A partially aromatic urethane dimethacrylate as a new substitute for Bis-GMA in restorative composites.

OBJECTIVES: The objective of this study was to investigate the use of a new, partially aromatic urethane dimethacrylate in visible-light cured resin-based composite restoratives. Selected mechanical properties, such as flexural strength and flexural modulus of elasticity, of model monomer mixtures and composites containing the new urethane dimethacrylate were investigated and compared to the properties of materials that are based on Bis-GMA, at present the most frequently used cross-linker in restorative composites. In addition, the polymerization shrinkage and the water sorption of selected composites were determined. METHODS: The flexural strength, flexural modulus of elasticity, and the water sorption were determined according to ISO 4049:2000. Test specimens (rods: 2 mmx2 mmx25 mm; discs: d=15 mm and h=1 mm) of the investigated composites were prepared in stainless steel molds and light-cured (150 mW/cm2, 2x180 s). The flexural strength and flexural modulus of rods were measured after the samples had been stored under 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. The water sorption was determined with discs. The polymerization shrinkage was calculated from the densities of the uncured composite pastes and cured composites. RESULTS: Visible light cured mixtures of dimethacrylate diluents with the new urethane dimethacrylate and composites based on these mixtures show a reactivity, flexural strength, flexural modulus of elasticity, polymerization shrinkage and water sorption similar to those of materials that are based on Bis-GMA. The composites did not show any strong deterioration of the mechanical properties after water storage.     

Sol-gel materials 2. Light-curing dental composites based on ormocers of cross-linking alkoxysilane methacrylates and further nano-components.

OBJECTIVES: The objective of this study was to investigate the use of ormocers, which were synthesized from amine or amide dimethacrylate trialkoxysilanes. Ormocers showed improved biocompatibility in dimethacrylate-diluent-free composite restoratives. Selected mechanical properties, such as flexural strength and flexural modulus of experimental composites containing ormocers were investigated. In addition, the influence of methacrylate-substituted ZrO2 clusters and SiO2 organosols on the mechanical properties of composites was studied. METHODS: The flexural strength and flexural modulus of elasticity were determined according to ISO 4049: 2000. For this purpose, test specimens (2mmx2mmx25mm) of the composites investigated were prepared in stainless steel moulds and light-cured (150mW/cm2, 2x180s). The flexural strength and flexural modulus of elasticity were measured after the samples had been stored in water for 24h at 37 degrees C. RESULTS: While visible light-cured dimethacrylate-diluent-free composite restoratives based on the investigated ormocers showed a similar flexural strength and flexural modulus of elasticity compared to composites that contain only dimethacrylates, their double bond conversion was considerable lower. The simultaneous addition of methacrylate-substituted ZrO2 clusters and SiO2 organosols to the ormocer composite improved the mechanical properties of the composites. SIGNIFICANCE: Ormocers of amine or amide dimethacrylate trialkoxysilanes enabled the preparation of dimethacrylate-diluent-free composite restoratives. Based on the lower cytotoxicity of the ormocers, the prepared restorative composites should show improved biocompatibility. With the addition of nanoparticles, such as methacrylate-substituted ZrO2 clusters or SiO2 organosols, the mechanical properties of composites can be improved.     

Benzoyl germanium derivatives as novel visible light photoinitiators for dental materials.

OBJECTIVES: The objective of this study was to investigate the use of benzoyl germanium derivatives as a novel visible light photoinitiator of resin-based dental composites. Selected mechanical properties, such as flexural strength and flexural modulus, setting time, storage stability, and UV light stability, of the composites based on the novel photoinitiators benzoyltrimethylgermane (BTMGe) or dibenzoyldiethylgermane (DBDEGe) were investigated and compared to the properties of materials that are cured with a mixture of camphorquinone (CQ) and ethyl 4-(N,N-dimethylamino)benzoate (EMBO). METHODS: The flexural strength and flexural modulus of elasticity were determined according to ISO 4049. 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 s x 180 s). The flexural strength and flexural modulus of elasticity were measured after immersing the cured specimens in water for 24h at 37 degrees C and in certain cases, after they had been boiled for 24h in water. In addition, the setting time, curing depth, storage and UV stability of selected composites were determined. RESULTS: The novel photoinitiators BTMGe or DBDEGe can be used to substitute the binary photoinitiator CQ/EMBO in visible light-cured restorative composites. Especially, DBDEGe showed a significantly higher photocuring activity in composites with a filler load of about 60 wt. % in comparison to that of CQ/EMBO. In addition, composites based on BTMGe or DBDEGe showed an improved UV stability and a storage stability comparable to that of CQ/EMBO-based composites.     

Influence of veneering composite composition on the efficacy of fiber-reinforced restorations (FRR)

This study investigated the influence of fiber reinforcement on the flexural properties of four commercial (Artglass, Belleglass HP, Herculite XRV and Solidex) veneering composites (Series A) and two experimental composites (Series B&C). This study investigated how the composition of the veneering composites influenced the enhancement of strength and modulus produced by fiber reinforcement. The formulation of the experimental composites were varied by changing the filler load (Series B) or the resin matrix chemistry (Series C) to assess the effect these changes would have on the degree of reinforcement. In Series A, the commercial veneering composites were reinforced by an Ultra-High-Molecular-Weight Polyethylene fiber (UHMW-PE/Connect) to evaluate flexural properties after 24 hours and six months. In Series B, experimental composites with the same organic matrix but with different filler loads (40% to 80% by weight) were also reinforced by Connect fiber to evaluate flexural properties. In Series C, experimental composites (Systems 1-4) with the same filler load (76.5% by weight) but with different organic matrix compositions were reinforced by Connect fiber to evaluate flexural properties. For Series B and C, flexural properties were evaluated after 24 hours water storage. All the samples were prepared in a mold 2 mm x 2 mm x 25 mm and stored in distilled water at 37 degrees C until they were ready for flexural testing in an Instron Universal Testing Machine using a crosshead speed of 1 mm/minute. The results showed no significant differences in the flexural strength (FS) between any of the commercial reinforced composites in Series A. The flexural modulus (FM) of the fiber-reinforced Belleglass HP group was significantly higher than for Artglass and Solidex. Water storage for six months had no significant (p>0.05) effect on the flexural strength of three of the four reinforced veneering composites. The flexural strength for Artglass was significantly reduced (p<0.05) by six-month water storage. In Series B, however, increasing the amount of filler loading improved the flexural modulus of the reinforced experimental composite but had no effect on its flexural strength. In Series C, changing the organic matrix formulation had no affect on flexural strength but affected the flexural modulus of the reinforced experimental composite.     

Effect of monomer structure on the mechanical properties of light-cured composite resins

The effects of monomer structure on the mechanical properties of visible light-cured composite resins based on the seven types of aromatic dimethacrylates were investigated. The results of this study suggested that the mechanical properties of the composite resins were dependent upon the chemical structure of the dimethacrylate monomers employed. The composites based on dimethacrylates with hydroxy groups showed a relatively significant decrease in flexural strength, elastic modulus, and compressive proportional limit under wet conditions. The segmental mobility of dimethacrylate monomers considerably influenced the nature of cured composites. Bis-GMA-F-based composite showed superior mechanical properties to a conventional Bis-GMA-based material. The SEM observation of fractured surfaces revealed that failure mainly occurred through the resin matrix of the composite resins.     

Properties of eight methacrylated beta-cyclodextrin composite formulations.

OBJECTIVES: Methacrylated beta-cyclodextrins (MCDs) are novel candidate dental monomers if all or some of the hydroxyl groups of beta-cyclodextrin are substituted with methacrylate groups. The main objective of this study was to evaluate mechanical properties of a number of composite formulations having MCDs as novel dental comonomers. The properties determined were flexural strength (FS), volumetric shrinkage (VS), and degree of conversion (DC). METHODS: A mass fraction of 50% of MCD monomers was mixed with a mass fraction of 50% each of a series of dimethacrylate or monomethacrylate diluent comonomers to produce consistent formulations of a workable viscosity. For comparison a resin mixture of a mass fraction of 50% Bis-GMA and a mass fraction of 50% triethyleneglycol dimethacrylate (a typical dental resin mixture) was also studied. The mixtures were activated with camphorquinone and ethyl 4-dimethylamino benzoate. One part by mass of each activated resin formulation was mixed with three parts by mass of glass filler. Samples for the FS tests were prepared in (2 x 2 x 25) mm3 molds by light-curing the composites for 2 min on each side. The cured samples were immersed in 37 degrees C water for 24 h, and FS was measured with an Instron machine at a crosshead speed of 0.5 mm/min. VS was measured by a computer-controlled mercury dilatometer. DC was measured by near-infrared spectroscopy. RESULTS: The properties of the MCD-based composites depended on the kind of diluent used. With these MCD monomers, diluents of triethyleneglycol dimethacrylate, 1,10-decamethylenediol dimethacrylate, or benzyl methacrylate yielded the best composite properties. SIGNIFICANCE: Although not yet fully optimized, MCD-based composite formulations containing triethyleneglycol dimethacrylate, 1,10-decamethylenediol dimethacrylate, or benzyl methacrylate yielded flexural strength and volumetric shrinkage values were comparable to those of the Bis-GMA/triethyleneglycol dimethacrylate controls. These findings lend support for further development and evaluations of polymerizable cyclodextrin derivatives for use in dental materials.     

Thermo-hydrolytic stability of core foundation and restorative composites

STATEMENT OF PROBLEM: The use of weak and less durable materials in restoring teeth may result in weak restorations unable to withstand intraoral conditions. PURPOSE: The purposes of this study were to evaluate the effect of thermo-hydrolytic stress on the flexural strength and flexural modulus of core foundation composites with direct restorative composites and determine mass percentage of filler content. MATERIAL AND METHODS: A total of 216 specimens, from 9 brands of commercially available composites (Coreflo, DC Core, Photocore, APX, Litefil II A, Surefil, TPH Spectrum, Z100, and Z250) were fabricated following ISO Standard 4049. Flexural strength (MPa) and flexural modulus (GPa) were determined on bar-shaped specimens (25 x 2 x 2 mm) before and after storage in boiling water for 24 hours (n=12). The filler content in composite was determined by incineration using a thermogravimetric analyzer. The data were analyzed using 2-way analysis of variance and the Student t test (alpha=.05). RESULTS: Filler content of the tested composites was 66.6 to 81.8 mass %. Significant differences in both flexural strength and flexural modulus existed among materials, the effect of boiling and interaction (P<.05). Coreflo, DC Core, Z100, and Z250 demonstrated a significant decrease in flexural strength after boiling (P<.05). Z250 showed a significant decrease in flexural modulus after boiling (P=.001), while Surefil showed a significant increase in flexural modulus (P=.007). CONCLUSION: Within the limitations of this study, it can be concluded that composites were affected differently by moist heat stress. Some composites showed a degradation of flexural properties while some retained flexural properties. Stability of the composites varied among brands.     

Comparison of flexural properties of composite restoratives using the ISO and mini-flexural tests

The purpose of this study was to investigate the flexural properties (flexural strength and flexural modulus) of four commercial composite restoratives (Silux Plus, Z100, Ariston and Surefil) using the ISO 4049 flexural test (IFT) and a mini-flexural test (MFT). Both tests involved the use of three-point loading and the same fixture. The difference between the tests was in the length of the composites specimens and the distance between the supports [20 mm (IFT) and 10 mm (MFT)]. Six specimens were made for each material and flexural test. Test specimens [25 x 2 x 2 mm (IFT) and 12 x 2 x 2 mm (MFT)] were fabricated according to manufacturers' recommendations. After light-polymerization, the specimens were stored in distilled water at 37 degrees C for 24 h. The specimens were subsequently blotted dry, measured and subjected to flexural testing using an Instron Universal Testing Machine with a crosshead speed of 0.75 mm min(-1). Data was analysed using anova/Scheffe's, paired samples test (P < 0.05) and Pearson's correlation (P < 0.01). For both IFT and MFT, results of statistical analysis of flexural strength were identical. Silux had significantly lower flexural strength compared with the other composites and the flexural strength of Ariston was significantly lower than Z100 and Surefil. For IFT, the flexural modulus of Z100 was significantly higher than Silux, Ariston and Surefil while for MFT, Silux had significantly lower modulus compared with Z100, Ariston and Surefil. A significant, strong and positive correlation (r = 0.95) was observed for flexural strength between IFT and MFT. Correlation for flexural modulus was also significant and positive but was weaker (r = 0.53). As MFT has the advantage of ease of specimen fabrication and is more clinically realistic, it is suggested for the testing of composite restoratives. CLINICAL RELEVANCE: The mini-flexural test may be better than the ISO flexural test for screening of composite restoratives for clinical applications.     

预浸润玻璃纤维强化复合树脂的力学性能

大学口腔医院　修复科;2.北京大学口腔医院　材料教研室,北京100081) [摘要]　目的　研究预浸润玻璃纤维对不同复合树脂的强化效果。方法　制作Sinfony和belleGlass两种复合树脂的加入和不加预浸润玻璃纤维的标准试件(25 mm×2 mm×2 mm),于(37±1)℃的蒸馏水环境中保存24 h后,在万能力学试验机上测试弯曲强度和弹性模量。结果　Sinfony复合树脂加入纤维后弯曲强度和弹性模量显著提高,分别为(555·76±67·31)MPa和(12·59±3·06)GPa,较不加玻璃纤维试件平均提高了4·9和2·5倍(P=0);belleGlass复合树脂加入纤维后弹性模量有提高,为(14·10±2·88)Gpa,较不加玻璃纤维试件平均提高了0·9倍(P=0),而弯曲强度提高不明显。结论　预浸润玻璃纤维可以显著提高复合树脂的力学性能,但对不同复合树脂的强化效果有明显差别。     

Synthesis and evaluation of modified urethane dimethacrylate resins with reduced water sorption and solubility

ObjectivesNew aliphatic and aromatic urethane dimethacrylate monomers containing pendant phenyl methoxy or ethyl substituents were synthesized in order to reduce the water sorption and solubility of urethane dimethacrylate systems. Selected properties including flexural strength, flexural modulus, water sorption and solubility, and water contact angle were evaluated. Hoy's solubility parameters were also calculated to rank copolymer hydrophilicity.MethodsFilled (20%) composite resins were formulated with each of the newly synthesized dimethacrylates as well as the commercially available urethane dimethacrylate monomer, UDMA. Flexural strength, flexural modulus, water sorption and solubility of the urethane composites were evaluated after light-cured specimens were immersed in water for seven days. Water contact angles were measured on the surface of each material. Data were analyzed using ANOVA and Ryan–Einot–Gabriel–Welsch multiple range tests (α = 0.05).ResultsA significant reduction of nearly 30% and 40% in water uptake was observed with composite polymers containing pendant ethyl and phenyl methoxy groups, respectively, compared to UDMA (p < 0.05). Urethane copolymers containing pendant ethyl groups also showed a significant reduction in water solubility (p < 0.05). A positive correlation was found between contact angle and water sorption as well as Hoy's δ_h for hydrogen bonding forces.SignificanceThe results of this study indicate that the incorporation of pendant hydrophobic substituents within the monomer backbone may be an effective method in reducing the water sorption and water solubility of urethane based dimethacrylate systems. The use of Hoy's solubility parameters to determine the relative hydrophilicity of a polymer may be limited by its three-dimensional chemical structure.     

Influence of shade and storage time on the flexural strength, flexural modulus, and hardness of composites used for indirect restorations

STATEMENT OF PROBLEM: Fracture resistance, elastic modulus, and hydrolytic degradation resistance are important properties of indirect composite restorations. Composite systems developed specifically for indirect application are said to have enhanced mechanical properties due to their elevated monomer conversion. PURPOSE: This study evaluated the influence of shade and the effect of 30-day water storage on the flexural strength, flexural modulus, and hardness of 4 commercially available indirect composite systems and 1 composite used with the direct technique. MATERIAL AND METHODS: A variety of commercially available indirect resin composites (Artglass, Belleglass, Sculpture, and Targis) and 1 directly placed composite (Z100, control) were used. Specimens made with either incisal or dentin shade (n = 10) were fractured with a 3-point bending test. Pre-failure loads corresponding to specific displacements of the crosshead were used for flexural modulus calculation. Knoop hardness was measured on fragments (n = 3) obtained after the flexural test. Tests were performed after 24 hours and after a 30-day water storage at 37 degrees C. Flexural strength data were analyzed with the Weibull distribution. Flexural modulus and Knoop hardness data were analyzed with 3-way ANOVA and Tukey's post-hoc test (alpha=0.05). RESULTS: In general, the directly placed composite (Z100) demonstrated flexural strength similar to that of Artglass, Targis, and Sculpture. Belleglass presented the highest flexural strength (221.7 MPa for incisal shade after 24 hours storage; 95% confidence interval: 208.3-235.4). Z100 demonstrated the highest flexural modulus (range: 10.9 +/- 0.6 to 12.0 +/- 0.9 GPa) and Targis the lowest (range: 5.1 +/- 0.5 to 5.9 +/- 0.9 GPa). Sculpture was the only material that showed differences in flexural strength with respect to shade (incisal-24 hours: 149.8 MPa; incisal-30 days: 148.7 MPa; dentin-24 hours: 200.0 MPa; dentin-30 days: 177.9 MPa). The flexural modulus and hardness of the dentin shade of Sculpture were higher than those of the incisal shade after 30 days. Belleglass also showed a significant difference in flexural modulus (dentin-24 hours: 11.1 GPa; incisal-24 hours: 9.6 GPa). The effect of water storage was more evident on hardness since all composite systems softened after 30 days. Prolonged water storage decreased flexural strength only for Artglass-dentin and Z100, both incisal and dentin shades. Water aging did not affect the flexural modulus of any composite tested. CONCLUSION: In general, indirect composites did not show enhanced mechanical properties compared to the directly placed composite. Property differences due to shade were more evident for Sculpture. Prolonged water storage had a deleterious effect on the hardness of all composites tested. However, water storage did not affect the flexural strength of most of the indirect composites or the flexural modulus of any composite tested.     

Carbon fiber reinforced root canal posts Mechanical and cytotoxic properties

The aim of this study was to compare the mechanical properties of a prefabricated root canal post made of carbon fiber reinforced composites (CFRC) with metal posts and to assess the cytotoxic effects elicited. Flexural modulus and ultimate flexural strength was determined by 3 point loading after CRFC posts had been stored either dry or in water. The bending test was carried out with and without preceding thermocycling of the CFRC posts. The cytotoxicity was evaluated by an agar overlay method after dry and wet storage. The values of flexural modulus and ultimate flexural strength were for dry stored CFRC post 82±6 GPa and 1154±65 MPa respectively. The flexural values decreased significantly after water storage and after thermocycling. No cytotoxic effects were observed adjacent to any CFRC post. Although fiber reinforced composites may have the potential to replace metals in many clinical situations, additional research is needed to ensure a satisfying life-span.     

Flexural properties of fiber reinforced composite using a vacuum/pressure or a manual adaptation manufacturing process

PURPOSE: This study investigated the influence of fiber content and water storage on the flexural strength of beams made of two fiber-reinforced composites (FRC), the Vectris and the FibreKor system. MATERIAL AND METHODS: A manual adaptation method (FibreKor, n=30) and a vacuum/pressure process (Vectris, n=30) were compared using 25x4x2mm(3) beams. One group of the Vectris (n=10) and the FibreKor beams (n=10) was stored in water for 24h, a further group was thermal-cycled (TC) 6000x5 degrees C/55 degrees C, and a third group was stored in water for 30days at 37 degrees C. All beams were then loaded to failure using a three-point bending test and the flexural strength was calculated. Finally, the fiber volume percent (vol%) was determined. RESULTS: Generally, the flexural strength decreased significantly with increasing storage time independent of the investigated fiber- and/or manufacturing system. With the parameters 24h/TC/30days, the mean of flexural strength for the Vectris beams was 618/579/545N/mm(2), and for FibreKor 585/534/499N/mm(2). A fiber content of 28.1+/-0.4vol% was assessed for the Vectris beams and 12.8+/-0.6vol% for the FibreKor beams. After 24h storage in water, the Vectris and the FibreKor beams demonstrated a statistically significant higher flexural strength than after 30days storage in water. CONCLUSIONS: A vacuum/pressure manufacturing process in contrast to manual adaptation, resulted in a markedly higher fiber content, but did not necessarily lead to significantly higher flexural strength. Not only the fiber content, but also matrix composition as well as the bond between fibers and matrix determined the properties of FRC.     

Flexural properties of fiber reinforced root canal posts.

OBJECTIVES: Fiber-reinforced composite (FRC) root canal posts have been introduced to be used instead of metal alloys and ceramics. The aim of this study was to investigate the flexural properties of different types of FRC posts and compare those values with a novel FRC material for dental applications. METHODS: Seventeen different FRC posts of various brands (Snowpost, Carbopost, Parapost, C-post, Glassix, Carbonite) and diameters, (1.0-2.1 mm) and a continuous unidirectional E-glass FRC polymerized by light activation to a cylindrical form (everStick, diameter 1.5 mm) as a control material were tested. The posts (n=5) were stored at room's humidity or thermocycled (12.000 x, 5 degrees C/55 degrees C) and stored in water for 2 weeks before testing. A three-point bending test (span=10 mm) was used to measure the flexural strength and modulus of FRC post specimens. RESULTS: Analysis of ANOVA revealed that thermocycling, brand of material and diameter of specimen had a significant effect (p<0.001) on the fracture load and flexural strength. The highest flexural strength was obtained with the control material (everStick, 1144.9+/-99.9 MPa). There was a linear relationship between fracture load and diameter of posts for both glass fiber and carbon fiber posts. Thermocycling decreased the flexural modulus of the tested specimens by approximately 10%. Strength and fracture load decreased approximately 18% as a result of thermocycling. SIGNIFICANCE: Considerable variation can be found in the calculated strength values of the studied post brands. Commercial prefabricated FRC posts showed lower flexural properties than an individually polymerised FRC material.     

Influence of polymerization mode on flexural properties of esthetic resin luting agents

STATEMENT OF PROBLEM: Dual-polymerized esthetic resin luting agents have become popular. However, it is not clear whether the autopolymerized versions of such products have adequate strength to meet clinical requirements. PURPOSE: The aim of this study was to investigate the effect of different polymerization modes on the flexural properties of esthetic resin luting agents. MATERIAL AND METHODS: Ten esthetic resin luting agents were studied. Materials with 3 polymerization modes (dual, auto, and light) were Appeal, Calibra, Illusion, Lute-It, and Variolink-II; those with 2 polymerization modes (dual and auto) were Bistite-II-DC, Cement-It-C&B, Clearfil-DC-Cement, Linkmax, and Nexus2-Dual-Syringe. Five flexural strength specimens (2 x 2 x 25 mm) were made for every available polymerization mode for each material. The specimens were stored in distilled water for 24 hours at 37 degrees C. The specimens were then tested for flexural strength (MPa) and flexural modulus (GPa) using the 3-point bending method on a universal material testing machine at a cross-head speed of 0.5 mm/min. Data were analyzed by Kruskal-Wallis and Mann-Whitney tests (alpha=.05). RESULTS: Flexural strength values were the highest for dual-polymerized Nexus2-Dual-Syringe (155 MPa), whereas the values were lowest for autopolymerized Bistite-II-DC (56 MPa) and light-polymerized Appeal (63 MPa). Flexural moduli values ranged from 4.3 to 10.0 GPa. The polymerization mode and luting agent influenced flexural strength and modulus significantly (P<.05). CONCLUSION: Dual-polymerized resin luting agents had higher or equal flexural strength compared to the autopolymerized mode. All the groups tested passed the flexural strength requirement of the ISO 4049 specification.     

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.     

Effect of diameter of glass fibers on flexural properties of fiber-reinforced composites

This study investigated the effect of the diameter of glass fibers on the flexural properties of fiber-reinforced composites. Bar-shaped test specimens of highly filled fiber-reinforced composites (FRCs) and FRC of 30 vol% fiber content were made from a light-cured dimethacrylate monomer liquid (mixture of urethane dimethacrylate and triethylene glycol dimethacrylate) with silanized E-glass fibers (7, 10, 13, 16, 20, 25, 30, and 45 microm in diameter). Flexural strength and elastic modulus were measured. The flexural strength of the highly filled FRCs increased with increasing fiber diameter. In particular, the strengths of highly filled FRCs with 20-, 25-, 30-, and 45-microm-diameter fibers was significantly higher than the others (p<0.05). The flexural strength of FRC of 30 vol% fiber content increased with increasing fiber diameter, except for the FRC with 45-microm-diameter fibers; FRCs with 20-, 25-, and 30-microm-diameter fibers were significantly stronger than the others (p<0.05). Therefore, it was revealed that the diameter of glass fibers significantly affected the flexural properties of fiber-reinforced composites.     

Characterization of urethane-dimethacrylate derivatives as alternative monomers for the restorative composite matrix

ObjectiveThe aim was accomplished by a comparative analysis of the physicochemical properties of urethane-dimethacrylate (UDMA) monomers and their homopolymers with regard to the properties of basic dimethacrylates used presently in dentistry. The homologous series of UDMA were obtained from four oligoethylene glycols monomethacrylates (HEMA, DEGMMA, TEGMMA and TTEGMMA) and six diisocyanates (HMDI, TMDI, IPDI, CHMDI, TDI and MDI).MethodsPhotopolymerization was light-initiated with the camphorquinone/tertiary amine system. Monomers were tested for viscosity and density. Flexural strength, flexural modulus, hardness, water sorption and polymerization shrinkage of the polymers were studied. The glass transition temperature and the degree of conversion were also discussed.ResultsHEMA/IPDI appeared to be the most promising alternative monomer. The monomer exhibited a lower viscosity and achieved higher degree of conversion, the polymer had lower water sorption as well as higher modulus, glass temperature and hardness than Bis-GMA. The polymer of DEGMMA/CHMDI exhibited lower polymerization shrinkage, lower water sorption and higher hardness, however it exhibited lower modulus when compared to HEMA/TMDI. The remaining monomers obtained from HEMA were solids. Monomers with longer TEGMMA and TTEGMMA units polymerized to rubbery networks with high water sorption. The viscosity of all studied UDMA monomers was too high to be used as reactive diluents.SignificanceThe systematic, comparative analysis of the homologous UDMA monomers and corresponding homopolymers along with their physico-mechanical properties are essential for optimizing the design process of new components desirable in dental formulations. Some of the studied UDMA monomers may be simple and effective alternative dimethacrylate comonomers.     

High refractive index monofunctional monomers as promising diluents for dental composites

ObjectivesTo evaluate high refractive index methacrylates as diluents for the formulation of radiopaque esthetic bulk-fill composites.Methods2-(4-Cumylphenoxy)ethyl methacrylate 1, 2-(2-phenylphenoxy)ethyl methacrylate 2 and 2-[2-(2-phenylphenoxy)ethoxy]ethyl methacrylate 3 were synthesized and characterized by ¹H NMR spectroscopy. The reactivity of each monomer was studied using photo-DSC. Bulk-fill composites based on monomers 1–3 were formulated. Translucency (before and after light cure) was measured using a spectrophotometer. The depth of cure and the water sorption of these materials were determined according to ISO 4049. The flexural strength and modulus of elasticity were measured using a three-point bending setup, according to ISO 4049. The shrinkage force was assessed based on a method described by Watts et al. using a universal testing machine.ResultsMonomers 1–3 were easily synthesized in two steps. They exhibit a low viscosity and a high refractive index (1.553–1.573). Monofunctional methacrylates 1–3 were found to be more reactive than triethylene glycol dimethacrylate (TEGDMA). Bulk-fill composites based on these monomers were successfully prepared. They exhibit a high depth of cure and excellent esthetic properties (low transparency). These composites provide higher flexural modulus as well as lower water sorption than a corresponding material based on TEGDMA. Methacrylates 1 and 3 are particularly interesting as they led to composites showing lower shrinkage force.SignificanceMethacrylates 1–3 are promising diluents for the formulation of highly esthetic radiopaque bulk-fill composites.     

Degree of cure and fracture properties of experimental acid-resin modified composites under wet and dry conditions.

OBJECTIVE: Evaluate the effects of core structure and storage conditions on the mechanical properties of acid-resin modified composites and a control material by three point bending and conversion measurements 15min and 24h after curing. METHODS: The monomers pyromellitic dimethacrylate (PMDM), biphenyldicarboxylic-acid dimethacrylate (BPDM), (isopropylidene-diphenoxy)bis(phthalic-acid) dimethacrylate (IPDM), oxydiphthalic-acid dimethacrylate (ODPDM), and Bis-GMA were mixed with triethyleneglycol dimethacrylate (TEGDMA) in a 40/60 molar ratio, and photo-activated. Composite bars (Barium-oxide-glass/resin=3/1 mass ratio, (2mmx2mmx25mm), n=5) were light-cured for 1min per side. Flexural strength (FS), elastic modulus (E), and work-of-fracture (WoF) were determined in three-point bending after 15min (stored dry); and after 24h under dry and wet storage conditions at 37 degrees C. Corresponding degrees of conversion (DC) were evaluated by Fourier transform infrared spectroscopy. Data was statistically analyzed (2-way analysis of variance, ANOVA, Holm-Sidak, p<0.05). RESULTS: Post-curing significantly increased FS, E and DC in nearly all cases. WoF did not change, or even decreased with time. For all properties ANOVA found significant differences and interactions of time and material. Wet storage reduced the moduli and the other properties measured with the exception of FS and WoF of ODPDM; DC only decreased in BPDM and IPDM composites. SIGNIFICANCE: Differences in core structure resulted in significantly different physical properties of the composites studied with two phenyl rings connected by one ether linkage as in ODPDM having superior FS, WoF and DC especially after 24h under wet conditions. As expected, post-curing significantly contributed to the final mechanical properties of the composites, while wet storage generally reduced the mechanical properties.