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PubMed1991

An evaluation of polishing agents for composite resins.

After the gross reduction and fine finishing of a composite resin restoration, selecting a system to create the smoothest polish is difficult because high magnification is necessary to compare the surface roughness. The surfaces of four anterior and posterior composite resins were compared using a Mylar strip, an unfilled resin as a glaze, polishing with three rubber polishers, and three different manufacturers' series of disks. This study suggested that pairing a specific composite resin with a matching polishing system produced the smoothest surface. Because of the differences in the size, shape, number of filler particles, and the type of resin, one system was incapable of creating the smoothest surface for all composite resins.

Acrylic Resins↗
PubMed1992

Shear strength of laboratory-processed composite resins bonded to a silane-coated nickel-chromium-beryllium alloy.

The shear bond strengths of three commercial laboratory curing composite resin veneers bonded to a nickel-chromium-beryllium alloy treated with the Silicoater system were evaluated. Two light-cured resins and one heat- and pressure-cured resin were evaluated. No statistically significant difference in bond strengths among the three resins was found. Microscopic analysis of the fracture surfaces indicated that all failures were complex and cohesive in nature within the resin and composite. On the basis of the shear bond strengths measured, any of the composite resin veneers tested appear to be clinically acceptable.

Acrylic Resins↗
PubMed2002

Effect of storage media upon the surface micromorphology of resin-based restorative materials.

The aim of this study was to evaluate the effect of different storage media upon the surface micromorphology of resin-based restoratives. One resin-modified glass-ionomer (Fuji II LC Improved), one polyacid-modified composite resin (Dyract AP), one microfilled composite resin (Durafill VS), and one hybrid composite resin (Filtek Z250) were tested. For each material, 45 standardized cylindrical specimens were randomly made. After 24 h, samples were finished and polished, and their surface roughness measured to obtain Ra (micro m) baseline values (Bv). Fifteen specimens of each material were then stored at 37 +/- 1 degrees C, for 24 h, either in distilled deionized water or in artificial saliva, or else subjected to a pH-cycling regimen. At the end of 10 days of storage, final readings (Fv) of surface roughness were obtained. The Analysis of Covariance (alpha=0.05), considering the covariate Bv showed a significant interaction between restorative materials and storage media (P value=0.0000). Multiple comparison Tukey's test revealed that the surface roughness of resin-based restoratives subjected to a pH-cycling model was significantly higher compared with both distilled deionized water and artificial saliva. Micromorphological changes were noticed in a situation of acid challenge.

Acids↗
PubMed1998

Shear bond strength of chemical and light-cured glass ionomer cements bonded to resin composites.

A bond between glass ionomer cements (GIC) and resin composites is desirable for the success of the 'sandwich' restoration. Chemically cured glass ionomer cements have been the traditional materials used in this technique since its development, but etching the GIC was necessary to obtain a bond to the composite facing. Producing a very smooth GIC surface has aided in better determining the magnitude of the chemical bond between glass ionomers and resin composites. Shear testing of bonded specimens has revealed that chemical bonding is minimal (0.21 MPa) in conventional glass ionomers, but does exist (4.92 MPa) between GIC and resin composite regardless of the filler content (microfilled vs hybrid) of the composite. Thermal stressing affects the bond to resin-modified glass ionomers, but has no significant effect on self-cured cements. Of all combinations tested. Vitremer/Scotchbond/Silux Plus showed the highest mean shear bond strength. Based on the clinical need for an adhesive bond between GIC liner/base and resin composite, the resin-modified glass ionomer would appear to be the material of choice.

Acid Etching, Dental↗
PubMed1996

Flexure strength of resin-modified glass ionomer cements and their bond strength to dental composites.

The flexure strength of three resin-modified glass ionomer cements and one conventional glass ionomer cement and their bond strength to dental composites were studied by measuring the three-point bending and the shear strengths. The bond strengths between the dental composite and the resin-modified glass ionomer cements were dependent on the curing modes. Resin-modified glass ionomer cements bonded significantly more strongly to cured dental composites than dental composites bonded to cured resin-modified glass ionomer cements. However, the dental composites showed a significantly stronger bonding to the resin-modified glass ionomer cements than to the cured conventional glass ionomer cement, to which the dental composite did not adhere without acid etching. The flexure strengths of the resin-modified glass ionomer cements were significantly improved compared with the conventional one but were still significantly lower than that of the dental composites.

Acid Etching, Dental↗
PubMed1992

Use of self-curing composite resins to facilitate amalgam repair.

Resin cements, which have been shown to adhere to various metal alloys, were investigated as possible repair adhesives for dental amalgam. Test bars of repaired amalgam, formed by condensing new alloy against previously set alloy with or without the use of "adhesive" resins, were subjected to three-point bending measurements of transverse fracture strength. The results indicated that application of adhesive resin did not improve the breaking strength of the repaired specimens from that of specimens prepared without the use of such resins. The breaking strength of all repaired specimens was approximately 15% of the transverse fracture strength of the original intact amalgam bars. Scanning electron microscopy revealed that there was an intermixing of fresh amalgam and unset interfacial resin, which led to mechanical bonding of these materials, but there was no evidence of adhesion of the resin to the previously set amalgam.

Acrylic Resins↗
PubMed1996

Marginal leakage of combinations of glass-ionomer and composite resin restorations.

This study compared the microleakage of four different combinations of glass-ionomer and composite resin restorations. Forty class V cavities were prepared in permanent posterior teeth. The gingival margin of the cavities were placed in cementum and the occlusal wall in enamel. The cavities were restored as either 1) light-cured glass-ionomer cement (LC-GIC); 2) chemically cured glass-ionomer cement (CC-GIC); 3) composite resin (with dentin bonding agent); or 4) light-cured glass-ionomer and composite resin (sandwich). Marginal microleakage was assessed by methylene blue dye penetration after thermocycling between 5 degrees C and 60 degrees C for 300 cycles. Microleakage of LC-GIC restorations and the dentin-bonded composite resin restorations were significantly lower than the CC-GIC and the LC-GIC sandwich technique restorations. There was no significant difference in the microleakage between the LC-GIC and the dentin-bonded composite resin restorations. The degree of microleakage of the sandwich restorations was significantly lower than the CC-GIC restorations. Light-cured glass-ionomer and dentin bonded composite resin restorations exhibited a lower degree of leakage than the glass-ionomer/composite sandwich and chemically cured glass-ionomer restorations at the gingival margins of class V restorations.

Analysis of Variance↗
PubMed1997

Strength of secondary-cured resin composite inlay repairs.

A study was designed to simulate the repair of an indirect resin composite restoration with conventionally cured resin composite. Two-part specimens were prepared to test the diametral tensile strength of the repair interface between the base material of an indirectly cured resin composite (Herculite XRV) and repairs carried out with three directly cured materials (Herculite XRV, TPH, and Charisma). The repairs were carried out with and without use of the bonding resin for the repair material. The diametral tensile strengths of all repaired specimens were significantly less than those of bulk unrepaired specimens. There were no significant differences between the diametral tensile strengths of repaired blocks when the repair materials were used without bonding resin. The use of an intermediate layer of bonding resin significantly increased the bond strengths obtained when Herculite XRV and TPH were used for repair. There was no significant difference between the strength values of Herculite XRV and TPH, but Charisma exhibited the lowest strengths of repaired specimens.

Acrylic Resins↗
PubMed1996

Marginal adaptation of resin-bonded light-cured glass ionomers in dentin cavities.

PURPOSE: To investigate the marginal adaptation of resin-modified glass ionomer cements in dentin cavities placed with or without additional application of resin bonding systems. MATERIALS AND METHODS: Three resin-modified materials (Fuji II LC, Photac-Fil, Vitremer), one compomer (Dyract) and as reference an adhesively bonded resin composite system (Gluma CPS-Pekafill) were used. Flat peripheral dentin surfaces on human molar teeth were produced by wet grinding on SiC paper. Cylindrical cavities, 3.5 mm wide, were prepared in these dentin areas and restored with the individual materials. Sixty cavities were pretreated and restored as requested by the respective manufacturers. Following water storage of the specimens for 15 minutes or 24 hours, excess was gently removed by wet grinding for microscopic inspection of the marginal area. Additionally, in 30 cavities an experimental one-component adhesive resin system, a proprietary dimethacrylate and HEMA mixture dissolved in acetone, was combined with each of the restoratives for evaluation after 15-minutes water storage. Finally, in six cavities each, Dyract was combined with Prime and Bond 2.0, and Vitremer with Scotchbond Multi-Purpose Plus for assessment after 15 minutes. Maximum marginal gap widths (MGW) were measured. One-way ANOVA by ranks (Kruskal-Wallis-Test) followed by Wilcoxon's Two-Sample test were used to study the statistical difference of MGW among the treatment groups at a rejection level P = 0.05. RESULTS: Neither the conventionally placed material systems nor the restorations in combination with adhesives showed consistently gap-free margins after 15-minute water storage. After 24-hour storage with Vitremer 4 of the 6 restorations were gap-free, whereas with all other materials only perfect margins were registered. There was, however, no significant difference between the groups. Application of the experimental and/or the specific resin bonding agents had no effect on early MGW except for the Photac-Fil group, which was significantly reduced.

Analysis of Variance↗
PubMed2006

Difference in color and color parameters between dental porcelain and porcelain-repairing resin composite.

The objective of this study was to measure the differences in color and color parameters between dental porcelain and porcelain-repairing resin composites. The colors of three shades (A2, A3, A3.5) of one brand of dental porcelain, three original shades (A2, A3, A3.5), and three combinations (A2/A3, A3/3.5, A2/A3.5) of three brands of porcelain-repairing resin composites (ABT, FSP, TCR) were measured. The specimens were 2 mm thick, and 1 mm of each shade was layered to make combined shades. Differences in color (DeltaE(ab) (*)), lightness (DeltaL*), chroma (DeltaC(ab) (*)), and hue (DeltaH(*)) between porcelain and resin composite were calculated. Color difference was calculated as DeltaE(ab) (*) = (DeltaL*(2) + Deltaa*(2) + Deltab*(2))(1/2), chroma difference was calculated as DeltaC(ab) (*) = (Deltaa*(2) + Deltab*(2))(1/2), and hue difference was calculated as DeltaH(ab) (*) = (DeltaE(ab) (*2) - DeltaL*(2) - DeltaC(ab) (*2))(1/2). The influence of porcelain shade, brand of resin composites, and shade of resin composites were analyzed by three-way analyses of variance, and the differential influence of color parameters on color difference was analyzed with multiple regression analysis (alpha = 0.05). Differences in color and color parameters were influenced by the porcelain shade, brand and shade of resin composites. The DeltaE(ab) (*) value was in the range of 2.2-16.9. The DeltaE(ab) (*) value was correlated with DeltaC(ab) (*) (standardized correlation coefficient, beta = - 0.85), DeltaL* (beta = - 0.52), and DeltaH(ab) (*) (beta = 0.08). Between the same shade designated pairs of porcelain and repairing composite, color difference was perceptible. Therefore, studies to improve the color matching between porcelain and repairing resin are recommended.

Color↗
PubMed2004

Headspace solid phase microextraction for screening for the presence of resins in Egyptian archaeological samples.

The aim of this study was to use headspace solid phase microextraction (SPME) to reveal the presence of resin in archaeological samples, such as mummification balms, from ancient Egypt. Experiments were first performed with fresh resins of known origin. The SPME fibre readily extracted mono- and sesquiterpenes and, to a lesser extent, diterpenes. Using mass spectra and retention indices of constitutive compounds, qualitative analysis of the volatile fraction allowed us to differentiate resins or gum-resins such as myrrh, olibanum, galbanum, labdanum, mastic, and conifer resins. SPME was then successfully applied to archaeological samples from ancient Egypt in which the presence of resins was detected. Volatile components were desorbed and trapped according to the same SPME procedure as was applied to fresh resins, after a sample preparation consisting of a fine grinding.

Journal Article↗
PubMed2002

Investigation on the wound healing activity of oleo-resin from Copaifera langsdorffi in rats.

The wound healing activity of oleo-resin from Copaifera langsdorffii Desf. (Leguminaceae) bark was evaluated in rats on experimental wounds. The oleo-resin was tested by monitoring wound contraction in excised wounds and by measuring tensile strength in healing incision wounds. The topical application of oleo-resin at a concentration of 4% accelerated wound contraction in open wounds. The mean values of wound contraction in oleo-resin treated rats on day 9 was 84.05% +/- 2.37% as against 51.29% +/- 9.54% seen in controls and the difference was statistically significant (p < 0.05). No significant differences in the rates of wound contraction were observed on days 12, 15, 18 and 21. Also, the tensile strength in healing incised wounds was found to be significantly higher in the group of animals treated with 4% oleo-resin on day 5 but not on days 7 and 12 (controls: 35.95 +/- 7.44 g/cm; oleo-resin: 71.48 +/- 5.77 g/cm; p < 0.05). These results indicate the beneficial effect of C. langsdorffii oleo-resin on wound healing and justify its traditional use for the treatment of wounds.

Administration, Cutaneous↗
PubMed1992

Physical and biochemical characterization of five commercial resins for immunoaffinity purification of factor IX.

The American Red Cross has developed an immunoaffinity chromatography method to purify human coagulation factor IX (FIX) to homogeneity using monoclonal antibodies (MAb) that bind FIX in the presence of divalent cations. The MAb is immobilized on Sepharose CL2B, a soft gel with a low pressure tolerance as well as poor large-scale performance characteristics, including low reusability, and resin crumbling and deterioration. In this study, we examined several commercially available resin supports. Aside from Sepharose CL2B, we studied two other cross-linked agaroses, as well as two synthetic polymer supports. Immobilization chemistries included cyanogen bromide activation of agarose, 2-fluoro-2 methylpyridinium toluene-4-sulfonate activation of one of the synthetic polymer as well as aldehyde group reduction by NaCNBH3 to form secondary amine linkages on one of the cross-linked agaroses. To determine the feasibility of using the resins in large-scale immunoaffinity chromatographic purification of FIX, we studied physical and biochemical properties of the resins. The physical characteristics studied included the crushability of the resins under pressure as well as ability to support increasing flow-rates at increasing pressures. The biochemical examination of the various resins focused on efficiency of antigen capture by the immobilized antibody ligand and the effect of flow-rate on MAb efficiency, where we found that very low flow-rates slightly increased the capacity of the MAb. The results demonstrate a straightforward method of assessing the feasibility of using particular resins in large-scale affinity purification.

Antibodies, Monoclonal↗
PubMed1987

Saliva contamination and resin bonding of etched metal retainers.

This study was performed to determine how preapplication of unfilled resin and subsequent saliva contamination would affect the shear strength of the etched-metal resin-bonded retainer. There was no significant difference in the shear strength of the metal-resin bond among experimental groups when the metal retainer was bonded in the routine manner, when unfilled resin was applied and allowed to polymerize before bonding of filled resin, or when saliva contamination occurred before the addition of filled resin. Preapplication of unfilled resin to etched metal retainers may serve as a means of protecting the etched metal surface for routine try-in of "Maryland bridges" before final cementation.

Acid Etching, Dental↗
PubMed2005

Comparison of standard methods and gas chromatography method in determination of formaldehyde emission from MDF bonded with formaldehyde-based resins.

Formaldehyde emissions from MDF bonded with urea-formaldehyde resin (UF), melamine-formaldehyde resin (MF) and the co-polycondensation resin of urea-melamine-formaldehyde (UMF) and melamine-formaldehyde, measured by the Japanese standard method of determining formaldehyde emission with a desiccator (JIS A 5908) and the DIN EN 120 (European Committee For Standardization, 1991) method using the perforator value, were used as the typical standard methods. While the UF resin showed a desiccator value of 7.05 ppm and a perforator value of 12.1 mg/100 g panel, the MF resin exhibited a desiccator value of 0.6 ppm and a perforator value of 2.88 mg/100 g panel. According to the Japanese industrial standard and the European standard, the formaldehyde emission level of the MDF panels made with UF resin in this study was E(2) grade. The formaldehyde emission level was dramatically reduced by the addition of MF resin. This is because the addition of formaldehyde to melamine occurs more easily and completely than its addition to urea, even though the condensation reaction of melamine with formaldehyde is similar to that between urea and formaldehyde. These two methods, the desiccator method and the perforator method, produced proportionally equivalent results. Gas chromatography, a more sensitive and advanced method, was also used. The samples used for gas chromatography were gathered during the experiment involving the perforator method. The formaldehyde emission levels obtained from gas chromatography were similar to those obtained from the perforator method. The formaldehyde contents measured by gas chromatography were directly proportional to the perforator values.

Chemistry Techniques, Analytical↗
PubMed1999

Effect of five woven fiber reinforcements on the impact and transverse strength of a denture base resin.

STATEMENT OF PROBLEM: Fracture strength of denture base resins is of great concern, and many approaches have been used to strengthen acrylic resin dentures. PURPOSE: This study measured the effect of 5 fiber strengtheners on the fracture resistance of denture base acrylic resin material. Impact strength, transverse strength, deflection, and elasticity modulus values of a heat-polymerized denture base resin (Trevalon), reinforced with glass, carbon, thin Kevlar, thick Kevlar, and polyethylene fibers in woven form were studied. MATERIAL AND METHODS: One hundred acrylic resin test specimens reinforced with woven fibers were fabricated. The control group consisted of 20 specimens with no fiber reinforcement. For the impact strength test, a Charpy-type impact tester was used. Transverse strength was assessed with a 3-point bending test by using a screw-driven mechanical testing machine. Ten specimens were used for each test. RESULTS: The highest impact test values were produced by polyethylene-reinforced group, and the lowest values were obtained from specimens containing no fibers. There were significant differences among the test groups, but no significant differences in transverse strength were found. The lowest transverse strength values were obtained for specimens strengthened with polyethylene fibers, which also insignificantly decreased transverse strength of the acrylic resin. CONCLUSION: The impact strength of denture base acrylic resins was increased with fibers in woven form. Tested fibers did not have a significant effect on the transverse strengths.

Analysis of Variance↗
PubMed2004

Heterogeneous catalysis using a nanostructured solid acid resin based on lyotropic liquid crystals.

The catalytic reactivity and selectivity of the first example of a nanostructured solid acid resin (1) are described. This new type of solid acid catalyst is formed by the self-assembly and copolymerization of two acidic lyotropic liquid crystals (LLCs), affording a columnar hexagonal polymer network with monodisperse nanochannels lined with sulfonic acid groups. The performance of this material as a heterogeneous catalyst was compared against that of two commercially available, amorphous sulfonic acid resins: Amberlyst-15 and Nafion NR50. Using the acid-catalyzed esterification of benzyl alcohol with 1-hexanoic acid in dry toluene as a test reaction, it was found that resin 1 displayed only slightly lower overall reactivity as compared to Amberlyst-15 and Nafion NR50 but more than an order of magnitude higher selectivity for the desired ester product over dibenzyl ether side-product. Control experiments revealed that the higher product selectivity is not due to differences in relative acidity between the nanostructured acid resin and the two amorphous resins. Instead, it appears that a large component of the enhanced selectivity is due to the regular nanostructure present in the LLC resin, which affords a much more uniform local acid microenvironment for reactions to occur. Resin 1 can also be recycled with almost complete recovery of catalytic activity and selectivity, and with essentially no leaching of reactive groups into the solution phase.

Journal Article↗
PubMed2002

Effect of thermal cycling on whisker-reinforced dental resin composites.

The mechanical properties of dental resin composites need to be improved in order to extend their use to high stress-bearing applications such as crown and bridge restorations. Recent studies used single crystal ceramic whiskers to reinforce dental composites. The aim of this study was to investigate the effects of thermal cycling on whisker-reinforced composites. It was hypothesized that the whisker composites would not show a reduction in mechanical properties or the breakdown of whisker-resin interface after thermal cycling. Silicon carbide whiskers were mixed with silica particles, thermally fused, then silanized and incorporated into resin to make flexural specimens. The filler mass fraction ranged from 0% to 70%. The specimens were thermal cycled in 5 degrees C and 60 degrees C water baths, and then fractured in three-point bending to measure strength. Nano-indentation was used to measure modulus and hardness. No significant loss in composite strength, modulus and hardness was found after 10(5) thermal cycles (family confidence coefficient=0.95; Tukey's multiple comparison test). The strength of whisker composite increased with filler level up to 60%, then plateaued when filler level was further increased to 70%; the modulus and hardness increased monotonically with filler level. The strength and modulus of whisker composite at 70% filler level were significantly higher than the non-whisker controls both before and after thermal cycling. SEM revealed no separation at the whisker-matrix interfaces, and observed resin remnants on the pulled-out whiskers, indicating strong whisker-resin bonding even after 10(5) thermal cycles. In conclusion, novel dental resin composites containing silica-fused whiskers possessed superior strength and modulus compared to non-whisker composites both before and after thermal cycling. The whisker-resin bonding appeared to be resistant to thermal cycling in water, so that no loss in composite strength or stiffness occurred after prolonged thermal cycling.

Journal Article↗