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Objective To evaluate the influence of tetrahydrofuran (THF) on the resin-to-dentin microtensile bond strength (μTBS) after water storage, for 24 h and 6 months, and to compare its behavior with that of traditional solvents. Methods Seven versions of monomer/solvent mixtures (primers) were prepared using the following solvent and water combinations: (1) THF, (2) acetone, (3) ethanol, (4) water, (5) THF/water, (6) acetone/water and (7) ethanol/water. An experimental adhesive resin was also synthesized to compare adhesive systems with the different primers. Forty-two bovine incisors, randomly separated into seven groups, had their superficial coronal dentin exposed. After acid-etching and rinsing, the excess water was removed from the surface with absorbent paper. Each experimental primer was applied with agitation (30 s) followed by a mild air stream (10 s). The experimental adhesive resin was applied and light-activated (20 s). Resin composite restorations were constructed incrementally. Restored teeth were stored in distilled water at 37 °C (24 h) and sectioned to obtain sticks with an area of 0.5 mm 2 . Half the specimens were subjected to the μTBS test immediately after being cut and the other half were tested after 6 months of water storage. Data (MPa) were analyzed by two-way ANOVA (solvent type and storage time as factors) and Tukey–Kramer's test at α = 0.05. Results Factors and interaction showed a statistical effect. After 6 months storage, acetone groups and primers containing THF showed similar μTBS to initial means. Significance THF seems to be a promising solvent for use in dental adhesive systems, maintaining bond strength on dentin substrate after storage.

To investigate the influence of different water concentrations in the solvents of self-etching primers on microtensile bond strength (LTBS) of an experimental adhesive system.Five experimental self-etching primers with 0, 5, 10, 20 and 40 (wt%) water as solvent were formulated. An experimental adhesive resin (AD-50) was also synthesized to create one experimental self-etching adhesive system. Clearfil SE Bond (CSEB) was used as the commercial reference. Sixty bovine incisors were randomly separated into 6 groups. Buccal enamel was removed to expose the superficial coronal dentin; this surface was polished wet to create a standardized smear layer. After rinsing, water was removed, leaving the surface visibly dried. The dentin surfaces were etched with primer and air dried, adhesive resin was applied and photoactivated, then the composite resin restoration was placed. After storage for 24 h, the specimens were sectioned with a cooled diamond saw at low speed. Microtensile bond strength was measured and data were analyzed with one-way ANOVA/Tukey's test (alpha = 0.05).ANOVA showed that primer composition was a significant factor for bond strength. There was no significant difference in bond strengths between the primers with a water concentration of 40% (53.9 +/- 12.7 MPa), 20% (51.1 +/- 11.5 MPa, and 10% (47.5 +/- 11.4 MPa), and CSEB (50.7 +/- 9.8 MPa). The groups with 5% (38.6 +/- 12.9 MPa) and 0% (31.5 +/- 7.5 MPa) water presented similar bond strengths amongst themselves but were statistically significantly lower than that of the other groups.The water concentration in the primer solvent exercises a significant influence on the bond strength of this experimental self-etching adhesive system.

The aim of this study was to evaluate the kinetics of conversion of Scotchbond Multi-purpose Plus (3M ESPE, St Paul, MN) and Prime&Bond NT (Dentsply De Trey, Konstanz, Germany) used in light-cured, self-cured, or dual-cured versions. The adhesive systems were used in the light-cured version (without the use of chemical initiator) or mixed with its respective chemical initiator either with light activation (dual-cured) or not (self-cured). The degree of conversion (DC) was monitored as a function of time during 5 minutes with a Fourier transform infrared spectrometer equipped with an attenuated total reflectance device. Light-cured and dual-cured modes of Scotchbond Multi-purpose Plus presented the highest DC at 5 minutes. The addition of the self-cure activator (dual-cured mode) to Prime&Bond NT reduced the DC. For the self-cured versions, only the Scotchbond Multi-purpose Plus presented any polymerization reaction at 5 minutes. For the two bonding systems tested, it appears that light curing of the adhesive is important in order to reach a high DC in the first moments after the bonding procedure.

This study evaluated the effect of organic solvent concentration on the polymerization kinetics for a model dental adhesive resin containing a ternary photoinitiator system. A monomer blend based on the bis-GMA, TEGDMA, and HEMA was used as a model dental adhesive resin, which was polymerized using a binary system [camphorquinone (CQ) and ethyl 4-dimethylamine benzoate (EDAB)] and a ternary system [CQ, EDAB, and diphenyliodonium hexafluorphosphate (DPIHFP)]. Additionally, these blends had 0, 10, 20, 30, and 40 wt % ethanol added. Real-time Fourier transform infrared spectroscopy was used to investigate the polymerization reaction over photoactivation time. Data were plotted, and Hill's three-parameter nonlinear regression was performed for curve fitting. The addition of a solvent to the monomer blends decreased the polymerization kinetics, directly affecting the rate of polymerization, delaying vitrification, and attenuating the Trommsdorf effect. The introduction of DPIHFP displayed a strong increase in reaction kinetics, reducing the solvent inhibition effect. After 10 s of photoactivation, the binary system obtained in 0, 10, 20, 30, and 40% of ethanol, a degree of conversion of 44.6, 26.3, 13.4, 1.15, and 0.0%, respectively, whereas when a ternary system was used, the values were 54.6, 40.5, 27.4, 14.5, and 3.4%. An improvement was observed in the polymerization kinetics of a model dental adhesive resin when using a ternary photoinitiation system, making the material less sensitive to the residual presence of a solvent before photoactivation.

Purpose: The aim of this study was to synthesize an alternative acidic monomer (polypropylene glycol phosphate methacrylate – Poly-P) to constitute experimental two-step self-etch adhesive systems and to evaluate its influence on the pH and microshear bond strength ( SBS) to enamel. Methods and materials: Four primers containing Poly-P (10, 15, 30 or 50wt%), 2-hydroxyethyl methacrylate (HEMA), ethanol, and water were prepared, which were allocated in two subgroups according to an adjusted (buffered) or non-adjusted (non-buffered) pH. One experimental control and one commercial (ClearfillTM SE Bond) references were used. SBS protocol was performed at human enamel, followed by mechanical testing (EMIC). Scanning Electron Microscopy (SEM) was performed after each primer application. Data was analyzed by One-Way Kruskall–Wallis and Student-Newman–Keuls tests (p