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dc.contributor.authorNam, Taehwan-
dc.contributor.authorPark, Sangjin-
dc.contributor.authorLee, Seung-Young-
dc.contributor.authorPark, Kyeongsoon-
dc.contributor.authorChoi, Kuiwon-
dc.contributor.authorSong, In Chan-
dc.contributor.authorHan, Moon Hee-
dc.contributor.authorLeary, James J.-
dc.contributor.authorYuk, Simseok Andrew-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorJeong, Seo Young-
dc.date.accessioned2024-01-20T19:33:31Z-
dc.date.available2024-01-20T19:33:31Z-
dc.date.created2021-09-02-
dc.date.issued2010-04-
dc.identifier.issn1043-1802-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/131611-
dc.description.abstractWe report tumor targeting nanoparticles for optical/MR dual imaging based on self-assembled glycol chitosan to be a potential multimodal imaging probe. To develop an optical/MR dual imaging probe, biocompatible and water-soluble glycol chitosan (M-w = 50 kDa) were chemically modified with 5 beta-cholanic acid (CA), resulting in amphiphilic glycol chitosan-5 beta-cholanic acid conjugates (GC-CA). For optical imaging near-infrared fluorescence (NIRF) dye, Cy5.5, was conjugated to GC-CA resulting in Cy5-labeled GC-CA conjugates (Cy5.5-GC-CA). Moreover, in order to dictate gadolinium (Gd(III)) in the Cy5.5-GC-CA conjugates, 1,4,7,10-tetraazacyclododecane1,4,7,10-tetraacetic acid (DOTA) was directly conjugated in Cy5.5-GC-CA. Finally, the excess GdCl3 was added to DOTA modified Cy5.5-GC-CA conjugates in distilled water (pH 5.5). The freshly prepared Gd(III) encapsulated Cy5.5-GC-CA conjugates were spontaneously self-assembled into stable Cy5.5 labeled and Gd(III) encapsulated chitosan nanoparticles (Cy5.5-CNP-Gd(III)). The Cy5.5-CNP-Gd(III) was spherical in shape and approximately 350 nm in size. From the cellular experiment, it was demonstrated that Cy5.5-CNP-Gd(III) were efficiently taken up and distributed in cytoplasm (NIRF lilter; red). When the Cy5.5-GC-Gd(III) were systemically administrated into the tail vein of tumor-bearing mice, large amounts of nanoparticles were successfully localized within the tumor, which was confirmed by noninvasive near-infrared fluorescence and MR imaging system simultaneously. These results revealed that the dual-modal imaging probe of Cy5.5-CNP-Gd(III) has the potential to be used as an optical/MR dual imaging agent for cancer treatment.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectCONTRAST AGENTS-
dc.subjectQUANTUM DOTS-
dc.subjectIN-VIVO-
dc.subjectDRUG-DELIVERY-
dc.subjectTHERAPY-
dc.subjectCARRIERS-
dc.subjectMR-
dc.titleTumor Targeting Chitosan Nanoparticles for Dual-Modality Optical/MR Cancer Imaging-
dc.typeArticle-
dc.identifier.doi10.1021/bc900408z-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOCONJUGATE CHEMISTRY, v.21, no.4, pp.578 - 582-
dc.citation.titleBIOCONJUGATE CHEMISTRY-
dc.citation.volume21-
dc.citation.number4-
dc.citation.startPage578-
dc.citation.endPage582-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000276817800002-
dc.identifier.scopusid2-s2.0-77951261362-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCONTRAST AGENTS-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusCARRIERS-
dc.subject.keywordPlusMR-
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