Initial adhesion of glass-fiber-reinforced composite to the surface of porcine calvarial bone

The aim of this preliminary study was to compare the initial bond strength of the glass-fiber-reinforced composite veil to the surface of the porcine calvarial compact bone using different adhesives. Fiber-reinforced composite (FRC) made of E-glass fiber veil with the BisGMA-PMMA resin system was used in the study. For the shear bond strength test, porcine calvarial bone cubes were mounted into resin matrix. FRC-veil discs were bonded to compact bone with different types of adhesives: (A) BisGMA-HEMA based (3M-ESPE Scotchbond Multi-Purpose Adhesive), (B) 4-META/UDMA/BisGMA based (Unifil Bond Bonding Agent) and MDP based (Clearfil Se Bond adhesive), (C) UDMA/BisGMA/PMMA-based experimental adhesive, and (D) silane-based (APS, ICS, MPS) experimental adhesives. The surface of the bone was mechanically roughened and was either used as such, treated with dental primers (Unifil Bond Self-etching Primer, Clearfil Se Bond Primer), or treated with an experimental silane mixture (APS, ICS, MPS), or with a mixture of the experimental silane liquid and Clearfil Se Bond Primer. The 3M-ESPE Scotchbond Multi-Purpose Adhesive and UDMA/BisGMA/PMMA experimental adhesive gave poor results in the shear bond test (0.58 and 0.40 MPa, respectively). Unifil Bond Bonding Agent and Clearfil Se Bond adhesive with respective primers markedly improved the shear bond strength; with Unifil the result was 3.40 MPa, and with Clearfil it was 6.19 MPa. When the bone surface was primed with a mixture of Clearfil Se Bond Primer and Clearfil Porcelain Bond Activator, the Clearfil Se Bond adhesive-impregnated FRC veil gave the best adhesion to the bone surface in this test: 9.50 MPa. The addition of bioactive glass granules between the veil and the bone lowered the shear bond strength in the test system described above to 6.72 MPa. The test systems with the silane mixture were also promising. In the SEM study, it was found that the mechanical treatment reveals the pores of the bone surface. Chemical treatments of the bone surface improved the adhesion of the FRC veil to the bone. The results showed that the adhesion of the FRC to the surface of the bone can be significantly improved with mechanical roughening and with special chemical treatments of the bone surface.     

Effects of environmental calcium and phosphate on wear and strength of glass ionomers exposed to acidic conditions

This study evaluated the effects of environmental calcium and phosphate on wear resistance, strength, and surface morphology of highly viscous glass-ionomers (HVGICs) (Fuji IX Fast [FN] and KetacMolar [KM]) when exposed to acidic conditions. Fabricated specimens were randomly divided into five groups and kept in acidic solutions (pH 3) with varied levels of calcium and phosphate ranging from 0 to 2.4 mM. After 4 weeks of conditioning, the specimens were subjected to wear testing, shear punch, and surface roughness testing as well as SEM evaluation. Multiple comparisons of wear depth (microm), shear strength (MPa), and surface roughness (Ra) between acidic conditions were performed using ANOVA/post-hoc Scheffe's test (p < 0.05). Results showed that FN and KM exposed to acidic conditions had varied wear resistance, shear strength, surface roughness, and structure depending on environmental phosphate level. Increased level of environmental phosphate led to rougher surface, greater wear resistance, and strength of FN and KM than the controls (acid of pH 3). Under SEM, the surface of both FN and KM specimens were covered by numerous small particles when environmental phosphate was high. Results suggest that environmental phosphate may improve wear resistance and shear strength of HVGICs when challenged by acids.     

Bonding of dual-cured resin cement to zirconia ceramic using phosphate acid ester monomer and zirconate coupler

This study evaluated the shear bond strength between dual-cured resin luting cement and pure zirconium (99.9%) and industrially manufactured yttrium-oxide-partially-stabilized zirconia ceramic, and the effect of MDP (10-methacryloyloxydecyl dihydrogen phosphate) primer (MP) and zirconate coupler (ZC) on bond strength. Two different-shaped pure zirconium and zirconia ceramic specimens were untreated or treated with various primers, including different concentrations of MP containing phosphoric acid ester monomer (MDP) in ethanol, ZC containing a zirconate coupling agent in ethanol, or a mixture of MP and ZC. The specimens were then cemented together with dual-cured resin luting cement (Clapearl DC). Half of the specimens were stored in water at 37 degrees C for 24 h and the other half were thermocycled 10,000 times before shear bond strength testing. The bond strengths of resin luting cement to both the zirconium and zirconia ceramic were enhanced by the application of most MPs, ZCs, and the mixtures of MP and ZC. For the group (MP2.0+ZC1.0) containing 2.0 wt % MP and 1.0 wt % ZC, no significant difference was observed between in shear bond strength before and after thermal cycling for both zirconium and zirconia ceramic (p > 0.05). For the other primers, statistically significant differences in shear bond strength before and after thermal cycling were observed (p < 0.05). The application of the mixture of MP and ZC (MP2.0+ZC1.0) was effective for bonding between zirconia ceramic and dual-cured resin luting cement. This primer may be clinically useful as an adhesive primer for zirconia ceramic restoration.     

氧化锆与纳米羟基磷灰石陶瓷的剪切实验

BACKGROUND: Nano-hydroxyapatite as a surface modification material that is bonded to the surface of the zirconia ceramics upon sintering at high temperature can improve bone-inducing activity and bone bonding strength of the zirconia ceramics. Moreover, the sintering temperature is crucial for performance and bonding of the composite. OBJECTIVE: To detect the shear strength of nano-hydroxyapatite ceramics coating bonded to zirconia ceramics at different sintering temperatures. METHODS: Nano-hydroxyapatite slurry was prepared using sol/gel technology. Thereafter, 20 zirconium green bodies were coated with nano-hydroxyapatite slurry and randomly divided into four groups. Then, the specimens were put into non-pressure sintering furnace and sintered at 1 300, 1 400, 1 500, and 1 550 ℃, respectively. At last, we measured the shear strength of all the specimens after sintering by universal testing machine, and analyze the type of fractures. RESULTS AND CONCLUSION: With the rising of sintering temperature, the shear strength of the specimens was gradually increased, and there were significant differences between the four groups [(4.04±1.19), (6.60±0.95), (16.51±1.93), (80.47±19.31) MPa, P < 0.05]. Within the scope of 1 550 ℃, the sintering temperature was positively relative to the shear strength of specimens. These findings indicate that in the certain temperature range, the higher the sintering temperature, the greater the shear strength of the bonding interface between zirconia and nano-hydroxyapatite. When the sintering temperature is 1 550℃, the shear strength of the bonding interface is the highest.      

Effect of temporary filling materials on repair bond strengths of composite resins

Endodontic access cavities sometimes can be prepared through a permanent composite restoration. Between the appointments, temporary cements are used to seal access cavities and may have negative effect on bonding of further composite restoration. The purpose of this study was to compare shear bond strength of composite to composite which had been in contact with various temporary filling materials. Standard cavities were prepared on 160 acrylic resin blocks, obturated with composite resin (Clearfil AP-X, Kuraray, Japan) and randomly divided into eight groups (n = 20). Group 1 received no treatment. From group 2-8, composite surfaces were covered with the following cements temporarily: Zinc-oxide/calcium-sulphate (Cavit-G, ESPE, Germany), two different Zinc-Oxide-Eugenol materials (ZnOE, Cavex, Holland and IRM, Dentsply, USA), Zinc-phosphate cement (Adhesor, Spofa-Dental, Germany), Zinc-polycarboxylate cement (Adhesor-Carbofine, Spofa-Dental, Germany), Glass-Ionomer-Cement (Argion-Molar, Voco, Germany), or light curing temporary material (Clip, Voco, Germany). The cements were removed mechanically after 1 week storage in distilled water at 37 degrees C and composite surfaces were treated with a self-etch adhesive system (SE-Bond, Kuraray, Japan). Composite resin build-ups were created on composite surfaces. Shear bond strength values were measured using universal testing machine at crosshead speed of 1 mm/min. The data was calculated in MPa and statistically analyzed using one-way ANOVA and Tukey tests. Eugenol-containing cements significantly reduced shear bond strengths of composite to composite (p < 0.05), while the other temporary materials had no adverse effect on shear bond strength (p > 0.05). These findings suggested that temporary filling materials except eugenol-containing materials have no negative effect on composite repair bond strengths.     

An investigation of the shear bond strength of compomer restorative material to enamel and dentine

The aim of this study was to investigate the effect of one step adhesives on the shear bond strength of a compomer restorative material to both enamel and dentine. Human extracted teeth were used for the study. Ten samples were prepared for both enamel and dentine specimens for each of the five groups: Tooth, no etch, Prime and Bond NT (P+B NT); tooth, Non-Rinse Conditioner (NRC), P+B NT; tooth, NRC, Prime and Bond 2.1 (P+B 2.1); tooth, etch, P+B NT; tooth, etch, P+B 2.1. The specimens were subjected to bond testing. The shear bond strength was measured using an Inston 1193 testing machine using a cross head speed of 1 mm/minute. The specimens were tested to destruction. The results show that for the enamel specimens the highest bond strength was recorded for those specimens subjected to Etch, P+B 2.1 (22.1 MPa) and Etch P+B NT (20.0 MPa). The groups of specimens which did not undergo etching had very low bond strengths ranging from 11.4 MPa for NRC, P+B 2.1, 8.5 MPa for NRC P+B NT to 6.9 MPa for P+B NT. For the dentine specimens, for all of the groups, the shear bond strengths were low. Those groups subjected to etching produced the highest values of 7.9 MPa for NRC P+B 2.1 with the lowest value of 6.1 MPa for NRC P+B NT. These bond strengths were significantly lower than those achieved for bonding to enamel. Prime and Bond NT and Prime and Bond 2.1, used in conjunction with acid etching, produce satisfactory bond strengths of compomer restorative material to enamel. Bond strengths to dentine were low.     

Deproteinized dentin: a favorable substrate to self-bonding resin cements?

The adhesive performance on deproteinized dentin of different self-adhesive resin cements was evaluated through microtensile bond strength (μTBS) analysis and scanning electron microscopy (SEM). Occlusal dentin of human molars were distributed into different groups, according to the categories: adhesive cementation with two-step bonding systems-control Groups (Adper Single Bond 2 + RelyX ARC/3M ESPE; One Step Plus + Duolink/Bisco; Excite + Variolink I/Ivoclar Vivadent) and self-adhesive cementation-experimental groups (Rely X Unicem/3M ESPE; Biscem/Bisco; MultiLink Sprint/Ivoclar Vivadent). Each group was subdivided according to the dentin approach to: α, maintenance of collagen fibers and β, deproteinization. The mean values were obtained, and submitted to ANOVA and Tukey test. Statistical differences were obtained to the RelyX Unicem groups (α = 13.59 MPa; β = 30.19 MPa). All the BIS Group specimens failed before the mechanical tests. Dentinal deproteinization provided an improved bond performance for the self-adhesive cement Rely X Unicem, and had no negative effect on the other cementing systems studied.     

Micromorphological changes in resin-dentin bonds after 1 year of water storage

The purpose of this study was to evaluate the degradation of resin-dentin bonds after 1 year of water storage. Resin-dentin-bonded specimens were prepared with the use of an adhesive resin system (One-Step: Bisco). Half of the experimental specimens were sectioned perpendicular to the adhesive interface to produce a beam (adhesive area: 0.9 mm(2)) before being stored in distilled water at 37 degrees C for 1 year. The remaining half of the bonded specimens were sectioned into beams of similar dimensions after 1 year of water storage. Additional bonded specimens that had been stored in water for 24 h before sectioning into beams were used as controls. The beams in the two experimental groups and the control group were subjected to microtensile bond testing. Fractography was performed on all fractured beams with the use of FE-SEM. There were significant (p <.05) differences in bond strength among the control specimens (55.9 +/- 12.9 MPa), specimens that had been sectioned into beams after water storage (68.9 +/- 18.6 MPa), and specimens that had been sectioned into beams before water storage (28.1 +/- 9.3 MPa). Fractography revealed that the resin material was gradually extracted from the periphery to the center portion of the beam. This probably accounted for the decrease in bond strength after 1 year of water storage.     

Adhesion of composite to enamel and dentin surfaces irradiated by IR laser pulses of 0.5-35 micros duration

The characteristics of laser-treated tooth surfaces depend on the laser wavelength, pulse duration, spatial and temporal laser beam quality, incident fluence, surface roughness, and the presence of water during irradiation. Ablated surfaces are most commonly restored with adhesive dental materials and the characteristics of the ablated surfaces influence adhesion of restorative materials. Previous studies suggest that high bond strengths can be achieved using shorter laser pulses that minimize peripheral thermal damage. In this study, Er:YSGG, Er:YAG, and CO(2) lasers were used at irradiation intensities sufficient to simulate efficient clinical caries removal to uniformly irradiate bovine enamel and human dentin surfaces using a motion control system with a microprocessor-controlled water spray. The degree of spatial overlap of adjacent pulses was varied so as to investigate the influence of irradiation uniformity and surface roughness on the bond strength. Composite resin was bonded to the irradiated surfaces and shear bond tests were used to obtain bond strengths in MPa. The highest results were obtained using the Er:YAG pulses with pulse durations less than 35 mus without the necessity for postirradiation acid etching. Some of these groups were not significantly different from nonirradiated, acid-etch-only positive control groups.     

Shear bond strength of a hot pressed Au-Pd-Pt alloy-porcelain dental composite

Objectives: The purpose of this study was to evaluate the effect of hot pressing on the shear bond strength of a Au-Pt-Pd alloy-porcelain composite. Methods: Several metal-porcelain composites specimens were produced by two different routes: conventional porcelain fused to metal (PFM) and hot pressing. In the latter case, porcelain was hot pressed onto a polished surface (PPPS) as well as a roughened one (PPRS). Bond strength of all metal-porcelain composites were assessed by the means of a shear test performed in a universal test machine (crosshead speed: 0.5?mm/min) until fracture. Interfaces of fractured specimens as well as undestroyed interface specimens were examined with optical microscope, stereomicroscope, Scanning Electron Microscope (SEM) and Energy Dispersive X-Ray Spectroscopy (EDS). The data were analyzed using one-way ANOVA followed by Tuckey's test (p<0.05). Results: Shear bond strength of conventional PFM specimens were in line with the upper range of literature data (83±14?MPa). Hot pressing proved to significantly increase bond strength between metal and porcelain (p<0.05). For both polished and roughened surface the shear bond strength values for hot pressed specimens were 120±16?MPa and 129±5?MPa, respectively, which represents an improvement of more than 50% relatively to a conventional PFM. Roughened surface did not have a significant effect on bond strength of hot pressed specimens (p>0.05). Significance: This study shows that it is possible to significantly improve metal-porcelain bond strength by applying an overpressure during porcelain firing.     

饰瓷温度烧结对氧化锆陶瓷与树脂黏结剂剪切强度的影响

背景：研究已证实硅烷偶联剂和喷砂等表面处理方式,以及增加氧化锆陶瓷表面的微裂纹可提高氧化锆陶瓷与树脂黏结剂间的黏结强度,但有关多次反复烧结是否会对氧化锆陶瓷黏结剪切强度产生影响尚缺少相关研究。 目的：测试饰瓷温度烧结对牙科氧化锆陶瓷与树脂黏结剂黏结剪切强度的影响。 方法：从40片氧化锆瓷片随机选择20片,分成 5组,按照常规烧结程序分别烧结0(对照组),2,4,6,8次,热处理起始温度为500 ℃,最终温度1 000 ℃,升温速率55 ℃/min,抽真空时间7 min。每次烧结最终温度恒定不变。将各组分别用树脂黏结剂与剩余未烧结的陶瓷片对位黏结,用万能材料试验机测黏结界面的剪切强度;使用扫描电镜观察剪切后的试件断面形貌。 结果与结论：烧结4,6,8次组试件剪切强度高于对照组(P < 0.05);烧结2次组试件剪切强度稍高于对照组,但差异无显著性意义(P > 0.05);烧结8次组试件剪切强度高于烧结4,6次组(P < 0.05)。未烧结氧化锆陶瓷表面未见裂纹;经过2次烧结后表面可见细微裂纹;经过4次烧结后表面可见裂纹增多;经过6次烧结后表面已经开始有明显变化,裂纹增多并伴有细微空隙产生,少量黏结剂残留;经过8次烧结后表面可见裂纹与空隙明显增多并有黏结剂残留。表明经过4,6,8次烧结后的氧化锆陶瓷对树脂黏结剂有较好的黏结剪切强度,烧结8次后的黏结剪切强度最强。中国组织工程研究杂志出版内容重点：生物材料;骨生物材料; 口腔生物材料; 纳米材料; 缓释材料; 材料相容性;组织工程全文链接：     

上釉技术对氧化钇稳定四方相氧化锆多晶陶瓷粘接及力学性能的影响

文题释义：氧化钇稳定四方相氧化锆多晶陶瓷：是以氧化钇为稳定剂、四方相为主要物相的氧化锆陶瓷，其具有较高的抗弯强度(900-1 200 MPa)和断裂韧性(9-10 MPa·m^1/2)。由于这些优异的机械性能，氧化钇稳定四方相氧化锆多晶陶瓷成为口腔冠桥修复中应用最广泛的陶瓷之一。 相变增韧机制：为氧化锆增韧的一种方法。稳定剂使四方相氧化锆在室温下可以处于亚稳态，但是在应力作用下亚稳态的四方相氧化锆易转化为单斜相氧化锆，同时伴有3%-5%的体积膨胀，这个过程能弥合微裂纹且消耗断裂能，提高氧化锆陶瓷的韧性。 背景：任何表面处理都应在不损害原有氧化钇稳定四方相氧化锆多晶陶瓷强度的前提下提高其粘接强度。目前缺乏上釉技术对氧化钇稳定四方相氧化锆多晶陶瓷粘接强度影响的资料，并且其对氧化钇稳定四方相氧化锆多晶陶瓷力学性能的影响尚不明确。 目的：评估上釉技术对氧化钇稳定四方相氧化锆多晶陶瓷力学行为及其与树脂水门汀粘接强度的影响。 方法：制作氧化钇稳定四方相氧化锆多晶陶瓷试件并随机分为4组：A组，表面不做任何处理；B组，110 μm氧化铝颗粒喷砂；C组，上釉+氢氟酸酸蚀；D组，上釉+氢氟酸酸蚀+硅烷化。检测每组试件的表面显微形貌、粗糙度、晶相结构、元素组成、剪切粘接强度和弯曲强度，并观察剪切粘接强度测试后所有断面的断裂模式。 结果与结论：①经表面处理后的试件粗糙度明显增大，降序排列依次为C组(0.62±0.01) μm、D组(0.55±0.02) μm、B组(0.11±0.02) μm、A组(0.05±0.01) μm，5组间粗糙度比较差异有显著性意义(P < 0.05)；②B组试件表面含有2.2%单斜相氧化锆，而其他组含量均为零；③除锆和氧2种元素外，B组还含有铝元素6.49%，C和D组分别含有硅元素18.67%和25.78%；④A、B、C、D组的剪切粘接强度分别为(3.11±0.40)，(4.23±0.45)，(6.62±0.60)，(10.46±0.83) MPa，组间两两比较差异均有显著性意义(P < 0.05)；⑤A、B、C和D组的三点弯曲强度分别为(961.07±75.53)，(1 234.73±114.09)，(1 024.28±120.51)，(1 036.09±80.10) MPa，其中A、C和D组两两比较差异无显著性意义(P > 0.05)，B组与A、C、D组比较差异有显著性意义(P < 0.05)；⑥结果表明，上釉技术未明显提升氧化钇稳定四方相氧化锆多晶陶瓷的弯曲强度，但上釉后经氢氟酸蚀刻并硅烷化处理可显著增强氧化钇稳定四方相氧化锆多晶陶瓷与树脂水门汀之间的粘接强度。 ORCID: 0000-0002-8066-2498(徐小敏) 中国组织工程研究杂志出版内容重点：生物材料；骨生物材料; 口腔生物材料; 纳米材料; 缓释材料; 材料相容性；组织工程     

Shear bond strength of experimental methacrylated beta-cyclodextrin-based formulations

Previous studies have shown that methacrylated beta-cyclodextrins (MCDs) can be used as comonomers in resin-based dental composites. These MCDs by virtue of having several polymerizable methacrylate groups and hydrophilic hydroxyl groups, may also promote bonding of dental composites to dentin. This study evaluated MCDs as adhesive comonomers, and optimized comonomer and polymerization initiator concentrations for maximum shear bond strength (SBS). Experimental MCD-based bonding formulations in acetone were prepared by mixing 33 mass fraction % MCDs with (10, 20, 30, 40, or 50) mass fraction % of 2-hydroxyethyl methacrylate (HEMA). The MCD/HEMA-based solutions were activated with varied amounts of camphorquinone (CQ) and ethyl 4-dimethylamino benzoate (4E). Samples for SBS were prepared by bonding a composite resin to acid-etched dentin surfaces of extracted human molars with the experimental bonding solutions. The specimens were immersed in 37 degrees C water for 24 h and bond strengths were determined in shear mode. With increasing HEMA concentration, the SBS values of MCD-bonding solutions increased to 16 MPa at a composition of 33% MCD, 30% HEMA, and 37% acetone by mass. Also, SBS values of MCD-bonding solutions varied as a function of the CQ and 4E concentrations and passed through a maximum SBS at 21 MPa, which was comparable to that of a commercial control. This preliminary study indicated that nonacidic MCD monomers could be used as an adhesion-promoting comonomer. Additional modification of MCDs having both polymerizable groups and anionic ligand groups, e.g., polymerizable acidic cyclodextrin derivatives should increase the SBS even further.     

In vitro effect of nanoleakage expression on resin-dentin bond strengths analyzed by microtensile bond test, SEM/EDX and TEM

This study evaluated the effect of multiple consecutive adhesive resin coatings of adhesive bonded to human dentin on nanoleakage and resin-dentin bond strength. Resin bonded dentin specimens were prepared using a total-etch adhesive (One-Step Plus) applied as multiple consecutive coating, or using two self-etch adhesive systems (iBond or Fluoro Bond). For the total-etch adhesive, resin application and air evaporation were performed 1, 2, 3, or 4 times. The self-etch adhesives were applied according to manufacturers' instructions. Resin-dentin bonded beams were prepared and immersed in water (control) or ammoniacal silver nitrate. After storage, microtensile bond strengths were measured. The fractured surfaces were examined by scanning and transmission electron microscopy (SEM and TEM), and energy-dispersive X-ray spectrometry (EDX). No significant differences in bond strength were found between water and silver nitrate storage groups. Several types of silver depositions (spotted, reticular, or water trees) were found in adhesive joints. The bond strengths of the single coated specimens of the total-etch adhesive were significantly lower than those receiving 2-4 coatings. Single coats produced more nanoleakage than multiple coats. However, no correlation was found between the bond strengths and nanoleakage between the different adhesives (total-etch adhesive with different conditions or self-etch adhesives).     

Bonding characteristics of newly developed all-in-one adhesives

This study evaluated the microtensile bond strength and the interfacial morphology of newer adhesives. The occlusal surfaces of extracted teeth were ground flat for random allocation to four equal groups. Resin composite was bonded to each surface using either Clearfil SE Bond [SEB], Clearfil Protect Bond [PB], G-Bond [GB], or an experimental adhesive, SSB-200 [SSB]. After storage for 24 h in water at 37 degrees C, they were sectioned into beams (cross-sectional area 1 mm(2)) for microtensile bond strength testing (muTBS) at a crosshead speed of 1 mm/min. The load at failure of each was recorded; the data were analyzed by one-way ANOVA and Games Howell tests. The surfaces of the fractured specimens were observed using SEM. For the ultra-morphology of the interface, the occlusal surfaces of four more teeth were prepared as before and a thin layer of flowable resin composite was bonded to each surface using one of the four adhesives.The mean muTBS ranged from 39.68 MPa (GB) to 64.97 MPa (SEB). There were no statistical differences between SEB and SSB, or between PB and GB (p > 0.05). The muTBS of SEB and SSB were significantly greater than that of PB and GB (p < 0.05). SEMs of the fractured surfaces revealed a mixed (cohesive/interfacial) failure. TEM examination highlighted differences in the hybrid layer; SEB had a thicker layer than the others. In conclusion, the newer all-in-one adhesives produced a thin hybrid layer but varied in their bond strengths. The 2-step self-etching adhesives do not necessarily produce higher bond strengths than that of the all-in-one systems.     

Study on Modification of Octyl-α-Cyanoacrylate Medical Adhesive

Objective：In order that the adhesive character could be improved to modify the octyl-α-cyanoacrylate（OCA） medical adhesive.Methods：Suitable modifiers involving polycaprolactone（PCL）,dibutyl phthalate （DBP）,dioctyl phthalate（DOP） and poly octyl methacrylat（POMA） have been chosen to modify the OCA adhesive,then tensile shear strength and adhesive strength are tested to evaluate the bond character of adhesives.Results：The PCL group＇s tensile shear strength and adhesive strength in normal temperature are descended while the other groups＇are all enhanced.Conclusion：The modification of properties of the other groups is effectively promoted in the aspect of the bond character,except the PCL group treated in normal temperature and the PCL modified group treated by rectification get a best improvement in the agglutinate intention, while the stability is expected to be improved.     

Effect of surface roughness, porosity, and a resorbable calcium phosphate coating on osseointegration of titanium in a minipig model

The aim of this study was to compare the osseointegration of four different implant surfaces in the G?ttingen minipig femur model. They were prepared by glasspearlblasting (A), sandblasting (B) and titaniumplasma spraying (C and D). Surface D received additionally an electrochemically deposited layer of a resorbable calcium phosphate (CaP) layer, made mainly of brushite. Sample size was n = 20 per group. Implants were placed in the intertrochanteric and intercondylar sites of both femora. After 12 weeks, implant anchorage was measured by the pull-out test and histomorphometry measurements were carried out at the bone-implant interface. Implant anchorage was 0.7 +/- 0.3 MPa for surface A, 3.2 +/- 0.6 MPa for surface B, 6.5 +/- 1.5 MPa for surface C and 7.3 +/- 1.9 MPa for surface D. The differences between surfaces were statistically significant, with exception of C and D. The stiffness of the bone-implant interface showed no statistically significant difference between surfaces. After pull-out, surface A and B showed nearly no bone spots, while on surfaces C and D bone remains were found. Bone-implant contact was 1.9 +/- 1.1% for surface A, 10.5 +/- 3.6% for surface B, 22.4 +/- 4.5% for surface C and 48.8 +/- 4.5% for surface D. The differences were statistically significant. Implant location, intertrochanteric and intercondylar, did not affect the data. In this minipig model, rougher surfaces showed better osseointegration. After 12 weeks of healing, the resorbable CaP layer enhanced significantly the bone-implant contact but not the level of anchorage. The findings also suggest that the pull-out test should be critically evaluated to determine the shear strength between bone and porous surfaces.     

不同表面处理对Ceramage聚合瓷黏结强度的影响

背景：长期以来修复材料与基牙的黏接技术一直是口腔修复学的研究热点,其中尤为引人关注的是黏结工件的表面处理工艺。 目的：对比观察8种表面处理方法对Ceramage聚合瓷黏结强度的影响,筛选适合Ceramage聚合瓷的表面处理方法。 方法：将Ceramage聚合瓷制成试件80个,随机分成8组,分别采用喷砂,酸蚀,偶联剂,喷砂+酸蚀,喷砂+偶联剂,酸蚀+偶联剂,喷砂+酸蚀+偶联剂处理聚合瓷表面并与树脂黏结剂黏结,对照组不进行任何处理。在37 ℃水浴24 h后测试样本剪切强度,并用扫描电镜观察处理后的聚合瓷表面形貌。 结果与结论：各组的剪切强度值由高到低分别为：喷砂+酸蚀+偶联剂处理组(31.12±2.81) MPa,喷砂+酸蚀组(27.62±1.70) MPa,酸蚀+偶联剂组(27.31±2.18) MPa,喷砂+偶联剂组(26.91±1.97) MPa,喷砂组(24.23±2.03) MPa,偶联剂组(23.50± 2.19) MPa,酸蚀组(17.61±2.14) MPa,对照组(8.13±0.63) MPa,除喷砂组、偶联剂组之间,喷砂+酸蚀组、喷砂+偶联剂组、酸蚀+偶联剂组之间比较差异无显著性意义外(P > 0.05),其余组间比较差异均有显著性意义(P  < 0.05)。结果显示7种表面处理方法都提高了黏结强度,喷砂、酸蚀联合硅烷偶联剂处理的聚合瓷黏结强度最高,是适合Ceramage聚合瓷黏结的表面处理方法。     

Influence of contamination on bonding to zirconia ceramic

The purpose of this study was to investigate the influences of contaminations and cleaning methods on bonding to dental zirconia ceramic. After saliva immersion and using silicone disclosing agent, airborne-particle abraded ceramic specimens were cleaned with isopropanol (AL), acetone (AC), 37% phosphoric acid (PA), additional airborne-particle abrasion (AA), or only with water rinsing (SS). Airborne-particle abraded specimens without contaminations (CL) were used as control group. For chemical analysis specimens of all groups were examined with X-ray photoelectron spectroscopy (XPS). Plexiglas tubes filled with composite resin were bonded to ceramic specimens using a phosphate-monomer containing composite luting resin. After 3-day water storage, tensile bond strengths (TBS) were tested. XPS analysis of group SS showed the presence of saliva and silicone (Si) contamination on the surface. The ratios of carbon/zirconium and oxygen/zirconium for groups PA and AA were comparable to those ratios obtained for group CL, indicating the removal of the organic saliva contamination. Airborne-particle abrasion and acetone completely removed Si contamination from ceramic surfaces. Isopropanol had little cleaning effect on the two contaminants. TBS (median +/- standard deviation) in MPa of the groups SS (11.6 +/- 3.1), AL (10.0 +/- 2.9), and AC (13.0 +/- 2.8) were statistically lower than those of groups PA (33.6 +/- 5.5), AA (40.1 +/- 3.6), and CL (47.0 +/- 8.1) (p < 0.001), while no differences were found in TBS between groups AA and CL (p > 0.5). Contamination significantly reduced bond strengths to zirconia ceramic. Airborne-particle abrasion was the most effective cleaning method.     

In vitro degradation of resin-dentin bonds analyzed by microtensile bond test,scanning and transmission electron microscopy

Our knowledge of the mechanisms responsible for the degradation of resin-dentin bonds are poorly understood. This study investigated the degradation of resin-dentin bonds after 1 year immersion in water. Resin-dentin beams (adhesive area: 0.9mm(2)) were made by bonding using a resin adhesive, to extracted human teeth. The experimental beams were stored in water for 1 year. Beams that had been stored in water for 24h were used as controls. After water storage, the beams were subjected to microtensile bond testing. The dentin side of the fractured surface was observed using FE-SEM. Subsequently, these fractured beams were embedded in epoxy resin and examined by TEM. The bond strength of the control specimens (40.3+/-15.1MPa) decreased significantly (p<0.01) after 1 year of water exposure (13.3+/-5.6MPa). Loss of resin was observed within fractured hybrid layers in the 1 year specimens but not in the controls. Transmission electron microscopic examination revealed the presence of micromorphological alterations in the collagen fibrils after 1 year of water storage. These micromorphological changes (resin elution and alteration of the collagen fibrils) seem to be responsible for the bond degradation leading to bond strength reduction.