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Multi-modal transfection agent based on monodisperse magnetic nanoparticles for stem cell gene delivery and tracking

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dc.contributor.authorPark W.-
dc.contributor.authorYang H.N.-
dc.contributor.authorDaishun Ling-
dc.contributor.authorYim H.-
dc.contributor.authorKim K.S.-
dc.contributor.authorTaeg Hwan Hyeon-
dc.contributor.authorNa K.-
dc.contributor.authorPark K.-H.-
dc.date.available2015-04-20T05:33:28Z-
dc.date.created2014-09-12-
dc.date.issued2014-08-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/929-
dc.description.abstractDirecting the controlled differentiation and tracking of stem cells is essential to achieve successful stem cell therapy. In this work, we describe a multi-modal (MR/optical) transfection agent (MTA) for efficient gene delivery and cell tracking of human mesenchymal stem cells (hMSCs). The MTA was synthesized through a facile two-step approach with 1) ligand exchange of a catechol-functionalized polypeptide (CFP) and 2) chemical immobilization of fluorescence labelled cationic polymer via aminolysis reaction. Cationic polymer-immobilized MTAs with size of ~40nm exhibit greatly enhanced colloidal stability in aqueous solution. In addition, the MTAs were capable of binding DNA molecules for transfection. The MTA/pDNA complex showed relatively good transfection efficiency in hMSCs (compared to the commercial transfection agent, Lipofectamine) and good biocompatibility. MTA-treated hMSCs were successfully visualized after transplantation via MR and optical imaging system over 14 days. These studies highlight the challenges associated with the potential advantages of designing multi-modal nanostructured materials as tools for genetic materials delivery and cell-tracking in stem cell therapy. © 2014 Elsevier Ltd.-
dc.description.uri1-
dc.language영어-
dc.publisherELSEVIER SCI LTD-
dc.subjectMultimodal imaging Magnetic resonance imaging Cell tracking Stem cells Catechol-
dc.titleMulti-modal transfection agent based on monodisperse magnetic nanoparticles for stem cell gene delivery and tracking-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000338386800054-
dc.identifier.scopusid2-s2.0-84902085523-
dc.identifier.rimsid53776ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorDaishun Ling-
dc.contributor.affiliatedAuthorTaeg Hwan Hyeon-
dc.identifier.doi10.1016/j.biomaterials.2014.05.010-
dc.identifier.bibliographicCitationBIOMATERIALS, v.35, no.25, pp.7239 - 7247-
dc.citation.titleBIOMATERIALS-
dc.citation.volume35-
dc.citation.number25-
dc.citation.startPage7239-
dc.citation.endPage7247-
dc.date.scptcdate2018-10-01-
dc.description.wostc27-
dc.description.scptc28-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusIRON-OXIDE NANOPARTICLES-
dc.subject.keywordPlusINORGANIC NANOPARTICLES-
dc.subject.keywordPlusBIOMEDICAL APPLICATIONS-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusPHOTOSENSITIZER-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusINTERNALIZATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPLATFORM-
dc.subject.keywordAuthorMultimodal imaging-
dc.subject.keywordAuthorMagnetic resonance imaging-
dc.subject.keywordAuthorCell tracking-
dc.subject.keywordAuthorStem cells-
dc.subject.keywordAuthorCatechol-
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Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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