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dc.contributor.authorHeo, Roun-
dc.contributor.authorYou, Dong Gil-
dc.contributor.authorUm, Wooram-
dc.contributor.authorChoi, Ki Young-
dc.contributor.authorJeon, Sangmin-
dc.contributor.authorPark, Jong-Sung-
dc.contributor.authorChoi, Yuri-
dc.contributor.authorKwon, Seunglee-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorJo, Dong-Gyu-
dc.contributor.authorKang, Young Mo-
dc.contributor.authorPark, Jae Hyung-
dc.date.accessioned2024-01-20T01:03:34Z-
dc.date.available2024-01-20T01:03:34Z-
dc.date.created2021-09-05-
dc.date.issued2017-07-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/122574-
dc.description.abstractWith the aim of developing nanoparticles for targeted delivery of methotrexate (MTX) to inflamed joints in rheumatoid arthritis (RA), an amphiphilic polysaccharide was synthesized by conjugating 5 beta-cholanic acid to a dextran sulfate (DS) backbone. Due to its amphiphilic nature, the DS derivative self-assembled into spherical nanoparticles (220 nm in diameter) in aqueous conditions. The MTX was effectively loaded into the DS nanoparticles (loading efficiency: 73.0%) by a simple dialysis method. Interestingly, the DS nanoparticles were selectively taken up by activated macrophages, which are responsible for inflammation and joint destruction, via scavenger receptor class A-mediated endocytosis. When systemically administrated into mice with experimental collagen-induced arthritis (CIA), the DS nanoparticles effectively accumulated in inflamed joints (12-fold more than wild type mice (WT)), implying their high targetability to RA tissues. Moreover, the MTX-loaded DS nanoparticles exhibited significantly improved therapeutic efficacy against CIA in mice compared to free MTX alone. Overall, the data presented here indicate that DS nanoparticles are potentially useful nanomedicines for RA imaging and therapy. (C) 2017 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.subjectHYALURONIC-ACID NANOPARTICLES-
dc.subjectMACROPHAGE SCAVENGER RECEPTOR-
dc.subjectCOLLAGEN-INDUCED ARTHRITIS-
dc.subjectIN-VIVO-
dc.subjectVITRO-
dc.subjectATHEROSCLEROSIS-
dc.subjectDOXORUBICIN-
dc.subjectCYTOKINES-
dc.subjectDELIVERY-
dc.subjectTHERAPY-
dc.titleDextran sulfate nanoparticles as a theranostic nanomedicine for rheumatoid arthritis-
dc.typeArticle-
dc.identifier.doi10.1016/j.biomaterials.2017.03.044-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOMATERIALS, v.131, pp.15 - 26-
dc.citation.titleBIOMATERIALS-
dc.citation.volume131-
dc.citation.startPage15-
dc.citation.endPage26-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000401393600002-
dc.identifier.scopusid2-s2.0-85016478906-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusHYALURONIC-ACID NANOPARTICLES-
dc.subject.keywordPlusMACROPHAGE SCAVENGER RECEPTOR-
dc.subject.keywordPlusCOLLAGEN-INDUCED ARTHRITIS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusVITRO-
dc.subject.keywordPlusATHEROSCLEROSIS-
dc.subject.keywordPlusDOXORUBICIN-
dc.subject.keywordPlusCYTOKINES-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordAuthorDextran sulfate-
dc.subject.keywordAuthorNanoparticles-
dc.subject.keywordAuthorDrug delivery-
dc.subject.keywordAuthorMacrophage-
dc.subject.keywordAuthorRheumatoid arthritis-
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