Document Type
Dissertation
Degree
Doctor of Philosophy (PhD)
Major/Program
Biomedical Engineering
First Advisor's Name
Dr. Sharan Ramaswamy
First Advisor's Committee Title
Committee Chair
Second Advisor's Name
Dr. Yen-Chih Huang
Second Advisor's Committee Title
Dissertation Committee Member
Third Advisor's Name
Dr. Norman Munroe
Third Advisor's Committee Title
Dissertation Committee Member
Fourth Advisor's Name
Dr. Arvind Agarwal
Fourth Advisor's Committee Title
Dissertation Committee Member
Fifth Advisor's Name
Dr. Lidia Kos
Fifth Advisor's Committee Title
Dissertation Committee Member
Keywords
Articular Cartilage, Engineered cartilage, osteochondral defects, Hydrogel, PEGDA, Hydroxyapatiye, nanoparticle, Biomechanics, Integration
Date of Defense
1-22-2014
Abstract
Articular cartilage injuries occur frequently in the knee joint. Several methods have been implemented clinically, to treat osteochondral defects but none have been able to produce a long term, durable solution. Photopolymerizable cartilage tissue engineering approaches appear promising; however, fundamentally, forming a stable interface between the tissue engineered cartilage and native tissue, mainly subchondral bone and native cartilage, remains a major challenge. The overall objective of this research is to find a solution for the current problem of dislodgment of tissue engineered cartilage at the defect site for the treatment of degraded cartilage that has been caused due to knee injuries or because of mild to moderate level of osteoarthritis. For this, an in-vitro model was created to analyze the integration of tissue engineered cartilage with the bone, healthy and diseased cartilage over time. We investigated the utility of hydroxyapatite (HA) nanoparticles to promote controlled bone-growth across the bone-cartilage interface in an in vitro engineered tissue model system using bone marrow derived stem cells. We also investigated the application of HA nanoparticles to promote enhance integration between tissue engineered cartilage and native cartilage both in healthy and diseased states. Samples incorporated with HA demonstrated significantly higher interfacial shear strength (at the junction between engineered cartilage and engineered bone and also with diseased cartilage) compared to the constructs without HA (p < 0.05), after 28 days of culture. These findings indicate that the incorporation of HA nanoparticles permits more stable anchorage of the injectable hydrogel-based engineered cartilage construct via augmented integration between bone and cartilage.
Identifier
FI14071120
Recommended Citation
Dua, Rupak, "Enhanced Anchorage of Tissue-Engineered Cartilage Using an Osteoinductive Approach" (2014). FIU Electronic Theses and Dissertations. 1459.
https://digitalcommons.fiu.edu/etd/1459
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