Intracellular translocation of superparamagnetic iron oxide nanoparticles encapsulated with peptide-conjugated poly(D,L lactide-co-glycolide)

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dc.contributor.authorLee, SJko
dc.contributor.authorJeong, JRko
dc.contributor.authorShin, Sung-Chulko
dc.contributor.authorHuh, YMko
dc.contributor.authorSong, HTko
dc.contributor.authorSuh, JSko
dc.contributor.authorChang, YHko
dc.contributor.authorJeon, BSko
dc.contributor.authorKim, Jong-Dukko
dc.date.accessioned2011-08-10T04:45:56Z-
dc.date.available2011-08-10T04:45:56Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2005-05-
dc.identifier.citationJOURNAL OF APPLIED PHYSICS, v.97, pp.1052 - 1057-
dc.identifier.issn0021-8979-
dc.identifier.urihttp://hdl.handle.net/10203/24822-
dc.description.abstractIn this study, we propose the use of iron oxide nanoparticle encapsulated with peptide-conjugated poly(D,L lactide-co-glycolide) (PLGA) as a potent intracellular carrier for diagnosis agent. The iron oxide (gamma-Fe2O3) nanoparticles were prepared by a chemical coprecipitation method of ferric and ferrous ions in an alkali solution. Arg peptide (RRRRRRRRCK-FITC) were conjugated to the PLGA via a simple coupling reaction between maleimide-derivatized PLGA and thiol-terminated Arg peptide. The gamma-Fe2O3-PLGA-Arg-FITC nanoparticle was then prepared by an emulsification-diffusion technique. A confocal laser scanning microscopy revealed that the gamma-Fe2O3-PLGA-Arg-FITC nanoparticle was effectively adsorbed onto the membrane of stem cells and delivered into the nuclei without cytotoxicity. Magnetic properties of the gamma-Fe2O3-PLGA-Arg-FITC nanoparticle were observed by measuring the zero-field-cooled/field-cooled magnetization and magnetic hysteresis loop using a superconducting quantum interference device magnetometer from 5 K to 300 K. (c) 2005 American Institute of Physics.-
dc.description.sponsorshipThis research was partially supported by Center for Ultramicrochemical Process Systems project and by Ministry of Science & Technology project through the Creative Research Initiatives Project.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherAMER INST PHYSICS-
dc.subjectMAGNETIC-PROPERTIES-
dc.subjectDRUG-DELIVERY-
dc.subjectNANOCLUSTERS-
dc.titleIntracellular translocation of superparamagnetic iron oxide nanoparticles encapsulated with peptide-conjugated poly(D,L lactide-co-glycolide)-
dc.typeArticle-
dc.identifier.wosid000230168500309-
dc.identifier.scopusid2-s2.0-20944443465-
dc.type.rimsART-
dc.citation.volume97-
dc.citation.beginningpage1052-
dc.citation.endingpage1057-
dc.citation.publicationnameJOURNAL OF APPLIED PHYSICS-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorShin, Sung-Chul-
dc.contributor.localauthorChang, YH-
dc.contributor.localauthorKim, Jong-Duk-
dc.contributor.nonIdAuthorLee, SJ-
dc.contributor.nonIdAuthorJeong, JR-
dc.contributor.nonIdAuthorHuh, YM-
dc.contributor.nonIdAuthorSong, HT-
dc.contributor.nonIdAuthorSuh, JS-
dc.contributor.nonIdAuthorJeon, BS-
dc.type.journalArticleArticle; Proceedings Paper-
dc.subject.keywordPlusMAGNETIC-PROPERTIES-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusNANOCLUSTERS-
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