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PubMed2005

The static strength and modulus of fiber reinforced denture base polymer.

OBJECTIVES: Partial fiber reinforcements have been employed to strengthen dentures both during repair and in the manufacturing process. The reinforcing fibers can be evenly distributed in the denture base polymer or alternatively fiber-rich phase in the denture base polymer can form a separate structure. The aim of this study was to determinate static three-point flexural strength and modulus of denture base polymer that had been reinforced with different fiber reinforcements. METHODS: The test specimens (3 x 5 x 50 mm) were made of auto-polymerized denture base polymer and reinforced with different fiber reinforcements. The test groups were: (A) no fibers; (B) non-impregnated polyethylene fibers; (C) light-polymerized monomer impregnated glass fibers; (D) porous polymer preimpregnated glass fibers and (E) light-polymerized monomer-polymer impregnated glass fibers. The fibers were oriented parallel to the long axis of the specimen and embedded into the denture base resin on the compression side (n=7) or tension side (n=7). Dry specimens were tested with three-point static flexural strength test set-up at crosshead speed of 5 mm/min. RESULTS: The statistical analysis by two-way analysis of variance showed that the brand and the location of the fiber reinforcements significantly influenced the flexural strength (p<0.0001). However, the location of the fiber reinforcements did not influence the flexural modulus (p<0.722). SIGNIFICANCE: The results suggest that impregnated and preimpregnated fibers reinforce denture base polymer more than non-impregnated fibers. Fiber reinforcements placed on the tensile side resulted in considerably higher flexural strength and flexural modulus values compared with same quantity of fibers placed on the compression side.

Acrylic Resins↗
PubMed2005

Influence of surface and heat treatments on the flexural strength of a glass-infiltrated alumina/zirconia-reinforced dental ceramic.

OBJECTIVES: The purpose of this study was to investigate the influence of sandblasting, grinding, grinding orientation and polishing before and after heat treatment, on the flexural strength of a glass-infiltrated alumina/zirconia-reinforced dental ceramic (In-Ceram Zirconia). METHODS: The uniaxial flexural strength was calculated on 160 bar-shaped specimens (20 x 4 x 1.2mm) divided equally into eight groups as follows: sandblasted; sandblasted heated; polished; polished heated; ground parallel to the tensile axis; ground parallel heated; ground perpendicular; and ground perpendicular heated. Data were analyzed with multiple regression analysis, one-way ANOVA and Tukey's pairwise multiple comparisons and Weibull analysis. The treated and fractured surfaces were observed with SEM. The relative content of the monoclinic phase was quantified with an X-ray diffraction analysis. RESULTS: A thin layer of glass was present on the surface of the specimens after heat treatment and contributed to an improvement of the flexural strength. Surface treatment (not followed by heat treatment) generated phase transformation which, however, was not sufficient to avoid strength degradation caused by the flaws introduced with the surface treatments. Sandblasting caused the most marked strength degradation. Polishing alone increased the reliability, but did not improve the strength. The orientation of grinding in respect of the direction of the tensile stresses did not influence the ultimate tensile strength. SIGNIFICANCE: The present study suggests that any surface treatment performed on In-Ceram Zirconia should always be followed by heat treatment to avoid strength degradation.

Aluminum Oxide↗
PubMed2004

A preliminary study of experimental polyacid-modified composite resins ('compomers') containing vinyl phosphonic acid.

OBJECTIVES: The aim of this investigation was to determine the properties of two novel compomers formulated with the monomer vinyl phosphonic acid (VPA). The setting properties, mechanical strength, wear characteristics and fluoride release of two experimental unshaded compomers containing VPA were determined, and compared with the commercial compomer Dyract A (shade C3). METHODS: Two novel compomers were prepared, containing, respectively, 0.24% (A) and 2.31% (B) by mass of VPA, and an appropriate amount of reactive glass filler. Their properties were compared with those of Dyract AP (shade A3). Depth of cure was determined according to the method of ISO 4049. Polymerization of model mixtures of bisGMA, TEGDMA and VPA was studied using FT Raman spectroscopy, by comparing the absorption at 1608cm(-1) (aromatic C-C bond) with that at 1313cm(-1) (CC aliphatic). Compressive and biaxial flexure strengths were determined for sets of 6 specimens stored either wet or dry. Wear was determined using a toothbrushing machine and an abrasive slurry, and fluoride release was determined following up to 6 weeks storage in aqueous media, using a fluoride-selective electrode. RESULTS: Of the model monomer mixtures, the one with the greater quantities of VPA showed lowest degrees of polymerization after irradiation for 40s. Compomer A had an acceptable depth of cure, and similar properties to Dyract AP in terms of compressive and biaxial flexure strength, and also fluoride release. Resistance to toothbrush abrasion of both of the experimental compomers was superior to that of Dyract AP. SIGNIFICANCE: These studies demonstrate that VPA can be used as the active monomer in experimental compomers, and is capable of yielding materials with properties equivalent to a commercial material, but with improved resistance to toothpaste abrasion. The level of VPA in the formulation is critical, because this monomer inhibits addition polymerization, hence must be used only in small amounts.

Analysis of Variance↗
PubMed2005

The effect of different light-curing units on fatigue behavior and degree of conversion of a resin composite.

OBJECTIVES: The aim of this study was to investigate the effect of different light-curing units and irradiation modes on the mechanical fatigue strength and degree of conversion of a restorative resin composite. METHODS: Conventional halogen, plasma arc and blue LED light-curing units were used for polymerization of a resin composite (Tetric) Ceram, Ivoclar, Vivadent, Liechtenstein). Initial fracture strength (FS) and flexural fatigue limit (FFL) as well as degree of conversion (DC) were measured. The FFL was determined under cyclic loading for 10(5) cycles in terms of a staircase approach. The specimens were stored for 14 days in 37 degrees C distilled water prior to testing. The curing efficiency was observed with Fourier transform infrared micromultiple internal reflectance spectroscopy. The measurements were carried out at 0.5 and 2.5 mm distance from the directly irradiated surface after 14 days storage in dark and dry conditions at 37 degrees C. RESULTS: The highest FS, FFL and DC were observed from high energy curing devices and from extended curing intervals. The conventional halogen light exhibited the most homogenous in-depth curing efficiency along with a low loss of mechanical resistance under cyclic fatigue. SIGNIFICANCE: Evaluation of flexural fatigue limit and curing efficiency correlate in terms of decreased mechanical strength due to insufficient light-curing intervals or light intensities. Initial promising fracture strengths do not correlate with a clinically more relevant fatigue loading and with the in-depth degree of conversion, both accounting for a significantly reduced strength performance.

Analysis of Variance↗
PubMed2004

Evaluation of dental restorative composites containing polyhedral oligomeric silsesquioxane methacrylate.

OBJECTIVES: The aim of this study was to explore novel polymeric dental restorative composites, in which polyhedral oligomeric silsesquioxane methacrylate monomer (POSS-MA) was used to partially (or completely) replace the commonly used base monomer 2,2'-bis-[4-(methacryloxypropoxy)-phenyl]-propane (Bis-GMA). METHODS: The composites were cured (hardened) by photo-initiated free radical polymerization. Mechanical properties (i.e. flexural strength, Young's modulus and diametral tensile strength) of the composites were tested by a universal mechanical testing machine; photopolymerization induced volumetric shrinkage was measured using a mercury dilatometer; and near infrared (NIR) technique was used to study the degree of methacrylate double bond conversion and photopolymerization rate. RESULTS: Small percentage POSS-MA substitution of Bis-GMA (i.e. mass fraction of 10% or less) in the resin system improved the mechanical properties of the composites; while large amount substitution led to less desirable mechanical properties, lower methacrylate double bond conversion, and slower photopolymerization rate. Statistical examinations showed the maximum flexural strength of the composites occurred when 10% (mass fraction) of Bis-GMA was replaced by POSS-MA, while the highest modulus occurred when the mass fraction of POSS-MA was 2%. SIGNIFICANCE: Polymeric dental restorative composites with improved mechanical properties may be designed by judicious choice of monomer (POSS-MA, Bis-GMA and TEGDMA) compositions.

Bisphenol A-Glycidyl Methacrylate↗
PubMed2005

Effect of coupling agents on the local mechanical properties of bioactive dental composites by the nano-indentation technique.

OBJECTIVES: To examine the use of nano-indentation as a method of determining the interfacial mechanics of bioactive composites for mandibular bone substitutes. METHODS: Three coupling agents (PMMA-MAA, PMMA-MA and silane) were used to treat hydroxyapatite (HA) particles before incorporation into a polymethylmethacrylate (PMMA) matrix. Nano-indentation was used to determine the hardness and Young's modulus on the HA particle surface, at the HA/PMMA interface and in the PMMA matrix region for each of the four groups. In addition bulk four-point bending tests were conducted on each of the four groups as a comparison. RESULTS: The findings resulted in significant differences in the local interfacial Young's modulus between the polymer-treated composites and the uncoupled control specimens with a marked improvement (50%) in modulus with either polymertreated group. Similarly, the bending modulus of the polymer-treated groups was significantly higher than the un-treated control group; however, these differences were not as pronounced (approximately 15%). SIGNIFICANCE: The co-polymer-treated composites resulted in improved interfacial modulus as compared to the un-treated controls and that the nano-indentation technique is a powerful tool for understanding the local interfacial mechanics of bioactive composites.

Analysis of Variance↗
PubMed2005

Influence of annealing temperature on the strength of dental glass ceramic materials.

OBJECTIVES: Dental glass ceramic components are always loaded by residual stresses because of the manufacturing process. For a reliable mechanical characterization, residual stress-free specimens are needed. Residual stresses can be removed by an annealing process. The hypothesis of this work was, that the annealing temperature must be individually chosen to reliably remove possible residual stresses without changing the characteristics of the glass ceramic material. METHODS: Knoop-indented specimens made of the glass ceramic materials Duceram Opaker (Degudent, Hanau, Germany, formerly Ducera, Rosbach, FRG), Empress 1 (Ivoclar Vivadent, Schaan, Liechtenstein), In-Ceram Alumina (Vita Zahnfabrik, Bad Säckingen, Germany), Optec OPC (Jeneric Pentron, Wellingford, USA), and Vita Omega Opaker (Vita Zahnfabrik, Bad Säckingen, Germany) were annealed at various temperatures below and above the respective glass transition temperature. The Weibull strength parameters and the lengths of the indentations before and after annealing were determined. RESULTS: A strength increase caused by relaxation of residual stresses was found after annealing at elevated temperatures. A local maximum of increased strength was determined after annealing at a temperature of 100K below the glass transition temperature. After annealing at temperatures above the glass transition temperature, microplasticity was observed. SIGNIFICANCE: It is recommended to anneal glass ceramic components that are intended to be mechanically characterized at a temperature 100K below the respective glass transition temperature before testing to determine 'true' mechanical values that are not influenced by possible residual stresses.

Aluminum Silicates↗
PubMed2005

3D FEA of cemented steel, glass and carbon posts in a maxillary incisor.

OBJECTIVES: A comparative study on the stress distribution in the dentine and cement layer of an endodontically treated maxillary incisor has been carried out by using Finite Element Analysis (FEA). The role of post and cement rigidity on reliability of endodontic restorations is discussed. METHODS: A 3D FEM model (13,272 elements and 15,152 nodes) of a central maxillary incisor is presented. A chewing static force of 10 N was applied at 125 degree angle with the tooth longitudinal axis at the palatal surface of the crown. Steel, carbon and glass fiber posts have been considered. The differences in occlusal load transfer ability when steel, carbon and glass posts, fixed to root canal using luting cements of different elastic moduli (7.0 and 18.7 GPa) are discussed. RESULTS AND SIGNIFICANCE: The more stiff systems (steel and carbon posts) have been evaluated to work against the natural function of the tooth. Maximum Von Mises equivalent stress values ranging from 7.5 (steel) to 5.4 and 3.6 MPa (respectively, for carbon posts fixed with high and low cement moduli) and to 2.2 MPa (either for glass posts fixed with high and low cement moduli) have been observed under a static masticatory load of 10 N. A very stiff post works against the natural function of the tooth creating zones of tension and shear both in the dentine and at the interfaces of the luting cement and the post. Stresses in static loading do not reach material (dentine and cement) failure limits, however, they significantly differ leading to different abilities of the restored systems to sustain fatigue loading. The influence of the cement layer elasticity in redistributing the stresses has been observed to be less relevant as the post flexibility is increased.

Bite Force↗
PubMed2005

Siloranes in dental composites.

OBJECTIVE: The purpose of this study was to compare the product profile of a Silorane based composite which polymerizes by a cationic ring opening process with the product profile of different methacrylate based restoratives. METHODS: Four methacrylate based materials Filtek Z250, Filtek P60,Tetric ceram, Spectrum TPH and a Silorane based material were investigated with regard to their compressive strength, flexural strength, E-Modulus and ambient light stability. The data were analyzed by 1-way ANOVA and 2 sample t test (p<0.05). Shrinkage data were determined by the Archimedes method and the bonded disk method. The reactivity of the Silorane and Tetric ceram were derived from the time resolved shrinkage behaviour and the development of the E-Modulus over time. RESULTS: The Silorane Composite revealed with 0.94 vol% (bonded disk method) and 0.99 vol% (Archimedes method) the lowest polymerization shrinkage among all tested composites. Its reactivity was comparable to the reactivity of Tetric Ceram. However, the ambient light stability of >10 min for Silorane was higher than the ambient light reactivity of the other tested methacrylates (55-90 s). SIGNIFICANCE: The ring opening chemistry of the Siloranes enables at the first time shrinkage values lower than 1 vol% and mechanical parameters as E-Modulus and flexural strength comparable to those of clinically well accepted methacrylate based composites.

Composite Resins↗
PubMed2005

The influence of short and medium-term water immersion on the hydrolytic stability of novel low-shrink dental composites.

OBJECTIVES: Differences in mechanical and physical properties exhibited by novel low-shrink resin-based composite (RBC) formulations compared with conventional methacrylate RBCs may contribute to the clinical success of the candidate material. The aim of the current study was to investigate the effect of water uptake characteristics and water solubility on the mechanical properties of two methacrylate (Z100 and Filtek Z250), an experimental oxirane (OXI) and silorane (SIL) RBC following short- and medium-term immersion. METHODS: The water sorption/solubility and associated diffusion coefficients of each material (n=5) were measured using gravimetric analysis following short- (0.1, 0.5, 1, 4, 24 and 48 h) and medium-term (1, 4, 12 and 26w) immersion. The bi-axial flexure strength, associated Weibull moduli (n=20) and fracture analysis using scanning electron microscopy (SEM) of each material for similar immersion periods was also investigated. RESULTS: Following 0.5h and each subsequent short- and medium-term immersion period the water sorption of Z100 and Filtek Z250 was decreased compared with OXI. A significant decrease in bi-axial flexure strength and associated increase in filler particle exfoliation identified through SEM was identified for OXI compared with Z100, Filtek Z250 and SIL following 26w immersion. SIL exhibited the significantly lowest water sorption, solubility and associated diffusion coefficient following each immersion period. SIGNIFICANCE: The increase in water sorption, solubility and the associated diffusion coefficient of the experimental oxirane RBC, OXI was manifested as a significant decrease in bi-axial flexure strength and attributed to the decrease in synergy between the filler particles and resin matrix. The decreased water sorption, solubility and associated diffusion coefficient of the experimental silorane RBC, SIL may potentially improve hydrolytic stability of RBC restorations demonstrated by the non-significant decrease in bi-axial flexure strength following medium-term immersion.

Absorption↗
PubMed2005

The reliability of standardized flexure strength testing procedures for a light-activated resin-based composite.

OBJECTIVES: To investigate the differences in the reliability of three-point flexure strength (TFS) and bi-axial flexure strength (BFS) data of a dental resin-based composite (RBC) irradiated by a hand-held or an oven light-curing unit (LCU). METHODS: Three-point bar-shaped (25 x 2 x 2 mm3) and bi-axial disc-shaped (12 mm diameter, 2 mm thick) specimens of Filtek Z250 were polymerized utilizing either a hand-held (n = 20) or an oven-LCU (n = 20). The mean TFS and BFS, associated Weibull moduli and degree of conversion (DC) for each curing regime were obtained following 24 h immersion in a light-proof water bath maintained at 37 +/-1 degrees C. RESULTS: A significant decrease in TFS (129 +/- 15 and 127 +/- 13 MPa) compared with BFS (140 +/- 12 and 148 +/- 13 MPa) was identified for specimens irradiated with both LCU types (P < 0.001). The Weibull moduli of TFS data associated with the hand-held--was significantly decreased compared with the oven-LCU since confidence intervals did not overlap (7.5-9.4 and 9.5-10.6, respectively). In contrast, the Weibull moduli of the BFS data associated with either LCU were not significant (11.3-12.4 and 11.3-13.5). A significant decrease in the DC of three-point and bi-axial flexure specimens irradiated with the hand-held compared with the oven-LCU was reported (P = 0.031). CONCLUSIONS: The improved experimental reliability combined with the increased clinical relevance in specimen geometry of disc-compared with bar-shaped specimens may advocate bi-axial flexure testing methodology as the standard to assess the strength of light-activated dental RBCs. The differences in extent of polymerization of RBC specimens cured with either LCU were not consistent with an equivalent dose of light energy density. This phenomenon may be attributed to differences in polymerization efficiency associated with the quantity of useful light energy emitted from the hand-held--compared with the oven-LCU.

Composite Resins↗
PubMed2005

The influence of calcium fluoride (CaF2) on biaxial flexural strength of apatite-mullite glass-ceramic materials.

OBJECTIVE: The aim of this study was to evaluate the effect of varying the molar percentage of calcium fluoride (CaF2) on the biaxial flexural strength (BFS) of apatite-mullite glass-ceramics. METHODS: Three apatite-mullite glass-ceramic materials were produced based on a formula of 4.5SiO(2)-3Al2O(3)-1.5P2O(5)-3CaO-XCaF2, where X=0.5, 1 and 3 and called HG 1-3, respectively. These materials were used to produce discs of 2 mm thickness and 12 mm diameter using the lost-wax casting process. 30 discs per material were produced, 10 discs per material were cast and then left to bench cool (glass state), 10 discs per material were given a heat treatment at 765, 679 and 629 degrees C for 1h and then heat treated at 890, 860 and 824 degrees C for the HG 1-3, respectively, for another hour to form apatite. Ten discs per material were heat treated as previously described (765, 679 and 629 degrees C) then heat treated for 1h at 1022, 987 and 892 degrees C for the HG 1-3, respectively, to form apatite-mullite. The heat treatment temperatures were obtained from differential thermal analysis data. A lithium disilicate glass-ceramic was used as a control. Biaxial flexural strength (BFS) was determined using a LIoyd 2000R tester. RESULTS: Data showed that the BFS increased as the fluoride content increased, and the apatite-mullite samples had significantly higher BFS values than the as cast glass or apatite samples (p<0.05), with the control having significantly higher BFS values than all the HG glass-ceramic materials for every condition (p<0.05). The fictive glass transition temperature (Tg) was observed to drop with increasing fluoride content. SIGNIFICANCE: Increasing the CaF2 content increased the BFS and decreased the Tg of the glass-ceramic materials tested.

Aluminum Silicates↗
PubMed2005

Novel amino acid modified zinc polycarboxylates for improved dental cements.

OBJECTIVE: The objective of this study was to develop a novel amino acid modified zinc/calcium polycarboxylate cement system, formulate the cements, and evaluate their mechanical strengths. MATERIALS AND METHODS: Acrylate and methacrylate derivatives of four amino acids were synthesized and characterized using FT-IR and 1HNMR spectroscopy. The derivatives were formulated with polymer having pendent methacrylate group, water, and synthesized novel filler. Compressive (CS) as well as flexural strengths (FS) and viscosities of the resin liquids were used as tools to evaluate the formulations and formed cements. The specimens for CS and FS tests were conditioned in distilled water at 37 degrees C for 24 h and 7 d, respectively, prior to testing. RESULTS: The measured CS and FS of the cements was in the decreasing order of methacryloyl beta-alanine > acryloyl glutamic acid = acryloyl beta-alanine > methacryloyl glutamic acid > 2-hydroxyethyl methacrylate. Methacryloyl beta-alanine was selected for further formulations due to its relatively low solution viscosity and high CS as well as FS. Effects of polymer content, P/L ratio, tartaric acid and initiator concentration were significant. During aging, the cement showed a constant increase in CS for up to 1 month and then kept constant for up to 3 months. CONCLUSIONS: This study developed a novel amino acid modified zinc/calcium polycarboxylate cement system. This system was 85% higher in CS, 98% higher in DTS and 183% higher in FS, compared to Durelon.

Amino Acids↗
PubMed2005

Effect of water storage, thermocycling, the incorporation and site of placement of glass-fibers on the flexural strength of veneering composite.

OBJECTIVES: To evaluate the effects of water storage, thermocycling, and the incorporation of glass-fibers, on the flexural strength of veneering composites. METHODS: Veneering composites with different fillers, matrices and polymerization methods (Belleglass Kerr Inc., Orange, CA, USA; Sculpture, Pentron Inc. Wallingford CT, USA; Sinfony, 3M Espe, Seefeld, Germany; SR Adoro LC and HP, Targis, Ivoclar Vivadent, Schaan, Liechtenstein), a glass-fiber framework material (Vectris Pontic VP, Ivoclar Vivadent) and a direct restorative composite control (Tetric Ceram, Ivoclar Vivadent) were selected. For the first part of the study, 30 bar specimens (25 x 2 x 2 mm3) per material were fabricated. Ten were stored for 24 h and 10 for 14 days in water at 37 degrees C. Ten were thermocycled (3000 x; 5-50-5 degrees C). Three-point bending tests (crosshead speed: 0.5 mm/min) were performed. For the second part of the study, all veneering materials were combined with a glass-fiber framework (VP). Sixty specimens were produced for each material (25 x 4 x 2 mm3) and treated as in the first part. Three-point bend tests were performed with the reinforcing glass-fiber framework either on the tension or the compression side. Data was evaluated by ANOVA and Weibull analysis. RESULTS: A decrease in flexural strength was observed after water storage or thermocycling for all veneering materials tested. None of the tested materials exhibited significant advantages compared to the control. The flexural strength of glass-fiber reinforced frameworks was ten times higher and not influenced by water storage or thermocycling. A significant reinforcing effect from glass fibers was observed when they were placed on the tension but not when placed on the compression side. SIGNIFICANCE: A glass-fiber framework on the tension side significantly improved the flexural strength of veneering composites. There was less deterioration due to water storage and thermocycling with the glass-fiber reinforced veneering composite compared to the non-reinforced materials.

Bisphenol A-Glycidyl Methacrylate↗
PubMed2005

Effects of silicon coating on bond strength of two different titanium ceramic to titanium.

OBJECTIVES: This study investigated the effect of silicon coating (SiO2) by magnetron sputtering on bond strength of two different titanium ceramics to titanium. METHODS: Sixty cast titanium specimens were prepared following the protocol ISO 9693. Titanium specimens were divided into two test and control groups with 15 specimens in each. Test groups were silicon coated by the magnetron sputtering technique. Two titanium ceramics (Triceram and Duceratin) were applied on both test (coated) and control (uncoated) metal specimens. The titanium-ceramic specimens were subjected to a three point flexural test. The groups were compared for their bond strength. SEM and SEM/EDS analyses were performed on the delaminated titanium surfaces to ascertain bond failure. RESULTS: The mean bond strength of Ti-Duceratin, Ti-Triceram, Si-coated Ti-Duceratin and Si-coated Ti-Triceram were 17.22+/-2.43, 23.31+/-3.18, 23.21+/-3.81 and 24.91+/-3.70 MPa, respectively. While the improvement in bond strength was 30% for Duceratin, it was statistically insignificant for Triceram. An adhesive mode of failure was observed in the Duceratin control group. In the silicoated Duceratin specimen, the bonded ceramic boundaries were wider but less than in the silicoated Triceram specimen. In the coated Triceram specimen, the ceramic retained areas were frequent and the failure mode was generally cohesive. SIGNIFICANCE: Silicon coating was significantly effective in both preventing titanium oxide layer formation and in improving bond strength for Duceratin. However, it was of less value for Triceram.

Adhesiveness↗
PubMed2005

Evaluation of two Bis-GMA analogues as potential monomer diluents to improve the mechanical properties of light-cured composite resins.

OBJECTIVES: The aim of this study was to investigate the influence of new diluent agents, diluent ratio and filler content, on relevant mechanical properties of several novel composite resins containing Bis-GMA as resin matrices, and to compare these with the properties of composites based on TEGDMA, a conventionally used diluent. METHODS: Two Bis-GMA analogues were synthesized and 20 experimental composite resins were prepared combining three monomer mixtures (Bis-GMA/TEGDMA, Bis-GMA/CH3 Bis-GMA and Bis-GMA/CF3 Bis-GMA), at three dilution rates (85/15, 10/90, 0/100) and three levels of hybrid filler content (barium aluminosilicate glass): 0, 10 and 35%. Flexural strength (FS), modulus of elasticity (ME) and microhardness (VHN) of the composites were evaluated. Five specimens of each material were prepared for each mechanical test, light-cured over 120 s and stored in water at 37 degrees C for 1 week. Three-point bending test was used for FS measurement and VHN was quantified by using a Vickers microindentor. Data were analyzed by ANOVA and Student-Newman-Keuls tests (P<0.05). RESULTS: Materials with CH3 Bis-GMA showed an enhanced VHN. Mean FS was higher for matrices containing TEGDMA. Overall, dilution favored FS and VHN but not ME. Filler loading specially improved ME and VHN. SIGNIFICANCE: Results correlate with an increase in the extent of polymerization due to the higher flexibility of the less viscous comonomer starting system and the hydrophobic character of the Bis-GMA analogues.

Aluminum Silicates↗
PubMed2005

Synthesis and photopolymerization of low shrinkage methacrylate monomers containing bulky substituent groups.

OBJECTIVES: This study was conducted to determine whether novel photopolymerizable formulations based on dimethacrylate monomers with bulky substituent groups could provide low polymerization shrinkage without sacrifice to degree of conversion, and mechanical properties of the polymers. METHODS: Relatively high molecular weight dimethacrylate monomers were prepared from rigid bisphenol A core groups. Photopolymerization kinetics and shrinkage as well as flexural strength and glass transition temperatures were evaluated for various comonomer compositions. RESULTS: Copolymerization of the bulky monomers with TEGDMA show higher conversion but similar shrinkage compared with Bis-GMA/TEGDMA controls. The resulting polymers have suitable mechanical strength properties for potential dental restorative materials applications. When copolymerized with PEGDMA, the bulky monomers show lower shrinkage, comparable conversion, and more homogeneous polymeric network structures compared with Bis-EMA/PEGDMA systems. SIGNIFICANCE: The novel dimethacrylate monomers with reduced reactive group densities can decrease the polymerization shrinkage as anticipated, but there is no significant evidence that the bulky substituent groups have any additional effect on reducing shrinkage based on the physical interactions as polymer side chains. The bulky groups improve the double bond conversion and help maintain the mechanical properties of the resulting polymer, which would otherwise decrease rapidly due to the reduced crosslinking density. Further, it was found that bulky monomers help produce more homogeneous copolymer networks.

Benzhydryl Compounds↗
PubMed2005

Compatibility between self-etching adhesive and self-curing resin by addition of anion exchange resin.

OBJECTIVE: The aim was to investigate whether anion exchange resin powder in the OH(-) form, added to the amine component of self-cured resin can deprotonize acid groups of a self-etching adhesive and thus eliminate incompatibility caused by amine neutralization. METHODS: Shear bond strength (SBS) of a self-cured CorePaste (COP), bonded either with all-in-one adhesive iBond (IBO) or with IBO coated with a self-cured experimental resin (SCR), loaded with 0, 8, 16, or 32 wt% of anion exchange resin powder (AER) in OH- form, were determined on 80 enamel and dentin surfaces each after 24 h water storage. IBO specimens were either light-activated or not. Flexural modulus and strength of the four SCR resins were determined by three-point bending. Data was analyzed by one-way ANOVA and Duncan's post hoc test (p<0.05). RESULTS: Enamel SBSs of COP on IBO were 20-25 MPa, in combination with SCR (0 up to 32%) >25 MPa for activated or non-activated IBO. COP on IBO produced no bond on dentin, with the non-loaded SCR 5-10 MPa SBS was achieved, and 15 and 21 MPa were measured with the three AER-loaded SCRs on activated and non-activated IBO, respectively. Flexural moduli of SCR with 0 and 8% AER were higher than with 16 and 32%. Flexural strengths were not significantly different. SIGNIFICANCE: Addition of anion exchange resin to the amine component of self-cured resin is an effective means of enhancing the bond strength on dentin and to prevent amine neutralization through the acid groups of self-etching primer adhesives.

Acid Etching, Dental↗