Efficacy of varying the NMEP concentrations in the NMGly-NMEP self-etching primer on the resin-tooth bonding

It is well understood that the application of a self-etching primer enhances the bonding at the resin-teeth interface. In this study, we designed a self-etching primer consisting of N-methacryloyl glycine (NMGly) and N-methacryloyl-2-aminoethyl phosphonic acid (NMEP). The demineralization effects on the hydroxyapatite or dentin by the carboxylic acid in the NMGly and by the phosphonic acid in the NMEP and their effects on the bond strength of the resin to the tooth were examined. The application of the NMGly-NMEP solution to the enamel resulted in an increase in the bond strength when additional amounts of NMEP were added to the NMGly aqueous solution. This increase was due to the phosphonic acid in the NMEP demineralizing the enamel. Conversely, the addition of the NMEP to the NMGly solution resulted in a decrease in the bond strength to the dentin. The optimal concentration of the NMEP in the NMGly-NMEP solution resulted in bond strengths of over 20 MPa for both the enamel and dentin.     

The pKa effects of the carboxylic acid in N-methacryloyl-omega-amino acid on the demineralization and bond strengths to the teeth

It is understood that the application of a self-etching primer to the tooth enhances the bonding of the resin to the tooth. In this study, we designed a self-etching primer consisting of a series of three N-methacryloyl-omega-amino acids (NMomegaA) with different methylene chain lengths. The demineralization aspect of the teeth components by the carboxylic acid in the NMomegaA and its effects on the bond strength of the resin to the tooth were examined. The amount of decalcification of the hydroxyapatite or dentin by the carboxylic acid in the NMomegaA was strongly dependent on the carboxylic acid's pKa value in the NMomegaA. However, the bond strength's mean values for both the enamel and dentin were not influenced by the degree of demineralization by the carboxylic acid in the NMomegaA. The greater mean value of the dentin's bond strength than with the enamel's was due to differences in the adhesion mechanism types, since the NMomegaA not only exhibited an etching efficacy but also a priming efficacy to the collagen that had been exposed by the NMomegaA conditioning.     

Hydrolytic stability of methacrylamide in acidic aqueous solution

In order to develop a more effective self-etching primer, with a longer lasting shelf life, we designed a self-etching primer comprised of methacrylamide, N-methacryloyl glycine, NMGly. In this study, the hydrolytic stability of the amide portion in the NMGly was examined. The difference in the hydrolytic stability between the methacrylamide and the methacrylate, 2-hydroxyethyl methacrylate, HEMA was then discussed. The addition of an acid to an aqueous solution allows for the hydrolysis of the ester portion in the methacrylate and for the production of methacrylic acid, MA and ethylene glycol, EG. From our study, the data clearly demonstrated that, if the storage duration of a commercially available self-etching primer is prolonged, then the functional methacrylates constituting the self-etching primer will be altered upon use. However, the hydrolytic stability of the amide portion in the methacrylamide, NMGly, designed as an acidic and/or hydrophilic monomer for the self-etching primer, was greater than the results achieved with the methacrylate, HEMA.     

Nanolayering of phosphoric acid ester monomer on enamel and dentin

Following the "adhesion-decalcification" concept, specific functional monomers possess the capacity to primary chemically interact with hydroxyapatite (HAp). Such ionic bonding with synthetic HAp has been demonstrated for 10-methacryloyloxydecyl dihydrogen phosphate (10-MDP), manifest as self-assembled "nanolayering". In continuation of that basic research this study aimed to explore whether nanolayering also occurs on enamel and dentin when a 10-MDP primer is applied following a common clinical application protocol. Therefore, the interaction of an experimental 10-MDP primer and a control, commercially available, 10-MDP-based primer (Clearfil SE Bond primer (C-SE), Kuraray) with enamel and dentin was characterized by X-ray diffraction (XRD), complemented with transmission electron microscopy interfacial ultrastructural data upon their reaction with enamel and dentin. In addition, XRD was used to study the effect of the concentration of 10-MDP on nanolayering on dentin. Finally, the stability of the nanolayers was determined by measuring the bond strength to enamel and dentin when a photoinitiator was added to the experimental primer or when interfacial polymerization depended solely on the photoinitiator supplied with the subsequently applied adhesive resin. XRD confirmed nanolayering on enamel and dentin, which was significantly greater on dentin than on enamel, and also when the surface was actively rubbed with the primer. Nanolayering was also proportional to the concentration of 10-MDP in the primer. Finally, the experimental primer needed the photoinitiator to obtain a tensile bond strength to dentin comparable with that of the control C-SE primer (which also contains a photoinitiator), but not when bonded to enamel. It is concluded that self-assembled nanolayering occurs on enamel and dentin, even when following a clinically used application protocol. The lower bonding effectiveness of mild self-etch adhesives to enamel should be ascribed in part to a lower chemical reactivity (nanolayering) with enamel HAp.     

Effect of addition of chitosan to self-etching primer: antibacterial activity and push-out bond strength to radicular dentin

The purpose of this study was to evaluate the antibacterial activity of a modified self-etching primer incorporating chitosan and whether this modification affected the bond strength to radicular dentin.A modified self-etching primer was prepared by adding chitosan solutions at 0.03%,0.06%,0.12% and 0.25%(W/W) to RealSeal selfetching primer.RealSeal primer without chitosan was used as the control.The antibacterial activity of the modified self-etching primer was evaluated using the direct contact test against Enterococcus faecalis.The bonding ability of the RealSeal system to radicular dentin was evaluated using the push-out bond strength test.The modes of failure were examined under a stereomicroscope.Data were analyzed using analysis of variance(ANOVA) and Tukey's test,with a P-value 0.05 indicating statistical significance.The results showed that the antibacterial properties of the freshly prepared and aged modified self-etching primer incorporating chitosan exhibited potent antibacterial effect against Enterococcus faecalis compared with the unmodified primer.The RealSeal system with the aged modified self-etching primer incorporating chitosan showed no significant differences in the bond strength as compared with the control(P = 0.99).The findings suggest that modified self-etching primer incorporating chitosan is a promising antibacterial primer which does not adversely affect the bond strength of the RealSeal system to radicular dentin.     

Adhesion of a self-etching system to dental substrate prepared by Er:YAG laser or air abrasion

The purpose of this study was to assess the microtensile bond strength of a self-etching adhesive system to enamel and dentin prepared by Er:YAG laser irradiation or air abrasion, as well as to evaluate the adhesive interfaces by scanning electron microscopy (SEM). For microtensile bond strength test, 80 third molars were randomly assigned to five groups: Group I, carbide bur, control (CB); II, air abrasion with standard tip (ST); III, air abrasion with supersonic tip (SP); IV, Er:YAG laser 250 mJ/4 Hz (L250); V, Er:YAG laser 300 mJ/4 Hz (L300). Each group was divided into two subgroups (n = 8) (enamel, E and dentin, D). E and D surfaces were treated with the self-etching system Adper Prompt L-Pop and composite buildups were done with Filtek Z-250. Sticks with a cross-sectional area of 0.8 mm(2) (+/-0.2 mm(2)) were obtained and the bond strength tests were performed. Data were submitted to ANOVA and Tukey's test. For morphological analysis, disks of 30 third molars were restored, sectioned and prepared for SEM. Dentin presented the highest values of adhesion, differing from enamel. Laser and air-abrasion preparations were similar to enamel. Dentin air-abrasion with standard tip group showed higher bond strength results than Er:YAG-laser groups, however, air-abrasion and Er:YAG laser groups were similar to control group. SEM micrographs revealed that, for both enamel and dentin, the air-abrasion and laser preparations presented irregular adhesive interfaces, different from the ones prepared by rotary instrument. It was concluded that cavity preparations accomplished by both Er:YAG laser energies and air abrasion tips did not positively influence the adhesion to enamel and dentin.     

Effect of self-etching primers containing N-acryloyl aspartic acid on dentin adhesion

The purpose of this study was to evaluate the feasibility of aspartic acid derivative, N-acryloyl aspartic acid (N-AAsp) when used as a self-etching primer prior to the application of a commercial bonding agent containing 10-methacryloxydecyl dihydrogen phosphate. N-AAsp was synthesized by the reaction of DL-aspartic acid and acryloyl chloride. N-AAsp can be dissolved in water up to 25 wt % and can adequately remove the smear layer. When 20 wt % N-AAsp was applied as a self-etching primer, the tensile bonding strength of resin composite to dentin doubled to 16.0 MPa compared with that of the nonetching group or the 40 wt % H(3)PO(4) etching/water rinse group. Scanning electron microscopic observations revealed that the formation of the hybrid layer at the interface between the resin composite and dentin and the thickness of the hybrid layer increased with N-AAsp concentration. The hybrid layer in the specimens treated with 20 wt % N-AAsp aqueous solution presented a uniform structure, whereas those treated with 5 wt % N-AAsp solution showed a porous structure. We conclude that 20 wt % N-AAsp aqueous solution has good potential value as a self-etching primer.     

Effects of a ferric chloride primer on collagen-depleted dentin bonding between tri-n-butylborane initiated self-curing resin and dentin

This study was designed to evaluate the micro-tensile bond strength between a carboxylic resin and dentin, when the dentin surface was modified with an experimental dentin primer. The three primers tested were ED primer II (ED), 0.3% ferric chloride aqueous solution (FE), and ED containing 0.3% ferric chloride (ED/FE). Three commercial dentin conditioners [40% phosphoric acid, 10% NaOCl, and 10% citric acid with 3% ferric chloride (10-3)] were also used. The coronal surfaces of extracted human molars were ground flat to dentin. The dentin surfaces were treated with phosphoric acid, NaOCl, or with one of the primers. The 10-3 was used without phosphoric acid or NaOCl as a control. A composite material rod was bonded to the dentin surface with 4-META/MMA-TBB resin. After 24-h immersion in 37 degrees C distilled water, 0.9 mm x 0.9 mm composite-dentin beams cut from the bonded specimens were stressed to failure in tension at 0.6 mm/min. The bond strengths were also evaluated after 5000 thermocycles. The bond strength of the group ED/FE was significantly higher than those of the 10-3, ED, and FE. After 5000 thermocycling, 10-3, ED and FE showed significant decrease in bond strength, although no significant decrease was seen for ED/FE. It was concluded that dentin surface treatment with phosphoric acid, NaOCl, and the ED/FE primer improved the bonding (p < 0.05) between 4-META/MMA-TBB resin and dentin, with or without thermocycling, while the bond strengths in the control group fell 34% following 5000 thermocycles.     

Bonding efficacy of polyalkenoic acids to hydroxyapatite,enamel and dentin

Previously, we introduced a methodology to determine the chemical bonding potential of polyalkenoic acids to mineralized tissues through quantification of the degree of ionic bond formation between the carboxyl groups of a polyalkenoic acid with calcium of hydroxyapatite. In a continuation of that study, we now investigated in how far the chemical bonding potential to synthetic hydroxyapatite is influenced by the molecular structure of the polyalkenoic acid and if this also may affect the self-adhesiveness to enamel and dentin. X-ray photoelectron spectroscopy and inductively coupled plasma atomic emission spectrometry were used to quantitatively analyze the chemical bonding efficacy of a polyalkenoic acid consisting of acrylic acid units (PAA) to synthetic hydroxyapatite (HAp) in comparison to the chemical bonding potential of the previously investigated synthesized polyalkenoic acid (s-PA) co-polymer consisting of 90w/w% acrylic and 10w/w% maleic acid units. In addition, the analysis was carried out for enamel and dentin samples. PAA revealed a significantly lower bonding effectiveness with only half of its carboxyl groups bonded to HAp versus about two-third of the carboxyl groups of s-PA. The difference in bonding potential was confirmed by the considerably lower adhesiveness of PAA to enamel and dentin as compared to that of s-PA The present findings indicate that the molecular structure of the polyalkenoic acid significantly influences the chemical bonding efficacy to Hap-based substrates.     

口腔粘接新型材料——磷酸二氢(甲基丙烯酰氧癸)酯的合成与应用

以甲基丙烯酸、1,10-癸二醇和三氯氧磷为主要原料合成出了磷酸二氢(甲基丙烯酰氧癸)酯.用1HNMR、MS和31P-NMR对产物结构进行了表征确认.通过剪切强度的测试评价了磷酸二氢(甲基丙烯酰氧癸)酯对复合树脂与牙釉质、牙本质、钛合金、钴铬合金和高含金合金之间的粘接性能的影响.结果表明磷酸二氢(甲基丙烯酰氧癸)酯能够促进复合树脂与牙釉质、牙本质、钛合金、钴铬合金的粘接,剪切强度分别达到13.5、11.2、16.2和18.1 MPa.     

Gluma脱敏剂对牙本质黏结强度影响的系统评价

BACKGROUND: Desensitization agent is widely used to relieve tooth sensitivity after tooth preparation. However, some components in the desensitization agent for certain affect the dentin bond strength between prosthesis and dentin. Given this, choosing a proper desensitization agent is under discussion. OBJECTIVE: To investigate the influence of Gluma desensitizing agents on bond strength to dentin by Meta-analysis. METHODS: A computer-based retrieval of PubMed, EMbase, EBSCO EDLINE, The chrane Library, ScienceDirect, Web Of Science, OVID, CBMbase, CJFD, CqVip and WanFang databases combined with manual searching was performed for randomized controlled trials or controlled clinical trials about effect of desensitizing agents on dentin bond strength. The retrieval time ranged from the creation date to June 18, 2016, without region and language limits. In accordance with inclusion/exclusion criteria, related data were extracted, and the qualitative and quantitative analysis of the included studies was performed by two researchers independently, and then the Meta-analysis was conducted using RevMan 5.2 software. RESULTS AND CONCLUSION: There was no significant difference in the shear bond strength of self-etching or total-etching adhesive to dentin between two groups, and the same results were found when comparing the shear bond strength of self-etching and total-etching adhesive to dentin. The Gluma had a beneficial effect on the shear bond strength of self-adhesive. These results indicate that when Gluma used as the desensitizing agent, self-adhesive materials are the first choice, and secondly the self-etching or total-etching adhesive materials containing acid or able to dissolve protein crystals are preferred.     

Release of aqueous calcium and phosphate from human dental enamel following administration of self-etching adhesives

Seven self-etching adhesives were studied on an experimental reconstituted human enamel model. The objective was to evaluate the acid dissociation step of the enamel minerals. The self-etching products were applied to the enamel specimens according to the manufacturers' instructions and then rinsed with distilled water. The aqueous calcium and phosphate released were analysed chemically by atomic absorption and ion chromatography, respectively. Results show widely varying concentrations related to pH, acid concentration and calcium binding capacity. All concentrations are less than reference values obtained with orthophosphoric acid. The effectiveness of self-etchants is discussed in terms of their ability to demineralise human enamel and incorporate the released ions in the subsequent HEMA co-polymer composing the hybrid layer.     

不同粘接系统对纤维桩粘接强度的影响

背景：粘接界面尤其是根管壁-粘接剂间是纤维桩修复后接构的薄弱环节,加强粘接剂与根管壁间粘接对提高纤维桩的修复成功率,有重要临床指导意义。 目的：比较自酸蚀粘接系统和全酸蚀粘接系统对纤维桩粘接强度的影响。 方法：选用30颗单根管前牙用于纤维桩粘接实验,每颗牙选用逐步后退法进行预备并进行根管充填。样本分为3组,自酸蚀粘接组、全酸蚀粘接组和空白对照组分别应用自酸蚀粘接系统、全酸蚀粘接系统、传统磷酸酸蚀法处理根管内壁。 结果与结论：自酸蚀粘接组、全酸蚀粘接组和空白对照组的粘接强度分别为(3.24±0.76),(4.09±0.54),(2.85±0.89) MPa。两两相比,不同粘接方法对纤维桩的粘接强度差异均有显著性意义(P < 0.05);扫描电镜观察发现全酸蚀粘接组混合层与牙本质和纤维桩粘接紧密,自酸蚀粘接组混合层只与纤维桩粘接紧密,与牙本质未形成有效连接。提示全酸蚀粘接系统的粘接强度优于自酸蚀粘接系统,具有良好的纤维桩固位性能。     

Release of aqueous calcium and phosphate from human dental enamel following administration of self-etching adhesives

Seven self-etching adhesives were studied on an experimental reconstituted human enamel model. The objective was to evaluate the acid dissociation step of the enamel minerals. The self-etching products were applied to the enamel specimens according to the manufacturers' instructions and then rinsed with distilled water. The aqueous calcium and phosphate released were analysed chemically by atomic absorption and ion chromatography, respectively. Results show widely varying concentrations related to pH, acid concentration and calcium binding capacity. All concentrations are less than reference values obtained with orthophosphoric acid. The effectiveness of self-etchants is discussed in terms of their ability to demineralise human enamel and incorporate the released ions in the subsequent HEMA co-polymer composing the hybrid layer.     

Evaluation of intermolecular interactions of self-etch dentin adhesive primer molecules with type 1 collagen: computer modeling and in vitro binding analysis

The objective of this investigation was to study adhesion of self-etch primer systems to dentin by computer-modeled docking simulations and in vitro binding assay methods. Computer modeling employed analysis of docking simulations of a self-etch primer molecule 10-methacryloxydecamethylene phosphoric acid (MDP) and its calcium salt (MDPCa) as ligands. Typical type 1 collagen segments were selected as targets to reflect potential differences in the amino acid residues in dentinal type 1 collagen triple helix motif. The binding assay involved immunochemical analysis of the modification of anti-collagen binding to collagen by prior exposure of the demineralized dentin to MDP. The estimated mean docking energy values ranged between -4.5 and -8.9kcalmol(-1). The results revealed significant differences in the docking energy estimates as a function of ligand and target structures (p<0.01). Van der Waals and electrostatic contributions were also significantly influenced by ligand selection and collagen structure. Both MDP and MDPCa appear to be important in the overall interactions. Binding assay studies also lend evidence of collagen-ligand intermolecular interactions. It is suggested that the ability of self-etch dentin primer systems to bond effectively to dentin is not limited to the interaction of the primer with the hydroxyapatite of dentin, but also due to the ability to prime dentin efficiently through intermolecular interactions between the primer and its calcium salt with the collagen matrix. Virtual screening methods may be very valuable to select primer molecules for dentin bonding.     

Adhesion/decalcification mechanisms of acid interactions with human hard tissues.

In order to study adhesion/decalcification mechanisms of acid interactions with human hard tissues such as bones and teeth, the chemical interaction of five carboxylic acids (acetic, citric, lactic, maleic, and oxalic) and two inorganic acids (hydrochloric and nitric) with enamel and two synthetic hydroxyapatite (HAp) powders with, respectively, a high and a low crystallinity were analyzed using X-ray photoelectron spectroscopy (XPS), atomic absorption spectrophotometry (AAS), and spectrophotometry (S). X-ray diffraction revealed that the crystallinity of the highly crystallized HAp was considerably higher than that of enamel while the crystallinity of the poorly crystallized HAp was similar to that of dentin and bone. XPS of acid-treated enamel demonstrated for all carboxylic acids ionic bonding to calcium of HAp. AAS and S showed for both HAps that all carboxylic and inorganic acids except oxalic acid extracted Ca significantly more than P, leading to a Ca/P ratio close to that of synthetic HAp (2.16 w/w). Oxalic acid extracted hardly any Ca, but substantially more P, leading to a significantly smaller Ca/P ratio than that of HAp. AAS showed that the calcium salt of oxalic acid hardly could be dissolved, whereas the calcium salts of all the other acids were very soluble in their respective acid solution. These results confirm the adhesion/decalcification concept (AD-concept) previously advanced. Depending on the dissolution rate of the respective calcium salts, acids either adhere to or decalcify apatitic substrates. It is concluded that the AD-concept that originally dictated the interaction of carboxylic acids with human hard tissues can be extended to inorganic acids, such as hydrochloric and nitric acid. Furthermore, HAp crystallinity was found not to affect the adhesion/decalcification behavior of acids when interacting with apatitic substrates, so that the AD-concept can be applied to all human hard tissues with varying HAp crystallinity.     

Etching kinetics of a self-etching primer

Self-etching primers are thought to offer significant advantages over total-etch adhesive systems. The hypothesis tested in this study was that there was no difference in etching characteristics between a self-etching primer and a phosphoric acid solution at the same pH. Etching was assessed using atomic force microscopy (AFM) evaluation of site-specific changes in the height of the peritubular and intertubular dentin as a function of exposure time. Human dentin disks (n = 6/group), prepared with an acid-resistant glass reference layer, were etched with a self-etching primer and with 0.0134 M phosphoric acid (both pH approximately egual to 1.94). Depth changes relative to the reference layer were measured with the AFM after each etching interval, at 15 different locations, each in the peritubular and intertubular dentin. The total demineralization depth was measured in a scanning electron microscope. Peritubular dentin etching rate was linear while it could be measured (up to 15 s) and was greater for the self-etching primer (p < 0.0001). Intertubular dentin displayed a similar demineralization pattern with both acids, ultimately reaching a plateau in the majority of specimens. The self-etching primer attained a plateau after less recession than phosphoric acid (p < 0.0001). Dentin demineralization appears to be affected by other factors in addition to the pH of the etchant solutions.     

Recent advances in the theory and mechanism of adhesive resin bonding to dentin: a critical review

Dentin bonding issues involving adhesive resins have attracted considerable research interest in recent years. An important advance due to the ongoing research is the concept of hybridization of the tissue with primer/adhesive systems. Hybridization involves permeation of primer monomer into the tissue substrate. Although the mechanism of adhesive permeation and interaction with tissue may be complex, significant advances have been made. In systems where etching precedes priming and bonding steps, the Hoy's solubility parameter compatibility of the primer formulation with that of demineralized dentin matrix may determine adhesive permeability. Monomer permeation brings the primer atoms in closer contact with the substrate atoms, leading to adhesive interactions through van der Waals, hydrogen bonding, and electrostatic interactions. In self-etch primer systems, stronger electrostatic interaction between primer monomers and hydroxyapatite has been used to explain the adhesion process. These interactions have been computer-modeled and analyzed. Such interactions and subsequent polymerization of the monomer promote improved bond strength and efficient margin sealing. Incomplete permeation of monomer into the full depth of demineralized region may, however, leave exposed collagen fibrils and cause nanoleakage of water into these regions through a 20-100 nm sized marginal gap, leading to subsequent hydrolytic degradation of these collagen fibrils and the hybrid layer. Microleakage is also a problem in some single step formulations. In this review, we analyze these current theoretical and mechanism-related issues of interest in adhesive resin bonding to dentin, and outline the continuing problems that need to be overcome in the future.     

Elemental distributions and microtensile bond strength of the adhesive interface to normal and caries-affected dentin

The aim of this study was to evaluate the microtensile bond strength (microTBS) and the elemental contents of the adhesive interface created to normal versus caries-affected dentin. Extracted human molars with coronal carious lesions were used in this study. A self-etching primer/adhesive system (Clearfil Protect Bond) was applied to flat dentin surfaces with normal and caries-affected dentin according to the manufacturer's instructions. After 24 h water storage, the bonded specimens were cross-sectioned and subjected to a microTBS test and electron probe microanalysis for the elemental distributions [calcium (Ca), phosphorus (P), magnesium (Mg), and nitrogen (N)] of the resin-dentin interface after gold sputter-coating. The microTBS to caries-affected dentin was lower than that of normal dentin. The demineralized zone of the caries-affected dentin-resin interface was thicker than that of normal dentin (approximately 3 microm thick in normal dentin; 8 microm thick in caries-affected dentin), and Ca and P in both types of dentin gradually increased from the interface to the underlying dentin. The caries-affected dentin had lost most of its Mg content. The distributions of the minerals, Ca, P, and Mg, at the adhesive interface to caries-affected dentin were different from normal dentin. Moreover, a N peak, which was considered to be the collagen-rich zone resulting from incomplete resin infiltration of exposed collagen, was observed to be thicker within the demineralized zone of caries-affected dentin compared with normal dentin.     

Effect of load cycling and in vitro degradation on resin-dentin bonds using a self-etching primer

The objective of this study was to evaluate the effect of in vitro degradation and mechanical loading on microtensile bond strength (MTBS) and microleakage (ML) of a resin composite to dentin using a self-etching primer adhesive [Clearfil SE Bond (SEB)] under two hydration statuses. Twenty-four flat dentin surfaces were divided in groups: 1) blot-dried, 2) air-dried. SEB was applied and resin buildups were performed with Tetric Ceram. Specimens were divided in four subgroups: a) sectioned into beams, b) load cycled, c) beams were immersed in NaOCl for 5 h, d) load cycled and immersed in NaOCl. Beams were tested in tension. For ML testing, 80 Class V cavities were prepared and molars divided in subgroups as described above (in group c and d, specimens were kept in distilled water for 1 year, instead of the 5-h NaOCl immersion). ML was assessed by dye penetration. Analysis of variance and multiple comparisons tests were used for MTBS. For ML, Mann-Whitney U and Wilcoxon matched pairs signed ranked were used (p<0.05). SEB applied to completely dehydrated dentin produced the highest MTBS, at 24-h evaluation. In vitro degradation always decreased MTBS, and fatigue loading only diminished MTBS on dehydrated dentin. Load cycling increased dye penetration on dentin margins. Degradation always increased ML in both enamel and dentin margins.