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Open pore biodegradable matrices formed with gas foaming

dc.contributor.authorHarris, Leatrese D.en_US
dc.contributor.authorKim, Byung-Sooen_US
dc.contributor.authorMooney, David J.en_US
dc.date.accessioned2006-04-28T16:36:18Z
dc.date.available2006-04-28T16:36:18Z
dc.date.issued1998-12-05en_US
dc.identifier.citationHarris, Leatrese D.; Kim, Byung-Soo; Mooney, David J. (1998)."Open pore biodegradable matrices formed with gas foaming." Journal of Biomedical Materials Research 42(3): 396-402. <http://hdl.handle.net/2027.42/38022>en_US
dc.identifier.issn0021-9304en_US
dc.identifier.issn1097-4636en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38022
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9788501&dopt=citationen_US
dc.description.abstractEngineering tissues utilizing biodegradable polymer matrices is a promising approach to the treatment of a number of diseases. However, processing techniques utilized to fabricate these matrices typically involve organic solvents and/or high temperatures. Here we describe a process for fabricating matrices without the use of organic solvents and/or elevated temperatures. Disks comprised of polymer [e.g., poly (D,L-lactic- co -glycolic acid)] and NaCl particles were compression molded at room temperature and subsequently allowed to equilibrate with high pressure CO 2 gas (800 psi). Creation of a thermodynamic instability led to the nucleation and growth of gas pores in the polymer particles, resulting in the expansion of the polymer particles. The polymer particles fused to form a continuous matrix with entrapped salt particles. The NaCl particles subsequently were leached to yield macropores within the polymer matrix. The overall porosity and level of pore connectivity were regulated by the ratio of polymer/salt particles and the size of salt particles. Both the compressive modulus (159 ± 130 kPa versus 289 ± 25 kPa) and the tensile modulus (334 ± 52 kPa versus 1100 ± 236 kPa) of the matrices formed with this approach were significantly greater than those formed with a standard solvent casting/particulate leaching process. The utility of these matrices was demonstrated by engineering smooth muscle tissue in vitro with them. This novel process, a combination of high pressure gas foaming and particulate leaching techniques, allows one to fabricate matrices with a well controlled porosity and pore structure. This process avoids the potential negatives associated with the use of high temperatures and/or organic solvents in biomaterials processing. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 42, 396–402, 1998.en_US
dc.format.extent560842 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.titleOpen pore biodegradable matrices formed with gas foamingen_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 Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109-2136en_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109-2136en_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109-2136 ; Department of Biologic and Materials Sciences, University of Michigan, Ann Arbor, Michigan 48109-2136 ; Department of Biologic and Materials Sciences, University of Michigan, Ann Arbor, Michigan 48109-2136en_US
dc.identifier.pmid9788501en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38022/1/7_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1097-4636(19981205)42:3<396::AID-JBM7>3.0.CO;2-Een_US
dc.identifier.sourceJournal of Biomedical Materials Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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