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Hydroxyapatite implants with designed internal architecture

dc.contributor.authorChu, Tien-Min Gabrielen_US
dc.contributor.authorHalloran, John W.en_US
dc.contributor.authorHollister, Scott J.en_US
dc.contributor.authorFeinberg, Stephen E.en_US
dc.date.accessioned2006-09-11T18:06:53Z
dc.date.available2006-09-11T18:06:53Z
dc.date.issued2001-06en_US
dc.identifier.citationChu, T.-M. G.; Halloran, J. W.; Hollister, S. J.; Feinberg, S. E.; (2001). "Hydroxyapatite implants with designed internal architecture." Journal of Materials Science: Materials in Medicine 12(6): 471-478. <http://hdl.handle.net/2027.42/46713>en_US
dc.identifier.issn0957-4530en_US
dc.identifier.issn1573-4838en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46713
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15348260&dopt=citationen_US
dc.description.abstractPorous hydroxyapatite (HA) has been used as a bone graft material in the clinics for decades. Traditionally, the pores in these HAs are either obtained from the coralline exoskeletal patterns or from the embedded organic particles in the starting HA powder. Both processes offer very limited control on the pore structure. A new method for manufacturing porous HA with designed pore channels has been developed. This method is essentially a lost-mold technique with negative molds made with Stereolithography and a highly loaded curable HA suspension as the ceramic carrier. Implants with designed channels and connection patterns were first generated from a Computer-Aided-Design (CAD) software and Computer Tomography (CT) data. The negative images of the designs were used to build the molds on a stereolithography apparatus with epoxy resins. A 40 vol% HA suspension in propoxylated neopentyl glycol diacrylate (PNPGDA) and iso-bornyl acrylate (IBA) was formulated. HA suspension was cast into the epoxy molds and cured into solid at 85 °C. The molds and acrylate binders were removed by pyrolysis, followed by HA green body sintering. With this method, implants with six different channel designs were built successfully and the designed channels were reproduced in the sintered HA implants. The channels created in the sintered HA implants were between 366 μm and 968 μm in diameter with standard deviations of 50 μm or less. The porosity created by the channels were between 26% and 52%. The results show that HA implants with designed connection pattern and well controled channel size can be built with the technique developed in this study. © 2001 Kluwer Academic Publishersen_US
dc.format.extent1209955 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherChemistryen_US
dc.subject.otherBiotechnologyen_US
dc.subject.otherPolymer Sciencesen_US
dc.subject.otherCharacterization and Evaluation Materialsen_US
dc.titleHydroxyapatite implants with designed internal architectureen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelDentistryen_US
dc.subject.hlbsecondlevelBiomedical Engineeringen_US
dc.subject.hlbsecondlevelRadiologyen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid15348260en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46713/1/10856_2004_Article_353879.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1011203226053en_US
dc.identifier.sourceJournal of Materials Science: Materials in Medicineen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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