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Investigations of step-growth thiol-ene polymerizations for novel dental restoratives.

OBJECTIVES: The goal of this work was to investigate the feasibility of formulating novel dental restorative materials that utilize a step-growth thiol-ene photopolymerization. Particularly, we are aiming to significantly reduce the polymerization shrinkage and shrinkage stress while retaining adequate physical properties as compared to current dimethacrylatre-based systems. METHODS: The thiol-ene system is composed of a 4:3 molar mixture of triallyl-1,3,5-triazine-2,4,6-trione (TATATO) and pentaerythritol tetramercaptopropionate (PETMP). The simultaneous measurement of shrinkage stress and functional group conversion was performed. Solvent extraction of unreacted monomers and dynamic mechanical analysis on the polymer networks that were formed were also studied. Flexural strength was measured for both filled and unfilled PETMP/TATATO and Bis-GMA/TEGDMA systems. RESULTS: Photopolymerization of PETMP/TATATO occurs at a much higher rate, with the maximum polymerization rate six times faster, than Bis-GMA/TEGDMA cured under the identical conditions. The results from the simultaneous measurement of shrinkage stress and conversion showed that the onset of shrinkage stress coincides with the delayed gel point conversion, which is predicted to be 41% for the 3:4 stoichiometric PETMP/TATATO resin composition. The maximum shrinkage stress developed for PETMP/TATATO was about 0.4 MPa, which was only approximately 14% of the maximum shrinkage stress of the Bis-GMA/TEGDMA system. Adequate flexural strength and flexural modulus values were obtained for both filled and unfilled PETMP/TATATO systems. SIGNIFICANCE: The dramatically reduced shrinkage stress, increased polymerization rate, significance increased functional group conversion, and decreased leachable species are all benefits for the use-of thiol-ene systems as potential dental restorative materials.

3-Mercaptopropionic Acid↗

Thiol-ene oligomers as dental restorative materials.

OBJECTIVE: The aim of this work was to prereact thiol-ene monomers to create reactive thiol or vinyl (ene)-functionalized oligomers, and to investigate the use of these materials as novel dental restorative material. Investigation has focused on the application of oligomeric thiol-ene materials as dental restorative resins with lower polymerization shrinkage and polymerization stress as compared to monomeric thiol-ene systems and particularly with respect to current dimethacrylate-based systems. METHODS: Reactive thiol-functionalized oligomers were created via photopolymerization using triallyl-1,3,5-triazine-2,4,6-trione (TATATO), trimethylolpropane tris(3-mercaptopropionate) (trithiol) and pentaerythritol tetramercaptopropionate (tetrathiol). Kinetic and mechanical investigation of Bis-GMA/TEGDMA, and oligomeric and monomeric thiol-ene systems were conducted. More specifically, polymerization shrinkage and stress, polymerization kinetics, glass transition temperature, flexural strength and flexural modulus were evaluated. RESULTS: Upon evaluation, the polymerization stress of oligomeric thiol-ene systems was dramatically reduced by as much as 33% when compared with the stress exhibited by monomeric thiol-ene systems and as much as a 92% reduction in stress relative to the current dimethacrylate-based dental restorative materials. Furthermore, the flexural strength and modulus of the monomeric and oligomeric thiol-ene resins were not significantly different. SIGNIFICANCE: Oligomeric thiol-ene systems offer potential as alternative dental restorative resins due to the significant reduction in polymerization shrinkage and stress while retaining the mechanical properties of monomer-based thiol-ene resins.

3-Mercaptopropionic Acid↗

The effect of ceramic and porous fillers on the mechanical properties of experimental dental composites.

OBJECTIVES: The purpose of this study was to investigate the effect of ceramic fillers (containing leucite crystals) and their porosity on the mechanical properties of a new experimental dental composite in order to compare with the properties of composites containing conventional glass fillers. METHODS: In this study, experimental composites were prepared by mixing the silane-treated fillers with monomers. Experimental composites were divided into four groups according to their filler type, amount and porosity. The monomers were composed of 70% Bis-GMA and 30% TEGDMA by weight for all groups. Glass and leucite-containing-ceramic were prepared as different filler types. In order to make fillers porous, leucite-containing-ceramic fillers were treated with HF acid. Camphorquinone and DMAEMA were used as photo initiator system. Post-curing was done for all groups before mechanical testing. Degree of Conversion of composites was measured using FTIR spectroscopy. The diametral tensile strength (DTS), flexural strength and flexural modulus were measured and compared among the groups. RESULTS: The results showed that the stronger and more porous filler has a positive effect on flexural strength. Porosity of filler increased flexural strength significantly. No significant difference was found in DTS tests among the groups. Flexural modulus was affected and increased by using ceramic fillers. The type of the filler affected the DC of the composite and DC increased by post-curing. SIGNIFICANCE: Flexural strength is one of the most important properties of restorative dental materials. Higher flexural strength can be achieved by stronger and more porous fillers. Investigation into the effect of filler on dental material properties would be beneficial in the development of restorative dental material.

Aluminum Silicates↗

Polymerization characteristics of light- and auto-curing resins for individual splints.

OBJECTIVES: The aim of this in vitro study was to assess different resins for occlusal splints regarding a number of polymerization characteristics. METHODS: One autopolymerizing resin (Palapress) and four light-curing resins (Acrylight, Primosplint, Triad TranSheet Colorless and Pink) were tested for flexural strength, modulus of elasticity, water sorption, volumetric shrinkage, and conversion of double bonds. These resins were polymerized for 10 and 15 min in a light oven at frequencies between 320 and 400 nm or 400 and 500 nm, respectively. Data were treated statistically by ANOVA and by Scheffé test. RESULTS: Concerning flexural strength and modulus of elasticity, Triad TranSheet Colorless showed significantly greater values than Primosplint and Palapress (p<0.05). The light curing resins Acrylight and Primosplint featured significantly higher water sorption when cured for 10 min compared to all other resins (p<0.05). Acrylight displayed significantly higher volumetric shrinkage and a higher quantity of remaining double bonds compared to all other light-curing resins (p<0.05). Primosplint, Triad TranSheet Colorless and Pink showed significantly lower shrinkage values than autopolymerizing Palapress (p<0.05). For all light curing resins, polishing of the samples resulted in a significantly lower quantity of remaining double bonds (p<0.05) compared to unpolished samples. SIGNIFICANCE: With respect to the polymerization properties evaluated, the light-curing resins reached similar material properties to the autopolymerizing resin or even surpassed them. Light-curing resins seem to be suitable for the fabrication of occlusal splints and can been seen as an alternative to autopolymerizing polymethylmethacrylates.

Acrylic Resins↗

Analyses of multilayered dental ceramics subjected to biaxial flexure tests.

OBJECTIVES: The purpose of this study was to formulate explicitly the equation to relate the biaxial strength of multilayered dental ceramics to the fracture load for multilayered discs subjected to biaxial flexure tests. METHODS: Analytical modeling showed that the solutions for multilayered discs subjected to biaxial flexure tests could be obtained from the existing solutions for monolayered systems by replacing the neutral surface position and the flexural rigidity of monolayers with those of multilayers. Finite element analyses were performed on porcelain/zirconia bilayered discs subjected to piston-on-ring and ring-on-ring tests to verify the analytical results. RESULTS: Good agreement was obtained between (i) present analytical results and Roark's formulas for stresses at the top and the bottom surfaces of bimetallic discs subjected to bending, and (ii) present analytical and finite element results for porcelain/zirconia bilayered discs subjected to piston-on-ring and ring-on-ring tests. SIGNIFICANCE: The present closed-form solutions provide a basis for evaluating the biaxial strength of multilayered dental ceramics. Depending upon the strength of the individual layers and the stress distribution through the thickness of the multilayer during tests, cracking can initiate from any layer under tension.

Crowns↗

Physical properties and microstructural characterization of dental porcelains mixed with distilled water and modeling liquid.

OBJECTIVE: The aim of this study was to microstructurally characterize and to make comparisons of the physical properties of sintered dental porcelains prepared by mixing with distilled water and with their modeling liquid. METHODS: Six commercial porcelain powders: IPS Classic (Ivoclar Vivadent AG, Schaan, Liechtenstein), IPS d.SIGN (Ivoclar Vivadent AG), IPS InLine (Ivoclar Vivadent AG), Vita VMK95 (Vita Zahnfabrik, Bad Sackingen, Germany), Vita OMEGA 900 (Vita) and Ceramco III (Ceramco-Dentsply, Burlington, NJ, USA) were used as starting powders. Following particle size and BET analyses of starting powders, each porcelain powder was mixed with distilled water and with its own modeling liquid. Disc specimens were sintered in accordance with each manufacturer's instructions. Specimens were characterized using X-ray diffraction (XRD), optical microscopy and SEM analysis and their physical properties such as bulk density, microhardness and biaxial flexural strength were determined. RESULTS: The sintered dental porcelains premixed with modeling liquid had density, biaxial flexural strength and microhardness values slightly higher than those premixed with distilled water. Mixing with distilled water and modeling liquid caused statistically significant differences between the density values of Vita VMK 95 and microhardness values of IPS d.SIGN and IPS InLine. Characterization investigations (XRD and SEM) revealed the coexistence of the tetragonal leucite (1-3 microm) and hexagonal fluorapatite crystals (0.4-1.2 microm) in a feldspathic glassy matrix in the microstructure of IPS d.SIGN and only leucite crystals (3-6 microm) in the microstructures of other porcelains. SIGNIFICANCE: Mixing the porcelain powders with distilled water or modeling liquid prior to sintering has no effect on the resultant sintered crystalline microstructure. On the other hand, significant differences exist between the physical properties of some porcelains.

Aluminum Silicates↗

The effects of thermocycling on the flexural strength and flexural modulus of modern resin-based filling materials.

OBJECTIVE: Evaluation of flexural strengths and flexural moduli of hybrids, packables, ormocers, compomers and flowables prior to, and after, thermocycling. MATERIALS AND METHODS: Twenty specimens, size (25 +/- 2) mm x (2 +/- 0.1) mm x (2+/-0.1) mm, of Herculite (HE), Point 4 (P4), TetricCeram (TC), Miris (MI), TetricCeram HB, (HB), Solitaire 2 (SO), Surefil A (SU), Definte (DE), Admira (AD), Dyract AP (DY), Compoglass (CO) and TetricFlow (TF) were made according to ISO 4049. A three-point-bending test was carried out for the first 10 specimens after 24 h water storage at 37 degrees C and for the second 10 specimens after 30-day water storage at 37 degrees C, followed by 5000 thermocycles between +5 and +55 degrees C. For each test series flexural strengths and flexural moduli were calculated. Statistical significance was p < 0.05. RESULTS: Flexural strengths of DY and CO missed the 80 MPa limit of ISO 4049 for occlusal fillings prior to and after thermocycling. AD missed it after thermocycling. HE, P4, TC, MI, HB, SO, SU, DE and TF did not significantly differ prior to and after thermocycling. Flexural strength of SO and AD significantly decreased after thermocycling. No change of the flexural moduli could be observed for any of the test materials. Only SU exceeded 10,000 MPa prior to and after thermocycling. SIGNIFICANCE: Only DY and CO missed the flexural strength limit of ISO 4049 for occlusal fillings. Only SU exceeded a flexural modulus of 10,000 MPa prior to and after thermocycling.

Analysis of Variance↗

Effect of food-simulating liquids on the mechanical properties of provisional restorative materials.

OBJECTIVES: The purpose of this study was to investigate the effects of food-simulating liquids (FSL) on the mechanical properties of provisional restorative materials. METHODS: Four provisional restorative materials were selected: (1) Dentalon Plus (DP), (2) Protemp II (PII), (3) Systemp C&B (SCB) and (4) Integrity (INTG). The specimens were fabricated in customized molds and each type was randomly divided into five groups (n = 10). The test groups were conditioned for 7 days at 37 degrees C as follows: water, 0.02 N citric acid, heptane and 75% ethanol in aqueous solution. Specimens in the control group were stored at room temperature in air. After conditioning, the flexural strength (FS) values were assessed using a universal testing machine (5 mm/min crosshead speed) and the fractured specimens were used for the determination of the Knoop hardness number (KHN) using a digital micro-hardness tester (100 gf/15 s). Kruskal-Wallis and Mann-Whitney U-tests were used for statistical analysis. RESULTS: In ethanol and heptane solutions, DP specimens were totally degraded, thus, FS/KHN for DP could not be measured. For all materials, the FS/KHN values were significantly lower than their control groups after conditioning in ethanol. After heptane conditioning, the decrease in FS for SCB and KHN for PII were statistically significant. After citric acid conditioning, KHN for PII and INTG were significantly higher than the controls and the decrease in FS for SCB and INTG were statistically significant. SIGNIFICANCE: The mechanical properties of provisional restorative materials are strongly influenced by food-simulating liquids.

Beverages↗

Network structure of Bis-GMA- and UDMA-based resin systems.

OBJECTIVES: The commonly used dental base monomers 2,2-bis[p-(2'-hydroxy-3'-methacryloxypropoxy)phenylene]propane (Bis-GMA) and 1,6-bis(methacryloxy-2-ethoxycarbonylamino)-2,4,4-trimethylhexane (UDMA) require the use of a diluent monomer, such as triethylene glycol dimethacrylate (TEGDMA). The aim of this study was to measure double bond conversion of UDMA/TEGDMA and Bis-GMA/TEGDMA polymeric systems, determine the leachable portion, and analyze network formation by evaluating crosslinking and pendant double bonds. METHODS: UDMA or Bis-GMA was combined with TEGDMA in systematic increments and irradiated to form light cured polymers. Fourier transform infrared spectroscopy in the near-infrared region was used to measure double bond conversion. The leachable sol fraction was analyzed by 1H NMR. Resin composites were formulated. Flexural strength was measured by three-point bending and volumetric shrinkage was determined with a mercury dilatometer. RESULTS: The amount of base monomer greatly influenced double bond conversion, sol fraction, and crosslinking. Increasing base monomer concentration decreased double bond conversion, increased the leachable fraction, and decreased crosslinking and network formation. At mole fractions higher than 0.125, the UDMA polymers had significantly higher conversion than the Bis-GMA polymers. Bis-GMA polymers had higher leachable amounts of unreacted monomer, while UDMA mixtures had more crosslinking than the Bis-GMA mixtures. In regards to the physical properties of resin composites, increasing the base monomer improved flexural strength and decreased volumetric shrinkage. SIGNIFICANCE: This systematic study for the evaluation of conversion, leachability, crosslinking, and network structure along with physical properties, like volumetric shrinkage and flexural strength, are required for the optimization of competing desirable properties for the development of durable materials.

Bisphenol A-Glycidyl Methacrylate↗

Prediction of permanent deformation in cast clasps for denture prostheses using a validated nonlinear finite element model.

OBJECTIVES: Permanent deformation is one of the most common mechanical complications that affect denture clasps. This can lead to loss of retention and stability of the prosthesis. The purpose of this study was to apply and validate a nonlinear finite element model for permanent deformation prediction in cast denture clasps. Such a model can enhance the process of design optimization and contribute to minimizing the possibility of this problem. METHODS: Cast clasps made from Ti-6Al-7Nb, Co-Cr and Type IV gold alloys were loaded in three different directions (outside, inside and outside inclined 30 degrees ), and the resulting permanent deformation values were recorded. Nonlinear finite element analysis simulations based on the maximum distortion energy criterion for yielding, were conducted for clasp models that were reproduced according to the dimensions of each experimental specimen. Linear regression analysis for the results of the experiment and simulation was performed to verify the validity of the mathematical models. RESULTS: Deflections required to produce specific amounts of permanent deformation were in close agreement with those recorded experimentally. The R2 value for all bending tests was 0.985 and the linear regression equation expressed in micrometers was [DeflectionFEA=0.976 (DeflectionReal)+34]. SIGNIFICANCE: Permanent deformation behavior in the cast clasps with a relatively wide range of deflections (0-2 mm) can be predicted using the proposed model, which shall enhance the design optimization process of cast clasps for denture prostheses.

Dental Alloys↗

The in vitro failure of all-ceramic crowns and the connector area of fixed partial dentures using bilayered ceramic specimens: the influence of core to dentin thickness ratio.

AIMS: To assess the effect of core to dentine thickness ratio on the bi-axial flexure strength and fracture mode and failure origin using bilayered ceramic specimens as an in vitro assessment for all-ceramic crowns and the connector area of fixed partial dentures (FPDs). METHODS: Sets of 30 bilayered composite discs, with a core layer thickness of 1mm and with core to dentine thickness ratios of 2:1, 1:1 and 1:2, were tested in bi-axial flexure with both the reinforcing core and veneering dentine loaded in tension. Mean flexure strengths, standard deviations and associated Weibull moduli (m) were determined. Optical microscopy was employed for identification of the fracture mode and failure origin for the failure all-ceramic crowns and the connector area of FPDs. RESULTS: For a core thickness of 1mm the core to dentine thickness ratio failed to influence the bi-axial flexure strength data when both the reinforcing core and veneering dentine porcelain were tested in tension. The number of fracture fragments, frequency of occurrence of specimen delaminations, Hertzian cone formations and sub-critical radial cracking in the bilayered dental ceramic composite disc-shaped specimens were dependent on the core to dentine thickness ratio and the surface loaded in tension. SIGNIFICANCE: The fracture mode and failure origin in bilayered ceramics tested to represent the failure mode of all-ceramic crowns and FPDs was dependent upon the core to dentine thickness ratio employed. However, the conventional wisdom regarding bilayered ceramic specimens with core thicknesses greater than 1mm are not followed when the core thickness was reduced to 1mm since the fracture resistance was not dependent on the core to dentine thickness ratio.

Aluminum↗

Influence of radiant exposure on contraction stress, degree of conversion and mechanical properties of resin composites.

OBJECTIVE: To verify the influence of radiant exposure (H) on contraction stress (CS), degree of conversion (DC) and mechanical properties of two restorative composites. METHODS: Filtek Z250 (3M ESPE) and Heliomolar (Ivoclar) were photoactivated with 6, 12, 24, or 36 J/cm2 at continuous irradiance of 600 mW/cm2. CS at 10 min was determined in a low compliance testing system. DC, flexural strength (FS), flexural modulus (FM) and Knoop microhardness (KHN) were measured after 24 h storage at 37 degrees C. KHN and DC measurements were conducted on the irradiated surface of 1mm thick disk-shaped specimens. Bar-shaped specimens were submitted to three-point bending to determine FS and FM. Data were analyzed by one-way ANOVA/Tukey's test (alpha = 0.05) separately for each composite. RESULTS: For Filtek Z250, no significant increase in CS was observed above 12 J/cm2. DC and FM were similar at all H values, while FS increased significantly between 6 and 24 J/cm2. KHN was significantly different among all H levels, except between 12 and 24 J/cm2. For Heliomolar, CS and KHN increased significantly with H, except between 24 and 36 J/cm2. DC, FM and FS did not vary, regardless of the radiant exposure. SIGNIFICANCE: Variables tested behaved differently. CS and KHN were more sensitive to increasing radiant exposures than the other properties evaluated. FS varied only for Filtek Z250, while, for both composites, DC and FM were not affected by different H values.

Acrylic Resins↗

Interphase structure-property relationships in thermoset dimethacrylate nanocomposites.

OBJECTIVES: The aim of this research was to better understand the relationships between interphase composition and the resultant mechanical properties of thermoset methacrylate nanocomposites, ultimately for the purpose of improving the properties of dental restorative materials through manipulation of the interphase. METHODS: Silica nanoparticles were silanized with three different silanes and blends of those silanes to generate six different interphase compositions. The silanes varied in their relative polarity, flexibility, and reactivity towards photo-polymerization. Composites containing 60% by mass of the silanized fillers were prepared and analyzed for uncured paste handling characteristics, vinyl conversion, biaxial flexure strength (BFS), modulus, and Knoop hardness. RESULTS: Dual silanization of the fillers improved the handling characteristics of the uncured composite pastes compared to those containing fillers silanized with 3-methacryloxypropyltrimethoxysilane. To obtain high BFS, functional groups reactive in free radical polymerization were needed in the composite interphase, but a high concentration of those groups was not necessary. Moduli were highest for composites with interphases that contained styrylethyltrimethoxysilane, a reactive aromatic silane. The hardness values of the composites with reactive interphases were all comparable. Methacrylate conversion was only modestly influenced by silane interphase composition. SIGNIFICANCE: This study suggests that dual silanization is a practical method for improving the handling characteristics of uncured dental restorative nanocomposites while maintaining or improving the mechanical properties of the cured composites.

Chemical Phenomena↗

Influence of environmental conditions on dental composite flexural properties.

OBJECTIVE: To determine if increased relative humidity and temperature simulating intraoral environmental conditions adversely affect flexural properties of dental composites. METHODS: Specimen fabrication followed ANSI/ADA specification 27 for resin-based filling materials, except that ambient laboratory conditions (47% relative humidity at 22 degrees C) or simulated intraoral conditions (90% relative humidity at 35 degrees C) were used when fabricating and polymerizing specimens. Ten specimens were made of each of three commercially available composites at each condition. As per the specification, after aging specimens in 10 ml of deionized water at 37 degrees C for 24 h, flexural properties were measured using a 3-point bend test. RESULTS: A two-factor ANOVA and Fisher's least significant difference (LSD) post hoc (alpha=0.05) indicated there were significant differences in flexural modulus and strength as a function of material, with Z250=TPH>Prodigy. However, neither flexural modulus nor flexural strength of any material was adversely influenced by fabrication conditions. SIGNIFICANCE: Although the flexural properties did not decrease with respect to fabrication conditions, the flexural modulus of some of the materials (TPH Spectrum and Z250) increased when specimens were fabricated at simulated intraoral temperature and relative humidity. Thus, simulation of these factors may be important in laboratory testing, since the resultant properties may better reflect flexural properties associated with dental composite restorations placed clinically.

Body Temperature↗

Effect of mechanical cycling on the flexural strength of densely sintered ceramics.

OBJECTIVES: The aim of this study was to evaluate the effect of mechanical cycling on the biaxial flexural strength of two densely sintered ceramic materials. METHODS: Disc shaped zirconia (In-Ceram Zirconia) and high alumina (Procera AllCeram) ceramic specimens (diameter: 15 mm and thickness: 1.2 mm) were fabricated according to the manufacturers' instructions. The specimens from each ceramic material (N=40, n=10/per group) were tested for flexural strength either with or without being subjected to mechanical cycling (20,000 cycles under 50 N load, immersion in distilled water at 37 degrees C) in a universal testing machine (1 mm/min). Data were statistically analyzed using two-way ANOVA and Tukey's test (alpha=0.05). RESULTS: High alumina ceramic specimens revealed significantly higher flexural strength values without and with mechanical cycling (647+/-48 and 630+/-43 MPa, respectively) than those of zirconia ceramic (497+/-35 and 458+/-53 MPa, respectively) (p<0.05). Mechanical cycling for 20,000 times under 50 N decreased the flexural strength values for both high alumina and zirconia ceramic but it was not statistically significant (p>0.05). SIGNIFICANCE: High alumina ceramic revealed significantly higher mean flexural strength values than that of zirconia ceramic tested in this study either with or without mechanical cycling conditions.

Aluminum Oxide↗

Formulation and characterization of a novel fluoride-releasing dental composite.

OBJECTIVES: The aims of this study were to formulate a novel fluoride-releasing dental composite and to evaluate its mechanical properties, fluoride release and recharge capabilities, water sorption and solubility. METHODS: A fluoride-releasing dimethacrylate monomer containing a ternary zirconium fluoride chelate was synthesized. Three experimental fluoride-releasing composites were fabricated with different monomer formulas (wt.%)-(1) Control A: 40 BisGMA/40 TEDMA/20 UEDMA; (2) EXPERIMENTAL: 20 F-releasing monomer/20 BisGMA/40 TEDMA/20 UEDMA; (3) Control B: the same formula as Control A except that it contained 10 wt.% (of total monomer) tetrabutylammonium fluoride (TBAF), which had a fluoride content equivalent to EXPERIMENTAL. All three materials had the same filler content: 55 wt.% silanized fluoroaluminosilicate particles (0.8 microm) and 10 wt.% silanized fumed silica (14 nm). All materials contained 0.17 wt.% camphorquinone (CQ) as a photoinitiator and 0.69 wt.% ethyl-4-dimethylaminobenzoate (4EDMAB) as an accelerator. The materials were tested for fluoride release (for 184 days), fluoride recharge, compressive and flexure strength, water sorption and solubility. The data were analyzed using ANOVA and Tukey-HSD tests, and Kruskal-Wallis test. RESULTS: The experimental composite had significantly higher fluoride release and fluoride recharge capabilities than both Control composites. It had significantly better physical and mechanical properties than Control B. SIGNIFICANCE: The combined use of the fluoride-releasing dimethacrylate monomer and fluoride-releasing filler can provide sustained high fluoride release and recharge as well as acceptable mechanical and physical properties. Simply adding organic fluoride salt in the monomer yields composites with poor mechanical and physical properties.

4-Aminobenzoic Acid↗

Bis-(acrylamide)s as new cross-linkers for resin-based composite restoratives.

OBJECTIVES: The objective of this study was to investigate the use of three new bis-(acrylamide)s as cross-linker in resin-based composite restoratives. Selected mechanical properties such as flexural strength and flexural modulus of model composites containing bis-(acrylamide)s were investigated and compared to the properties of composites that are based on only conventional dimethacrylates. In addition, the hydrolytic stability of composites containing an acidic monomer was examined. METHODS: The flexural strength and flexural modulus of elasticity were determined according to ISO 4049:2000. For this purpose, test specimens (2 mm x 2 mm x 25 mm) of the composites investigated were prepared in stainless steel moulds and light-cured (150 mW/cm2, 2 x 180 s). The flexural strength and flexural modulus were measured after the samples had been stored in dry conditions or in water for 24 h at 37 degrees C as well as after they had been stored in water for 7 days at 37 degrees C, and in certain cases, after they had been boiled for 24 h in water. RESULTS: Visible light cured mixtures of dimethacrylates with bis-(acrylamide)s and composites based on these mixtures show a similar reactivity, flexural strength and flexural modulus of elasticity compared to materials that contain only dimethacrylate. The composites did not show any deterioration of the mechanical properties after water storage. Only when strongly acidic monomers were added to the composites containing dimethacrylates or bis-(acrylamide)s did the flexural strength and flexural modulus of the samples decrease after they were stored in water. SIGNIFICANCE: Bis-(acrylamide)s were similarly reactive than dimethacrylates and therefore can be used as diluents to substitute dimethacrylate diluents in composites. Although the bis-(acrylamide)s are entirely soluble in water, non-ionic materials based on bis-(acrylamide)s did not strongly change their mechanical properties during storage in water.

Acrylamides↗

Characterization of nanofilled compared to universal and microfilled composites.

OBJECTIVES: The purpose of this study was to compare the inorganic fraction and the mechanical properties of three nanofilled composites with four universal hybrid and two microfilled composites. The degrees of conversion of the materials photopolymerized using halogen and LED units were also investigated. METHODS: Three nanofilled (Supreme, Grandio and Grandio Flow), four universal hybrid (Point-4, Tetric Ceram, Venus, Z 100) and two microfilled (A 110, Durafill VS) composites were used in this study. Their filler weight content was measured by thermogravimetric analysis. The morphology of the filler particles was determined using scanning-electron microscopy (SEM). Mechanical properties were measured: dynamic and static elastic moduli, flexural strength and Vickers microhardness. The degree of conversion in relation with the depth of polymerization of every material tested was evaluated using Raman spectrophotometry. RESULTS: Nanofilled resin composites show higher elastic moduli than those of universal and microfilled composites, except for the Z-100. The microfilled composites exhibit by far the lowest mechanical properties. The flexural strength does not appear as a discriminating factor in this study. The degrees of polymerization obtained with the halogen lamp are higher than those obtained with the LED lamp. SIGNIFICANCE: Nanofilled resin composites show mechanical properties at least as good as those of universal hybrids and could thus be used for the same clinical indications as well as for anterior restorations due to their high aesthetic properties.

Composite Resins↗