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Functional Bone Engineering Using ex Vivo Gene Therapy and Topology-Optimized, Biodegradable Polymer Composite Scaffolds

dc.contributor.authorLin, Chia-Yingen_US
dc.contributor.authorSchek, Rachel M.en_US
dc.contributor.authorMistry, Amit S.en_US
dc.contributor.authorShi, Xinfengen_US
dc.contributor.authorMikos, Antonios G.en_US
dc.contributor.authorKrebsbach, Paul H.en_US
dc.contributor.authorHollister, Scott J.en_US
dc.date.accessioned2009-07-10T18:59:15Z
dc.date.available2009-07-10T18:59:15Z
dc.date.issued2005-09-01en_US
dc.identifier.citationLin, Chia-Ying; Schek, Rachel M.; Mistry, Amit S.; Shi, Xinfeng; Mikos, Antonios G.; Krebsbach, Paul H.; Hollister, Scott J. (2005). "Functional Bone Engineering Using ex Vivo Gene Therapy and Topology-Optimized, Biodegradable Polymer Composite Scaffolds." Tissue Engineering 11(9-10): 1589-1598 <http://hdl.handle.net/2027.42/63144>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/63144
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=16259612&dopt=citationen_US
dc.description.abstractBone tissue engineering could provide an alternative to conventional treatments for fracture nonunion, spinal fusion, joint replacement, and pathological loss of bone. However, this approach will require a biocompatible matrix to allow progenitor cell delivery and support tissue invasion. The construct must also support physiological loads as it degrades to allow the regenerated tissue to bear an increasing load. To meet these complex requirements, we have employed topology-optimized design and solid free-form fabrication to manufacture biodegradable poly(propylene fumarate)/ β-tricalcium phosphate composites. These scaffolds were seeded with primary human fibroblasts transduced with an adenovirus expressing bone morphogenetic protein-7 and implanted subcutaneously in mice. Specimens were evaluated by microcomputed tomography, compressive testing, and histological staining. New bone was localized on the scaffold surface and closely followed its designed contours. Furthermore, the total stiffness of the constructs was retained for up to 12 weeks after implantation, as scaffold degradation and tissue invasion took place.en_US
dc.format.extent330661 bytes
dc.format.extent2489 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherMary Ann Liebert, Inc., publishersen_US
dc.titleFunctional Bone Engineering Using ex Vivo Gene Therapy and Topology-Optimized, Biodegradable Polymer Composite Scaffoldsen_US
dc.typeArticleen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.identifier.pmid16259612en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/63144/1/ten.2005.11.1589.pdf
dc.identifier.doidoi:10.1089/ten.2005.11.1589en_US
dc.identifier.sourceTissue Engineeringen_US
dc.identifier.sourceTissue Engineeringen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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