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Tumor Targeting Chitosan Nanoparticles for Dual-Modality Optical/MR Cancer Imaging

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dc.contributor.authorNam, Taehwan-
dc.contributor.authorPark, Sangjin-
dc.contributor.authorLee, Seung-Young-
dc.contributor.authorPark, Kyeongsoon-
dc.contributor.authorSong, In Chan-
dc.contributor.authorLeary, James J.-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorJeong, Seo Young-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorYuk, Simseok Andrew-
dc.contributor.authorHan, Moon Hee-
dc.contributor.authorChoi, Kuiwon-
dc.date.accessioned2012-07-04T05:01:40Z-
dc.date.available2012-07-04T05:01:40Z-
dc.date.issued2010-03-04-
dc.identifier.citationBIOCONJUGATE CHEMISTRY; Vol.21 4; 578-582ko_KR
dc.identifier.issn1043-1802-
dc.identifier.urihttps://hdl.handle.net/10371/78402-
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 GdCl(3) 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.ko_KR
dc.language.isoenko_KR
dc.publisherAMER CHEMICAL SOCko_KR
dc.titleTumor Targeting Chitosan Nanoparticles for Dual-Modality Optical/MR Cancer Imagingko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor남태환-
dc.contributor.AlternativeAuthor박상진-
dc.contributor.AlternativeAuthor이승영-
dc.contributor.AlternativeAuthor박경순-
dc.contributor.AlternativeAuthor최귀원-
dc.contributor.AlternativeAuthor송인찬-
dc.contributor.AlternativeAuthor한문희-
dc.contributor.AlternativeAuthor권익찬-
dc.contributor.AlternativeAuthor김광명-
dc.contributor.AlternativeAuthor정서영-
dc.identifier.doi10.1021/bc900408z-
dc.citation.journaltitleBIOCONJUGATE CHEMISTRY-
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