(1/474) Steric effects of N-acyl group in O-methacryloyl-N-acyl tyrosines on the adhesiveness of unetched human dentin.
We have prepared various O-methacryloyl-N-acyl tyrosines (MAATY) to reveal the relationship between molecular structure near carboxylic acid and adhesive strength of MAATY-HEMA type adhesive resin to unetched dentin. In this study, we attempted to change the steric hindrance effect without changing the HLB value, i.e., introducing an iso-acyl group instead of n-acyl group into MAATY. O-methacryloyl-N-ethylbutyryl tyrosine (MIHTY) showed significantly lower adhesive strength when compared with O-methacryloyl-N-hexanoyl tyrosine even though both MAATY have the same HLB value. The possible explanation of the significantly different adhesive strength was that the 2-ethylbutyryl group in MIHTY was bulky, resulting in inhibition of the hydrogen bonding of the carboxylic group. The HLB value is independent of the steric effect of molecular structure, and thus the steric factor should be taken into consideration for the explanation of different adhesive strengths within the adhesive monomers having the same HLB value but different molecular structures. (+info)
(2/474) Marginal adaptation of commercial compomers in dentin cavity.
The dentin cavity adaptation and setting characteristics of four commercial compomers were evaluated by measuring the wall-to-wall contraction gap width in the cylindrical dentin cavity and measuring the compressive strength for a maximum of 14 days after setting. The dentin cavity wall was pretreated by the dentin adhesives according to each manufacturer's instructions or the experimental contraction gap-free dentin bonding system. Complete marginal integrity was obtained in only one compomer and two resin composites which were combined with the experimental dentin bonding system. The compressive strength of two resin composites and two compomers ten minutes after setting was comparable to that after 14 days which indicated that the compomers exhibited setting characteristics as rapidly as the resin composite. It was concluded that a high efficacy dentin bonding system is required for commercial compomers to prevent gap formation during irradiation caused by the rapid setting shrinkage. (+info)
(3/474) An ex vivo investigation into the bond strength of orthodontic brackets and adhesive systems.
The aim of this study was to compare the shear bond strength of Adhesive Precoated Brackets (APC) with that of two types of uncoated bracket bases, Straight-Wire and Dyna-Lock. Two types of orthodontic adhesives were used, Transbond XT and Right-On. Three different curing times were evaluated with the APC brackets in order to find the best. Adhesive remnants on the enamel surface following debond were evaluated using the Adhesive Remnant Index (Artun and Bergland, 1984). Bond strengths ranged from 11.00 to 22.08 MPa. For both types of brackets Transbond produced a significant increase in bond strength compared to Right-On. The Dyna-Lock/Right-On combination produced the poorest results. APC brackets cured for 40 s had similar bond strengths to uncoated brackets fixed by means of Transbond. Overall, 79 per cent of specimens had less than half the tooth surface covered with adhesive following debond. Significantly more adhesive remained on tooth surfaces following debond of the Straight-Wire/Right-On group than any other bracket/adhesive combination. Bond strengths were higher with light-cured Transbond than with chemically-cured Right-On. When Transbond is used in association with APC brackets a 40-second cure time is recommended. (+info)
(4/474) Factors affecting the shear bond strength of orthodontic brackets to porcelain.
The aim of this investigation was to establish a regime for orthodontic bonding to feldspathic porcelain, which ensures adequate bond strength (6-8 MPa) with minimal damage on debond and consisted of an ex vivo investigation measuring the effects of porcelain surface preparation and thermocycling on shear bond strength of orthodontic brackets. One-hundred-and-twenty feldspathic porcelain bonded crown surfaces were divided into 12 equally-sized groups to assess the effects of: (1) glaze removal, (2) application of hydrofluoric acid, phosphoric acid, or omission of acid treatment, and (3) silane priming upon the bond strength of premolar brackets bonded with Right-on (TM) composite resin adhesive. Specimens were subjected to thermocycling and then to shear debonding forces on an Instron machine. Removal of the porcelain glaze, or use of hydrofluoric acid, prior to bonding were found to be unnecessary to secure the target bond strength. Hydrofluoric acid application was associated with increased porcelain surface damage. Thermocycling caused a significant reduction in shear bond strength to porcelain (P < 0*001). The best regime for orthodontic bonding to feldspathic porcelain was to apply phosphoric acid for 60 seconds, and prime with silane prior to bonding. Usually the porcelain surfaces could be repolished. Refereed Paper (+info)
(5/474) Effects of composite thickness on the shear bond strength to dentin.
The manufacturers of some condensable posterior composites claim that their products can be placed in bulk and light-cured in 5-mm-thick increments. This study compared the shear bond strengths of three composite resins when bonded to dentin in 2- and 5-mm-thick increments. Overall the bond strengths were adversely affected by the composite thickness (p < 0.0001). The shear bond strength of each composite tested was much lower when polymerized in a 5-mm increment than in a 2-mm increment of composite (p < or = 0.0005). The two condensable composites tested had a lower bond strength than the conventional composite when polymerized in a 5-mm bulk increment (p < or = 0.01). (+info)
(6/474) Effect of cavosurface angle on dentin cavity adaptation of resin composites.
The effect of the cavosurface angle of dentin cavities prepared in extracted human molars on the cavity adaptation of a resin composite was evaluated by measuring the gap width between the resin composite and the dentin cavity wall. Cavities with cavosurface angles of 90 degrees, 120 degrees, 135 degrees, or 150 degrees were pretreated with one of two commercial dentin bonding systems or an experimental dentin bonding system. The contraction gap width was measured at both the cavity margin and the section cavity using a light microscope. Complete cavity adaptation was obtained with pretreatment of the experimental groups regardless of the cavosurface angle. The contraction gap observed at the cavity margin was prevented with the two commercial dentin bonding systems when the cavosurface angle was increased to 150 degrees. A high correlation was observed between the contraction gap width and the proportion of the free surface to the adhesive surface of the resin composite restoration. (+info)
(7/474) Effectiveness of the addition of water-soluble photoinitiator into the self-etching primers on the adhesion of a resin composite to polished dentin and enamel.
The effectiveness of the addition of a photoinitiator into self-etching primer was investigated by measuring the tensile bond strength between a resin composite and dentin or enamel. The addition of camphorquinone to 5 M (5 wt% MDP -35 wt% HEMA aqueous solution) or 30 M (30 wt% MDP -35 wt% HEMA aqueous solution) did not increase the bond strengths of resin composite to dentin or enamel. On the other hand, the bond strength to dentin was increased by the addition of a water-soluble photoinitiator, 2-hydroxy-3-(3,4-dimethyl-9-oxo-9H-thioxanthen-2-yloxy)-N,N, N-trimethyl-1- propanaminium chloride (QTX) to 5 M or 30 M. The bond strengths to enamel were not influenced by the addition of QTX to 5 M or 30 M. (+info)
(8/474) Correlation of dentin bond durability with water absorption of bonding layer.
In order to understand the relationship between the durability of adhesive strength in the oral cavity and water absorption, a series of O-methacryloyl-N-acyl tyrosines (MAATY)-2-hydroxyethyl methacrylate (HEMA) bond system samples was prepared and their bonding strength to unetched human dentin was measured as a function of immersion period in water. Also, bulk polymerization was carried out to measure the amount of water absorption as a function of time. All specimens absorbed water suddenly when they were immersed into water. The amount of absorbed water was large when the carbon number in the acyl group was small or the number of carboxylic groups was large. The adhesive strength of the MAATY-HEMA system to unetched dentin decreased significantly when the MAATY-HEMA absorbed a larger amount of water. We concluded, therefore, that preparation of MAATY which absorbs less water may improve durability even when immersed in water. (+info)