Hisashi Hisamitsu

Self-etching dentin primers containing phenyl-P.

The dentin bonding efficacies of two commercial dentin bonding systems and experimental self-etching dentin primers composed of methacryloxyethyl hydrogen phenyl phosphate (Phenyl-P) and either hydroxyethyl methacrylate (HEMA) or glyceryl methacrylate (GM, 2,3-dihydroxypropyl methacrylate) were examined. The wall-to-wall polymerization contraction gap width of a commercial light-activated resin composite in a cylindrical dentin cavity and the tensile bond strength to a flat dentin surface were measured. Changes in dentin hardness were determined by Micro Vickers Hardness measurement, and an SEM observation was performed after priming. Formation of a contraction gap was completely prevented by the application of Phenyl-P diluted in HEMA or GM solution combined with a commercial dentin bonding agent, although gap formation was evident in nearly half of the specimens with both commercial dentin bonding systems. The mean tensile bond strengths of the tested groups varied from 16.3 to 20.7 MPa, and there were no significant differences between groups. Based on the measurement of Micro Vickers Hardness and SEM observation after priming, a slight reduction in dentin hardness was observed. However, this reduction in dentin hardness due to self-etching priming did not significantly correlate with either contraction gap width or tensile bond strength.

In vitro inhibition of caries around a resin composite restoration containing antibacterial filler.

Class V cavities were prepared and restored with resin composite containing antibacterial filler powder (Apacider-AW, Ap-AW) using experimental restorations. The restored teeth were incubated in vitro with the cariogenic bacteria Streptococcus mutans IFO 13955. Ground sections were then prepared and examined using macrophotography. Lesions of the outer and inner wall were noted, and the depths of which the lesions penetrated were measured. We found that, in restorations containing 1-5 wt% Ap-AW, caries penetrated the marginal area, while in restorations containing 10 wt% Ap-AW the margin remained free of caries out to a distance of about 1.1 and 1.8 mm on the occlusal and gingival sides, respectively.

A study on the adsorption structure of an adhesive monomer for precious metals by surface-enhanced Raman scattering spectroscopy

In order to clarify the role of a primer on the adhesion between dental precious metals and resin, surface-enhanced Raman scattering (SERS) technique has been applied to the structural analysis of the adhesive monomer, 6-(N-(4-vinylbenzyl)propylamino)-1,3,5-triazine-2, 4-dithione (VBATDT) adsorbed on colloidal Au surfaces. VBATDT is one of the major components of commercial primers. A mixture of a methanol solution of VBATDT and aqueous Au colloid was illuminated by the 647.1 nm line from a Kr ion laser to obtain the SERS. The most intense peak at 458 cm-1 due to C = S stretching in the Raman spectrum of solid VBATDT disappears completely in the SERS, while all the other peaks due to vinylbenzyl group vibrations remain unchanged. It suggests that some structural change occurs in VBATDT upon adsorption on Au which involves the C = S bonds and that the molecule undergoes thione-thiol-type tautomerization in the adsorption process. The SERS spectrum of a commercial primer containing VBATDT exhibits a similar spectral pattern. The present results lead us to conclude that some specific interactions exist between the sulfur atoms of VBATDT and Au surface to form chemical bond likes, which are effective to improve the bond strength between dental precious metals and resin. The ambivalent properties of the primer, chemical stability in storage and chemical affinity to Au, are also explained by the thione-thiol-type tautomerization of VBATDT on the basis of the spectroscopic evidence.

Efficacy of various commercial dentin bonding systems

OBJECTIVES The purpose of this study was to test the bonding efficacy of fifteen commercial dentin bonding systems and also to determine the effect of various commercial dentin cleaners on bonding and dentin hardness. METHODS Each commercial bonding system was examined by two methods: 1) measuring the maximum contraction gap of a light-cured composite in a cylindrical dentin cavity; and 2) determine the tensile bond strength to a flat dentin surface. In addition, various commercial dentin cleansers were investigated to determine if dentin hardness was reduced after cleaning. As a control, the dentin surface was cleaned with neutralized EDTA prior to the combined application of an experimental dentin primer, a commercial bonding agent, and a commercial light-cured composite. RESULTS The study demonstrated that complete marginal adaptation was obtained by the experimental dentin bonding system used as the control. However, it was not possible to completely prevent gap formation with the commercial dentin bonding systems tested. A high correlation (R = 0.88) was observed between maximum contraction gap width and reduction of hardness only in the group in which the dentin was rinsed after cleaning. SIGNIFICANCE It is very important to combine optimal dentin cleansers, primers, and bonding agents to compensate for the polymerization contraction stress of the composite. Therefore, it was speculated that the commercial dentin bonding systems tested in this study consisted of unsuitable materials.

Factors affecting tensile bond strength of composite to dentin

Five factors which might affect the tensile bond strength of an experimental dentin bonding system to extracted human dentin were evaluated. Flat dentin surfaces of extracted human teeth were cleaned with 0.5 mol/L EDTA and pretreated with 35% glyceryl methacrylate solution. A commercial light-activated composite was then bonded using a commercial bonding agent. The five evaluated factors were: 1) embedding or not embedding the specimens in an epoxy resin, 2) thickness of the specimens, 3) crosshead speed during measurement, 4) storage time of the specimens, and 5) dentin substrate depth. Measurements were made of the bond strengths that resulted from the effects of these varied factors. These measurements were compared to a control group. Only the specimen thickness significantly affected the measured bond strength, and extremely thin specimens (about 1 mm) showed the lowest bond strength.

Bonding efficacy and interfacial microstructure between resin and dentine primed with glyceryl methacrylate

OBJECTIVES To evaluate the effect of two experimental primers based on glyceryl methacrylate (GM, 2,3-dihydroxypropyl methacrylate) and 2-hydroxyethyl methacrylate (2-HEMA) on the marginal adaptation of light-cured composite placed into cylindrical dentine cavities and to study the interfacial microstructure. METHODS The bonding efficacy of two experimental dentine primers combined with a dentine cleanser composed of either 0.5 mol l-1 EDTA neutralized to pH 7.4 by sodium hydroxide or 10% citric acid containing 3% ferric chloride (10-3 solution), and a commercial dentine bonding agent containing phosphate ester, were examined by measuring the wall-to-wall polymerization contraction gap of a commercial light-activated resin composite placed into cylindrical dentine cavities. The adhesive interface between the dentine and the dentine adhesive was observed using a transmission electron microscope (TEM). RESULTS The formation of a contraction gap was completely prevented by priming with GM, regardless of the dentine cleanser used. However, in groups primed with 2-HEMA, gap formation was observed in three and four specimens out of 10 in the groups that were cleaned with the EDTA and 10-3 solution, respectively. In samples primed with GM, a high-density layer was observed by TEM at the superficial dentine in the hybrid layer, which may have indicated a high monomer content, whereas no density variations were observed in the hybrid layer in samples primed with 2-HEMA.

A delayed hypersensitivity reaction to dentine primer in the guinea-pig.

OBJECTIVE This study was undertaken to examine the possibility of a delayed hypersensitivity reaction or contact dermatitis occurring in the guinea-pig in response to methacrylate derivatives used as experimental dentine primers. METHODS The dentine primers 2-HEMA, GM, MA and MMA were tested in a guinea-pig maximization test. RESULTS All the dentine primers tested produced positive delayed hypersensitivity reactions in the guinea-pig. MMA produced the most severe reaction. CONCLUSION It is concluded that in the clinical situation, clinicians and other members of the dental team should be aware of the need for careful handling of the dentine primers tested.

The efficacy of dentine adhesive to sclerotic dentine

OBJECTIVE To evaluate the effect of a dentine bonding system to sclerotic dentine in comparison with normal dentine. METHODS The efficacy of the dentine bonding system to sclerotic dentine was examined by measuring wall-to-wall polymerization contraction gap width. The dentine cavity wall was pretreated with an experimental dentine bonding system with and without a dentine primer. The dentine primer was glyceryl mono-methacrylate (Blemmer GLM, NOF Corp., Tokyo, Japan) (GM), which contained esterified methacrylate with a polyvalent alcohol, which is similar to 2-HEMA. The structure of sclerotic dentine and the changes to that structure caused by etching were observed using a scanning electron microscope (SEM). RESULTS With GM priming, complete marginal integrity was obtained regardless of the type of dentine. Without GM priming, complete marginal integrity was obtained in half of the specimens of the sclerotic dentine, and was not obtained in any of the specimens of normal dentine. In the SEM study, the structure of sclerotic dentine was considered to be viable for adhesion. However, this was not the case when etched with phosphoric acid. CONCLUSION It was concluded that sclerotic dentine had a clear advantage over normal dentine with regard to the adaptation of resin composites. Therefore the structure of sclerotic dentine possesses a naturally derived structure to which a primer may attach. Sclerotic dentine is part of the bodys natural defenses and should be preserved. It should not be exposed to acid etching which would damage its structure.

Effects of polyvalent alcohol solutions as dentine primers

OBJECTIVES The purpose of this study was to examine the bonding effect of polyvalent alcohols as dentine primers without a methacrylate group, which may cause contact dermatitis. METHODS The efficacy of polyvalent alcohols as dentine primers was estimated by measuring the wall-to-wall polymerization contraction gap width of a light-activated resin composite filled in a cylindrical dentine cavity in an extracted human tooth. A dentine cavity was cleaned with ethylenediaminetetraacetic acid (EDTA) and primed with an aqueous solution of either ethylene glycol, glycerol, erythritol, xylitol or sorbitol at concentrations of between 25 and 75 wt%. A light-cured resin composite was filled after the application of a commercial dual-cured bonding agent. RESULTS Contraction gap formation was completely prevented only in the group in which the dentine cavity had been primed with an aqueous solution of 62.5% wt% ethylene glycol. Furthermore, in the measurement of a tensile bond strength to a flat dentine surface, high tensile bond strength (17.5 +/- 4.4 MPa) was observed in the group that was primed with 62.5% ethylene glycol solution. CONCLUSION These results suggest that it is not necessary to dissolve methacrylates in a dentine primer when the primer is dried with a blast of compressed air before application of a polymerizable, suitable bonding agent. It is concluded that a dentine primer composed of polyvalent alcohol solutions without a methacrylate group which may cause contact dermatitis, is effective as a dentine primer, affects the dentine surface, and promotes the efficacy of the dentine bonding system.

A study on adsorption structures of methacryloyloxyalkyl dihydrogen phosphates on silver substrates by infrared reflection absorption spectroscopy

10-Methacryloyloxydecyl dihydrogen phosphate (M10P) for use in dentistry has recently been noted as an adhesive monomer contained in a metal primer. Although the treatment of a metal surface with primer before the application of resin is recognized to improve the adhesion between metal and resin, the role of M10P in the adhesion process has not been clarified. In this study, infrared reflection absorption (IRA) spectroscopy was employed to study the adsorption structures of M10P as well as 2-methacryloyloxyethyl dihydrogen phosphate (M2P) on evaporated silver substrates. The IRA spectra of the self-assembled films of those phosphates verified the adsorption of M10P or M2P on silver substrates from the methyl methacrylate solutions (5 x 10(-5) mol/L). The saturation coverages of M10P and M2P were completed after about 50 and 25 min, respectively. Two characteristic bands around 980 and 1080 cm-1 due to the PO(2-)3 stretching vibrations were observed. These results indicate that the phosphate groups of both monomers are adsorbed to silver surfaces in the dissociated form, -PO(2-)3, and form hydrophobic monolayers. The monolayer of M10P was found to be more durable against thermocycling in water than that of M2P by IRA measurements. The roles of M10P in the metal primer are presumably to form such a monolayer with appreciable durability and to promote polymerization with resin monomers.