The overall objective of this proposal is to develop novel polymer networks for tissue engineering that elicit desired physicochemical properties for the repair or replacement of craniofacial and orthopaedic cartilage. In particular, this proposal focuses on the development stage of intelligent matrices with controlled architectures and gelling techniques that allow imprinting of the cellular structure in the final network microstructure. The global hypothesis to be tested is that matrix materials will provide superior performance in tissue engineering cartilage when they are engineered to: 1) match the physical and mechanical properties of native cartilage; 2) incorporate cellular structural information in the hydrogel pores; and 3) allow easy structural and chemical modification through photochemistry. Specifically, the aims of the research are as follows.
Specific Aim 1 : to develop hydrogel matrices based on poly (vinyl alcohol) (PVA) which have controlled molecular architecture that allows intelligent engineering of properties such as mesh size, mechanical behavior, hydrophilicity, and degradability.
Specific Aim 2 : to modify further the aforementioned PVA hydrogels with a novel photografting technique which facilitates initiator free gelation and grafting of hydrophilic monomers to improve the immunoprotective properties and mechanical stabilization.
Specific Aim 3 to evaluate these materials for their cellular compatibility (e.g., chondrocyte proliferation and extracellular matrix formation) and their performance in the correction of a cartilage defect to restore function (e.g., mechanical and eventual integrated tissue formation).

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
1R01DE012998-01
Application #
2796493
Study Section
Special Emphasis Panel (ZHL1-CSR-F (M2))
Project Start
1998-09-01
Project End
2001-06-30
Budget Start
1998-09-01
Budget End
1999-06-30
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Colorado at Boulder
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
City
Boulder
State
CO
Country
United States
Zip Code
80309
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Sridhar, Balaji V; Doyle, Nicholas R; Randolph, Mark A et al. (2014) Covalently tethered TGF-?1 with encapsulated chondrocytes in a PEG hydrogel system enhances extracellular matrix production. J Biomed Mater Res A 102:4464-72
Papadopoulos, Anestis; Bichara, David A; Zhao, Xing et al. (2011) Injectable and photopolymerizable tissue-engineered auricular cartilage using poly(ethylene glycol) dimethacrylate copolymer hydrogels. Tissue Eng Part A 17:161-9
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Salinas, Chelsea N; Anseth, Kristi S (2009) Decorin moieties tethered into PEG networks induce chondrogenesis of human mesenchymal stem cells. J Biomed Mater Res A 90:456-64
Salinas, C N; Anseth, K S (2009) Mesenchymal stem cells for craniofacial tissue regeneration: designing hydrogel delivery vehicles. J Dent Res 88:681-92
Fairbanks, Benjamin D; Schwartz, Michael P; Bowman, Christopher N et al. (2009) Photoinitiated polymerization of PEG-diacrylate with lithium phenyl-2,4,6-trimethylbenzoylphosphinate: polymerization rate and cytocompatibility. Biomaterials 30:6702-7
Salinas, Chelsea N; Anseth, Kristi S (2008) The influence of the RGD peptide motif and its contextual presentation in PEG gels on human mesenchymal stem cell viability. J Tissue Eng Regen Med 2:296-304

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