diacetate incorporated into polymethyl methacrylate.

OBJECTIVE: This study aimed to evaluate the physical properties and antifungal activities of polymethyl methacrylate (PMMA) acrylic resins after the incorporation of chlorhexidine diacetate salt (CDA). METHODOLOGY: First, acrylic resin specimens were fabricated with Vipi Cor® and DuraLay® resins with and without the incorporation of 0.5%, 1.0% or 2.0% CDA. The residual monomer and CDA release were measured at intervals ranging from 2 hours to 28 days using ultraviolet spectrometry combined with high-performance liquid chromatography. The antifungal activity against C. albicans was evaluated with the agar diffusion method. Fourier transform infrared spectroscopy was used to analyze the degree of resin conversion. Finally, the water sorption values of the resins were also measured. RESULTS: The incorporated CDA concentration significantly changed the rate of CDA release (p<0.0001); however, the brand of the material appeared to have no significant influence on drug release. Subsequently, the inhibition zones were compared between the tested groups and within the same brand, and only the comparisons between the CDA 2% and CDA 1% groups and between the CDA 1% and CDA 0.5% groups failed to yield significant differences. Regarding the degrees of conversion, the differences were not significant and were lower only in the CDA 2% groups. Water sorption was significantly increased at the 1.0% and 2.0% concentrations. CONCLUSIONS: We concluded that the incorporation of CDA into PMMA-based resins enabled the inhibition of C. albicans growth rate, did not alter the degrees of conversion of the tested resins and did not change the release of residual monomers.

Evaluation of the physical and antifungal effects of chlorhexidine diacetate incorporated into polymethyl methacrylate

Abstract This study aimed to evaluate the physical properties and antifungal activities of polymethyl methacrylate (PMMA) acrylic resins after the incorporation of chlorhexidine diacetate salt (CDA). Methodology: First, acrylic resin specimens were fabricated with Vipi Cor® and DuraLay® resins with and without the incorporation of 0.5%, 1.0% or 2.0% CDA. The residual monomer and CDA release were measured at intervals ranging from 2 hours to 28 days using ultraviolet spectrometry combined with high-performance liquid chromatography. The antifungal activity against C. albicans was evaluated with the agar diffusion method. Fourier transform infrared spectroscopy was used to analyze the degree of resin conversion. Finally, the water sorption values of the resins were also measured. Results: The incorporated CDA concentration significantly changed the rate of CDA release (p<0.0001); however, the brand of the material appeared to have no significant influence on drug release. Subsequently, the inhibition zones were compared between the tested groups and within the same brand, and only the comparisons between the CDA 2% and CDA 1% groups and between the CDA 1% and CDA 0.5% groups failed to yield significant differences. Regarding the degrees of conversion, the differences were not significant and were lower only in the CDA 2% groups. Water sorption was significantly increased at the 1.0% and 2.0% concentrations. Conclusions: We concluded that the incorporation of CDA into PMMA-based resins enabled the inhibition of C. albicans growth rate, did not alter the degrees of conversion of the tested resins and did not change the release of residual monomers.

The use of clays for chlorhexidine controlled release as a new perspective for longer durability of dentin adhesion.

The adhesive systems have the function to establish the connection between the restorative material and dental tissue, therefore it is of fundamental importance, because failures in the adhesive interface can reduce the life of a dental restoration. This study investigated the possibility of using the adhesive layer as a chlorhexidine modified release system evaluating their impact on the properties of these systems as well as evaluating the impact of these systems on immediate and post-aging dentin adhesion. Were used a matrix with BisGMA, UDMA, HEMA and TEGDMA copolymer and clay particles (Dellite 67G); associated with a chlorhexidine and a camphorquinone photoinitiator system. The properties of these systems were evaluated by the XRD, FTIR spectrophotometer, flexural strength, elasticity modulus, drug release, enzymatic inhibition and dentin adhesion resistance. The presence of the clay can raise the mechanical properties of the adhesive systems engendering a more resistant hybrid layer and led to a more sustained release of chlorhexidine in the systems, allowing a longer effective period of MMP-2 inhibition. The hypothesis that the addition of clays as release modulators could increase the effectiveness of these drugs in inhibiting the dentin's MPPs and consequently enhancing the adhesive durability was confirmed. These results indicate that the controlled release of chlorhexidine is able to reduce the process of loss of adhesion presenting itself as a promising system to increase the longevity of dental restorations.

Aesthetic solution for ceramic restoration on cast metal core

Introduction: In order to satisfy the aesthetic desires of the population, by masking the restorations was the search for the evolution of restorative materials enabling the introduction of metal-free materials. But previous studies that have been made with metal structures often cannot be removed and therefore require devices that can be masked, because there is no desire for a total passage of light avoiding dim reflection of these funds. For these situations, you must opt for a ceramic system to provide a degree of opacity, without losing its characteristics of light transmission, reflectance and saturation. Case report: In case the patient had clinical a metal ceramic crown on the molten core element 21, it was confirmed radiographically the core could not be removed because it would fracture risk to the tooth. We chose to use an opaquer ceramic framework to prevent the passage of light over dark metal. The material of choice was zirconia ceramic by high flexural strength, allowing it to function as a framework for crowns. Conclusion: With the correct application of ceramic coverage on Caquetá noted that it is possible to mask the gray color of the metal through the knowledge of the optical material, the correct use of these properties, opacity and translucidus, and a close contact between dentists and prosthetic.

Introdução: A fim de satisfazer os anseios estéticos, da população, por mascarar as restaurações houve a busca pela evolução dos materiais restauradores possibilitando a introdução de materiais livres de metais. Porém trabalhos prévios que foram confeccionados com estruturas metálicas muitas vezes não podem ser removidos e, portanto, necessitam de artifícios para que possam ser mascarados, pois não há o desejo de uma total passagem de luz evitando a reflexão desses fundos escurecidos. Para estas situações, é necessário optar por um sistema cerâmico que apresente um grau de opacidade, sem perda de suas características de translucidez, refletância e saturação. Relato do caso: A paciente possuía uma coroa metalo-cerâmica sobre núcleo fundido no elemento 21, constatou-se radiograficamente que o núcleo não podia ser retirado, pois traria risco de fratura ao dente. Optou-se por utilizar uma cerâmica mais opaca de arcabouço para evitar a passagem de luz sobre o metal escurecido. O material de escolha foi à cerâmica de zircônia por apresentar alta resistência à flexão, permitindo que funcione como arcabouço para coroas unitárias. Conclusão: Com a correta aplicação de cerâmicas de cobertura sobre o casquete observou- se que é possível mascarar a cor acinzentada do metal através dos conhecimentos ópticos do material, a correta utilização dessas propriedades, opacidade e translucides, e um estreito contato entre dentista e protético.

Preparation of Poly(D,L-lactic-co-glycolic acid) Nanoparticles Through Solvent Displacement and Structural Evaluation Using Time-Domain Nuclear Magnetic Resonance.

The present study obtained coated poly(lactic-co-glycolic acid) nanoparticles using the solvent displacement method aiming to evaluate the effect of the polymer concentration in the pharmaceutical formulations' and polymer properties. Nanosuspensions were evaluated by fourier-transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), zeta potential (ZP), thermogravimetric analysis (TGA), X-ray diffraction (XRD) and time-domain nuclear magnetic resonance (TD-NMR). Uniform nanoparticles could be obtained using this method and higher polymer concentrations led to an increase in particle size and negatively charged surfaces were observed. However typical PLGA halo was observed in XRD, diffractograms revealed the Pluronic chains behavior when PLGA concentration changed. Additionally, samples' spin-lattice relaxation times, dipolar interaction and correlation times were evaluated using time-domain nuclear magnetic resonance (TD-NMR), which revealed the interference of PLGA chain packing when Pluronic was incorporated as well as Pluronic chains organization and its behavior around the particle.

Effect of monomer type on the CC degree of conversion, water sorption and solubility, and color stability of model dental composites.

OBJECTIVE: This study has investigated the influence of BisGMA, BisEMA, BisEMA 30, and two UDMA-based monomers (UDMA and Fit 852), with TEGDMA as co-monomer, on the degree of conversion, water sorption, water solubility, and optical properties of experimental dental composites. METHODS: Materials were formulated at 70/30 molar rations using BisGMA, BisEMA, BisEMA 30, UDMA or FIT 852, as base monomers, combined with TEGDMA. 60wt% of silanated-glass particles was added. Degree of conversion (DC) and polymerization kinetics were monitored using Fourier-transformed infrared spectroscopy in the near-IR range. Water sorption (Wsp) and solubility (Wsl) were assessed using mass variation after 60days water storage. Color was evaluated using a digital spectrophotometer, applying the CIELab parameters 24h after dry storage and 60days after water immersion to calculate ΔE values. All data were analyzed using ANOVA and Tukey's test (pre-set alpha=0.05). RESULTS: The BisGMA-based co-monomer mixture presented the lowest DC (62±1%), whereas BisEMA 30 had the highest DC value (95±2%). The highest Wsp was observed for BisEMA 30 (12.2±0.8%), and the lowest for BisEMA (0.4±0.1%). BisEMA has shown the lowest Wsl (0.03±0.01%) and BisEMA 30 the highest one (0.97±0.1%). The ΔE values showed that BisEMA 30 (7.3 color units) and Fit 852 (3.8 color units) altered the color stability providing ΔE>3.3, which is considered clinically unacceptable. CONCLUSIONS: The chemical composition and structure of the base monomer influenced the degree of conversion, water sorption, water solubility, and color stability. Considering the overall results, it is possible to state that the base monomer BisEMA mixed with the co-monomer TEGDMA presented the best performance in terms of all the parameters tested. SIGNIFICANCE: The resin matrix composition might influence physical property degradation processes and color stability of dental resin composites. Formulations based on BisEMA seem most promising for materials' development.

Effect of Nanofiller Loading on Cure Efficiency and Potential Color Change of Model Composites.

OBJECTIVES: To evaluate the effect of nanofiller loading on cure efficiency and potential color change of experimental composites. MATERIALS AND METHODS: Four different polymeric materials were produced using the same organic matrix blend. To this matrix, different amounts of 0.05 µm fumed silica filler were added: no filler, 13, 52, and 65wt%. Fourier transform infrared spectroscopy was used to evaluate the degree of conversion (DC) for each composite using near-IR analysis, and spectrophotometry according to CIELab chromatic space was used to evaluate the color change.To induce color change, composites were artificially aged with exposure to cycles of UV-B light for 300 hours. Trasmission electron microscopy was used to illustrate nanoffiler aglomeration in the resin matrix. Data were analyzed using correlation analysis (α = 0.05). RESULTS: There was an excellent inverse linear correlation between filler wt% and either DC or color change. Greater changes to red (+Δa) and yellow (+Δb) were observed as the filler wt% increased. CONCLUSIONS: A higher percentage of nano-sized filler particles in dental resin composites directly affects their cure efficiency and potential for color change. CLINICAL SIGNIFICANCE: The increase in filler particle loading negatively affected monomer conversion and color stability of resin-based composites. As reduced filler loading results in poorer mechanical properties, to enhance color stability, resin-based composites should be formulated by making the refractive index of the polymeric matrix more closely match that of the filler throughout the polymerization process. (J Esthet Restor Dent, 2016).

Influência da camada híbrida na resistência à microtração de sistemas adesivos após armazenamento / Hibrid layer influence in bond systems microtensile test after storage

O objetivo deste estudo foi avaliar a resistência à microtração de sistemas adesivos em função da presença ou não da camada de colágeno e do tempo de armazenamento. Para tanto foram utilizados 24 terceiros molares restaurados utilizando-se diferentes sistemas adesivos, com ou sem tratamento prévio com NaOCl, e armazenados por 24 horas e 12 meses. Os valores de resistência foram submetidos à análise estatística. O tratamento prévio com NaOCl não foi significativo em 24 horas. Entretanto, este tratamento manteve resultados satisfatórios de adesão após 12 meses para todos os sistemas adesivos, com exceção apenas do Prime & Bond NT.

The aim of the present study was to evaluate the microtensile bond strength of different bond systems due to presence or absence of the collagen layer and storage time. Therefore, 24 third molars were restored using different bond systems, with or without pretreatment with NaOCl, and stored for 24 hours and 12 months. The microtensile strength values were subjected to statistical analysis. The pretreatment with NaOCl was not significant in 24 hours. However, this pretreatment remained satisfactory bond results after 12 months for all bond systems, except for Prime & Bond NT.

The effect of time between handling and photoactivation on self-adhesive resin cement properties.

PURPOSE: To evaluate the degree of conversion, absorption, and solubility in water of self-adhesive resin cements subjected to different time intervals between material preparation and the photoactivation procedure. MATERIALS AND METHODS: Two dual self-adhesive resin cements were tested: RelyX Unicem and SmartCem2. The degree of conversion as a function of time was evaluated by Fourier-transformed infrared spectroscopy using the attenuated total reflectance technique. Three time intervals between handling and photoactivation were applied: Group 1 = immediately; Group 2 = a 1-minute interval; Group 3 = a 4-minute interval. All specimens were irradiated with a light-emitting diode source for 40 seconds. Thirty discs of each cement (1 mm thick × 6 mm diameter, n = 10) were prepared for the absorption and solubility tests. These specimens were stored in distilled water at 37°C for 90 days. The results were subjected to ANOVA with two factors (material and activation time intervals) and Tukey's test (95% significance). RESULTS: The 4-minute interval significantly reduced the degree of conversion of SmartCem2 (30.6% ± 8.3%). No other significant changes were observed for the degree of conversion; however, the time intervals before photoactivation interfered significantly in the water absorption of the RelyX Unicem specimens but not the SmartCem2 specimens. The time intervals did not affect the solubility of either cement. In all cases, SmartCem2 had higher solubility than RelyX Unicem. CONCLUSION: The time interval between handling and photoactivation significantly influenced the degree of conversion and water sorption of the resin-based cements. In general, one can say that the self-adhesive resin cements should be photoactivated as soon as possible after the material handling process.