Temple University. Libraries
SPECTROSCOPIC ASSESSMENT OF TISSUE ENGINEERED CARTILAGE: A PATHWAY FOR BENCH TO BEDSIDE EVALUATION OF CARTILAGE DEVELOPMENT AND REPAIR
Abstract
dc:description.abstractCartilage tissue engineering is a promising approach for the repair of chondral defects. Engineering of cartilage combines a three-dimensional scaffold with chondrogenic cells and appropriate external stimuli, and ideally results in constructs with properties that resemble, as closely as possible, native cartilage. Once implanted to repair a cartilage defect, the integration of tissue engineered cartilage (TEC) to surrounding native tissue is critical for a successful clinical outcome. However, this depends in part on the initial maturity of the engineered construct, which is challenging to assess a priori. Another challenge relates to the assessment of the longitudinal repair of cartilage defects after tissue engineering approaches are applied. Currently, evaluation is qualitative, based on visual and tactile observations using arthroscopic hook probes which can be a very subjective approach. Furthermore, gold standard techniques (histological, mechanical and biochemical evaluation) to determine compositional and mechanical properties of constructs in vitro and ex vivo are generally destructive.In this thesis, we are proposing the use of a spectroscopic fiber optic probe approach that spans the visible-near infrared (Vis-NIR) regions. This would be a novel, non-destructive technique based on high frequency nonionizing radiation that causes vibrations in the NIR region (750-2500 nm or 12000 to 4000 cm-1), and electronic transitions in the VIS region (400-750 nm) that result in a unique spectrum of the sampled tissues. Previously, we have shown that NIR spectral data collected in a non-destructive manner correlate to compositional and biomechanical properties of tissue engineered cartilage. Additionally, using an arthroscopic fiber optic probe, Vis-NIR spectra can be collected from repairing cartilage tissue in situ. The overarching hypothesis of this thesis is that Vis-NIR fiber optic spectroscopy can be utilized to assess engineered cartilage development in vitro, and in vivo to assess repair in a pre-clinical model of chondral defect. This hypothesis was tested in the following three aims: 1. Assessment of the mid and NIR spectral features of scaffold and extracellular matrix components of cartilage and TECs for in vitro monitoring of TEC development by fiber optic NIR spectroscopy; 2. Assessment of the Vis-NIR spectral features of tissues present in the mini-pig stifle joint during the chondral repair process to facilitate interpretation of in vivo repair; 3. Model-informed design and analysis of an arthroscopic probe for spectral collection during the cartilage repair process in preclinical models and clinical scenarios. Together these studies contribute to an overall approach for spectroscopic assessment of tissue engineered cartilage as a pathway for bench to bedside evaluation of cartilage development and repair.
Degree
thesis:*- Grantor dc:publisher
- Temple University. Libraries
- Year dc:date.issued
- 2021
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Kandel, Shital
- Advisor dc:contributor.advisor
-
- Pleshko, Nancy
- Committee members dc:contributor.committeemember
-
- Patil, Chetan Appasaheb
- Orrego, Santiago
- Mauck, Robert L.
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- IN COPYRIGHT- This Rights Statement can be used for an Item that is in copyright. Using this statement implies that the organization making this Item available has determined that the Item is in copyright and either is the rights-holder, has obtained permission from the rights-holder(s) to make their Work(s) available, or makes the Item available under an exception or limitation to copyright (including Fair Use) that entitles it to make the Item available.
- Licence dc:rights.uri
- Language dc:language.iso
- eng
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/20.500.12613/7653
- OAI identifier oai:identifier
- oai:scholarshare.temple.edu:20.500.12613/7653