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Development of collagen scaffolds to address biomechanical design criteria for tendon–to–bone repair
Mozdzen, Laura C
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https://hdl.handle.net/2142/100414
Description
- Title
- Development of collagen scaffolds to address biomechanical design criteria for tendon–to–bone repair
- Author(s)
- Mozdzen, Laura C
- Issue Date
- 2016-07-07
- Director of Research (if dissertation) or Advisor (if thesis)
- Harley, Brendan A. C.
- Doctoral Committee Chair(s)
- Harley, Brendan A. C.
- Committee Member(s)
- Kong, Hyunjoon
- Leckband, Deborah E.
- Wagoner-Johnson, Amy J.
- Department of Study
- Chemical & Biomolecular Engr
- Discipline
- Chemical Engineering
- Degree Granting Institution
- University of Illinois at Urbana-Champaign
- Degree Name
- Ph.D.
- Degree Level
- Dissertation
- Keyword(s)
- collagen scaffold
- orthopedic tissue engineering
- mesenchymal stem cells
- biomechanics
- Abstract
- The tendon-bone junction (TBJ) is a unique, mechanically dynamic and structurally graded anatomical zone which transmits tensile loads between tendon and bone. The TBJ repeatedly transmits high tensile loads to result in movement without failure by effectively dissipating stress concentrations which arise between mechanically dissimilar materials (tendon, bone). Upon injury, surgical repair techniques rely on mechanical fixation, and the local heterogeneities of the TBJ do not reform, causing poor functional outcomes (re-failure >90%). Biomaterial platforms and tissue engineering methods offer an alternative approach to address these injuries. Although current methods are moving towards multi-tissue regenerative approaches to address these injuries, it remains a challenge to fully characterize local mechanical and cellular heterogeneities within a single biomaterial using traditional techniques. Herein we describe a variety of collagen biomaterials which incorporate local changes and patterns in composition to create multi-compartment and composite scaffolds for the purpose of orthopedic regeneration. We demonstrate that these biomaterials exhibit enhanced, locally tunable mechanical properties, and are capable of providing mesenchymal stem cells (MSCs) signals in a spatially selective manner. We highlight tradeoffs and synergies in local cellular and mechanical behavior, which give rise to the mechanisms behind observed differences in bulk cellular and biomaterial behavior. This work provides key insights into design elements under consideration for mechanically competent, multi-tissue biomaterial platforms which drive MSCs towards spatially distinct lineages for orthopedic regeneration.
- Graduation Semester
- 2016-08
- Type of Resource
- text
- Permalink
- http://hdl.handle.net/2142/100414
- Copyright and License Information
- Copyright 2016 Laura Mozdzen
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Graduate Dissertations and Theses at Illinois PRIMARY
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