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Cited 39 time in webofscience Cited 44 time in scopus
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dc.contributor.authorJo, H-
dc.contributor.authorYoun, H-
dc.contributor.authorLee, S-
dc.contributor.authorBan, C-
dc.date.accessioned2015-06-25T02:27:15Z-
dc.date.available2015-06-25T02:27:15Z-
dc.date.created2015-02-04-
dc.date.issued2014-08-14-
dc.identifier.issn2050-750X-
dc.identifier.other2015-OAK-0000031444en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/10989-
dc.description.abstractAlthough various studies related to nanoparticles-based photothermal therapy have been actively performed, an epoch-making photothermolysis therapy exhibiting both high selectivity and efficiency has yet not been discovered. For the first time, we have developed novel valuable therapeutic complexes, namely, dual aptamer-modified gold nanostars, for the targeting of prostate cancers, including PSMA(+) and PSMA(-) cells. The synthesized probes were characterized through several techniques, including UV-VIS spectral analysis, DLS analysis, zeta potential measurements, and TEM imaging, and were subsequently subjected to cytotoxicity tests, cell uptake confirmation, and in vitro photothermat therapy. The homogeneously well-fabricated nanostars presented high selectivity to prostate cancer cells and extremely high efficiency for therapy using an 808 nm laser under an irradiance of 0.3 W cm(-2), which is lower than the permitted value for skin exposure (0.329 W cm(-2)). It is anticipated that this novel photothermal agent will become the general platform for targeted therapy.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.relation.isPartOfJOURNAL OF MATERIALS CHEMISTRY B-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleUltra-effective photothermal therapy for prostate cancer cells using dual aptamer-modified gold nanostars-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1039/C4TB00643G-
dc.author.googleJo, Hen_US
dc.author.googleYoun, Hen_US
dc.author.googleBan, Cen_US
dc.author.googleLee, Sen_US
dc.relation.volume2en_US
dc.relation.issue30en_US
dc.relation.startpage4862en_US
dc.relation.lastpage4867en_US
dc.contributor.id10085220en_US
dc.relation.journalJOURNAL OF MATERIALS CHEMISTRY Ben_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF MATERIALS CHEMISTRY B, v.2, no.30, pp.4862 - 4867-
dc.identifier.wosid000339469000010-
dc.date.tcdate2019-01-01-
dc.citation.endPage4867-
dc.citation.number30-
dc.citation.startPage4862-
dc.citation.titleJOURNAL OF MATERIALS CHEMISTRY B-
dc.citation.volume2-
dc.contributor.affiliatedAuthorBan, C-
dc.identifier.scopusid2-s2.0-84904167419-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc18-
dc.description.scptc19*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusANTIBODIES-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordPlusNANOCAGES-
dc.subject.keywordPlusABLATION-
dc.subject.keywordPlusBINDING-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-

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반창일BAN, CHANGILL
Dept of Chemistry
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