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dc.contributor.authorLee, JE-
dc.contributor.authorKim, SE-
dc.contributor.authorKwon, IC-
dc.contributor.authorAhn, HJ-
dc.contributor.authorCho, H-
dc.contributor.authorLee, SH-
dc.contributor.authorKim, HJ-
dc.contributor.authorSeong, SC-
dc.contributor.authorLee, MC-
dc.date.accessioned2024-01-21T06:34:22Z-
dc.date.available2024-01-21T06:34:22Z-
dc.date.created2021-09-04-
dc.date.issued2004-09-
dc.identifier.issn0160-564X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/137290-
dc.description.abstractThe objectives of this study were (1) to develop a three-dimensional chitosan scaffold in combination with transforming growth factor-beta1 (TGF-beta1)-loaded chitosan microspheres and (2) to evaluate the effect of the TGF-beta1 release on the chondrogenic potential of rabbit chondrocytes in the scaffolds. TGF-beta1 was loaded into chitosan microspheres using an emulsion-crosslinking method, resulting in spherical shapes with a size ranging from 0.3 to 1.5 mum. Controlled release of TGF-beta1, as measured by enzyme-linked immunosorbent assay (ELISA), was observed with chitosan microspheres over 7 days. Chitosan solutions (2% and 3%) were fabricated into two types of scaffolds with different pore morphologies and mechanical properties using a freeze-drying technique, with the result that scaffold with higher concentrations showed smaller pores and lower porosity, leading to a much stronger scaffold. The TGF-beta1 microspheres were incorporated into the scaffolds at a concentration of 10 ng TGF-beta1/scaffold and then chondrocytes seeded into each scaffold and incubated in vitro for 2 weeks. The 2% chitosan scaffolds showed higher cell attachment levels than the 3% chitosan scaffolds (P < 0.01), regardless of the TGF-beta1 microspheres. Both the proliferation rate and glycosaminoglycan (GAG) production were significantly higher for scaffolds incorporating TGF-beta1 microspheres than for the control scaffolds without microspheres 10 days after incubation. Extracellular matrix staining by Safranin O and immunohistochemistry for type II collagen both significantly increased in scaffolds containing TGF-beta1 microspheres. These results suggest that the TGF-beta1 microsphere incorporated in scaffolds have the potential to enhance cartilage formation.-
dc.languageEnglish-
dc.publisherWILEY-
dc.subjectGROWTH-FACTOR BETA-1-
dc.subjectARTICULAR-CARTILAGE-
dc.subjectCONTROLLED-RELEASE-
dc.subjectGENE DELIVERY-
dc.subjectMATRIX-
dc.subjectOSTEOBLASTS-
dc.subjectHYDROGEL-
dc.titleEffects of a chitosan scaffold containing TGF-beta 1 encapsulated chitosan microspheres on in vitro chondrocyte culture-
dc.typeArticle-
dc.identifier.doi10.1111/j.1525-1594.2004.00020.x-
dc.description.journalClass1-
dc.identifier.bibliographicCitationARTIFICIAL ORGANS, v.28, no.9, pp.829 - 839-
dc.citation.titleARTIFICIAL ORGANS-
dc.citation.volume28-
dc.citation.number9-
dc.citation.startPage829-
dc.citation.endPage839-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000223367600007-
dc.identifier.scopusid2-s2.0-4344685878-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryTransplantation-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaTransplantation-
dc.type.docTypeArticle; Proceedings Paper-
dc.subject.keywordPlusGROWTH-FACTOR BETA-1-
dc.subject.keywordPlusARTICULAR-CARTILAGE-
dc.subject.keywordPlusCONTROLLED-RELEASE-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusMATRIX-
dc.subject.keywordPlusOSTEOBLASTS-
dc.subject.keywordPlusHYDROGEL-
dc.subject.keywordAuthorchitosan-
dc.subject.keywordAuthorscaffold-
dc.subject.keywordAuthorchondrocyte-
dc.subject.keywordAuthortissue engineering-
dc.subject.keywordAuthorcartilage-
dc.subject.keywordAuthormicrosphere-
dc.subject.keywordAuthorgrowth factor-
dc.subject.keywordAuthorcontrolled release-
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KIST Article > 2004
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