Bisphenol A Glycol Dimethacrylate Research Articles

Strength of Fiber Posts with Experimental TiO2 and ZrO2 Particle Bonding—An SEM, EDX, Rheometric and Push-Out Strength Study

The present study aimed to prepare experimental adhesives (EAs): 5 wt.% titanium dioxide (TiO2) adhesive; and 5 wt.% zirconium oxide (ZrO2) adhesive; and analyze their impact on bond integrity of fiber posts to root dentin, and viscosity. The EA was composed of: bisphenol A glycol dimethacrylate (BisGMA); triethylene glycol dimethacrylate (TEGDMA); 2-hydroxyethyl methacrylate (HEMA); and ethyl 4-dimethylamino benzoate and camphorquinone. TiO2 and ZrO2 particles were individually incorporated into the EA at 5 wt.%, to form two groups (5% TiO2 and 5% ZrO2). The adhesives, with particles, were characterized using scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy. The bonded interface was evaluated for adhesive–dentin penetration at the interface, using SEM. The study adhesive groups (EA, 5% TiO2 and 5% ZrO2) were analyzed for rheology and push-out bond strength of the fiber post to root dentin. Data were analyzed using analysis of variance and post hoc comparison. Both TiO2 and ZrO2 particles had irregular, non-uniform shapes. The EDX mapping showed the elemental presence of Ti (TiO2), Zr (ZrO2) and oxygen in formulated adhesives. The 5% TiO2 and 5% ZrO2 adhesives showed a decrease in viscosity, compared with the EA. Bond strength among the 5% TiO2 and 5% ZrO2 adhesives was statistically comparable (p > 0.05), but higher than the control group (10.57 ± 1.45 MPa) (p < 0.05). Reinforcement of the experimental dentin adhesive with 5% TiO2 or 5% ZrO2 increased the push-out bond strength of the fiber post to root dentin, in comparison with the EA. Particle-incorporated adhesives (5% TiO2 and 5% ZrO2) displayed decreased viscosity, compared with the EA (without particles).

Influence of TiO2 and ZrO2 Nanoparticles on Adhesive Bond Strength and Viscosity of Dentin Polymer: A Physical and Chemical Evaluation.

The present study aimed to formulate an experimental adhesive (EA) and reinforce it with 5 wt.% titanium dioxide (TiO2) or zirconium oxide (ZrO2) to yield 5% TiO2 and 5% ZrO2 adhesives, respectively, and then analyze the impact of this reinforcement on various mechanical properties of the adhesives. The EA contained a blend of monomers such as bisphenol A glycol dimethacrylate (BisGMA), triethylene glycol dimethacrylate (TEGDMA), 2-hydroxyethyl methacrylate (HEMA), and ethyl 4-dimethylamino benzoate and camphorquinone. The EA included ethyl 4-dimethylamino benzoate and camphorquinone photo-initiators, and diphenyliodonium hexafluorophosphate (DPIHP) was also included to act as an electron initiator. The TiO2 and ZrO2 nanoparticles were incorporated into the EA post-synthesis. To characterize the filler nanoparticles, scanning electron microscopy (SEM) and line-energy dispersive X-ray (EDX) spectroscopy were performed. The adhesives were characterized by analyzing their rheological properties, shear-bond strength (SBS), and interfacial failure types. Further, the resin–dentin interface was also analyzed via SEM. The TiO2 nanoparticles were spherically shaped on the SEM micrographs, while the ZrO2 nanoparticles were seen as non-uniformly shaped agglomerates. The EDX mapping demonstrated the presence of Ti and oxygen for TiO2 and Zr and oxygen for the ZrO2 nanoparticles. Both 5% TiO2 and 5% ZrO2 adhesives revealed decreased viscosity as compared with the EA. The 5% TiO2 adhesive demonstrated higher SBS values for both non-thermocycled (NTC) and thermocycled samples (NTC: 25.35 ± 1.53, TC: 23.89 ± 1.95 MPa), followed by the 5% ZrO2 adhesive group (NTC: 23.10 ± 2.22, TC: 20.72 ± 1.32 MPa). The bulk of the failures (>70%) were of adhesive type in all groups. The SEM analysis of the resin–dentin interface revealed the development of a hybrid layer and resin tags (of variable depth) for the EA and 5% TiO2 groups. However, for the 5% ZrO2 group, the hybrid layer and resin tag establishment appeared compromised. Reinforcement of the EA with TiO2 or ZrO2 caused an increase in the adhesive’s SBS (with the 5% TiO2 group demonstrating the highest values) in comparison with the EA (without nanoparticles). However, both nanoparticle-containing adhesives revealed decreased viscosity compared with the EA (without nanoparticles). Further studies investigating the impact of diverse filler concentrations on the properties of adhesives are suggested.

The effects of the dental methacrylates TEGDMA, Bis-GMA, and UDMA on neutrophils in vitro.

ObjectivesThe prevalent usage of methacrylates in modern dentistry demands good knowledge of their biological impacts. While there have been several studies demonstrating the effects of different methacrylic monomers on mononuclear white blood cells, very little is known about the effects caused by these monomers on neutrophilic granulocytes. The objective of this study was to add novel knowledge about how neutrophils are affected by exposure to triethylene glycol dimethacrylate (TEGDMA), urethane dimethacrylate (UDMA), and bisphenol A glycol dimethacrylate (Bis‐GMA) alone or in combinations.Materials and MethodsIsolated neutrophils were cultured in the presence or absence of methacrylates. The IL‐8 release was measured using a DuoSet ELISA development kit. Apoptosis and necrosis were analyzed using flow cytometry. The formation of neutrophil extracellular traps (NETs) was investigated using Sytox green DNA staining combined with microscopically examination of released DNA and myeloperoxidase (MPO).ResultsThe release of IL‐8 was significantly increased after exposure to TEGDMA, Bis‐GMA, UDMA, or TEGDMA in combination with Bis‐GMA or UDMA compared to the unstimulated controls. Exposure to TEGDMA, UDMA, and Bis‐GMA for 24 hr separately or in combination did not affect apoptosis or necrosis of the exposed neutrophils. NET structures were formed by neutrophils after exposure to the different combinations of the methacrylates.ConclusionThe combination of TEGDMA and Bis‐GMA had a synergistic proinflammatory effect on neutrophils by increasing the release of IL‐8 and the formation of NET structures. The changes in the normal functions of neutrophils caused by methacrylate exposure may lead to altered inflammatory response and relate to previously reported adverse immune reactions caused by these substances.

The effect of UDMA and Bis-GMA irradiation period on residual monomers in resin packable composite

Background: Residual monomers are non-polymerized monomers which can cause clinical harm, for example inflammation, to oral cavity tissue while the remaining monomers can potentially be carcinogenic. The more residual monomers that remain due to an imperfect polymerization processes, the lower the compressive strength level and the higher the number of micro slits that can cause secondary caries and tooth sensitivity. Urethane dimethacrylate (UDMA) and bisphenol A glycol dimethacrylate (Bis-GMA) constitute two of the resins most frequently used in packable composites. During the short irradiaton period forming part of the polymerization process, UDMA and Bis-GMA have the potential to produce residual monomers. Purpose: This study aimed to compare the number of residual monomers in packable composite resin following irradiation lasting 1x20 seconds and 2x20 seconds. Methods: 28 samples of cylindrical packable composite with a thickness of 2 mm and a diameter of 5 mm were divided into four groups. Groups 1 and 2 were irradiated for 1x20 seconds, and groups 3 and 4 for 2x20 seconds with the composite subsequently being immersed in ethanol solution for 24 hours. The number of residual monomers using high-performance liquid chromatography (HPLC) devices was calculated and the results statistically analyzed using a Mann-Whitney Test. Results: Repeated irradiation had no effect on the amount of residual monomers in packable composite resins. However, there were differences in the number of residual monomers in the material contained in packable composite resins Bis-GMA and UDMA, while the remaining monomers in UDMA outnumbered those in Bis-GMA. Conclusion: The number of residual monomers in Bis-GMA is lower than in the remaining UDMA after 1x20 seconds irradiation, while the number of residual monomers in Bis-GMA and UDMA following 2x20 seconds irradiation was no different to that after irradiation of 1x20 seconds duration.

Influence of zinc oxide quantum dots in the antibacterial activity and cytotoxicity of an experimental adhesive resin

ObjectiveTo evaluate the influence of zinc oxide quantum dots (ZnOQDs) into an experimental adhesive resin regarding the antibacterial activity against Streptococcus mutans and the cytotoxicity against pulp fibroblasts. Materials and methodsZnOQDs were synthesized by sol-gel process and were incorporated into 2-hydroxyethyl methacrylate (HEMA). An experimental adhesive resin was formulated by mixing 66.6 wt.% bisphenol A glycol dimethacrylate (BisGMA) and 33.3 wt.% HEMA with a photoinitiator system as control group. HEMA containing ZnOQDs was used for test group formulation. For the antibacterial activity assay, a direct contact inhibition evaluation was performed with biofilm of Streptococcus mutans (NCTC 10449). The cytotoxicity assay was performed by Sulforhodamine B (SRB) colorimetric assay for cell density determination using pulp fibroblasts. Data were analyzed by Student’s t-test (α = 0.05). ResultsThe antibacterial activity assay indicated statistically significant difference between the groups (p = 0.003), with higher values of biofilm formation on the polymerized samples of control group and a reduction of more than 50% of biofilm formation on ZnOQDs group. No difference of pulp fibroblasts viability was found between the adhesives (p = 0.482). ConclusionZnOQDs provided antibacterial activity when doped into an experimental adhesive resin without cytotoxic effect for pulp fibroblasts. Thus, the use of ZnOQDs is a strategy to develop antibiofilm restorative polymers with non-agglomerated nanofillers. Clinical significanceZnOQDs are non-agglomerated nanoscale fillers for dental resins and may be a strategy to reduce biofilm formation at dentin/restoration interface with no cytotoxicity for pulp fibroblasts.

Triazine Compound as Copolymerized Antibacterial Agent in Adhesive Resins.

The aim of this study was to formulate and evaluate an experimental adhesive resin with the addition of 1,3,5-triacryloylhexahydro-1,3,5-triazine at different concentrations. Experimental adhesive resins were obtained by mixing 50% wt bisphenol A glycol dimethacrylate (BisGMA), 25% wt triethylene glycol dimethacrylate (TEGDMA), 25% wt 2-hydroxyethyl methacrylate (HEMA) and photoinitiator system. The triazine compound was added in 1, 2.5 and 5% wt to a base adhesive resin and one group remained with no triazine as control group. The experimental adhesive resins were analyzed for antibacterial activity (n=3), degree of conversion (n=3) and softening in solvent (n=3). Data distribution was evaluated by Kolmogorov-Smirnov test, paired t test, one-way ANOVA and Tukey's with a 0.05 level of significance. All groups with added triazine compound showed antibacterial activity against Streptococcus mutans (p<0.05). All groups achieved more than 70% degree of conversion, but there was no difference in this chemical property (p>0.05). The initial Knoop hardness was higher in 2.5 and 5% wt groups (p<0.05) and both groups present lower percentage variation of Knoop hardness after solvent degradation. The present study formulated an antibacterial adhesive resin with a non-releasing agent able to copolymerize with the comonomeric blend, improving the restorative material's properties.

Fluoridated hydroxyapatite nanorods as novel fillers for improving mechanical properties of dental composite: Synthesis and application

Abstract Fluoridated hydroxyapatite (FHA) in nanorod morphology and hexagonal cross section were synthesised via hydrothermal process using Apricot Tree Gum (ATG) as a surfactant. The synthesised FHA nanorods were then used as reinforcement in bisphenol A-glycol dimethacrylate (Bis-GMA) as base monomer of composite matrix. The FHA nanorods with different ratios were incorporated in the matrix to examine fluoride ion release and pH changes in the Simulated Body Fluid (SBF) and their mechanical properties. The resin without FHA reinforcement was used as the control sample. The Diametral Tensile Strength (DTS), Flexural Strength (FS), and Flexural Modulus (FM) of the reinforced composite were found to be higher compared to the control sample; the values increased from 34.8 to 45.4 MPa, 76.5 to 99.4 MPa, and 1.7 to 2.5 GPa, respectively. Moreover, findings revealed that the pH is reduced by releasing the fluoride ions into the SBF which can be effective for preventing secondary caries. The most optimum mechanical properties were achieved with 0.2 wt% of FHA reinforcement. The FHA nanocomposite meets the minimum standard requirements for dental applications and compared to other dental composites has advantage of preventing formation of secondary caries due to release of fluoride.

Effect of incorporating BisGMA resin on the bonding properties of silane and zirconia primers

Some silane primers and some zirconia primers contain extra resins such as bisphenol A glycol dimethacrylate (BisGMA) in their formulations for better wetting. No studies exist on the bonding properties of zirconia and silane primers, which contain extra resins. The purpose of this study was to investigate the effect of incorporating BisGMA resin on the bonding properties of silane and zirconia primers. Silica-base lithium disilicate was etched and treated with BisGMA-incorporated Porcelain Primer, unmodified Porcelain Primer, or resin-containing Kerr Silane. Zirconia ceramic was airborne-particle abraded and treated with BisGMA-incorporated Monobond Plus, unmodified Monobond Plus, or BisGMA-containing ZPrime Plus. After primer treatment and cleaning with ethanol, the contact angles were measured to determine surface change (n=10). Shear bond strength tests were also performed to measure the adhesion strength between resin cements and ceramic surfaces (n=10). Data were statistically analyzed by 1-way ANOVA followed by the Tukey multiple comparison as a post hoc test (significance level .05). The incorporation of BisGMA resin did not significantly influence the bond strength or contact angle of the zirconia primer (P>.05), but it did significantly reduce those of the silane primer (P<.05). Resin-containing Kerr Silane (22 degrees, 23 MPa) had a similar contact angle and higher bond strength than the control (21 degrees, 18 MPa), but lower than Porcelain Primer (88 degrees, 34 MPa). Resin-containing ZPrime Plus (75 degrees, 29 MPa) had a similar contact angle and higher bond strength than both Monobond Plus (74 degrees, 18 MPa) and the control (15 degrees, 4 MPa). The addition of BisGMA resin significantly inhibited the efficacy of silane-containing porcelain primers but did not affect that of phosphate-containing zirconia primers.

Measurement of Solubility and Water Sorption of Dental Nanocomposites Light Cured by Argon Laser

Different parameters used for photoactivation process and also composition provide changes in the properties of dental composites. In the present work the effect of different power density of argon laser and filler loading on solubility (SL) and water sorption (WS) of light-cure dental nanocomposites was studied. The resin of nanocomposites was prepared by mixing bisphenol A glycol dimethacrylate (Bis-GMA) and triethylene glycol dimethacrylate (TEGDMA) with a mass ratio of 65/35. 20 wt.% and 25 wt.% of nanosilica fillers with a primary particle size of 10 nm were added to the resin. Camphorquinone (CQ) and DMAEMA were added as photoinitiator system. The nanocomposites were cured by applying the laser beam at the wavelength of 472 nm and power densities of 260 and 340 mW/cm(2) for 40 sec. Solubility and water sorption were then measured according to ISO 4049, which in our case, the maximums were 2.2% and 4.3% at 260 mW/cm(2) and 20% filler, respectively. The minimum solubility (1.2%) and water sorption (3.8%) were achieved for the composite containing 25% filler cured at 340 mW/cm(2). The results confirmed that higher power density and filler loading decreased solubility of unreacted monomers and water sorption and improved physico-mechanical properties of nanocomposites.

Synthesis and characterization of cross-linked polymeric nanoparticles and their composites for reinforcement of photocurable dental resin

Reactive polymeric nanoparticles were formed for reinforcement of photocurable dental resin. Cross-linked polymeric nanoparticles were synthesized by emulsion polymerization of mono- (methyl methacrylate; MMA) and trifunctional (trimethylol propane trimethacrylate; TMPTMA) monomers. The nanoparticles were dispersed in bisphenol A glycol dimethacrylate (Bis-GMA) based dental resin matrix in the range of 5–25wt% to form photocurable nanocomposites.The effect of reactive polymeric particles on the mechanical properties of photocurable dental resin was investigated. Polymerization shrinkage, polymerization shrinkage stress, viscosity, diametral tensile strength, compressive, and flexural strength of the nanocomposites have been studied.It was observed that the cross-linked nanoparticles significantly influenced the mechanical properties of the reinforced dental resin nanocomposites.

Simultaneous determination of components released from dental composite resins in human saliva by liquid chromatography/multiple‐stage ion trap mass spectrometry

Dental composite resins are widely used for fixing teeth; however, the monomers used in dental composite resins have been found to be cytotoxic and genotoxic, namely triethylene glycol dimethacrylate (TEGDMA), urethane dimethacrylate (UDMA), and bisphenol A glycol dimethacrylate (Bis-GMA). In this study, we incubated dental composite resins with human saliva for demonstrating the released monomers and biodegradation products. A simple saliva sample dilution method without purification or derivatization was used for quantification. We found that liquid chromatography coupled with multiple-stage ion trap mass spectrometry (LC-MS(n) ) operated in selected reaction monitoring (SRM) mode was able to separate the three monomers within 10 min. The calibration curves were linear (R² >0.996) over a wide range for each monomer in saliva: TEGDMA, 5-500 ppb; UDMA, 5-100 ppb, and Bis-GMA, 5-700 ppb. Furthermore, several biodegradation products were discovered with data-dependent MS/MS scan techniques. Although TEGMA degradation products have previously been reported, we identified two previously unknown UDMA degradation products. The LC-MS/MS method developed in this study was able to successfully quantify monomers and their principal biodegradation products from dental composite resins in human saliva.

Sorption and desorption parameters of water or ethanol in light‐cured dental dimethacrylate resins

AbstractTwo cycles of sorption/desorption of water or ethanol by light‐cured dental resins of bisphenol A glycol dimethacrylate (Bis‐GMA), bisphenol A ethoxylated dimethacrylate (Bis‐EMA) urethane dimethacrylate (UDMA) triethylene glycol dimethacrylate and decanediol dimethacrylate (D3MA) were studied. The experimental curves mt = f(t) taken for the first water sorption by poly‐Bis‐GMA, poly‐Bis‐EMA and poly‐UDMA showed a maximum. A maximum was also observed in the curve obtained for first sorption of ethanol by poly‐Bis‐GMA. In all other cases, the curves for sorption or desorption of water or ethanol showed Fickian behavior. The experimental data obtained for first sorption of water or ethanol were perfectly fitted to a new proposed equation, which predicts water or ethanol sorption with simultaneous extraction of unreacted the monomer. This equation gave us the possibility for the determination of the diffusion coefficient of the extraction of the unreacted Bis‐GMA during the water and ethanol sorption, as well as the diffusion coefficient of the extraction of the unreacted Bis‐EMA and UDMA during the water sorption. The maximum water or ethanol absorbed at equilibrium and the diffusion coefficient are determined from the second sorption/desorption cycle during which the extraction of the monomer is negligible. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008

Relation between Degree of Conversion and Post-Cured Properties of Light Cured Composite Systems Used as Filling Materials

The composite, based on a polymer matrix such as Bisphenol A glycol dimethacrylate (Bis-GMA), urethane dimethacrylate (UDMA), and triethyleneglycoldimethacrylate (TEGDMA) and a reinforced-ceramic filler has been used in dental restorative materials. The light curing composite consists of Bis-GMA, TEGDMA, UDMA, Bis-GMA/TEGDMA, Bis-GMA/UDMA, or UDMA/TEGDMA polymer systems and a fumed silica filler with 35 weight ratio loading was synthesized using camphorquinone (CQ) and 2-(dimet6hyloamino)ethyl methacrylate (DMAEMA) as an initiator system. FTIR spectroscopy was used to determine the degree of conversion (DC) of the composites. Polymerization shrinkage and physical properties such as hardness strength and flexural strength were correlated with the composites containing different polymer systems.

Sorption kinetics of ethanol/water solution by dimethacrylate‐based dental resins and resin composites

In the present investigation the sorption-desorption kinetics of 75 vol % ethanol/water solution by dimethacrylate-based dental resins and resin composites was studied in detail. The resins examined were made by light-curing of bisphenol A glycol dimethacrylate (Bis-GMA), triethylene glycol dimethacrylate (TEGDMA), urethane dimethacrylate (UDMA), bisphenol A ethoxylated dimethacrylate (Bis-EMA), and mixtures of these monomers. The resin composites were prepared from two commercial light-cured restorative materials (Z100 MP and Filtek Z250), the resin matrix of which is based on copolymers of the above-mentioned monomers. Ethanol/water sorption/desorption was examined in both equilibrium and dynamic conditions in two adjacent sorption-desorption cycles. For all the materials studied, it was found that the amount of ethanol/water sorbed or desorbed was always larger than the corresponding one reported in literature in case of water immersion. It was also observed that the chemical structure of the monomers used for the preparation of the resins directly affects the amount of solvent sorbed or desorbed, as well as sorption kinetics, while desorption rate was nearly unaffected. In the case of composites studied, it seems that the sorption/desorption process is not influenced much by the presence of filler. Furthermore, diffusion coefficients calculated for the resins were larger than those of the composites and were always higher during desorption than during sorption. Finally, an interesting finding concerning the rate of ethanol/water sorption was that all resins and composites followed Fickian diffusion kinetics during almost the whole sorption curve; however, during desorption the experimental data were overestimated by the theoretical model. Instead, it was found that a dual diffusion-relaxation model was able to accurately predict experimental data during the whole desorption curve. Kinetic relaxation parameters, together with diffusion coefficients, are reported for all resins and composites.

Elution study of unreacted Bis‐GMA, TEGDMA, UDMA, and Bis‐EMA from light‐cured dental resins and resin composites using HPLC

In the present work the elution of residual monomers from light-cured dental resins and resin composites into a 75% ethanol:water solution was studied using High-Performance Liquid Chromatography (HPLC). The resins studied were made by light-curing of bisphenol A glycol dimethacrylate (Bis-GMA), triethylene glycol dimethacrylate (TEGDMA), urethane dimethacrylate (UDMA), ethoxylated bisphenol A glycol dimethacrylate [Bis-EMA(4)] and mixtures of these monomers. The resin composites were made from two commercial light-cured restorative materials (Z100 MP and Filtek Z250), the resin matrix of which is based on copolymers of these monomers. The effect of the curing time on the amount of monomers eluted was investigated. The concentration of the extractable monomers was determined at several immersion periods from 3 h to 30 days. For all the materials studied, it was observed that the chemical structure of the monomers used for the preparation of the resins, which defines the chemical and physical structure of the corresponding resin, directly affects the amount of eluted monomers, as well as the time needed for the elution of this amount. In the case of composites, it seems that the elution process it is not influenced by the presence of filler.

Kinetics of the Benzoyl Peroxide/Amine Initiated Free-Radical Polymerization of Dental Dimethacrylate Monomers: Experimental Studies and Mathematical Modeling for TEGDMA and Bis-EMA

The kinetics of the benzoyl peroxide/amine initiated free-radical cross-linking polymerization of dimethacrylate monomers used as dental materials was studied. The monomers examined were triethylene glycol dimethacrylate (TEGDMA) and ethoxylated bisphenol A glycol dimethacrylate (Bis-EMA). As co-initiator to the benzoyl peroxide (BPO) the new amine 4-(N,N-dimethylamino)phenethyl alcohol was used. The polymerization rate vs time for several initial initiator concentrations was measured using differential scanning calorimetry. Differences in the polymerization kinetics of the two monomers are discussed in connection with the chemical structure of dimethacrylates Furthermore, a mathematical model was developed to simulate the BPO/amine initiated free-radical polymerization of dimethacrylate monomers. In the elementary reaction mechanism besides initiation, propagation, and termination reactions, also inhibition, primary radical termination, radical trapping, and secondary initiator chain transfer reactions w...

Water sorption characteristics of light-cured dental resins and composites based on Bis-EMA/PCDMA

The water uptake characteristics of resins and composites based on an ethoxylated bisphenol A glycol dimethacrylate (Bis-EMA) and a polycarbonate dimethacrylate (PCDMA) were studied in detail. Polydimethacrylate resins were prepared by photopolymerization of the neat monomers and mixtures of them with various weight ratios, using the camphoroquinone/ N, N-dimethylaminoethyl methacrylate system as initiator, while the composites were prepared from the light-curing of commercial samples (Sculpt-It and Alert). Water sorption/desorption was examined both in equilibrium and dynamic conditions in two adjacent sorption–desorption cycles. The equilibrium water uptake from all resins was very small with a trend to increase as the amount of PCDMA was increased. The inverse effect was observed in the solubility values. The composites studied exhibited also very low water uptake values in comparison to other composite materials reported in the literature. It was also observed that the equilibrium uptake decreased with increasing filler loading. Slightly larger equilibrium water uptake and much smaller solubility values were obtained during the second sorption–desorption cycle in comparison to the first one. Concerning the sorption rate data, it was observed that the resin materials followed Fickian diffusion during almost the whole sorption or desorption curve, while the composites showed this behavior until only M t / M ∞≅0.5. The diffusion coefficients calculated for the resins were larger than those of the composites and always higher during desorption compared to sorption. The values of the diffusion coefficients for both resins and composites were in the same order of magnitude with the values of the corresponding materials reported in the literature.

PHYSICAL PROPERTY EVALUATIONS OF PERFLUOROTRIETHYLENE GLYCOL DIMETHACRYLATE AS A POTENTIAL REACTIVE DILUENT IN DENTAL COMPOSITE RESINS

Perfluorotriethylene glycol dimethacrylate (FTEGDMA), a fluoro analog of triethylene glycol dimethacrylate (TEGDMA), was evaluated in dental composites. Curing, physical properties, and water sorption of FTEGDMA-ethoxylated bisphenol A dimethacrylate (BisEMA) and bisphenol A glycol dimethacrylate (BisGMA) – TEGDMA as well as TEGDMA - BisEMA blends were evaluated and compared. BisEMA and FTEGDMA viscosities were lower than BisGMA and TEGDMA. FTEGDMA has the lowest refractive index and contact angle on silanated or nonsilanated glass. Polymerization studies showed that FTEGDMA did not significantly alter the decrease of C˭C conversion of the various formulations. Further, the experimental FTEGDMA resins absorbed much less water than the control formulations.

EFFECT OF FLUORINATED TRIETHYLENE GLYCOL DIMETHACRYLATE ON THE PROPERTIES OF UNFILLED, LIGHT-CURED DENTAL RESINS

ABSTRACT The fluorinated triethylene glycol dimethacrylate (FTEGDMA) was used to improve the properties of Bisphenol A glycol dimethacrylate (BisGMA)/triethylene glycol dimethacrylate (TEGDMA) based dental resin system. Physical properties such as contact angle, polymerization shrinkage and water sorption, thermal properties such as glass transition temperature, dynamic modulus and thermal expansion, and mechanical properties such as compressive and diametral tensile strengths of the experimental neat resins and conventional controls were investigated and compared, using methods described in the text. Results showed that the FTEGDMA modified neat resins exhibited significant less water sorption and lower polymerization shrinkage and the 2,2'-bis(4-methacryloxy ethoxy phenyl) propane (BisEMA) also contributed significantly towards reducing water sorption. The resin containing FTEGDMA and BisEMA(10:90 molar ratio) (or F1E9) showed the highest values in mechanical strengths, due to its higher glass transition temperature (Tg), while the F5E5 (50:50) showed the least water sorption, based on the results of contact angle tests and water sorption measurements. The F5E5 resin exhibited the highest dynamic modulus. The F3E7 (30:70) resin showed the lowest polymerization shrinkage.