Pilot evaluation of resin composite cement adhesion to zirconia using a novel silane system

OBJECTIVE: In this study, we evaluated the effect of two silane coupling agents and their blends with a cross-linker silane on the bond strength of a dimethacrylate-based resin composite cement to surface-conditioned zirconia. MATERIAL AND METHODS: A total of 40 planar zirconia specimens were used for 8 test groups. After alumina particle abrasion, followed by tribochemical silica-coating, the specimens were randomly assigned to four silanizations: with 1.0 vol% 3-methacryloyloxypropyltrimethoxysilane or 1.0 vol% 3-mercaptopropyltrimethoxysilane or their blends with 1.0 vol% 1,2-bis-(triethoxysilyl)ethane (all in ethanol/water). The resin composite (RelyX ARC, 3M ESPE) stubs (n=10/group) were light-polymerized onto zirconia specimens. Four test groups were tested without water storage and 4 thermo-cycled at 6000 cycles (5+/-1 degrees C to 55+/-1 degrees C), with a dwelling time of 30 s. The shear bond strength of the cement stubs to zirconia was measured using a universal testing machine at a constant cross-head speed of 1 mm/min. Scanning electron microscopy was employed for imaging the zirconia surface after conditioning and testing. Failure mode was evaluated visually. A surface chemical analysis was carried out with the EDXA system. RESULTS: The highest shear bond strength was 21.9+/-8.7 MPa, obtained with a blend of 3-mercaptopropyltrimethoxysilane and 1,2-bis-(triethoxysilyl)ethane (dry storage), and 16.0+/-1.5 MPa, with 3-methacryloyloxypropyltrimethoxysilane (thermo-cycled). Thermo-cycling decreased the bond strengths significantly (ANOVA, p<0.01), and the silanes differed significantly (p<0.005). Some specimens suffered from spontaneous debonding during thermo-cycling. CONCLUSIONS: The luting cement adhesion might be promoted to silica-coated zirconia with 1.0 vol% 3-methacryloyloxypropyltrimethoxysilane and with a blend of 1.0 vol% 3-mercaptopropyltrimethoxysilane and 1.0 vol% 1,2-bis-(triethoxysilyl)ethane.     

Evaluation of five dental silanes on bonding a luting cement onto silica-coated titanium

OBJECTIVES: Five commercial dental silanes were evaluated in vitro as adhesion promoters bonding a luting cement to silica-coated titanium surfaces. METHODS: Titanium slides (n=20) were cleaned with alumina sand and then silica-coated with a special sand consisting of alumina particles coated with silica. The bonding of a resin composite cement (3M ESPE, Seefeld, Germany) to silica-coated and silanized titanium was evaluated by using the dental silane (RelyX Ceramic Primer) that belongs to the RelyX ARC cementing kit, and comparing it to four other dental silanes (Bisco Porcelain Primer, Cimara, ESPE Sil, and Pulpdent Silane Bond Enhancer). The resin composite cement stubs (n=8) were light-polymerized onto a silanized silica-coated titanium surface. The shear bond strength of the cement stubs was measured after dry storage and thermo-cycling 6000 times between 5 and 55 degrees C. The silanes and their reactions were chemically monitored by using Fourier transform infrared analysis. RESULTS: Statistical analysis using ANOVA revealed that the brand of silanes and the types of storage condition differ significantly (p<0.005). The highest shear bond strength was obtained with RelyX ceramic silane in dry conditions (19.5+/-4.3 MPa), and after thermo-cycling (16.6+/-3.5 MPa). The lowest results were obtained using Pulpdent Silane Bond Enhancer, in dry conditions (7.8+/-2.2 MPa), and after thermocycling (5.3+/-2.4 MPa). The analysis showed that silanes had different pH values. Some differences were detected between the silanes and their reactions. CONCLUSIONS: Dental silanes provide different bonding strengths and have differences in their pH, solvent system and silane concentration.     

The effect of five silane coupling agents on the bond strength of a luting cement to a silica-coated titanium.

OBJECTIVES: The adhesive performance of five silane coupling agents in adhering resin composite cement (3M ESPE) to silica-coated titanium was evaluated. Titanium was tribochemically silica-coated by using the Rocatec system. METHODS: Two volume percent solutions of 3-acryloyloxypropyltrimethoxysilane (Toray Dow Corning Silicone), N-[3-(trimethoxysilyl)propylethylenediamine] (Dow Corning), 3-mercaptopropyltrimethoxysilane (Toray Dow Corning Silicone) and bis-[3-(triethoxysilyl)propyl]polysulfide (Dow Corning) were prepared in 95 vol.% acidified ethanol and allowed to activate (hydrolyze). A pre-activated ca. 2 vol.% 3-methacryloyloxypropyltrimethoxysilane (ESPE Sil) was used as a control. The silanes were applied onto silica-coated titanium slides. Chemical activation reactions of the silanes were monitored by Fourier transform infrared spectrometry (Perkin-Elmer Spectrum One). RelyX ARC (3M ESPE) resin composite cement stubs were applied and photo-polymerized onto silica-coated titanium. The specimens were thermo-cycled (6000 cycles, 5-55 degrees C). RESULTS: Statistical analysis (ANOVA) showed that the highest shear bond strength (n=8 per group) value after thermocycling, 14.8 MPa (S.D. 3.8 MPa), was obtained with 2.0 vol.% 3-acryloyloxypropyltrimethoxysilane. Silanization and results with 3-methacryloyloxypropyltrimethoxysilane (control, ESPE Sil) did not statistically differ from 3-acryloyloxypropyltrimethoxysilane, 14.2 MPa (S.D. 5.8). The lowest shear bond strength was 7.5 (S.D. 1.9) MPa for N-[3-(trimethoxysilyl)propylethylenediamine] and 7.5 (S.D. 2.5) MPa for bis-[3-(triethoxysilyl)propyl]polysulfide. Both the type of silane (p<0.001) and storage conditions affected significantly the shear bond strength values (p<0.001). All silanes became activated according to the infrared spectroscopic analysis. SIGNIFICANCE: Silanization with 3-acryloyloxypropyltrimethoxysilane or 3-mercaptopropyltrimethoxysilane might offer an alternative for bonding a luting cement to silica-coated titanium.     

Isocyanato- and methacryloxysilanes promote Bis-GMA adhesion to titanium

In dentistry, adhesion promotion with 3-methacryloyloxypropyltrimethoxysilane is usually sufficient, but its hydrolytic stability is a continuous concern. The hydrolytic stability of an alternative, 3-isocyanatopropyltriethoxysilane, was compared with that of conventional 3-methacryloyloxypropyltrimethoxysilane. Two silanes, both in 0.1 and 1.0 vol-% in ethanol-water, were evaluated in the attachment of an experimental bis-phenol-A-diglycidyldimethacrylate (Bis-GMA) resin to grit-blasted (with two different systems) titanium. Silane hydrolysis was monitored by FTIR spectrometry. Bis-GMA resin was applied and photo-polymerized on titanium. The specimens were thermocycled (6000 cycles, 5-55 degrees C). Surface analysis was carried out with scanning electron microscopy. Statistical analysis (ANOVA) showed that the highest shear bond was achieved with 0.1% 3-isocyanatopropyltriethoxysilane (12.5 MPa) with silica-coating, and the lowest with 1.0% 3-methacryloyloxypropyltrimethoxysilane (3.4 MPa) with alumina-coating. The silane, its concentration, and the grit-blasting method significantly affected the shear bond strength (p < 0.05). SEM images indicated cohesive failure of bonding, and, in conclusion, 3-isocyanatopropyltriethoxysilane is a potential coupling agent.     

The effect of a novel silane blend system on resin bond strength to silica-coated Ti substrate

OBJECTIVES: The adhesive performance of 3-acryloyloxypropyltrimethoxysilane and a silane blend consisting of 3-acryloyloxypropyltrimethoxysilane and 1,2-bis(triethoxysilyl)ethane, adhering an experimental dendrimer-based resin to a silica-coated titanium surface, conditioned by CoJet method, was evaluated in vitro. METHODS: 3-Acryloyloxypropyltrimethoxysilane (1.0 vol%) and a blend of 3-acryloyloxy-propyltrimethoxysilane and 1,2-bis(triethoxysilyl)ethane (both 1.0 vol%) were prepared in acidified 95 vol% ethanol. A commercial 3-methcryloyloxypropyltrimethoxysilane (ESPE Si) was used as control. The silanes were applied onto tribochemically silica-coated titanium surfaces. Fresh silane solution hydrolysis (activation) was monitored by Fourier transform infrared (FTIR) spectrometry. Experimental dendrimer resin stubs were applied and photo-polymerized on titanium. The specimens were thermocycled (6000 cycles, 5-55 degrees C). Before measuring shear bond strength of the resin to titanium, surface imaging was carried out with a scanning electron microscope (SEM) with elemental analysis applying energy dispersive X-ray analysis (EDXA). RESULTS: Statistical analysis (ANOVA) showed that the highest shear bond was obtained with 1.0 vol% 3-acryloyloxypropyltrimethoxysilane+1.0 vol% 1,2-bis(triethoxysilyl)ethane blend (5.2+/-1.3 MPa), and the lowest result with fresh commercial 3-methacryloyloxypropyltrimethoxysilane, ESPE Sil (2.1+/-0.8 MPa). 3-Acryloyloxypropyltrimethoxysilane yielded 4.1+/-1.0 MPa. The type of silane affected significantly the shear bond strength (ANOVA, p<0.001). All silanes were activated according to the infrared spectra. The SEM/EDXA analysis revealed an uneven distribution of titanium, silicon, and aluminum on silica-coated Ti surfaces. CONCLUSION: Silanization with 3-acryloyloxypropyltrimethoxysilane might offer better bonding of a novel dendrimer resin to silica-coated titanium than using a pre-hydrolyzed 3-methacryloyloxypropyltrimethoxysilane.     

Enhanced resin-composite bonding to zirconia framework after pretreatment with selected silane monomers

Objective

To evaluate the effect of five experimental silane monomer primers in vitro on the shear bond strength of a phosphate ester resin-composite cement bonded to a silicatized zirconia framework.

Methods

A total of 144 planar zirconia (Procera AllZircon) specimens were subjected to tribochemical silica treatment, randomly divided into 12 sub-groups (n = 12), and silanized with 1.0% (v/v) activated solutions of 3-acryloxypropyltrimethoxysilane, 3 glycidoxypropyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, styrylethyltrimethoxysilane, and 3-isocyanatopropyltriethoxysilane, which had been prepared in 95% ethanol (pH 4.5). A ready-to-use 3-methacryloxypropyltrimethoxysilane (RelyX™ Ceramic Primer) was used as the control. One resincomposite cement (RelyX™ Unicem) stub was bonded to each silicatized and silanized zirconia specimen. Half of the specimen groups were dry-tested and half were thermo-cycled at 6000 cycles between 5 °C and 55 °C, with a constant dwelling time of 30 s. The shear bond strengths of the cement stubs bonded to zirconia were measured using a universal testing machine using a constant cross-head speed of 1 mm/min. The silane primer activation was evaluated using Fourier-transform infrared spectroscopy.

Results

The highest shear bond strength was obtained for 3-acryloxypropyltrimethoxysilane in dry storage, 11.7 MPa (SD, 2.3 MPa) and after thermo-cycling 17.6 (4.1) MPa for glycidoxypropyltrimethoxysilane. The lowest shear bond strength values were obtained with control silane: in dry storage, 4.5 (1.3) MPa, after thermo-cycling 6.5 (2.6) MPa. Thermo-cycling increased the bond strengths significantly (ANOVA, p < 0.001) and differently for each type of silane (ANOVA, p < 0.001).

Significance

Silanization with five experimental silane primers in vitro produced significantly greater shear bond strengths than the ready-to-use control silane.     

The effect of three silane coupling agents and their blends with a cross-linker silane on bonding a bis-GMA resin to silicatized titanium (a novel silane system)

OBJECTIVES: Three activated organofunctional silane coupling agents alone and blended with a non-functional cross-linker silane were evaluated as adhesion promoters in an experiment where a bis-GMA (bis-phenol-A-diglycidyldimethacrylate) resin was bonded to silicatized titanium. The adhesive performances of the silanes were assessed as shear bond strength values. MATERIALS AND METHODS: 3-Methacryloyloxypropyltrimethoxysilane, N-[3-(trimethoxysilyl)propyl]ethylenediamine and [3-(triethoxysilyl)propyl]urea were prepared as 1.0vol.% solutions in 95 vol.% ethanol. They were each also blended with 1.0 vol.% 1,2-bis-(triethoxysilyl)ethane solutions that were activated for 1 or 24 h. Titanium slides were cleaned, silicatized, distributed randomly to study groups and silanized with nine silane solutions. After silanization experimental bis-GMA resin stubs were photo-polymerized and post-polymerized in a light-curing unit. The shear bond strength was measured as 'dry samples' and after thermo-cycling (6000 cycles at 5-55 degrees C). RESULTS: The type of silane affected significantly the shear bond strength (p<0.001) and the use of cross-linker silane (p<0.005) according to the statistical analysis (ANOVA). It showed that the highest shear bond strength for thermo-cycled resin stub samples (n=8/group) was obtained with a blend of 1.0vol.% 3-methacryloyloxypropyltrimethoxysilane+1.0 vol.% 1,2-bis-(triethoxysilyl)ethane blend (10.4+/-3.5 MPa). The lowest results were obtained with 1.0 vol.% [3-(triethoxysilyl)propyl]urea (4.5+/-1.0 MPa), and with 1.0 vol.% N-[3-(trimethoxysilyl)propyl]ethylenediamine (4.5+/-1.4 MPa). CONCLUSIONS: Silanization with a blend of a functional silane and a cross-linker silane (a novel silane system) might improve the hydrolytic stability of a siloxane film between silicatized titanium and a bis-GMA resin.     

Extrusion shear strength between an alumina-based ceramic and three different cements

STATEMENT OF PROBLEM: Surface treatment is an essential step in bonding a ceramic to resin. Alumina ceramics are particularly difficult to prepare for adequate bonding to composite resin cements. PURPOSE: The purpose of this study was to evaluate the bond strength between a densely sintered alumina ceramic and bovine dentin with 2 adhesive resin cements and a resin-modified glass ionomer cement using an extrusion shear strength test. MATERIAL AND METHODS: Alumina cones (n=30), 4 mm in height, 3 mm in diameter at the small end, and with an 8-degree taper, were fabricated. Without any treatment, the cones were cemented in a standardized cavity in 2.5-mm-thick bovine dentin discs using 1 of 3 cement systems: Panavia F, RelyX ARC, or RelyX Luting. The cements were manipulated following the manufacturers' instructions. After 24 hours of storage at 37 degrees C, an extrusion shear test was performed in a universal testing machine at 0.5 mm/min until bonding failure. The data were analyzed using 1-way ANOVA and Tukey HSD test (alpha=.05). All fractured specimens were examined at x25 magnification and classified by fracture mode. Representative specimens were selected for SEM observation. RESULTS: The highest strength values were obtained with Panavia F, and they were significantly higher (P<.05) than each of the other 2 cements, which were not significantly different from each other. Panavia F resulted in predominantly mixed failure and RelyX ARC and RelyX Vitremer showed primarily adhesive failure. CONCLUSIONS: An MDP-containing adhesive system (Panavia F) provides better extrusion bond strength to a high-density alumina ceramic than a Bis-GMA resin luting agent system (RelyX ARC) or a resin-modified glass ionomer cement system (RelyX Luting).     

Shear bond strength of Bis-GMA resin and methacrylated dendrimer resins on silanized titanium substrate.

OBJECTIVES: The study compared the bond strengths of three resins, Bis-GMA and two novel experimental methacrylated polyester dendrimer resins to grit-blasted titanium substrate with three silanes. METHODS: Two commercial dental silanes (ESPE Sil and Monobond-S) and an experimental 0.5 vol% 3-methacryloxypropyltrimethoxysilane were applied to grit-blasted Ti substrates. Light-polymerizable resins of Bis-GMA and methacrylated dendrimer were applied to the grit-blasted Ti substrate with polyethylene molds. The substrates with resin stubs (n = 10) were thermocycled (6000 cycles, 5-55 degrees C) or kept in water (37 degrees C, 24 h). The shear bond strength of the resin was measured at a crosshead speed of 1.0 mm min(-1). The surface examination, before and after silanization, was made with a scanning electron microscope (SEM). The silane reactions on the Ti surface were monitored by Fourier transform infrared spectrometry. RESULTS: Statistical analysis (ANOVA) showed that the highest shear bond for thermocycled samples was obtained for Bis-GMA with Monobond-S (19.4 MPa, standard deviation (SD) 7.1 MPa), and after water storage with a laboratory-made silane (26.4 MPa, SD 8.1 MPa). The dendrimer and Bis-GMA resins conferred equal bonding properties to grit-blasted titanium after thermocycling. The silane, resin type, and storage conditions significantly affected the shear bond strength (p < 0.001 for all factors). SEM images suggested a mainly cohesive type of bonding failure. SIGNIFICANCE: A dendrimer based resin and the Bis-GMA resin systems conferred statistically equivalent bonding properties to silica-coated Ti after thermocycling.     

Effect of surface conditioning methods on the bond strength of luting cement to ceramics

OBJECTIVES: This study evaluated the effect of three different surface conditioning methods on the bond strength of a Bis-GMA based luting cement to six commercial dental ceramics. METHODS: Six disc shaped ceramic specimens (glass ceramics, glass infiltrated alumina, glass infiltrated zirconium dioxide reinforced alumina) were used for each test group yielding a total number of 216 specimens. The specimens in each group were randomly assigned to one of the each following treatment conditions: (1) hydrofluoric acid etching, (2) airborne particle abrasion, (3) tribochemical silica coating. The resin composite luting cement was bonded to the conditioned and silanized ceramics using polyethylene molds. All specimens were tested at dry and thermocycled (6.000, 5-55 degrees C, 30 s) conditions. The shear bond strength of luting cement to ceramics was measured in a universal testing machine (1 mm/min). RESULTS: In dry conditions, acid etched glass ceramics exhibited significantly higher results (26.4-29.4 MPa) than those of glass infiltrated alumina ceramics (5.3-18.1 MPa) or zirconium dioxide (8.1 MPa) (ANOVA, P<0.001). Silica coating with silanization increased the bond strength significantly for high-alumina ceramics (8.5-21.8 MPa) and glass infiltrated zirconium dioxide ceramic (17.4 MPa) compared to that of airborne particle abrasion (ANOVA, P<0.001). Thermocycling decreased the bond strengths significantly after all of the conditioning methods tested. SIGNIFICANCE: Bond strengths of the luting cement tested on the dental ceramics following surface conditioning methods varied in accordance with the ceramic types. Hydrofluoric acid gel was effective mostly on the ceramics having glassy matrix in their structures. Roughening the ceramic surfaces with air particle abrasion provided higher bond strengths for high-alumina ceramics and the values increased more significantly after silica coating/silanization.     

Effect of the cross-linking silane concentration in a novel silane system on bonding resin-composite cement

Objective. Four experimental blends of an organo-functional silane monomer with a non-functional cross-linking silane monomer (a novel silane system) were evaluated as adhesion promoters in an experiment in which a resin-composite cement was bonded to silica-coated titanium. Material and Methods. 3-Acryloyloxypropyltrimethoxysilane (as constant 1.0 vol%) was blended with 1,2-bis-(triethoxysilyl)ethane, where its concentration was 0.1, 0.2, 0.3, or 0.5 vol%. Titanium slides (n=20) were grit-blasted, silica-coated, and silanized with four experimental silane solutions, with a pre-activated silane Cimara? (VOCO, Germany) as control. After silanization, resin-composite cement stubs (Bifix? QM; VOCO, Germany) were photo-polymerized. The shear bond strength was measured after dry storage (24 h) or after thermo-cycling (6000 cycles between 5°C and 55°C). The resin stub failure mode was determined. Results. Statistical analysis (ANOVA) showed that type of storage (p <0.05) and concentration of cross-linker silane (p<0.005) both significantly affected the shear bond strength. The highest shear bond strength was obtained with a blend of 1.0 vol% 3-acryloyloxypropyltrimethoxysilane+0.3 vol% 1,2-bis-(triethoxysilyl)ethane, 15.9 MPa (standard deviation SD 3.4 MPa) for both the thermo-cycled group and after dry storage (24 h), 14.3 MPa (SD 4.1 MPa) (n=8/group). The lowest values were obtained with Cimara? silane 7.3 MPa (SD 2.2 MPa) in dry storage and 7.9 MPa (SD 2.0 MPa) obtained with 1.0 vol% 3-acryloyloxypropyltrimethoxysilane+0.1 vol% 1,2-bis-(triethoxysilyl)ethane. The failure type was mainly cohesive. Conclusion. A novel silane system with an optimal concentration of the cross-linking silane may produce significantly higher shear bond strength between silica-coated titanium and resin-composite cement compared to a pre-activated silane product.     

The shear bond strength between luting cements and zirconia ceramics after two pre-treatments

This study evaluated the shear-bond strength of 11 luting cements from different material classes to manufactured pre-treated zirconia ceramics (Lava: 97% ZrO2, stabilized with 3% Y2O3). In addition, the influence of the curing method on shear-bond strength was investigated. The cements examined were one zinc-phosphate cement (Fleck's zinc cement), two standard glass-ionomer cements (Fuji I, Ketac-Cem), three resin-modified glass-ionomer cements (Fuji Plus, Fuji Cem, RelyX Luting), four standard resin cements (RelyX ARC, Panavia F, Variolink II, Compolute) and one self-adhesive universal resin cement (RelyX Unicem). The ceramic surface was sand-blasted with 100-microm alumina or tribochemically coated with silica. After bonding procedure, one group was tested after 30 minutes (Time I), the other group was stored in distilled water at 37 degrees C for 14 days and subsequently thermocycled 1000 times (Time II). Statistical analysis was performed by multifactorial ANOVA models with interactions. For multiple pairwise comparisons, the Tukey method was used. After sandblasting, the highest shear-bond strength was obtained for the self-adhesive universal resin cement at 9.7 MPa (Time I) and 12.7 MPa (Time II), respectively. When using the Rocatec system, the highest values were found for one of the resin cements at 15.0 MPa (Time I) and for the self-adhesive universal resin cement at 19.9 MPa (Time II).     

Effect of endodontic sealer and resin luting strategies on pull-out bond strength of glass fiber posts to dentin

The aim of this study was to evaluate the influence of eugenol-containing endodontic sealers and luting strategy on the pull-out bond strength of glass fiber posts to dentin. Sixty-four bovine incisors were randomly assigned into two groups of 32 specimens each for obturation procedure with gutta-percha only, or with Pulp Canal Sealer EWT Subsequently, the roots were prepared for the fiber post Reforpost and all specimens of each endodontic sealing procedure were allocated to four groups (n = 8), according to the strategies for post cementation: A) Single Bond 2 and RelyX ARC; B) All Bond 2 and C&B cement; C) All Bond 2 and RelyX ARC; D) Single Bond 2 and C&B Cement. The posts were cemented immediately after the endodontic treatment. The pull-out test was performed at a cross-head speed of 0.5 mm/min in a universal testing machine (EMIC). Data (Kgf) were submitted to a two-way ANOVA and Tukey test (p < or = 0.05). The eugenol-based sealer did not influence the pull-out bond strength of fiber posts regardless of the luting strategy. RelyX ARC showed higher bond strength than C&B Cement when used with Single Bond 2 adhesive system, when the eugenol-based sealer was present. All Bond 2, when associated to all cements studied, promoted similar bond strength, regardless of the eugenol-containing endodontic sealer In conclusion, eugenol-containing sealer did not influence the pull-out bond strength values of the resin luting systems for glass fiber post cementation. The bond system and resin cement association from the same manufacturer had similar bond strength values for dentin.     

3种树脂水门汀对CAD/CAM全瓷-牙本质剪切强度的比较

目的:评价3种树脂水门汀对CAD/CAM全瓷-牙本质剪切强度的影响。方法:选取新鲜拔除的人磨牙30颗,制备牙本质黏结面,随机分为3组(n=10),分别选用全酸蚀树脂水门汀RelyX ARC、自酸蚀树脂水门汀Clearfil DCBond和自黏结树脂水门汀RelyX Unicem对CAD/CAM硅酸锂玻璃全瓷进行黏结,测试3种树脂水门汀对CAD/CAM全瓷-牙本质的剪切强度,并通过立体显微镜观察牙本质的黏结界面。采用SPSS11.0软件包对数据进行统计学分析。结果:RelyX ARC组的剪切强度为(15.90±6.15)MPa,Clearfil DC Bond组的剪切强度为(14.41±5.07)MPa,而RelyXUnicem组的剪切强度为(23.29±7.39)MPa,与前2组相比有显著性差异(P<0.05)。立体显微镜观察显示,3组黏结断面均位于牙本质与树脂水门汀之间。结论:自酸蚀树脂水门汀及自黏结树脂水门汀与CAD/CAM硅酸锂玻璃陶瓷修复体的黏结强度不低于传统全酸蚀树脂水门汀,且临床操作简便,为临床全瓷黏结提供了更多便利与选择。     

Bonding of resin composite luting cements to zirconium oxide by two air-particle abrasion methods

OBJECTIVE: This study evaluated the shear bond strength of two resin composite luting cements to zirconium oxide ceramic substrate using two air-particle abrasion methods. METHODS: Two resin composite cements, RelyX Unicem (3M ESPE) and Panavia F (Kuraray), each with an acidic composition, were used in combination with a zirconium oxide (DCS Dental AG) substrate containing Al2O3 and SiO2 (Rocatec system, 3M ESPE) and two air-particle abrasion methods. The shear bond strength of the resin composite cement to the substrate was tested after the samples were either water-stored for one week or thermocycled following 24 hours of water storage. RESULTS: The RelyX Unicem resin composite cement specimens with the Rocatec treatment (20.9 +/- 4.6 Mpa and 20.1 +/- 4.2 MPa, respectively, n = 12) demonstrated the highest shear bond strength. Alternatively, the lowest values were obtained for the Panavia F resin cement samples, with Al2O3 air-particle abrasion in both storage conditions, water storage for one week (17.7 +/- 8.9MPa) or thermocycling after 24 hours of water storage (16.3 +/- 4.9 MPa). Neither storage condition or particle abrasion system significantly affected shear bond strengths (ANOVA, p > 0.05). CONCLUSION: It was concluded that two different surface conditioning methods and storage conditions did not significantly affect the bonding properties of Panavia F and RelyX Unicem resin composite luting cements to Zirconia.     

氧化锆陶瓷与三种树脂粘接剂粘接剪切强度比较

目的探讨适合牙科氧化锆陶瓷的粘接材料。方法将烧结后的氧化锆陶瓷片分为3组,每组32片,分别采用三种自酸蚀粘接剂RelyX Unicem、PanaviaTM F、Superbond C﹠B与喷砂后的氧化锆陶瓷片粘接,水浴24h和水浴30d后,测试其粘接剪切强度。数据用SAS9.12软件进行统计学分析,粘接断面用扫描电镜观察。结果 PanaviaTMF树脂粘接材料粘接强度最好,分别为（31.36±3.49）MPa（水浴24h）、（29.52±3.44）MPa（水浴30d）。Superbond C﹠B能够取得较好的初期粘接强度（31.85±3.61）MPa（水浴24h）,但水浴30d后明显下降至（21.32±2.58）MPa,P〈0.05。RelyX Unicem的初期（水浴24h）粘接强度最小为（13.29±3.05）MPa,P〈0.0001,但水浴30d后粘接强度为（12.06±2.28）MPa,未见明显降低,P（0.05。结论含有MDP磷酸单体的树脂粘接材料可以使牙科氧化锆陶瓷获得最好的粘接效果。使用不含无机填料的化学固化型纯树脂粘接剂可以取得较好的初期粘接强度但长期效果欠佳。一步法自酸蚀树脂粘接剂虽然没有很高的初期粘接强度,但粘接效果尚能持久。     

三种树脂粘接剂对可切削复合树脂与牙本质粘接强度的比较研究

目的 通过比较3种树脂粘接剂对聚甲基丙烯酸甲酯-纳米二氧化硅-二氧化锆(polymethylmecrylate/nano SiO2-ZrO2,PNSZ)可切削复合树脂与牙本质的粘接强度的差异,寻找适合PNSZ可切削复合树脂的树脂粘接剂,为临床应用提供参考.方法 使用树脂粘接剂A(RelyX ARC)、B(Panavia-F)和c(Variolink II)粘接PNSZ可切削复合树脂与牙本质,测试剪切粘接强度和微拉伸粘接强度(各分为A、B、C 3组,每组10个试件),并采用50倍立体显微镜观察断裂模式.结果 剪切测试中A、B、C组试件的粘接强度分别为(14.07±4.67)、(13.17±4.63)、(12.10±2.18)MPa,差异无统计学意义(P＞0.05);微拉伸测试中A、B、C组试件的粘接强度分别为(11.49±4.90)、(9.66±4.15)、(10.11±4.20)MPa,差异无统计学意义(P＞0.05).立体显微镜观察显示,3种粘接剂的断裂模式均以牙本质-粘接剂界面的断裂为主.结论 3种树脂粘接剂对PNSZ可切削复合树脂与牙本质的粘接效果相近.PNSZ可切削复合树脂一粘接剂界面的粘接优于牙本质-粘接剂界面.     

Bond strength between polymer resin-based cement and porcelain-dentin surfaces: influence of polymerization mode and early cyclic loading

PURPOSE: The objective of this study was to verify the influence of resin cement polymerization mode and early cyclic loading on the bond strength of porcelain-dentin specimens. MATERIALS AND METHODS: Two cementation systems, Choice/One-Step and RelyX ARC/Single Bond, were tested. Porcelain truncated cones were bonded into cavities prepared in sections of bovine root dentin. Each system was tested with the resin cement in dual-cure and self-cure mode (with and without photoactivation, respectively). Half of the specimens were load cycled 15 minutes after cement mixing (60 N, 20 times). The other half were not submitted to mechanical loading (control). After 24-hour storage in distilled water (37 degrees C), the extrusion shear test was performed. Data were analyzed by three-way ANOVA. RESULTS: With both systems, some specimens built with the cement in self-cure mode debonded during cyclic loading (RelyX ARC/Single Bond 47%; Choice/One-Step 13%). No significant system effects were detected. Mean bond strength under the dual-cure mode (13.4 MPa, SD 3.6) was significantly higher than the corresponding mean for the self-cured specimens (5.7 MPa, SD 2.6). No reduction in bond strength was observed for the specimens that survived the early cyclic loading. CONCLUSION: Resin cements in dual-cure mode presented higher bond strengths than self-cured materials. Early load cycling caused debonding of some self-cured specimens. However, the bond strength of the survivor specimens was not affected by load cycling.     

通用型粘接剂和树脂水门汀对氧化锆剪切粘接强度的影响

目的 研究通用型粘接剂和树脂水门汀对氧化锆陶瓷剪切粘接强度和耐久性的影响。方法 氧化锆陶瓷烧结制作20 mm×10 mm×10 mm和10 mm×10 mm×10mm两种尺寸的试件,实验分为12组,将这2种试件分别采用不同的树脂水门汀（RelyX Ultimate树脂水门汀、Clearfil SAC自粘接树脂水门汀）和通用粘接剂（无粘接剂、Scotchbond通用粘接剂、Clearfil SE One粘接剂）在不同的储存条件（水浴、水浴+冷热循环）下进行粘接。测试剪切粘接强度,分析断裂形态。结果 水门汀（F=8.41,P<0.01）和粘接剂（F=30.34,P<0.01）对氧化锆剪切粘接强度的影响有统计学意义;储存条件对剪切粘接强度的影响无统计学意义（F=1.83,P=0.18）。RelyX Ultimate树脂水门汀、无粘接剂、水浴+冷热循环储存时的剪切粘接强度最低（14.02 MPa±6.86 MPa）,RelyX Ultimate树脂水门汀、Scotchbond通用粘接剂、水浴+冷热循环储存时的剪切粘接强度最高（54.12 MPa±8.37 MPa）。结论 通用型粘接剂可提高树脂水门汀对氧化锆的粘接耐久性。非自粘接的树脂水门汀如不使用通用型粘接剂则其粘接耐久性下降。     

通用型粘接剂和树脂水门汀对氧化锆 剪切粘接强度的影响

目的 研究通用型粘接剂和树脂水门汀对氧化锆陶瓷剪切粘接强度和耐久性的影响。方法 氧化锆陶瓷烧结制作20 mm×10 mm×10 mm和10 mm×10 mm×10mm两种尺寸的试件,实验分为12组,将这2种试件分别采用不同的树脂水门汀（RelyX Ultimate树脂水门汀、Clearfil SAC自粘接树脂水门汀）和通用粘接剂（无粘接剂、Scotchbond通用粘接剂、Clearfil SE One粘接剂）在不同的储存条件（水浴、水浴+冷热循环）下进行粘接。测试剪切粘接强度,分析断裂形态。结果 水门汀（F=8.41,P<0.01）和粘接剂（F=30.34,P<0.01）对氧化锆剪切粘接强度的影响有统计学意义;储存条件对剪切粘接强度的影响无统计学意义（F=1.83,P=0.18）。RelyX Ultimate树脂水门汀、无粘接剂、水浴+冷热循环储存时的剪切粘接强度最低（14.02 MPa±6.86 MPa）,RelyX Ultimate树脂水门汀、Scotchbond通用粘接剂、水浴+冷热循环储存时的剪切粘接强度最高（54.12 MPa±8.37 MPa）。结论 通用型粘接剂可提高树脂水门汀对氧化锆的粘接耐久性。非自粘接的树脂水门汀如不使用通用型粘接剂则其粘接耐久性下降。