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Engineering new bone tissue in vitro on highly porous poly(Α-hydroxyl acids)/hydroxyapatite composite scaffolds

dc.contributor.authorMa, Peter X.en_US
dc.contributor.authorZhang, Ruiyunen_US
dc.contributor.authorXiao, Guozhien_US
dc.contributor.authorFranceschi, Renny T.en_US
dc.date.accessioned2006-04-19T13:33:28Z
dc.date.available2006-04-19T13:33:28Z
dc.date.issued2001-02en_US
dc.identifier.citationMa, Peter X.; Zhang, Ruiyun; Xiao, Guozhi; Franceschi, Renny (2001)."Engineering new bone tissue in vitro on highly porous poly(Α-hydroxyl acids)/hydroxyapatite composite scaffolds." Journal of Biomedical Materials Research 54(2): 284-293. <http://hdl.handle.net/2027.42/34419>en_US
dc.identifier.issn0021-9304en_US
dc.identifier.issn1097-4636en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34419
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11093189&dopt=citationen_US
dc.description.abstractEngineering new bone tissue with cells and a synthetic extracellular matrix (scaffolding) represents a new approach for the regeneration of mineralized tissues compared with the transplantation of bone (autografts or allografts). In the present work, highly porous poly( L -lactic acid) (PLLA) and PLLA/hydroxyapatite (HAP) composite scaffolds were prepared with a thermally induced phase separation technique. The scaffolds were seeded with osteoblastic cells and cultured in vitro . In the pure PLLA scaffolds, the osteoblasts attached primarily on the outer surface of the polymer. In contrast, the osteoblasts penetrated deep into the PLLA/HAP scaffolds and were uniformly distributed. The osteoblast survival percentage in the PLLA/HAP scaffolds was superior to that in the PLLA scaffolds. The osteoblasts proliferated in both types of the scaffolds, but the cell number was always higher in the PLLA/HAP composite scaffolds during 6 weeks of in vitro cultivation. Bone-specific markers (mRNAs encoding bone sialoprotein and osteocalcin) were expressed more abundantly in the PLLA/HAP composite scaffolds than in the PLLA scaffolds. The new tissue increased continuously in the PLLA/HAP composite scaffolds, whereas new tissue formed only near the surface of pure PLLA scaffolds. These results demonstrate that HAP imparts osteoconductivity and the highly porous PLLA/HAP composite scaffolds are superior to pure PLLA scaffolds for bone tissue engineering. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res 54: 284–293, 2001en_US
dc.format.extent1695230 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherChemistryen_US
dc.subject.otherPolymer and Materials Scienceen_US
dc.titleEngineering new bone tissue in vitro on highly porous poly(Α-hydroxyl acids)/hydroxyapatite composite scaffoldsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelBiomedical Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biologic and Materials Sciences, 1011 North University Ave., Room 2211, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan 48109 ; Macromolecular Science and Engineering Center, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Biologic and Materials Sciences, 1011 North University Ave., Room 2211, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Biologic and Materials Sciences, 1011 North University Ave., Room 2211, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Periodontics/Prevention/Geriatrics, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Periodontics/Prevention/Geriatrics, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.identifier.pmid11093189en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34419/1/16_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/1097-4636(200102)54:2<284::AID-JBM16>3.0.CO;2-Wen_US
dc.identifier.sourceJournal of Biomedical Materials Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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