The objective of the materials testing project is to guide the evolution, refinement and fabrication of developing resin composites throughout the stages of their development. The general hypotheses is that a low shrinkage nanofilled resin composite will have mechanical and physical properties superior to a commercially available resin composite. Thus, in this project, 6 specific aims are proposed each with an underlying subsidiary hypothesis. The transverse strength and fracture toughness of the nanofiller particles in 1:1 Bis-GMA/TEGMA will be used as the screening test for specific aim 1 - It is hypothesized in specific aim 1 that the use of nanofiller particles in the resin will impart a transverse strength and fracture toughness that is equal to or greater than 80% of that of a commercially available resin composite.
Specific aim 2 will screen the Bis-acrylate and -methacrylate terminated nematic liquid crystal monomers(NLCM)using the polymerization shrinkage test.
In specific aim 2, it is hypothesized that the NLCM will have polymerization shrinkage that is less than 80% of the shrinkage of a clinically successful, commercially available resin composite. NLCM and nanofiller particles showing sufficient promise will be blended into various formulations of resin composite; and microstructural analyses, and mechanical and physical properties (specific aims 3, 4, and 5) will be used to characterize them. It is hypothesized in specific arms 3-5 that the nanofiller particles will be homogeneously distributed and that selected mechanical and physical properties will be superior to a commercially available resin composite. formulations showing promise will be subjected to shear bond testing using a commercially available dentin bonding agent in specific aim 6 and after dentin treatment with OP1/TGF-beta1 in specific aim 7. It is hypothesized in specific aims 6 and 7 that the shear bond strength of a prototype resin composites using a commercially available dentin bonding agent and after OP-l/TGF-beta1 treatment will be superior to the bond strength using a commercially available resin composite. It is through comprehensive tests that the ultimate formulation of the model resin composites will be selected for eventual scale up and biocompatibility evaluation.

Project Start
1997-06-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
5
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Type
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Chan, Kwai S; Chan, Candace K; Nicolella, Daniel P (2009) Relating crack-tip deformation to mineralization and fracture resistance in human femur cortical bone. Bone 45:427-34
Shin, Dong-Hoon; Rawls, H Ralph (2009) Degree of conversion and color stability of the light curing resin with new photoinitiator systems. Dent Mater 25:1030-8
Furman, Benjamin R; Wellinghoff, Stephen T; Thompson, Paul M et al. (2008) Preparation, characterization, and modeling of alpha-zirconium phosphonates with ether-functional surfaces. Chem Mater 20:5491-5499
Chan, K S; Lee, Y-D; Nicolella, D P et al. (2007) Improving fracture toughness of dental nanocomposites by interface engineering and micromechanics. Eng Fract Mech 74:1857-1871
Boland, Edward J; Carnes, David L; MacDougall, Mary et al. (2006) In vitro cytotoxicity of a low-shrinkage polymerizable liquid crystal resin monomer. J Biomed Mater Res B Appl Biomater 79:1-6
Satsangi, Neera; Rawls, H Ralph; Norling, Barry K (2005) Synthesis of low-shrinkage polymerizable methacrylate liquid-crystal monomers. J Biomed Mater Res B Appl Biomater 74:706-11
Satsangi, Neera; Rawls, H Ralph; Norling, Barry K (2004) Synthesis of low-shrinkage polymerizable liquid-crystal monomers. J Biomed Mater Res B Appl Biomater 71:153-8
Papagerakis, P; MacDougall, M; Hotton, D et al. (2003) Expression of amelogenin in odontoblasts. Bone 32:228-40
Knight, C; Papagerakis, P; Simmons, D et al. (2002) Genomic organization and localization of mouse Nma/BAMBI: possible implications related to ameloblastoma formation. Connect Tissue Res 43:359-64
MacDougall, M; Unterbrink, A; Carnes, D et al. (2001) Utilization of MO6-G3 immortalized odontoblast cells in studies regarding dentinogenesis. Adv Dent Res 15:25-9

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