Effects of tributylborane-activated adhesive and two silane agents on bonding computer-aided design and manufacturing (CAD/CAM) resin composite

The present study was conducted to evaluate the effects of an experimental adhesive agent [methyl methacrylate-tributylborane liquid (MT)] and two adhesive agents containing silane on the bonding between a resin composite block of a computer-aided design and manufacturing (CAD/CAM) system and a light-curing resin composite veneering material. The surfaces of CAD/CAM resin composite specimens were ground with silicon-carbide paper, treated with phosphoric acid, and then primed with either one of the two silane agents [Scotchbond Universal Adhesive (SC) and GC Ceramic Primer II (GC)], no adhesive control (Cont), or one of three combinations (MT/SC, MT/GC, and MT/Cont). A light-curing resin composite was veneered on the primed CAD/CAM resin composite surface. The veneered specimens were subjected to thermocycling between 4 and 60 °C for 10,000 cycles, and the shear bond strengths were determined. All data were analyzed using analysis of variance and a post hoc Tukey–Kramer HSD test (α = 0.05, n = 8). MT/SC (38.7 MPa) exhibited the highest mean bond strengths, followed by MT/GC (30.4 MPa), SC (27.9 MPa), and MT/Cont (25.7 MPa), while Cont (12.9 MPa) and GC (12.3 MPa) resulted in the lowest bond strengths. The use of MT in conjunction with a silane agent significantly improved the bond strength. Surface treatment with appropriate adhesive agents was confirmed as a prerequisite for veneering CAD/CAM resin composite restorations.     

不同硅烷偶联剂对瓷和树脂之间黏接强度的影响

目的：比较瓷表面不同酸蚀状态下,4种硅烷偶联剂对瓷和树脂之间黏接强度的影响。方法：将64个瓷试件按照所使用硅烷偶联剂的不同分为4组,每组包括磷酸和氢氟酸处理两个亚组。表面处理完成后将瓷试件与复合树脂黏接,测试剪切强度。结果：氢氟酸与两种双组分偶联剂相配合产生的黏接强度最高（p〈O．05）,两种单组分偶联剂与氢氟酸配合使用的效果同两种双组分偶联剂与磷酸配合使用的效果没有显著差异如〉O．05）。结论：不同种类偶联剂对瓷和树脂之间的黏接强度有明显影响,选用合适的双组分硅烷偶联剂与磷酸处理相配合,足以产生满足临床要求的黏接强度。     

三种酸蚀剂联合偶联剂对Cerinate瓷与树脂粘结强度的影响

目的：评价三种陶瓷酸蚀剂联合偶联剂对Cerinate瓷与树脂粘结强度的影响。方法：将252个Cerinate瓷试件分为3组,每组84个试件,分别用自制A配方（含2.5%氢氟酸）﹑B配方（含6%氢氟酸）、C配方（含10%氢氟酸）陶瓷酸蚀剂处理0 s﹑30 s﹑60 s﹑90 s、120 s、150 s、180 s后,一半使用偶联剂,另一半不使用偶联剂,与树脂粘结后测试其粘结强度。结果：无偶联剂组酸蚀30 s后C配方的剪切强度为27.46 MPa,偶联剂组在酸蚀30 s后C配方剪切强度可达31.08 MPa,酸蚀时间对粘结强度无明显影响。结论：C配方配合偶联剂较短酸蚀时间内可获得较理想的粘结强度。     

Shear bond strength of a new self-adhering flowable composite resin for lithium disilicate-reinforced CAD/CAM ceramic material

PURPOSE

The purpose of this study was to evaluate and compare the effects of different surface pretreatment techniques on the surface roughness and shear bond strength of a new self-adhering flowable composite resin for use with lithium disilicate-reinforced CAD/CAM ceramic material.

MATERIALS AND METHODS

A total of one hundred thirty lithium disilicate CAD/CAM ceramic plates with dimensions of 6 mm × 4 mm and 3 mm thick were prepared. Specimens were then assigned into five groups (n=26) as follows: untreated control, coating with 30 µm silica oxide particles (Cojet™ Sand), 9.6% hydrofluoric acid etching, Er:YAG laser irradiation, and grinding with a high-speed fine diamond bur. A self-adhering flowable composite resin (Vertise Flow) was applied onto the pre-treated ceramic plates using the Ultradent shear bond Teflon mold system. Surface roughness was measured by atomic force microscopy. Shear bond strength test were performed using a universal testing machine at a crosshead speed of 1 mm/min. Surface roughness data were analyzed by one-way ANOVA and the Tukey HSD tests. Shear bond strength test values were analyzed by Kruskal-Wallis and Mann-Whitney U tests at α=.05.

RESULTS

Hydrofluoric acid etching and grinding with high-speed fine diamond bur produced significantly higher surface roughness than the other pretreatment groups (P<.05). Hydrofluoric acid etching and silica coating yielded the highest shear bond strength values (P<.001).

CONCLUSION

Self-adhering flowable composite resin used as repair composite resin exhibited very low bond strength irrespective of the surface pretreatments used.     

Effect of silane primers and unfilled resin bonding agents on repair bond strength of a prosthodontic microfilled composite

This study examined the effect of silane primers and bonding agents on bonding between layers of a light-activated composite material when repaired in the laboratory process. Disk specimens were prepared with the dentin portion of a composite material (Dentacolor DA-30) and abraded with a silicon carbide rotary cutting instrument. The specimens were conditioned with either one of the two silane primers (Porcelain Liner M and Silicer) or one of the two unfilled resin bonding agents (Dentacolor Opaker liquid and New Metacolor Photo Opaque liquid), or one of four combinations of two primers and two bonding agents. An intact surface with a thin air-inhibited unpolymerized layer, and an unprimed surface with only silicone carbide abrasion were also used for references. After placement of the enamel portion of the same brand of composite material (Dentacolor SA-30) on each surface of the dentin material, the specimens were light-exposed, and stored for 24 h in either dry or wet condition. Shear bond strengths were then determined with a mechanical testing device. The results showed that combined use of a silane primer and a bonding agent generally showed the greatest magnitude of bond strength regardless of material variation. The use of an unfilled resin bonding agent after application of a silane primer (Porcelain Liner M) is recommended to ensure adequate repair bonding between layers of the composite material.     

Tensile bond strength of two ceramic and three resin composite inlay materials placed using a resin luting agent.

The tensile bond strength of inlay materials to dentin was evaluated. Five materials, two direct resin composite inlay products, one hybrid resin composite, a preformed ceramic block, and a conventional porcelain material were bonded to bovine dentin and bonded together using a dual-polymerizing resin luting agent. Specimens were tested with and without thermocycling. Some bar-to-bar bonding groups fractured through the bar. Significantly higher (P < .05) bar-to-bar bonds were recorded than the bar-dentin bonds, irrespective of the inlay materials. VitaDur N showed the lowest bar-to-bar failure values (7.6 MPa) compared to the four other inlay materials (14.4 MPa to 22.2 MPa), but had the highest dentin bond strength (4.5 MPa). Unexpectedly, thermal loading increased the bond strength to bovine dentin, although this was only statistically significant for VitaDur N. The dentin bond strength of Charisma (1.4 MPa) was inferior (P < .02) to all other materials (2.6 MPa to 4.5 MPa) when thermocycled before testing.     

冷热循环老化对可切削复合树脂表面粗糙度的影响

目的：研究冷热循环老化对可切削复合树脂材料粗糙度的影响。方法以可切削复合树脂A( Lava Ultimate ,3M ESPE)、B(High-Class, AMBORINO)、C(Hyramic 润瓷, Upcera)为实验组,以光固化复合树脂 D ( Ceramage, Shofu)和二硅酸锂玻璃陶瓷E( UP-CAD, Upcera)为对照组,分别在老化前和经5000及10000次冷热循环后测量表面粗糙度( Ra),并观察表面形貌,进行统计学分析。结果在老化前,D和E组间Ra值差异有统计学意义(P<0.05),其余各组间Ra值差异均无统计学意义。经冷热循环老化实验,A、B、C和E四组材料冷热循环前后材料表面粗糙度Ra值的差异均无统计学意义;D组材料冷热循环前后,材料表面粗糙度Ra值的差异有显著统计学意义(P<0.001)。结论经冷热循环老化后,可切削复合树脂和玻璃陶瓷表面粗糙度较为稳定,而光固化复合树脂粗糙度增加。     

Microtensile bond strength testing of luting cements to prefabricated CAD/CAM ceramic and composite blocks.

OBJECTIVES: To investigate the Microtensile bond strength (microTBS) and failure mode of resin cements bonded to composite and ceramic CAD/CAM blocks following various surface treatments. METHODS: Paradigm composite blocks and Cerec Vitablocs received three surface treatments following the control treatment of surface grinding with 600 SiC grit. (1) Application of adhesive resin (Adh), (2) etching with hydrofluoric acid and silanization (HF+S) or (3) combination of the previous two treatments (HF+S+Adh). Three resin cements (Tetric Flow, Nexus 2, RelyX ARC) were applied to these surfaces and built-up in layers. After 24 h water storage at 37 degrees C, the non-trimming version of microTBS test was used to produce 1 mm(2) microbars. The Microbars were subjected to a tensile load using a modified testing device. The broken specimens were examined with a stereomicroscope and SEM to determine the failure mode. RESULTS: All control and adhesive treated groups of the ceramic substrate showed premature debonding during cutting. The overall mean microTBS for the three resin cements bonded to ceramic following HF+S and HF+S+Adh surface treatment, was 27 and 29.2 MPa and for the resin cements bonded to composite substrate was 42.3 and 54.2 MPa, respectively. The mode of failure was 98% adhesive with composite as a substrate and 68% mixed failures with ceramic as a substrate. CLINICAL SIGNIFICANCE: CAD/CAM restorations fabricated from processed composite blocks may have advantage over the ceramic blocks with regard to the higher bond strength with resin cements.     

Examining the effects of acid etching duration on the bond strength between two CAD/CAM materials and one composite resin

This study aimed to evaluate the effect of three hydrofluoric acid (HF) etching periods on the micro-tensile bond strength between two CAD–CAM ceramic systems [Vita Suprinity (VS) and feldspathic CEREC blocs (CB)] and a composite resin. The ceramics were categorized into six groups based on the surface conditioning protocol used, as follows: G1: CB-HF 5% for 20 s; G2: CB-HF 5% for 40 s; G3: CB-HF 5% for 60 s; G4: VS-HF 5% for 20 s; G5: VS-HF 5% for 40 s; G6: VS-HF 5% for 60 s. Scotchbond Universal was applied onto the pretreated ceramic surfaces and covered with Filtek Z350 XT composite resin. After 24 h, the specimens were cut into microbars (n?=?16) and a micro-tensile bond strength test (μTBS) was carried out. An optical microscope was used to examine the fractured microbars. The results showed statistically significant differences between the factors tested (p?<?0.01). Moreover, the mean MPa of G1(17.27), G2(13.03), G3(12.82), G4(15.83), G5(21.66), and G6(14.50) was seen to significantly differ. The predominant failure type observed was adhesive, and all three periods of HF etching produced satisfactory bonding between the composite resin and CB. An etching time of 40 s provided the highest μTBS value for VS.

     

2种粘结剂及粘结方法对CAD/CAM全瓷冠抗折强度的影响

目的 研究不同粘结方法及冷热循环对Cerec全瓷冠粘结后抗折强度的影响。 方法 选择离体前磨牙80颗,进行Cerec全瓷冠预备及制作。随机分为1~4组,每组20颗,分别使用Variolink N树脂粘结剂+硅烷偶联剂粘结、Variolink N树脂粘结剂粘结、Bisco Choice TM 2树脂粘结剂＋硅烷偶联剂粘结、Bisco Choice TM 2树脂粘结剂粘结;每组再分为A、B小组,分别不进行和进行冷热循环。8组试件均用万能力学实验机测试其全瓷冠最大抗折裂强度,观察所有标本粘结破坏形式;进行统计分析。 结果 使用Variolink N树脂粘结剂+硅烷偶联剂组粘结的Cerec全瓷冠抗折裂强度最高;全瓷冠抗折强度A组(非冷热循环)高于B组。差异有统计学意义(P<0.05)。 结论 双重固化树脂粘结系统是牙科长石质陶瓷粘结的理想选择,可以获得较高的抗折裂强度。冷热循环降低Cerec全瓷冠抗折裂强度。     

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.     

Effectiveness of two-liquid silane primers on bonding sintered feldspathic porcelain with a dual-cured composite luting agent

The purpose of the current study was to evaluate the effect of two-component ceramic primers on the bond strength of a composite material joined to a sintered porcelain material. Two sizes of porcelain discs (VMK 68; 10 and 8 mm in diameter by 2.5 mm thick) were ground (No. 1000 SiC), and surface-conditioned using one of the following systems: (i) unprimed, (ii) Liquid A of the Porcelain Liner M material (PLM-A), (iii) Liquid B of Porcelain Liner M (PLM-B), (iv) Liquids A and B of Porcelain Liner M (PLM-AB), (v) Liquid A of the Tokuso Ceramics Primer material (TCP-A), (vi) Liquid B of Tokuso Ceramics Primer (TCP-B) and (vii) Liquids A and B of Tokuso Ceramics Primer (TCP-AB). All specimens were bonded with the Bistite II dual-cured composite luting agent, and shear bond strengths were determined both after 24 h immersion in water and after subsequent thermocycling (4-60 degrees C, 1 min each, 20,000 cycles). Of the seven groups assessed, two groups (PLM-AB and TCP-AB) showed the greatest bond strength both before (30.7 MPa for PLM-AB and 29.7 MPa for TCP-AB) and after (19.7 MPa for PLM-AB and 22.4 MPa for TCP-AB) thermocycling (P < 0.05). No significant differences were found between the PLM-AB and TCP-AB groups regardless of the application of thermocycling (P > 0.05). It can be concluded that both of the acid-catalysed two-liquid ceramic primers showed superior bonding to the unhydrolysed single-liquid silane agents (PLM-B and TCP-A) when the feldspathic porcelain was bonded with the Bistite II luting composite.     

Comparison of the shear bond strength of a titanium composite resin material with dentinal bonding agents versus glass ionomer cements.

This study compared the in vitro shear bond strength of an autopolymerizing composite resin system (CR) (Ti-Core) with two third-generation dentinal bonding agents (DBA) (Tenure and Scotchbond 2) to glass ionomer cements (GIC) (Ketac-Silver, GC Miracle Mix, and Ketac-Cem). The experiment was divided in five groups. The shear bond strengths were evaluated on a universal testing apparatus at three different intervals; 15 minutes, 24 hours, and 7 days. Statistically, (two-way analysis of variance), the shear bond strengths from the greatest to least were: Ti-Core CR with Tenure DBA > Ti-Core CR with Scotchbond 2 DBA > Ketac-Silver GIC, GC Miracle Mix GIC > Ketac-Cem GIC. There were no differences in shear bond strengths according to time, and no interactions between groups and time. The shear bond strengths for Tenure DBA with Ti-Core CR were two and a half to three times greater than the silver-filled glass ionomers, Ketac-Silver GIC and GC Miracle Mix GIC. Tenure DBA with Ti-Core CR also had consistently greater shear bond strengths than Scotchbond 2 DBA with Ti-Core CR, and this trend is in agreement with similar research.     

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。     

Porcelain laminate veneer restorations bonded with a three-liquid silane bonding agent and a dual-activated luting composite

This clinical report describes the fabrication and bonding of porcelain laminate veneer restorations in a patient with anterior open spaces. Laminate veneer restorations made of feldspathic porcelain were etched with 5% hydrofluoric acid, rinsed under tap water, ultrasonically cleaned with methanol, and primed with a chemically activated three-liquid silane bonding agent (Clearfil Porcelain Bond). The enamel surfaces were etched with 40% phosphoric acid, rinsed with water, and primed with a two-liquid bonding agent (Clearfil New Bond) that contained a hydrophobic phosphate (10-methacryloyloxydecyl dihydrogen phosphate; MDP). The restorations were bonded with a dual-activated luting composite (Clapearl DC). The veneers have been functioning satisfactorily for an observation period of one year. Combined use of the Clearfil bonding agents and Clapearl DC luting composite is an alternative to conventional materials for seating porcelain laminate veneer restorations, although the system is inapplicable to dentin bonding.