Highly open porous biodegradable microcarriers: In vitro cultivation of chondrocytes for injectable delivery

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dc.contributor.authorChung, Hyun Jungko
dc.contributor.authorKim, In Kyoungko
dc.contributor.authorKim, Taek Gyoungko
dc.contributor.authorPark, Tae Gwanko
dc.date.accessioned2009-11-23T07:04:51Z-
dc.date.available2009-11-23T07:04:51Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2008-05-
dc.identifier.citationTISSUE ENGINEERING, v.14, no.5, pp.607 - 615-
dc.identifier.issn2152-4947-
dc.identifier.urihttp://hdl.handle.net/10203/13131-
dc.description.abstractInjectable cell therapy would provide a patient-friendly procedure for treatment of degenerated or wounded tissue. Biodegradable injectable porous microspheres were fabricated to use as dual-purpose microcarriers for cell culture and injectable scaffold for tissue regeneration. Gas foaming in a water-in-oil-in-water double emulsion was performed for fabricating the well-interconnected porous microcarriers using poly(lactic-co-glycolic acid) (PLGA). The gas foaming conditions were finely tuned to control the structural and morphological characteristics. Porous microcarriers with a mean size of approximately 175 mu m and an average pore diameter of approximately 29 mu m were produced for cell cultivation and injectable delivery. To promote cell seeding, amine-functionalized porous microcarriers were prepared by blending amine-functionalized PLGA with unreacted PLGA. To assess the porous microcarriers for chondrocyte cultivation, bovine articular chondrocytes were seeded and cultured in vitro in spinner flasks for 4 weeks. Visualization and biochemical analyses of the microcarrier-cell constructs were performed to demonstrate cell proliferation and phenotypic expression. Quantification of deoxyribonucleic acid, glycosaminoglycan, and collagen content showed that much greater cell proliferation and expression of cartilage-specific phenotype were observed for cultures in the following order: amine-functionalized porous microcarriers, porous microcarriers, nonporous microcarriers, and monolayer culture.-
dc.description.sponsorshipMinistry of Commerce, Industry and Energy (10011366) and from the Ministry of Science and Technology, National Research Laboratory Program, Republic of Korea.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherMARY ANN LIEBERT INC-
dc.titleHighly open porous biodegradable microcarriers: In vitro cultivation of chondrocytes for injectable delivery-
dc.typeArticle-
dc.identifier.wosid000256239800004-
dc.identifier.scopusid2-s2.0-43649096860-
dc.type.rimsART-
dc.citation.volume14-
dc.citation.issue5-
dc.citation.beginningpage607-
dc.citation.endingpage615-
dc.citation.publicationnameTISSUE ENGINEERING-
dc.identifier.doi10.1089/tea.2007.0263-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorChung, Hyun Jung-
dc.contributor.localauthorPark, Tae Gwan-
dc.contributor.nonIdAuthorKim, In Kyoung-
dc.contributor.nonIdAuthorKim, Taek Gyoung-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCELL ATTACHMENT-
dc.subject.keywordPlusPOLYMERIC MICROSPHERES-
dc.subject.keywordPlusROTATING BIOREACTOR-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordPlusCULTURE-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusEXPANSION-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusACID)-
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