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Effective delivery of immunosuppressive drug molecules by silica coated iron oxide nanoparticles

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dc.contributor.authorHwang, Jang Sun-
dc.contributor.authorLee, Eunwon-
dc.contributor.authorKim, Jieun-
dc.contributor.authorSeo, Youngmin-
dc.contributor.authorLee, Kwan Hong-
dc.contributor.authorHong, Jong Wook-
dc.contributor.authorGilad, Assaf A.-
dc.contributor.authorPark, Hansoo-
dc.contributor.authorChoi, Jonghoon-
dc.date.available2019-03-08T12:56:51Z-
dc.date.issued2016-06-
dc.identifier.issn0927-7765-
dc.identifier.issn1873-4367-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/6842-
dc.description.abstractIron oxide nanoparticles have been used in a wide range of biomedical applications, including drug delivery, molecular imaging, and cellular imaging. Various surface modifications have been applied to the particles to stabilize their surface and to give them a moiety for anchoring tags and/or drug molecules. Conventional methods of delivering immunosuppressant drugs often require a high dose of drugs to ensure therapeutic effects, but this can lead to toxic side effects. In this study, we used silica-coated iron oxide nanoparticles (IOSs) for a drug delivery application in which the nanoparticles carry the minimum amount of drug required to be effective to the target cells. IOSs could be loaded with water-insoluble immunosuppressive drug molecules (MPA: mycophenolic acid) and be used as a contrast agent for MRI. We characterized the IOSs for their physicochemical properties and found their average hydrodynamic diameter and core size to be 40.5 nm and 5 nm, respectively. Following the introduction of MPA-loaded IOSs (IOS/M), we evaluated the secretion dynamics of cytokines from peripheral blood mononuclear cells stimulated with phytohemagglutinin (PHA). The results showed that IOS/M effectively inhibited the secretion of the cytokines interleukin-2 and tumor necrosis factor a, with a minimal concentration of MPA. In conclusion, IOW may have potential applications in both efficient drug delivery and MRI. (C) 2016 Elsevier B.V. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titleEffective delivery of immunosuppressive drug molecules by silica coated iron oxide nanoparticles-
dc.typeArticle-
dc.identifier.doi10.1016/j.colsurfb.2016.01.040-
dc.identifier.bibliographicCitationCOLLOIDS AND SURFACES B-BIOINTERFACES, v.142, pp 290 - 296-
dc.description.isOpenAccessN-
dc.identifier.wosid000375169600035-
dc.identifier.scopusid2-s2.0-84960123324-
dc.citation.endPage296-
dc.citation.startPage290-
dc.citation.titleCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.citation.volume142-
dc.type.docTypeArticle-
dc.publisher.location네델란드-
dc.subject.keywordAuthorIron oxide nanoparticles-
dc.subject.keywordAuthorMycophenolic acid-
dc.subject.keywordAuthorImmunosuppressive drug-
dc.subject.keywordAuthorMagnetic resonance imaging-
dc.subject.keywordAuthorDrug delivery-
dc.subject.keywordPlusMYCOPHENOLIC-ACID-
dc.subject.keywordPlusBIOMEDICAL APPLICATIONS-
dc.subject.keywordPlusMAGNETIC NANOPARTICLES-
dc.subject.keywordPlusDENDRITIC CELLS-
dc.subject.keywordPlusCONTRAST AGENTS-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusIL-2-
dc.subject.keywordPlusCYCLOSPORINE-
dc.subject.keywordPlusSURFACE-
dc.subject.keywordPlusSYSTEM-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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