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

DC Field Value Language
dc.contributor.authorPark, Wooram-
dc.contributor.authorYang, Han Na-
dc.contributor.authorLing, Daishun-
dc.contributor.authorYim, Hyeona-
dc.contributor.authorKim, Kyoung Sub-
dc.contributor.authorHyeon, Taeghwan-
dc.contributor.authorNa, Kun-
dc.contributor.authorPark, Keun-Hong-
dc.date.accessioned2020-04-27T13:44:19Z-
dc.date.available2020-04-27T13:44:19Z-
dc.date.created2018-01-10-
dc.date.issued2014-08-
dc.identifier.citationBiomaterials, Vol.35 No.25, pp.7239-7247-
dc.identifier.issn0142-9612-
dc.identifier.other11831-
dc.identifier.urihttps://hdl.handle.net/10371/166098-
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 MIAs with size of 40 nm 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. (C) 2014 Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.publisherPergamon Press Ltd.-
dc.titleMulti-modal transfection agent based on monodisperse magnetic. nanoparticles for stem cell gene delivery and tracking-
dc.typeArticle-
dc.contributor.AlternativeAuthor현택환-
dc.identifier.doi10.1016/j.biomaterials.2014.05.010-
dc.citation.journaltitleBiomaterials-
dc.identifier.wosid000338386800054-
dc.identifier.scopusid2-s2.0-84902085523-
dc.citation.endpage7247-
dc.citation.number25-
dc.citation.startpage7239-
dc.citation.volume35-
dc.identifier.sci000338386800054-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorHyeon, Taeghwan-
dc.type.docTypeArticle-
dc.description.journalClass1-
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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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Chemistry, Materials Science

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