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Sulforaphane-PLGA microspheres for the intra-articular treatment of osteoarthritis

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dc.contributor.authorKo, Ji-Yun-
dc.contributor.authorChoi, You-Jeong-
dc.contributor.authorJeong, Geun-Jae-
dc.contributor.authorIm, Gun-Il-
dc.date.accessioned2024-08-08T05:01:24Z-
dc.date.available2024-08-08T05:01:24Z-
dc.date.issued2013-07-
dc.identifier.issn0142-9612-
dc.identifier.issn1878-5905-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/18400-
dc.description.abstractSulforaphane (SFN) is a member of the isothiocyanate family that has anti-inflammatory action as well as anti-carcinogenic properties. The authors have devised an intra-articular injectable SFN PLGA microsphere system that can be used for treating osteoarthritis (OA). The purpose of this study was to evaluate the in vitro and in vivo efficacy of the SFN PLGA microsphere system. Articular chondrocytes were obtained from knee OA patients and were cultured in monolayers. The optimal concentration of SFN was obtained and the dose of SFN PLGA microspheres was determined based on the concentration. The in vitro anti-inflammatory effect on markers such as cyclooxygenase (COX)-2, a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)-5, and matrix metalloproteinase (MMP)-2 was assessed by real-time PCR and Western blotting. The in vivo therapeutic effect of SFN PLGA microspheres was investigated using surgically-induced rat OA model. Treatment with SFN PLGA microspheres inhibited the mRNA and protein expression of COX-2, ADAMTS-5 and MMP-2 induced by LPS in articular chondrocytes. Intraarticular SFN PLGA microspheres delayed the progression of surgically-induced osteoarthritis in rats. In conclusion, SFN PLGA microspheres can be a useful injectable delivery system for treating osteoarthritis. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCI LTD-
dc.titleSulforaphane-PLGA microspheres for the intra-articular treatment of osteoarthritis-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.biomaterials.2013.03.066-
dc.identifier.scopusid2-s2.0-84877062207-
dc.identifier.wosid000319630000045-
dc.identifier.bibliographicCitationBIOMATERIALS, v.34, no.21, pp 5359 - 5368-
dc.citation.titleBIOMATERIALS-
dc.citation.volume34-
dc.citation.number21-
dc.citation.startPage5359-
dc.citation.endPage5368-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusNATURALLY-OCCURRING ISOTHIOCYANATE-
dc.subject.keywordPlusEXPERIMENTAL ARTHRITIS-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusCARTILAGE-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusRABBITS-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusINJECTION-
dc.subject.keywordAuthorSulforaphane-
dc.subject.keywordAuthorPLGA microspheres-
dc.subject.keywordAuthorIntra-articular injection-
dc.subject.keywordAuthorOsteoarthritis-
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