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A multifunctional core-shell nanoparticle for dendritic cell-based cancer immunotherapy

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dc.contributor.authorCho, Nam-Hyuk-
dc.contributor.authorCheong, Taek-Chin-
dc.contributor.authorMin, Ji Hyun-
dc.contributor.authorWu, Jun Hua-
dc.contributor.authorLee, Sang Jin-
dc.contributor.authorKim, Daehong-
dc.contributor.authorYang, Jae-Seong-
dc.contributor.authorKim, Sanguk-
dc.contributor.authorKim, Young Keun-
dc.contributor.authorSeong, Seung-Yong-
dc.date.accessioned2021-09-07T07:44:00Z-
dc.date.available2021-09-07T07:44:00Z-
dc.date.created2021-06-19-
dc.date.issued2011-10-
dc.identifier.issn1748-3387-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/111436-
dc.description.abstractDendritic cell-based cancer immunotherapy requires tumour antigens to be delivered efficiently into dendritic cells and their migration to be monitored in vivo. Nanoparticles have been explored as carriers for antigen delivery, but applications have been limited by the toxicity of the solvents used to make nanoparticles, and by the need to use transfection agents to deliver nanoparticles into cells. Here we show that an iron oxide-zinc oxide core-shell nanoparticle can deliver carcinoembryonic antigen into dendritic cells while simultaneously acting as an imaging agent. The nanoparticle-antigen complex is efficiently taken up by dendritic cells within one hour and can be detected in vitro by confocal microscopy and in vivo by magnetic resonance imaging. Mice immunized with dendritic cells containing the nanoparticle-antigen complex showed enhanced tumour antigen specific T-cell responses, delayed tumour growth and better survival than controls.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherNATURE PUBLISHING GROUP-
dc.subjectIRON-OXIDE NANOPARTICLES-
dc.subjectIN-VIVO TRACKING-
dc.subjectCARCINOEMBRYONIC ANTIGEN-
dc.subjectMELANOMA PATIENTS-
dc.subjectLYMPH-NODES-
dc.subjectZINC-OXIDE-
dc.subjectMIGRATION-
dc.subjectIMMUNITY-
dc.subjectDISPLAY-
dc.titleA multifunctional core-shell nanoparticle for dendritic cell-based cancer immunotherapy-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Young Keun-
dc.identifier.doi10.1038/NNANO.2011.149-
dc.identifier.scopusid2-s2.0-80455164555-
dc.identifier.wosid000295923800017-
dc.identifier.bibliographicCitationNATURE NANOTECHNOLOGY, v.6, no.10, pp.675 - 682-
dc.relation.isPartOfNATURE NANOTECHNOLOGY-
dc.citation.titleNATURE NANOTECHNOLOGY-
dc.citation.volume6-
dc.citation.number10-
dc.citation.startPage675-
dc.citation.endPage682-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusIRON-OXIDE NANOPARTICLES-
dc.subject.keywordPlusIN-VIVO TRACKING-
dc.subject.keywordPlusCARCINOEMBRYONIC ANTIGEN-
dc.subject.keywordPlusMELANOMA PATIENTS-
dc.subject.keywordPlusLYMPH-NODES-
dc.subject.keywordPlusZINC-OXIDE-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusIMMUNITY-
dc.subject.keywordPlusDISPLAY-
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