It is known that resin-modified glass-ionomer cement (RMGIC) is an attractive dental restorative because it has enhanced mechanical strength, bonding and handling properties. However, a disadvantage of this cement is that it contains a large quantity of 2-hydroxyethyl methacrylate (HEMA). Since unreacted HEMA is cytotoxic to pulp and surrounding tissues, elimination of HEMA could make this """"""""intelligent"""""""" cement more attractive for both dental and orthopedic applications. We have demonstrated that new and novel amino acid-modified and non-HEMA containing RMGICs exhibit significantly improved mechanical strengths, adhesion and self-etching capabilities. The objective of this research is to develop these novel amino acid based glass-ionomers for both dental and orthopedic applications, in response to NIBIB's RFA for development of novel biomaterials with improved biological and mechanical properties. In this research, inexpensive and biostable amino acid-based polycarboxylic acid will be synthesized and formulated with amino acid derivatives to form an innovative non-HEMA containing RMGIC system. Design of Experiment (DOE) methodology will be applied to optimize molar ratio, molecular weight, grafting ratio of synthesized poly(amino acid), formulations and filler contents. Mechanical strengths and other physical properties of the new cements will be evaluated. The proposed amino acid-based cements will provide extra salt-bridges, thus enhancing adhesion and mechanical strengths. In vitro direct cell contact as well as methylthiazolyldiphenyl tetrazolium (MTT) studies and in vivo bone response will be conducted to determine the biocompatibility and bioactivity of the new cements. Novel restoratives for both dentistry and orthopedics should be an outcome of this basic research to establish commercial biomaterials for future industrial development. Successful achievement of the goal of this project will significantly impact the field of restorative dentistry and orthopedic surgery. This project will create a university-wide collaboration between synthetic polymer chemist, biomaterials scientist, biomechanical engineer and clinical dentist. This project will also provide an ideal training environment for biomedical engineering students because it will allow them, through close interactions with the collaborators from different disciplines, to develop a broad perspective on biomaterials research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
1R01EB003162-01
Application #
6737905
Study Section
Special Emphasis Panel (ZRG1-SSS-M (55))
Program Officer
Moy, Peter
Project Start
2003-09-19
Project End
2004-07-31
Budget Start
2003-09-19
Budget End
2004-07-31
Support Year
1
Fiscal Year
2003
Total Cost
$277,313
Indirect Cost
Name
University of Alabama Birmingham
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Xie, Dong; Zhao, Jun; Park, Jong-Gu (2007) A novel light-cured glass-ionomer system for improved dental restoratives. J Mater Sci Mater Med 18:1907-16
Xie, Dong; Yang, Youyun; Zhao, Jun et al. (2007) A novel comonomer-free light-cured glass-ionomer cement for reduced cytotoxicity and enhanced mechanical strength. Dent Mater 23:994-1003
Xie, Dong; Park, Jong-Gu; Zhao, Jun (2007) Synthesis and preparation of novel 4-arm star-shape poly(carboxylic acid)s for improved light-cured glass-ionomer cements. Dent Mater 23:395-403
Xie, Dong; Park, Jong-Gu; Faddah, Mona et al. (2006) Preparation, formulation and evaluation of novel photo-cured glass ionomers based on co-polymers of (meth)acrylated amino acids. J Biomater Sci Polym Ed 17:303-22
Xie, Dong; Park, Jong-Gu; Faddah, Mona et al. (2006) Novel amino acid-constructed polyalkenoates for dental glass-ionomer restoratives. J Biomater Appl 21:147-65
Xie, Dong; Faddah, Mona; Park, Jong-Gu (2005) Novel amino acid modified zinc polycarboxylates for improved dental cements. Dent Mater 21:739-48