The long-term objective is to make it possible to repair tooth defects by applying solutions and then composite materials which will bond to the surface. When composites can be durably bonded to both dentin and enamel by adhesion, the amount of """"""""drilling"""""""" (and therefore the need for local anesthetics) will be lessened, because there will no longer be the necessity to cut away vital supportive dentin to make undercuts and mechanically lock the filling material in place. A recent breakthrough in this project suggests that this goal is a real possibility.
The specific aims of the project are to determine the essential mechanisms of the new bonding method and to optimize variables in its materials and methods. The work plan is to characterize the surface modification of dentin and enamel which results from the application of the aqueous ferric oxalate (or alternative) mordant solution. This microstructure will be detailed with scanning and transmission electron microscopies, and the components determined by X-ray, secondary ion mass spectroscopy, and other techniques. The role played by N-phenylglycine will be revealed by functional comparisons of chemically related alternatives. The surface interpenetration by the polar difunctional monomer of this system will be characterized by transmission electron microscopy. The methodology will include the use of ultraviolet, infrared, and electron-spin resonance spectroscopies. Once the source and nature of the polymerization are known for the present system, it will then become possible to make substitutions for the various components, broaden the scope of the capability, and facilitate the transfer of this technology to clinical usefulness. Success will improve treatments of cervical and root lesions as well as repairs of tooth crowns, and it will become possible to provide protective coatings of exposed root surfaces where there has been gingival recession.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE005129-09
Application #
3219251
Study Section
(SSS)
Project Start
1977-12-01
Project End
1988-07-31
Budget Start
1986-08-01
Budget End
1987-07-31
Support Year
9
Fiscal Year
1986
Total Cost
Indirect Cost
Name
American Dental Association Foundation
Department
Type
DUNS #
789085941
City
Chicago
State
IL
Country
United States
Zip Code
60611
Bowen, Rafael L; Schumacher, Gary E; Giuseppetti, Anthony A et al. (2009) Adhesive Bonding to Dentin Improved by Polymerizable Cyclodextrin Derivatives. J Res Natl Inst Stand Technol 114:11-20
Bowen, Rafael L; Carey, Clifton M; Flynn, Kathleen M et al. (2009) Synthesis of Polymerizable Cyclodextrin Derivatives for Use in Adhesion-Promoting Monomer Formulations. J Res Natl Inst Stand Technol 114:1-9
Hussain, Latiff A; Dickens, Sabine H; Bowen, Rafael L (2005) Properties of eight methacrylated beta-cyclodextrin composite formulations. Dent Mater 21:210-6
Hussain, Latiff A; Dickens, Sabine H; Bowen, Rafael L (2005) Shear bond strength of experimental methacrylated beta-cyclodextrin-based formulations. Biomaterials 26:3973-9
Hussain, Latiff A; Dickens, Sabine H; Bowen, Rafael L (2004) Effects of polymerization initiator complexation in methacrylated beta-cyclodextrin formulations. Dent Mater 20:513-21
Richards, N D; Eichmiller, F; Dickens, S V et al. (1993) The effect of two initiator/stabilizer concentrations in a metal primer on bond strengths of a composite to a base metal alloy. Dent Mater 9:91-4
Miniotis, N J; Bennett, P S; Johnston, A D (1993) Molar efficiency study of chlorinated NPG substitutes in dentin bonding. J Dent Res 72:1045-9
Simpson, M D; Horner, J A; Brewer, P D et al. (1992) Effects of aluminum oxalate/glycine pretreatment solutions on dentin permeability. Am J Dent 5:324-8
Farahani, M; Johnston, A D; Bowen, R L (1991) The effect of catalyst structure on the synthesis of a dental restorative monomer. J Dent Res 70:67-71
Webb, R E; Johnston, A D (1991) Dentin-bonding molar efficiency using N-phenylglycine, N-phenyl-beta-alanine, or N-methyl-N-phenylglycine. J Dent Res 70:211-4

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