A study on disintegration of posterior composite resins caused by long-term water immersion

The purpose of this study is to clarify a cause of disintegration for posterior composite resins by long-term immersion in distilled water during the 3-year period. Three kinds of posterior composite resins [Bellfirm P (BP), Clearfil Posterior (CP) and Micro Jar (MJ)] and one conventional anterior composite resin [Clearfil FII (FII)] were prepared as to specimens with 20 mm diameter, and 1 mm in thickness. These specimens were immersed in distilled water at 37 +/- 1 degree C for 3 years. These specimens were observed by scanning electron microscope (SEM). The residuces in distilled water were analyzed by X-ray microdiffractometry, infrared (IR) and nuclear magnetic resonance (NMR) spectrometers. One posterior composite resin (microparticle filled resin) was eluted in water more than the other posterior and anterior composite resins with conventional fillers. In SEM observations, many air bubbles were found inside all sections of the four composite resins, because of all mixing type composite resins. The subsurface layer of all four composite resins showed signs of disintegration, but the center layer of the specimens was not disintegrated. Three cured composite resins except MJ had crystalline X-ray diffraction patterns before water immersion, but the cured MJ alone was amorphous. These peaks of crystals showed fillers of these composite resins respectively. X-ray diffraction patterns of the dissolved substances for three composite resins except BP were also crystalline, but the peaks of the crystals except CP were different from the peaks of the fillers respectively. In IR and 1H-NMR spectra of dissolved substances, an unreacted monomer could be detected in one posterior composite resin (BP), but not in the other composite resins. In 1H-NMR spectra of dissolved substances, new signals not found originally were observed in all four composite resins. Therefore, the progress of disintegration was demonstrated clearly. The dissolved substances of all four composite resins were shown as the disintegrated substances between resin matrixes and silane coupling agents. It is suggested that the disintegration of these composite resins by long-term water immersion is derived from hydrolysis.     

Durability of commercial composite resin. Chronological change in transverse strength and transverse elastic modulus of composite resin immersed in MeOH

The durability of visible light-cured composite resin was examined. Five kinds of commercial redox type composite resin and 7 kinds of visible light-cured composite resin were used and their base monomers were analyzed by HPLC. After the set products were immersed in MeOH, transverse strength and transverse elastic modulus were measured. Furthermore, the MeOH sorption, solubility in MeOH and main soluble component were examined. The main component of the base monomer in all 5 kinds of redox type was Bis-GMA. Seven kinds of visible light-cured composite resin consisted of 4 kinds of Bis-GMA (including BMPEPP) and 3 kinds of UDMA. Both cases of redox type and visible light-cured type of composite resin, when they were immersed in MeOH, transverse strength and transverse elastic modulus decreased. In the case of redox type (Clearfil posterior new bond), the decrease of transverse strength and transverse elastic modulus was small, that is, its base monomer was Bis-GMA, and large quantities of hybrid type filler were mixed. In the case of redox type, transverse strength and transverse elastic modulus showed a tendency to decrease with the increase of MeOH sorption. Solubility of 12 kinds of these composite resins was 0.25-4.78% and its main component in Pyrofil light bond A was BMPEPP, the residual were coincident with the main component of base monomer.     

Effect of dentin primers containing N-methylolacrylamide or N-methylolmethacrylamide on dentin pretreatment.

The effect of experimental dentin primers containing N-methylolacrylamide (MEAA) or N-methylolmethacrylamide (MEMA) on the bonding of three commercial light-cured resin composite systems [Restorative Z 100 (Scotchbond), Palfique Estelite (Macbond) and Photo Clearfil A (Clearfil Photobond)] to etched dentin was investigated. Water solutions of 35% hydroxyethyl methacrylate (HEMA). 50% MEAA or 30% MEMA were used as dentin primers. The dentin etched with 10% phosphoric acid solution was pretreated with dentin primers for 30 s. The resin composite systems were applied in a Teflon tube positioned onto pretreated dentin surfaces. After water immersion for 1 day, the shear bond strengths were measured. The thicknesses of hybrid layers at dentin-resin interfaces treated with 6 mol/l HCl and 1% NaOCl were measured by scanning electron microscopy. The dentin primer pretreatment increased the bond strengths of all resin composite systems. For Macbond and Clearfil Photobond, the bond strengths (14.2-26.5 MPa) with MEAA and MEMA were higher than those (10.5 and 17.8 MPa) with HEMA. All hybrid layer thicknesses were 1-1.5 microns after HCl immersion. The hybrid layers after NaOCl immersion become narrower. The main fracture pattern of specimens exhibiting high bond strengths (more than 14.2 MPa) was dentin cohesive fracture after bond test. For Macbond and Clearfil Photobond, the layers of specimens pretreated with MEAA and MEMA were clearly thicker than those pretreated with HEMA after NaOCl immersion. MEAA and MEMA solutions were more effective in improving the bond strength of Macbond and Clearfil Photobond to etched dentin than was HEMA. Macbond and Clearfil Photobond created good hybrid dentin layers which could resist NaOCl-attack when MEAA and MEMA solutions were used as dentin primers.     

Surface hardness of light-cured and self-cured composite resins.

The surface microhardness of eight visible light-cured and self-cured composite resin materials was measured from 10 minutes after polymerization to 12 months. After the last measurement, a 250 microns layer was removed by grinding and the surface was reexamined. There was a progressive increase of microhardness for 4 weeks in all specimens (dry or wet), followed by stabilization. These results reflected the continual polymerization of composite resins after initial hardening for both self-cured and light-cured composite resins. The surfaces of specimens stored in water were softened compared with the surfaces of dry specimens. All the composite resins demonstrated substantially higher hardness after grinding, but different results among materials were attributed to varying compositions.     

The effect of application sustained seating pressure on adhesive luting procedure.

OBJECTIVES: To evaluate the effect of short versus long application seating pressure on the bond strength of resin blocks, luted with a dual-cured resin cement (Panavia F) to pre-coated or non pre-coated dentin with an hydrophobic light-cured adhesive (Clearfil Protect Bond). METHODS: Sixteen non-carious human third molars were randomly divided into six Groups (four teeth each). Cylindrical composite blocks were luted with Panavia F (Group Ia) and with Clearfil Protect Bond with Panavia F (Group IIa) and seating pressure was applied for 5s. In Groups Ib and IIb, the two bonding procedures were respectively repeated, but the resin cylinder was maintained under constant pressure during the entire 3min polymerization period for the resin cement. After storing in distilled water for 24h, 0.9mmx0.9mm sticks were produced from these luted specimens for microtensile bond testing and SEM examination. RESULTS: The use of Clearfil Protect Bond with Panavia F produced higher bond strengths than the use of Panavia F (p<0.05). Extending the time of pressure application up to 3min increased the bond strength (p<0.001) and improved the integrity of the interfacial quality. SIGNIFICANCE: The application of sustained seating pressure during luting procedures and the additional use of a hydrophobic light-cured adhesive both improve the final bond strength of the resin cement.     

Adhesion to root canal dentine using one and two-step adhesives with dual-cure composite core materials

The regional tensile bond strengths of two dual-cure composite resin core materials to root canal dentine using either a one or two-step self-etching adhesive were evaluated. Extracted premolar teeth were decoronated and their root canals prepared to a depth of 8 mm and a width of 1.4 mm. In one group, a one-step self-etching adhesive (Unifil Self-etching Bond) was applied to the walls of the post-space and light-cured for 10 s. After which, the post-spaces were filled with the a dual-cure composite resin (Unifil Core) and then half the specimens were light-cured for 60 s and the other half placed in darkness for 30 min. In the second group, a self-etching primer (ED Primer II) was applied for 30 s, followed by an adhesive resin (Clearfil Photo Bond), which was light-cured for 10 s. The post-spaces were filled with a dual-cure composite resin (DC Core) and then half the specimens were light-cured for 60 s and the other half placed in darkness for 30 min. Chemical-cure composite resin was placed on the outer surfaces of all the roots, which were then stored in water for 24 h. They were serially sliced perpendicular to the bonded interface into 8, 0.6 mm-thick slabs, and then transversely sectioned into beams, approximately 8 x 0.6 x 0.6 mm, for the microtensile bond strength test (muTBS). Data were divided into two (coronal/apical half of post-space) and analysed using three-way anova and Scheffe's test (P < 0.05). Failure modes were observed under an scanning electron microscope (SEM) and statistically analysed. Specimens for observation of the bonded interfaces were prepared in a similar manner as for bond strength testing, cut in half and embedded in epoxy resin. They were then polished to a high gloss, gold sputter coated, and after argon ion etching, observed under an SEM. For both dual-cure composite resins and curing strategies, there were no significant differences in muTBS between the coronal and apical regions (P > 0.05). In addition, both dual-cure composite resins exhibited no significant differences in muTBS irrespective of whether polymerization was chemically or photoinitiated (P > 0.05). Both dual-cure composite resins exhibited good bonding to root canal dentin, which was not dependent upon region or mode of polymerization.     

Effects of storage media on mechanical properties of adhesive systems

PURPOSE: To evaluate the effects of water vs. oil storage on the mechanical properties of dental adhesives over 3 and 6 months. METHODS: Adhesive resin sheets were prepared by pouring either Single Bond (SB), One-Step (OS) or Clearfil Liner Bond 2V (CL) into a mold measuring 15 x 15 x 0.8 mm. After solvent evaporation, the adhesives were light-cured, removed from the mold and trimmed to either hourglass or I-beam shapes that were used to determine the true stress (TS) and modulus of elasticity (E), respectively. Control adhesive specimens were subjected to tensile testing at 0.6 mm/minute after 24 hours of immersion in distilled water. Experimental specimens were stored at 37 degrees C in either distilled water or mineral oil and tested after 3 and 6 months. The data were analyzed by two-way ANOVA and Tukey's test. RESULTS: Storage in water significantly decreased the TS and E of SB and OS specimens after 3 and 6 months (P < 0.05), but did not cause significant changes in either TS or E of CL specimens in the same periods (P > 0.05). Storage in oil significantly increased the TS of the three adhesives after 3 and 6 months (P > 0.05), and the same trend was observed for E value of CL sample (P > 0.05). CLINICAL SIGNIFICANCE: Exposure of cured adhesive systems to long-term immersion in water caused marked reduction in their mechanical properties. Reduced mechanical properties of the adhesive system may compromise resin/dentin bonds and have a clinical implication on the longevity of adhesive restorations.     

An evaluation of self-cured and visible light-cured denture base materials when used as a denture base repair material

summary The aim of this study was to compare some of the physical properties of a heat-cured, a self-cured and a visible light-cured acrylic resin, and to evaluate the suitability of visible light-cured resin as a repair material for dentures made of heat-cured acrylic resin. Transverse strength, surface hardness and impact strength were determined for the three materials and the efficiencies of light-cured and self-cured resins, when used as a repair material, were evaluated by testing the transverse strength of repaired heat-cured specimens 1 hour, 1 week and 1 month after repair. The results showed that the rigidity of specimens repaired with light-cured resin improved with longer water storage. However, their transverse strength reached a maximum after one day and was reduced after 1 month. The rigidity and transverse strength of specimens repaired with self-cured resin were not influenced significantly by water storage and the transverse strength was significantly higher than the light-cured repaired specimens.     

Shear bond strength of provisional restoration materials repaired with light-cured resins

This study evaluated the repair bond strengths of light-cured resins to provisional restoration materials with different chemical compositions and polymerization techniques. Fifty discs (10 mm in diameter and 1.5 mm thick) were fabricated for each provisional resin base material, including a self-cured methacrylate (Alike), self-cured bis-acrylate (Protemp 3 Garant), light-cured bis-acrylate (Revotek LC) and a heat-cured methacrylate (Namilon). All specimens were stored in distilled water at 37 degrees C for seven days before undergoing repair with one of four light-cured resins, including AddOn, Revotek LC, Dyractflow and Unifast LC and a self-cured resin (Alike), according to the manufacturers' instructions, for a total of 200 specimens. After 24 hours of storage in 37 degrees C water, the shear bond strengths were measured with a universal testing machine and fracture surfaces were examined under a stereomicroscope. Two-way ANOVA revealed that provisional resin-base material (p < 0.001), repair material (p < 0.001) and their interactions (p < 0.001) significantly affected the repair strength. Tukey's multiple comparisons showed that the lowest bonding strengths were found in specimens of heat-cured methacrylate resin materials repaired with bis-acryl resins, with their failure modes primarily being of the adhesive type. The highest bond strengths were recorded when the provisional resin-base materials and repairing resins had similar chemical components and the failure modes tended to be of the cohesive type.     

家庭漂白剂对复合树脂表面粗糙度、显微硬度的影响

目的:评价10%过氧化脲家庭漂白剂对直接和间接复合树脂材料表面粗糙度和显微硬度的影响。方法:实验选用2种直接复合树脂材料(Filtek Z350,Clearfil Majesty Esthetic)和2种间接复合树脂材料(Ceramage,Adoro SR)。每种树脂材料在粗糙度和显微硬度试验中分别制作20个盘形试样(直径10 mm、厚1.0 mm),随机分为10%过氧化脲漂白组和去离子水对照组(n=10)。漂白凝胶处理漂白组试样每天使用8 h,共2周。测量树脂试样漂白处理前、后表面粗糙度和显微硬度值。结果:10%过氧化脲漂白剂处理前后,树脂材料表面粗糙度变化无统计学差异(除外Clearfil Majesty Esthetic)。4种树脂材料漂白前后试样的显微硬度值变化不大,且没有统计学差异。结论:10%过氧化脲漂白剂没有改变树脂材料的显微硬度,但树脂材料表面粗糙度的改变取决于树脂材料的类型。     

Properties of microfilled and visible light-cured composite resins.

Physical and mechanical properties of four commercial micro-filled composite resins, a visible light-cured composite resin, and a conventional composite resin were investigated. Isocap, Isopast, and Superfil were similar in most properties. Compared with Concise, they had lower values of inorganic filler content and modulus of elasticity and higher values of water sorption, depth of indentation, and linear coefficient of thermal expansion. The properties of Silar were between those of Concise and the other microfilled composite resins. Fotofil had lower values of modulus of elasticity, water sorption, and linear coefficient of thermal expansion than Concise.     

10种复合树脂颜色稳定性与吸水溶解性研究

目的 评价10种光固化复合树脂在不同溶液中的颜色稳定性及吸水溶解性能。方法 10种光固化复合树脂分别为：BeautifilⅡ(B2)、Ceram. X One Universal (CXU)、Charisma (CS)、Charisma Diamond (CD)、Denfil (DF)、DX. Universal (DXU)、Filtek Z250 (Z250)、Filtek Z350 XT (Z350)、FS-1 (FS)、Magnafill Putty(MP)。每种树脂材料各制作20个试件,随机分为4组(n=5),分别浸入蒸馏水(对照组)、咖喱、咖啡和红酒28 d,分光光度计测量试件浸入前及浸入后1、7、14、21和28 d的色度值(CIE L^*a^*b^*),计算染色前后色差值。根据ISO 4049:2019标准,每种材料制作3个试件,测量材料的吸水性和溶解性。采用三因素方差分析评估树脂材料、染液、染色时间对染色前后色差值(ΔE)的影响,采用单因素方差分析比较不同材料的吸水值和溶解值变化。结果 随着染色时间增加,所有试...     

Microtensile bond strength of adhesive systems to dentin with or without application of an intermediate flowable resin layer

This study evaluated the effect of flowable composite resin application on the microtensile bond strength (muTBS) of adhesive systems to dentin. Occlusal surfaces of human third molars were ground to obtain flat dentin surfaces. The crown of each tooth was sectioned occluso-gingivally into four quarters with a water-cooled diamond saw. One of the following adhesive systems was applied to dentin surface in each quarter of the same tooth, following manufacturers' instructions: Scotchbond Multipurpose, Single Bond Adper Prompt and Clearfil SE Bond. Experimental and control groups received the same treatment, except for the fact that a layer of flowable composite (Filtek Flow) was placed and light-cured on top of the adhesive layer in the specimens of the experimental groups. Resin composite (Filtek Z250) crown buildups were then made on the bonded surfaces and incrementally light-cured for 20 s. The restored teeth were stored in water at 37 masculineC for 24 h. Each tooth quarter was serially cut in a longitudinal direction in order to obtain several bonded sticks (0.9-mm(2) in cross-section). Maximal microtensile stress (in MPa) at failure was recorded using a universal testing machine. Data were analyzed by two-way ANOVA and Tukey's test at 5% significance level. Placement of a low-viscosity resin to the hybridized dentin increased the muTBS for all tested adhesive systems. However, such increase was significant only for Clearfil SE Bond (p<0.05). When the restorations were placed without low-viscosity resin, Clearfil SE Bond presented higher muTBS than Adper Prompt (p<0.05). For the groups treated with flowable composite, Clearfil SE Bond produced the highest muTBS means to dentin. In conclusion, the effect of the addition of an intermediate flowable composite layer on muTBS to dentin was material-dependent and resulted in an increased adhesion for all tested materials, though with significance only for Clearfil SE Bond.     

The effect of additional etching and curing mechanism of composite resin on the dentin bond strength

PURPOSE

The aim of this study was to evaluate the effects of additional acid etching and curing mechanism (light-curing or self-curing) of a composite resin on the dentin bond strength and compatibility of one-step self-etching adhesives.

MATERIALS AND METHODS

Sixteen human permanent molars were randomly divided into eight groups according to the adhesives used (All-Bond Universal: ABU, Clearfil S3 Bond: CS3), additional acid etching (additional acid etching performed: EO, no additional acid etching performed: EX), and composite resins (Filtek Z-250: Z250, Clearfil FII New Bond: CFNB). Group 1: ABU-EO-Z250, Group 2: ABU-EO-CFNB, Group 3: ABU-EX-Z250, Group 4: ABU-EX-CFNB, Group 5: CS3-EO-Z250, Group 6: CS3-EO-CFNB, Group 7: CS3-EX-Z250, Group 8: CS3-EX-CFNB. After bonding procedures, composite resins were built up on dentin surfaces. After 24-hour water storage, the teeth were sectioned to make 10 specimens for each group. The microtensile bond strength test was performed using a microtensile testing machine. The failure mode of the fractured specimens was examined by means of an optical microscope at ×20 magnification. The data was analyzed using a one-way ANOVA and Scheffe''s post-hoc test (α=.05).

RESULTS

Additional etching groups showed significantly higher values than the no additional etching group when using All-Bond Universal. The light-cured composite resin groups showed significantly higher values than the self-cured composite resin groups in the Clearfil S3 Bond.

CONCLUSION

The additional acid etching is beneficial for the dentin bond strength when using low acidic one-step self-etch adhesives, and low acidic one-step self-etch adhesives are compatible with self-cured composite resin. The acidity of the one-step self-etch adhesives is an influencing factor in terms of the dentin bonding strength and incompatibility with a self-cured composite resin.     

Bond strength and failure analysis of light-cured denture resins bonded to denture teeth

This study examined the tensile bond strength and failure sites of one heat-cured (Microlon) and two visible light-cured (Triad and Extoral) denture resins to two types of denture teeth. The resins were processed into cylinders against denture teeth milled to the same size. Half of the specimens were thermocycled. After tensile testing, statistical analysis (p 0.05) showed that the strongest bond was achieved with the heat-cured resin Microlon, whereas Triad resin displayed the stronger bond between the two light-cured resins. Scanning electron microscopic analysis showed that the nature and location of the fracture sites was different among the three resins tested.     

Effects of mechanical properties of adhesive resins on bond strength to dentin.

OBJECTIVES: The purpose of this study was to evaluate the relationship between the micro-tensile bond strength to dentin and mechanical properties of the cured adhesive resins. METHODS: Coronal dentin surfaces of extracted human teeth were treated with four commercial self-etching priming systems (Clearfil SE Bond; UniFil Bond; Tokuso Mac-Bond II; and Imperva Fluoro Bond) and bonded with a resin composite. After 24h storage in water at 37 degrees C, the bonded specimens were trimmed and subjected to micro-tensile bond strength testing at a cross-head speed of 1mm/min. Debonded surfaces were observed under a FE-SEM. For testing mechanical properties, 0.7-mm thick slabs of each adhesive resin were prepared, light-cured, and stored dry at the room temperature for 24h. After trimming, ultimate micro-tensile strength was measured. The nano-hardness and Young's modulus were also evaluated using cured adhesives that were prepared in the same manner as described above. RESULTS: The micro-tensile bond strengths to dentin and ultimate micro-tensile strengths of the resins were not significantly different among all systems (P>0.05). However, the nano-hardness and Young's modulus of Clearfil SE Bond and Imperva Fluoro Bond adhesive resins were significantly higher than those of UniFil Bond and Tokuso Mac-Bond II resins (P<0.05). The micro-tensile bond strength significantly correlated with the ultimate micro-tensile strength of the resins (r(2)=0.77; P<0.05), but was not correlated with the nano-hardness or Young's modulus (P>0.05). SEM observation of the debonded surfaces revealed a mixed type of fracture with a combination of interfacial and cohesive failure within the adhesive resin. SIGNIFICANCE: The four self-etching priming systems exhibited similar dentin bond strengths, which also correlates with the ultimate strength of the adhesive resins.     

Effect of blood contamination with 1-step self-etching adhesives on microtensile bond strength to dentin

This study evaluated the effect of blood contamination and decontamination methods on the microtensile bond strength of 1-step self-etching adhesive systems to dentin contaminated after adhesive application and light curing. Three commercially available "all-in-one" adhesives (One Up Bond F, Xeno III and Adper Prompt L-Pop) and 1 resin composite (Clearfil AP-X) were used. Third molars that had been stored in distilled water with 0.5% thymol at 4 degrees C were ground with #600 SiC paper under running water to produce a standardized smear layer. The specimens were randomly divided into groups according to the 3 adhesive systems. The adhesive systems were used under 3 conditions: no contamination, which was the control (C); contamination of the light-cured adhesive surface with blood and reapplication of adhesive (Contamination 1) and contamination of the light-cured adhesive surface with blood, then washing, drying and reapplication of the adhesive (Contamination 2). Following light curing of the adhesive, the resin composite was placed in 3 increments up to a 5-mm-thick layer on the bonded surface. All specimens were stored in distilled water at 37 degrees C for 24 hours. The microtensile bond strength was measured using a universal testing machine (EZ test), and data were analyzed by 1-way ANOVA followed by the Duncan test to make comparisons among the groups (p=0.05). After debonding, 5 specimens were selected from each group and examined in a scanning electron microscope to evaluate the modes of fracture. For all adhesives, contamination groups showed lower bond strength than the control (p<0.05). There was no statistically significant difference among the control groups (p>0.05). For Xeno III and Adper Prompt L-Pop, contamination group #2 showed the lowest bond strength among the groups (p<0.05). For One Up Bond F, contamination group #2 showed higher bond strength than contamination group #1 but showed no statistical significance between them (p>0.05).     

Effect of light-activation methods and water storage on the flexural strength of two composite resins and a compomer

The present study evaluated the flexural strength of three composite resins recommended for direct esthetic restorations: a polyacid modified composite (Dyract AP), a unimodal composite resin (Filtek Z250) and a hybrid composite resin (Point 4). The variation factors, apart from the type of composite resin, were the light activation method and the water storage period. The composite resins were light-cured in continuous mode (40 s, 500 mW/cm2) or in ramp mode (0-800 mW/cm2 for 10 s followed by 30 s at 800 mW/cm2) and stored for 24 hours or 30 days in distilled water at 37 degrees C. The data were analyzed by ANOVA and Tukey test for multiple comparisons (alpha = 0.05). The composite resin Z250 presented the highest mean flexural strength (166.74 MPa) and Dyract AP presented the lowest one (129.76 MPa). The storage for 30 days decreased the flexural strength in ramp mode (24 h: 156.64 MPa; 30 days: 135.58 MPa). The light activation method alone did not lead to different flexural strength values.     

Mechanical stability of resin-dentin bond components.

OBJECTIVES: To evaluate the effects of long-term storage on the mechanical properties of the components of resin-dentin bonds, that is, resin composite, adhesive system, demineralized and mineralized dentin. METHODS: Specimens of resin composite (Z250) and adhesive systems (Single Bond-SB; One-Step-OS and Clearfil Liner Bond 2V-CL) were cast in molds. Dentin specimens were prepared from dentin discs obtained from the crowns of extracted human molars. Specimens of demineralized dentin were obtained by immersion of dentin discs for 6 days in 0.5 mol/l EDTA (pH 7.0). Both dentin and resin-based substrates were shaped to hourglass or I-beam specimens that were used to determine the true stress (TS) or apparent modulus of elasticity (E), respectively. Control specimens were subjected to tensile testing at 0.6 mm/min after 24 h of immersion in distilled water. Experimental specimens were stored at 37 degrees C in either distilled water or mineral oil and tested after 12 months. The data of each group were individually analyzed by ANOVA and Tukey's test. RESULTS: Both TS and E of the resin-based materials decreased significantly after 12 months of storage in water (p < 0.05) except the TS of SB (p > 0.05). No changes were observed for specimens of mineralized dentin, regardless of storage condition (p > 0.05). Storage of demineralized dentin in water did not cause any significant effect in either TS or E (p > 0.05), however, significant reductions of TS and E of demineralized dentin occurred after storage in oil for 1 year (p < 0.05). SIGNIFICANCE: Storage time and medium may be deleterious to the mechanical properties of the resin-dentin bond components, which ultimately could compromise the durability of resin-dentin bonds.     

渗透树脂与前牙美学树脂颜色稳定性的比较研究

目的 通过分析不同树脂材料对饮料色素的着色效果,比较渗透树脂与前牙美学树脂颜色稳定性的差异。方法 选择3种前牙美学树脂（Filtek Z250、Filtek Z350 XT、Beautiful Flow Plus F00）及人工早期龋渗透树脂（Icon）处理样本各20例,不同树脂样本分别分为2组（每组10例）分别置于咖啡溶液及蒸馏水中浸泡1、2、3周。应用Crystaleye分光光度比色仪进行样本颜色分析。结果 人工早期龋渗透树脂处理表面的着色明显高于其他前牙美学树脂（P<0.05）。所有实验树脂及渗透树脂处理表面的着色均随时间延长而增加,但第1周的着色最为显著,明显高于第2周及第3周的着色（P<0.05）。结论 人工早期龋渗透树脂处理表面较前牙美学树脂更易发生颜色改变。