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Effect of adherend temperature on bond strengths of resin bonding systems to denture base resin and a semi-precious alloy
Abstract
This study investigated the effect of adherend temperature on shear bond strengths of auto-polymerizing resin to denture base resin and 4-META/MMA-TBBO resin to silver-palladium-copper-gold (Ag-Pd-Cu-Au) alloy. Bonding procedure was carried out when adherend temperature was 10, 23, 37, or 55°C, and shear bond strengths (SBSs) were measured before and after thermocycling. Before thermocycling, there were no significant differences in bond strength among the four adherend temperatures for each adhesive resin: 31.59±6.11-32.89±2.12 MPa for auto-polymerizing resin; 35.43±2.2-38.38±0.61 MPa for 4-META/MMA-TBBO resin. After thermocycling, optimal adherend temperature to achieve the highest bond strength was 37°C for auto-polymerizing resin to denture base resin (30.02±2.29 MPa) and 10ºC for 4-META/MMA-TBBO resin to Ag-Pd-Cu-Au alloy (37.14±2.17 MPa).
... The shear bond strengths of the acrylic resin and two types of zirconia ceramic (Y-TZP and Ce-TZP/A) were evaluated after traditional surface pretreatment, air-abrasion with 50 µm and 0.3 MPa Al 2 O 3 particles (CON) [23], and a novel pretreatment, using a laser to create microslits (MS). Despite the fact that studies on the bonding strength between acrylic resin and metal alloys [32,33] postulate that bonding strength is sufficient for clinical dentistry, the durability after thermal cycling as a means of artificial aging, requires discussing. The results confirmed that the SBS values of MS were higher than that of CON, regardless of artificial aging. ...
Heightened aesthetic considerations in modern dentistry have generated increased interest in metal-free “zirconia-supported dentures.” The lifespan of the denture is largely determined by the strength of adhesion between zirconia and the acrylic resin. Thus, the effect on shear bond strength (SBS) was investigated by using an acrylic resin on two types of zirconia ceramics with differently sized microslits. Micromechanical reticular retention was created on the zirconia surface as the novel treatment (microslits (MS)), and air-abrasion was used as the control (CON). All samples were primed prior to acrylic resin polymerization. After the resin was cured, the SBS was tested. The obtained data were analyzed by using multivariate analysis of variance(α = 0.05). After the SBS test, the interface failure modes were observed by scanning electron microscopy. The MS exhibited significantly higher bond strength after thermal cycles (p < 0.05) than the CON. Nevertheless, statistically comparisons resulted in no significant effect of the differently sized microslits on SBS (p > 0.05). Additionally, MS (before thermal cycles: 34.8 ± 3.6 to 35.7 ± 4.0 MPa; after thermal cycles: 26.9 ± 3.1 to 32.6 ± 3.3 MPa) demonstrated greater SBS and bonding durability than that of CON (before thermal cycles: 17.3 ± 4.7 to 17.9 ± 5.8 MPa; after thermal cycles: 1.0 ± 0.3 to 1.7 ± 1.1 MPa), confirming that the micromechanical retention with laser-milled microslits was effective at enhancing the bonding strength and durability of the acrylic resin and zirconia. Polycrystalline zirconia-based ceramics are a newly accessible material for improving removable prosthodontic treatment, as the bond strength with acrylic resin can be greatly enhanced by laser milling.
... The adhesive strength between the PEEK and acrylic resin significantly influences the probability of denture fracture. Many studies have analyzed the adhesive strength of metal surface treatments to denture base resins [7][8][9][10][11][12][13][14][15][16], suggesting that such treatments lead to improvement in the bending strength of the denture, while providing protection from microleakage between the interface, discoloration, and denture fracture. Studies on the bond strength of PEEK to luting cement or veneering resins for fixed prostheses have been reported [17][18][19][20][21][22][23][24][25]; however, information on the bonding strength between PEEK (applied to the clasp) and acrylic resin is lacking. ...
These days, new prosthodontic materials are appearing with the development of digitalization. Among these, the use of polyetheretherketone (PEEK) as the clasp of removable partial dentures has been proposed. The adhesive strength between the PEEK and acrylic resin influences the probability of denture fracture. To investigate the effect of PEEK surface treatments on the shear bond strength to acrylic resin, five surface treatment conditions of PEEK were analyzed: 1. no treatment; 2. ceramic primer application; 3. Al2O3 sandblasting; 4. Rocatec; and 5. Rocatec with ceramic primer application, comparing with a metal primer-treated Co-Cr alloy. Two kinds of autopolymerizing resin (Unifast II and Palapress Vario) were used as bonding materials. The specimens were evaluated to determine the bond strength. Rocatec treatment with ceramic primer application yielded the highest bond strengths (12.71 MPa and 15.32 MPa, respectively, for Unifast II and Palapress Vario). When compared to a metal primer-treated Co-Cr alloy, the bond strength of PEEK to Unifast II was similar, whereas it was about 60% of that to Palapress Vario. Rocatec treatment, combined with ceramic primer, showed the highest bond strength of PEEK to acrylic resin. Treatment of PEEK will enable its use as the clasp of removable dentures and the fixation of PEEK prostheses.
... Substitute substrate of bovine teeth, which has already been reported to be capable of providing similar bond strength to that of human dentin, was used in this study. [17][18] Spohr et al. studied the tensile bond strength of three adhesive systems to dentin after being stored at room temperature and in refrigerator for 6 months before being used; [19] one of which was Adper single bond that revealed no significant difference in the two conditions. As with refrigeration, evaporation of the solvents could not be completed, because little or no significant change was observed in the bond strength. ...
Monomer viscosity and solvent evaporation can be affected by the adhesive system temperature. Higher temperature can elevate the vapor pressure in solution and penetration of adhesive in smear layer. Bonding mechanism may be influenced by the adhesive temperature.
This study aimed to evaluate the effect of pre-heating on shear bond strength of etch-and-rinse and self-etching adhesives to ground bovine dentin surfaces, at temperatures of 4˚C, 25˚C and 40˚C.
In this experimental study, 60 maxillary bovine incisors were randomly divided into 6 groups (n=10). The central part of labial dentin surfaces was exposed with a diamond bur and standardized smear layer was created by using silicon carbide paper (600 grit) under water-coolant while the specimens were mounted in acrylic resin. Two adhesive systems, an etch-and-rinse (Adper single bond) and a self-etch (Clearfil SE Bond) were stored at temperatures of 4˚C, 25˚C and 40˚C for 30 minutes and were then applied on the prepared labial surface according to the manufacturer's instructions. The composite resin (Z350) was packed in Teflon mold (5 mm in diameter) on this surface and was cured. The shear bond strength (MPa) was evaluated by universal testing machine (Zwick/Roell Z020, Germany) at cross head speed of 1mm/min. The results were statistically analyzed by using ANOVA and Tukey tests (p< 0.05).
No significant difference was found between the shear bond strength of Clearfil SE Bond adhesive in different temperature and single Bond adhesive system at 25 ˚C and 40 ˚C. However, there were significant differences between 4 ˚C of Adper single bond in comparison with 25˚C and 40˚C (p= 0.0001).
Pre-heating did not affect the shear bond strength of SE Bond, but could promote the shear bond strength of Adper Single Bond.
To evaluate the effect of adhesive temperature on the resin-dentin bond strength (μTBS), nanoleakage (NL), adhesive layer thickness (AL), and degree of conversion (DC) of ethanol/water- (SB) and acetone-based (PB) etch-and-rinse adhesive systems.
The bottles of the two adhesives were kept at each temperature (5°C, 20°C, 37°C, and 50°C) for 2 hours before application to demineralized dentin surfaces of 40 molars. Specimens were prepared for μTBS testing. Bonded sticks (0.8 mm(2)) were tested under tension (0.5 mm/min). Three bonded sticks from each tooth were immersed in silver nitrate and analyzed by scanning electron microscopy. The DC of the adhesives was evaluated by Fourier transformed infrared spectroscopy.
Lower μTBS was observed for PB at 50°C. For SB, the μTBS values were similar for all temperatures. DC was higher at 50°C for PB. Higher NL and thicker AL were observed for both adhesives in the 5°C and 20°C groups compared to the 37°C and 50°C groups. The higher temperatures (37°C or 50°C) reduced the number of pores within the adhesive layer of both adhesive systems.
It could be useful to use an ethanol/water-based adhesive at 37°C or 50°C and an acetone-based adhesive at 37°C to improve adhesive performance.
The influence of temperature and relative humidity (RH) on the bond strength of orthodontic adhesives was investigated. Two self-etching/composite type, one acid-etching/composite type, and one acid-etching/PMMA type of adhesives were examined under different temperature and RH conditions. Orthodontic brackets were bonded to bovine enamel, and shear bond strength test was performed at a crosshead speed of 1.0 mm/min after 24-hour storage in 37 degrees C water. Data were analyzed by Tukey's HSD test. Each specimen was assigned an ARI score. All the materials tested exhibited their highest bond strength under room conditions at a range of 10.4-17.0 MPa. Conversely, when under a lower RH condition, bond strength for all the systems ranked the lowest within a range of 6.8-12.0 MPa, with bond failure at the bracket-adhesive interface. These results demonstrated that care should be exercised when using orthodontic adhesive systems in the oral environment.
Fracture of a repaired denture base often occurs at the junction of the base and repair materials rather than within these materials.
The purpose of the study was to evaluate the shear bond strengths of 4 denture base acrylic resins following the use of 3 chemical solvents and to examine treated acrylic resin surfaces under a field emission scanning electron microscope (SEM).
Forty discs (15 mm in diameter and 3 mm thick) were fabricated for each denture base material (a conventionally molded, heat-polymerized [Meliodent, M], an injection-molded, heat-polymerized [SR-Ivocap, I], and a microwave-polymerized [Acron MC, A]) repaired with an autopolymerizing acrylic resin (Meliodent), for a total of 120 specimens, processed according to manufacturers' instructions, embedded in acrylic resin blocks, and divided into 4 groups of 10. One of the groups served as control and had no surface treatment. In the 3 experimental groups, specimen surfaces were treated with chemical etchants by immersion in acetone (ac) for 30 seconds, in methylene chloride (mc) for 30 seconds, or in MMA (mo) for 180 seconds, respectively. Then autopolymerizing acrylic resin (Meliodent) was placed on the treated surfaces using a brass ring (6 mm in diameter and 2 mm in height) to confine the material to a standardized dimension. After 24 hours of storage at 37 degrees C, the shear bond strength (MPa) of the specimens was measured in a universal testing machine. A 2-way analysis of variance and the Tukey HSD test were performed to identify significant differences (alpha=.05). The nature of the failure was noted as adhesive, cohesive, or mixed. The effect of the chemical treatments on the surface of base resins was examined under an SEM.
Chemical treatments increased the bond strength of repair material significantly. Significant differences were found between the control and experimental groups (P<.001). In the control group, M showed the highest (16.7 MPa) bond strength, and A showed the lowest (9.4 MPa). No significant differences were detected between M (18.9 MPa) and A (19.9 MPa) with acetone treatment, or between M (19.3 MPa) and A (20.3 MPa) with methylene chloride treatment. The SEM observations showed that application of chemical etchants produced smoother surfaces than controls.
Chemical treatment prior to denture base repair showed significant improvement on the bond strength of the base materials. Although the microwave-polymerized acrylic resin, A, showed the lowest shear bond strength compared to the control groups, the highest percentage increase was obtained with A after chemical treatments.
The aim of this study was tested the effect of adhesive temperature on the bond strength to dentin (μTBS) and silver nitrate uptake (SNU) of an ethanol/water (Adper Single Bond 2 [SB]) and an acetone-based (Prime & Bond 2.1 [PB]) etch-and-rinse
adhesive systems. The bottles of each adhesive were kept in each temperature (5.C, 20.C, 37.C and 50.C) for one hour previously to its application in the occlusal demineralized dentin of forty molars. Bonded sticks (0.8 mm2) were tested in tension (0.5 mm/min) immediately (IM) or after 6 months (6M) of water storage. Two bonded sticks from each hemi-tooth were immersed in silver nitrate and analyzed by SEM. Data were analyzed by two-way repeated measures ANOVA and Tukey’s test (α=0.05). Results: No significant difference in μTBS was detected for both adhesives at 5.C and 20.C. The highest bond strength for PB was observed in the 37.C group while for SB it was in the 50.C. Significant reductions of bond strengths were observed for PB at 37.C and SB at 50.C after 6M of water storage. Silver nitrate deposition was seen in all hybrid layers, irrespective of the group. Lower silver nitrate deposition (water trees) in the adhesive layer was seen for PB and SB at higher temperatures. Conclusions: The heating or refrigeration of the adhesives did not improve their resin dentin bond resistance to water degradation over time.
An interpenetrating polymer network (IPN) is a material containing two polymers, each in network form. In biomaterials used in dentistry, the IPN-like nanostructures are used in denture base polymers, denture teeth and fibre-reinforced composites. IPN structures provide the specific and desired properties for the resin system prior to and after polymerization. At adhesive interfaces, IPN polymers and composites provide good interfacial adhesion for adhering and veneering resin composites based on the so-called secondary-IPN bonding formation due to swelling of the IPN nanostructure. Good interfacial adhesion is a requirement for the success of modern adhesive dentistry.
Objectives:
The aim of this study was to test the effect of adhesive temperature on the bond strength to dentin (muTBS) and silver nitrate uptake (SNU) of an ethanol/water (Adper Single Bond 2 [SB]) and an acetone-based (Prime&Bond 2.1 [PB]) etch-and-rinse adhesive system.
Methods:
The bottles of each adhesive were kept in various temperatures (5 degrees C, 20 degrees C, 37 degrees C and 50 degrees C) for 1h previously to its application in the occlusal demineralized dentin of 40 molars. Bonded sticks (0.8 mm(2)) were tested in tension (0.5 mm/min) immediately (IM) or after 6 months (6 M) of water storage. Two bonded sticks from each hemi-tooth were immersed in silver nitrate and analyzed by SEM. Data were analyzed by two-way repeated measures ANOVA and Tukey's test (alpha=0.05).
Results:
No significant difference in muTBS was detected for both adhesives at 5 degrees C and 20 degrees C. The highest bond strength for PB was observed in the 37 degrees C group while for SB it was in the 50 degrees C. Significant reductions of bond strengths were observed for PB at 37 degrees C and SB at 50 degrees C after 6 M of water storage. Silver nitrate deposition was seen in all hybrid layers, irrespective of the group. Lower silver nitrate deposition (water trees) in the adhesive layer was seen for PB and SB at higher temperatures.
Conclusions:
The heating or refrigeration of the adhesives did not improve their resin-dentin bond resistance to water degradation over time.
To test in vitro the shear bond strength of resin teeth to an acrylic resin denture base given different ridgelap surface treatments.
Ninety rectangular dies were made with wax and traditionally invested in metallic or plastic flasks. The stone molds were covered with silicone, in which were included an acrylic molar with a wax stick fixed on the ridge lap surface. After deflasking, the wax sticks were removed, the teeth were cleaned with detergent, the ridge lap surface was submitted to different treatments (unmodified, bur-cut grooves, aluminum oxide particle sandblasting, monomer swelling, and primer swelling), and the teeth were replaced in the silicone molds. Metallic flasks were placed in a thermopolymerizing unit to polymerize heat-curing denture-base polymer, and plastic flasks were placed in a domestic microwave oven at 900 W to polymerize microwaveable denture base polymer. After deflasking, the specimens were submitted to the shear bond test in an Instron machine at a cross-speed of 1 mm/min. Results were submitted to ANOVA and Tukey's test (5%).
Shear bond strength values were influenced by the ridge-lap surface treatments only in the microwaved polymer. Sandblasting + monomer swelling and sandblasting + primer swelling interactions yielded lower strengths for microwaved polymer. Only the unmodified surfaces presented a significant difference when the resins were compared, where the microwaved polymer showed a higher value.
Different tooth ridge-lap surface treatments promoted different strengths of the tooth/resin bond.
Unlabelled:
This study evaluated the microtensile bond strength test (pT), micromorphology of resin-enamel interface (RET) and etching patterns (EP) promoted by the etch-and-rinse adhesive, Prime&Bond NT (PB), and two self-etching adhesives, Clearfil SE Bond (SE) and Adper Prompt L-Pop (APR), to ground bovine enamel surfaces, when applied at temperatures of 5 degrees C (C), 40 degrees C (H) and 20 degrees C (R). MATERIALS AND METHODS. Sixty-three bovine incisors were randomly divided into nine experimental groups (n = 7) according to adhesive systems and temperatures. The buccal enamel surfaces were flattened with 600-grit SiC paper and abraded with a diamond bur under water-cooling. The adhesive systems were applied according to the manufacturer's instructions. After the restorative procedures, the specimens were sectioned into five slabs. Four slabs were prepared for pT and one for interface analysis. For etching pattern analysis, the remaining 16 bovine enamel fragments were used (n = 2). The adhesives were applied and the surfaces were rinsed with organic solvents after application. The specimens for RET and EP analysis were prepared for SEM analysis.
Results:
No significant differences among the adhesives were found at R temperature. However, at 5 degrees C, PB and APR presented lower bond strength than SE. At H temperature, higher bond strength was observed for PB than for APR and SE. At C and H temperature, formation of the interdiffusion zone was impaired and the treated enamel surfaces presented an undefined EP.
Conclusion:
The variation of temperature of bonding agents affected microT, RET and EP for all materials tested.
To assess whether the bonding potential to dentin of self-adhesive resin cements was affected by their pre-cure temperature.
Composite overlays (Paradigm MZ100, 3M ESPE) were luted on 100 extracted molars with G-Cem (GC Corp.), BisCem (Bisco), Multilink Sprint (Ivoclar Vivadent), SAC-A (Kuraray Co.), XP Bond/Calibra (Detrey Dentsply). The cements were used at pre-cure temperatures that recur in their handling (4 degrees C refrigerator, 24 degrees C room and 37 degrees C intraoral), as well as following pre-heating up to 60 degrees C. Microtensile bond strengths to dentin were measured and compared with statistical tests. Scanning electron microscope observations of cement-dentin interfaces were performed.
The bond strength of G-Cem and Calibra was not significantly affected by temperature changes from refrigerator storage to intraoral application. At any assessed pre-cure temperature the total-etch luting agent Calibra achieved a significantly stronger adhesion than the auto-adhesive cements. Limited to null adhesion was yielded by BisCem and SAC-A. The procedure of 60 degrees C pre-heating, proposed in previous studies for restorative resin composites, was of no use for the tested luting agents. Only the total-etch luting agent Calibra developed a distinct hybrid layer. The self-adhesive cements exhibited a more superficial interaction with dentin.
Regardless of the pre-cure temperature, the bonding potential of the self-adhesive resin cements was inferior to that of the total-etch luting agent tested as control. The adhesive properties of the BisCem and SAC-A were extremely scarce.
The bond strength of a composite resin bonded to various dental casting alloys with three adhesive systems--Silicoater, Panavia, and Superbond C&B--was investigated. The metal surfaces were treated solely with aluminum oxide blasting before application of the adhesive. Thermal cycling caused a reduction in bond strength for all combinations of the adhesive systems and alloys, but the Silicoater system recorded the greatest bond strength. The 4-META system was equivalent to Panavia system in bond strengths to most metals and exhibited greater strength with others.
This study investigated the transverse strength of repaired test specimens of heat-cured acrylic resin. The repair surfaces of the specimens were wetted with methyl methacrylate for various amounts of time before the autopolymerizing acrylic resin was applied to the joint space. A three-point loading test was used to determine the transverse strength of the test specimens, and the morphologic changes in the methyl methacrylate-wetted repair surface was analyzed by scanning electron microscopy. Visual inspection was used to determine whether the failures were adhesive or cohesive. The results revealed that repaired test specimens were weaker than those unrepaired (p < 0.001). The strength of the test specimens increased as the duration of methyl methacrylate wetting of the repair surfaces increased (p < 0.001). Furthermore, the number of adhesive failures was small if the repair surfaces were adequately wetted with methyl methacrylate. Scanning electron micrographs revealed that after 60- and 180-second wetting periods, the poly(methyl methacrylate) was noted to be dissolved with a smooth surface texture. This study suggests that proper wetting of the repair surface makes an important contribution to the strength of repaired acrylic resin.
The aim of this study was to evaluate early tensile bond strengths of three commercial resin cements (a dual-cured and two chemically cured) to bovine dentin. Bonding was performed in two environmental conditions, namely room environment (23 degrees C/50% RH) and oral environment (30 degrees C/80% RH). Tensile bond strengths were recorded at 10 minutes, 1 hour, and 1 day after the bonding procedure was completed and were analyzed using one-way ANOVA, Fisher's PLSD test, and Student's t-test. The results showed that bond strengths were statistically greater for all materials (P < 0.05) over time, except for Bistite Resin Cement between 10 minutes and 1 hour (P > 0.05). Variation between the bonding environments was observed only for Bistite Resin Cement at both 10 minutes and 1 hour, and Panavia 21 at 10 minutes. It was concluded that bond strengths were initially weak for the chemically cured materials, and all materials showed significantly greater bond strengths over the first 24 hours, but bonding environment had little influence.
To investigate the influence of contamination by water, human saliva, and blood on the bonding of metal brackets with a 4-META/MMA/TBB resin to etched enamel.
For compressive shear bond strength measurements, the surfaces of bovine enamel were prepared either by etching with 37% phosphoric acid solution for 10, 30, or 60 s and then dried with oil-free compressed air for 10 s, or by contaminating with water, human saliva, and blood. Brackets were applied with Super Bond under loads of 200, 400, or 600 g. The bonded samples were immersed in water for 1 d or thermo-cycled for 500 cycles, and the mean shear bond strengths were compared using two-way ANOVA and Scheffé's multiple comparisons test at P = 0.05.
The bond strengths to enamel etched for 60 s were independent of the variable load, regardless of the type of contamination. A short etching duration provided higher bond strengths than extended etching of samples contaminated with saliva and blood. The bond strengths to enamel etched for 10 s after thermal stress and immersion in water were from 11.4 to 30.4 MPa. The samples contaminated by saliva showed the lowest bond strength, and thermal stress did not reduce the bond strengths.
Breakage is a potential problem of provisional resin restorations. A method that effectively increases the strength of the resin is desirable.
This study examined the effects of the curing environment, air or water, and water temperature during polymerization on the mechanical properties of autopolymerizing resin.
After mixing the autopolymerizing methyl methacrylate resin for 10 seconds, it was placed in a stainless steel mold (2 x 2 x 25 mm). One minute and 50 seconds after the start of mixing, the mold containing the resin was placed under the following conditions: in air at 23 degrees C; or in water at 10 degrees C, 23 degrees C, 30 degrees C, 40 degrees C, 60 degrees C, and 80 degrees C. Six minutes after mixing began, the resin specimen was removed from the mold and the transverse test (3-point flexural test) was performed.
Alteration of conditions during polymerization revealed a significant effect on both the transverse strength and modulus of the resin (P <.0001). Both increased with an increase in water temperature. Water conditions of 60 degrees C to 80 degrees C produced more than 2 times greater transverse strength and modulus of the resin compared with polymerization in 23 degrees C air (P <.0001).
Polymerization of the resin in hot water greatly increased its mechanical properties. The method of placing resin restorations in hot water during polymerization may be useful for improving mechanical requirements and obtaining long-lasting performance.
A study was conducted to investigate the influence of temperature and relative humidity (RH) on the bond strengths of several recently developed dentin bonding systems. Six environmental conditions, (A) 25+/-0.5 degrees C, 50+/-5% RH, (B) 25+/-0.5 degrees C, 80+/-5% RH, (C) 25+/-0.5 degrees C, 95+/-5 % RH, (D) 37+/-0.5 degrees C, 50 +/-5 % RH, (E) 37+/-0.5 degrees C, 80+/-5% RH, (F) 37+/-0.5 degrees C, 95+/-5 % RH were used. Bovine mandibular incisors were mounted in self-curing resin and the facial surfaces were ground on wet #600 SiC paper to expose the dentin. After the tooth surface had been treated according to each manufacturer's instructions, adhesives were applied, followed by condensation of resin composites into a mold placed on the dentin surface. Fifteen specimens per group were stored in distilled water at 37 degrees C for 24 h, and then shear-tested at a cross-head speed of 1.0 mm/min. Statistical analysis was carried out with two-way ANOVA followed by Tukey's test (P<0.05). Dentin bond strengths decreased with increasing relative humidity but were not influenced by environmental temperature. Even though one-bottle adhesive systems require a wet dentin surface, their bond strengths are affected by an increase in environmental humidity.
Residual monomer contents and surface hardness are important factors in determining the serviceability of provisional restorations. The intent of this study was to systemically evaluate the effects of curing conditions on provisional polymethyl methacrylate (PMMA) resins which utilize a free-radical polymerization reaction. Combinations of the three curing factors of temperature, pressure, curing environment (water/air) were adjusted during the fabrication of autopolymerized specimen disks. The initial hardness of tested materials was measured with a microhardness tester 1 h after disc fabrication, and the amounts of residual methyl methacrylate (MMA) released into water were analyzed by reverse-phase HPLC after 7 d of water immersion. Results from multiple regressions showed that curing temperature was the dominant factor in improving resin surface hardness, whereas curing in water was the key factor for reducing the quantity of residual monomer. The pressure factor, which was thought to be critical for managing autopolymerized resins, showed no significant influences on the properties tested. ANOVA results showed that provisional PMMA resins cured in hot water, with or without pressure, significantly reduced the amount of residual MMA elution (up to 80%) and increased the microhardness values (up to 50%).
Although resin composite restorations may undergo relatively extreme temperature changes in the oral cavity, little is known about the effects of temperature on their adhesion to tooth structure. This study evaluated the effect of temperature on shear bond strength to dentin of three commercial resin dentin adhesives through testing of matured specimens over the 20 degrees to 55 degrees C temperature range. A significant difference (p < 0.05) was observed between 20 degrees C and 55 degrees C for all the materials, and for one of the materials, a significant difference was also observed between 20 degrees C and 37 degrees C.
Bonding failures of repair resin to denture base resin occurs when denture base resin is wet, however, little is known of how water relates to failures.
This study evaluated the influence of water absorbed in denture base resin on the bond strength and resistance to cyclic thermal stresses of autopolymerizing resins bonded to denture base resin.
Denture base resin disks (n = 180; 12 mm diameter and 3 mm thick) were fabricated from heat-polymerized acrylic resin (Lucitone 199). The disks were divided into groups (n = 60) with 3 conditions of water content: (1) complete water saturation (control), (2) superficial desiccation by blowing air on the specimen, or (3) complete desiccation. Each denture base specimen received 1 of 3 surface treatments (n = 20) including: (1) no treatment, (2) airborne-particle abrasion, or (3) methylene chloride application. An autopolymerizing repair resin (Repair Material, n = 10) or reline resin (Tokuso Rebase Normal set, n = 10) was applied to the bonding area (5 mm diameter) and polymerized at 37 degrees C for 10 minutes. The resistance to cyclic thermal stress was determined after subjecting the specimens to 50,000 thermal cycles between 4 degrees C and 60 degrees C water baths with a 1-minute dwell time (n = 5 per group). Bond strength (MPa) was measured by shear bond testing at a 1.0 mm/min crosshead speed until the applied resin debonded from denture base resin. Data were statistically analyzed by 3-way analysis of variance and multiple comparisons among the groups were performed with Bonferroni test (alpha = .05).
The mean bond strengths of repair resin to airborne-particle-abraded denture base specimens were not significantly influenced by either thermal cycling or water content. The mean bond strengths of reline resin significantly decreased after thermal cycling (P < .0001) regardless of the conditions of surface treatment and water content. For methylene chloride treated specimens, bond strengths of both repair and reline resins to completely water saturated specimens were significantly higher than those of completely desiccated specimens (P = .0048 for repair resin, P < .0001 for reline resin) after thermal cycling.
Bond strengths of autopolymerizing resin to denture base resin were not significantly influenced by water content of denture base resin but were significantly influenced by resin type, thermal cycling, and surface treatment.
Adhesion promoting monomers -5-(4-vinylbenzyl)-2-thiobarbituric acid (5VS), 9,10-epithiodecyl methacrylate (EP8MA), 9,10-epithiodecyl 4-vinylbenzoate (EP8VB), and 3,4-epithiobutyl 2,2-bis(methacryloyloxymethyl)propionate (EP2BMA)--were added to the MMA liquid of a MMA-PMMA/TBBO resin. Three dental precious metal alloys were butt-jointed together with the MMA-PMMA/TBBO adhesive resin, and tensile bond strength was measured after 2,000 thermocycles in water. Polymerization kinetics of MMA by 2,2'-azobis (isobutyronitrile) at 70 degrees C in the presence of 5VS, EP8MA, EP8VB, or EP2BMA were examined quantitatively using a DSC to clarify the relationship between the adhesive properties of MMA-PMMA/TBBO adhesive resin and the kinetic polymerization behavior thereof. Obtained kinetic parameters indicated that 5VS was not suitable as an adhesive monomer for adhesive resin formulations and that EP2BMA possessed the latent potential as an adhesive monomer. Further, tensile test results revealed the applicability of EP8MA, EP8VB, and EP2BMA as an adhesive monomer component of adhesive resin formulations.
To assess whether the pre-cure temperature of resin cements significantly influenced the bonding potential to dentin.
Forty extracted molars were randomly divided into 8 groups (n=5): Groups (1-4) RelyX Unicem (RU, 3 M ESPE) and Groups (5-8) Panavia F 2.0 (PF, Kuraray Co.), at pre-cure temperatures of 4, 24, 37, and 60 degrees C, respectively. Cements were used in dual-cure mode for luting composite overlays (Paradigm MZ100, 3 M ESPE) to dentin. Microtensile bond strength testing and scanning electron microscope (SEM) observations of cement-dentin interfaces were performed.
Group 4 had to be eliminated as RU at 60 degrees C underwent such an accelerated curing that was already set at the time of dispensing. The bond strengths (MPa) measured at refrigerator, room, and intraoral temperature were, respectively: RU 5.4+/-1.7, 11.4+/-6.1, 10.6+/-4.2; PF 7.4+/-3.7, 13.9+/-6.2, 12+/-5.2. The statistical analysis revealed that both luting agents developed a significantly weaker adhesion when used at refrigerator temperature (p<0.05). No statistically significant differences in bond strength were recorded when either cement was used at 24 or 37 degrees C (p>0.05). Pre-heating of PF to 60 degrees C resulted in a significant increase in bond strength (20.7+/-9.4 MPa; p<0.05). SEM observations disclosed an enhanced potential of PF to form a hybrid layer as the temperature increased over 4 degrees C. RU exhibited a less porous and more homogeneous layer at intraoral than at refrigerated temperature.
It is advisable to let refrigerator-stored resin cements warm up to at least room temperature prior to clinical use. Pre-heating to 60 degrees C enhances the bonding potential of PF.
In vitro evaluation of the influence of repairing condition of denture base resin on the bonding of autopolymerizing resins
- H Minami
- S Suzuki
- Y Minesaki
- H Kurashige
- T Tanaka
Influence of environmental conditions on orthodontic bracket bonding of self-etching systems
- A Rikuta
- T Toshida
- K Tsubota
- H Tsuchiya
- A Tsujimoto
- M Ota
- M Miyazaki
Rikuta A, Toshida T, Tsubota K, Tsuchiya H, Tsujimoto A,
Ota M, Miyazaki M. Influence of environmental conditions
on orthodontic bracket bonding of self-etching systems. Dent
Mater J 2008; 27: 654-659.