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dc.contributor.authorLee, Jangwook-
dc.contributor.authorJeong, Eun Ju-
dc.contributor.authorLee, Yeon Kyung-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorLee, Kuen Yong-
dc.date.accessioned2024-01-20T04:34:04Z-
dc.date.available2024-01-20T04:34:04Z-
dc.date.created2021-09-04-
dc.date.issued2016-03-02-
dc.identifier.issn1613-6810-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124300-
dc.description.abstractRecently, targeted delivery systems based on functionalized polymeric nanoparticles have attracted a great deal of attention in cancer diagnosis and therapy. Specifically, as neuroblastoma occurs in infancy and childhood, targeted delivery may be critical to reduce the side effects that can occur with conventional approaches, as well as to achieve precise diagnosis and efficient therapy. Thus, biocompatible poly(D,L-lactide-co-glycolide) (PLG) nanoparticles containing an imaging probe and therapeutic gene are prepared, followed by modification with rabies virus glycoprotein (RVG) peptide for neuroblastoma-targeting delivery. RVG peptide is a well-known neuronal targeting ligand and is chemically conjugated to PLG nanoparticles without changing their size or shape. RVG-modified nanoparticles are effective in specifically targeting neuroblastoma both in vitro and in vivo. RVG-modified nanoparticles loaded with a fluorescent probe are useful to detect the tumor site in a neuroblastoma-bearing mouse model, and those encapsulating a therapeutic gene cocktail (siMyc, siBcl-2, and siVEGF) significantly suppressed tumor growth in the mouse model. This approach to designing and tailoring of polymeric nanoparticles for targeted delivery may be useful in the development of multimodality systems for theranostic approaches.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectNICOTINIC ACETYLCHOLINE-RECEPTORS-
dc.subjectDRUG-DELIVERY-
dc.subjectMULTIFUNCTIONAL NANOPARTICLES-
dc.subjectPLGA NANOPARTICLES-
dc.subjectCANCER-THERAPY-
dc.subjectCELLS-
dc.subjectGLYCOPROTEIN-
dc.subjectPEPTIDE-
dc.subjectNANOTECHNOLOGY-
dc.subjectPROLIFERATION-
dc.titleOptical Imaging and Gene Therapy with Neuroblastoma-Targeting Polymeric Nanoparticles for Potential Theranostic Applications-
dc.typeArticle-
dc.identifier.doi10.1002/smll.201501913-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSMALL, v.12, no.9, pp.1201 - 1211-
dc.citation.titleSMALL-
dc.citation.volume12-
dc.citation.number9-
dc.citation.startPage1201-
dc.citation.endPage1211-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000372008600012-
dc.identifier.scopusid2-s2.0-84960115074-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusNICOTINIC ACETYLCHOLINE-RECEPTORS-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusMULTIFUNCTIONAL NANOPARTICLES-
dc.subject.keywordPlusPLGA NANOPARTICLES-
dc.subject.keywordPlusCANCER-THERAPY-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusGLYCOPROTEIN-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusNANOTECHNOLOGY-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordAuthorneuroblastoma-
dc.subject.keywordAuthorrabies virus glycoprotein peptides-
dc.subject.keywordAuthortargeted delivery-
dc.subject.keywordAuthortheranostics-
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