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Highly Sensitive Diagnosis of Small Hepatocellular Carcinoma Using pH-Responsive Iron Oxide Nanocluster Assemblies

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dc.contributor.authorJingxiong Lu-
dc.contributor.authorJihong Sun-
dc.contributor.authorFangyuan Li-
dc.contributor.authorJIn Wang-
dc.contributor.authorJianan Liu-
dc.contributor.authorDokyoon Kim-
dc.contributor.authorChunhai Fan-
dc.contributor.authorTaeghwan Hyeon-
dc.contributor.authorDaishun Ling-
dc.date.available2019-01-03T05:33:34Z-
dc.date.created2018-09-17-
dc.date.issued2018-08-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/5241-
dc.description.abstractIron oxide nanoparticle (IONP)-based magnetic resonance imaging (MRI) contrast agents have been widely used for the diagnosis of hepatic lesions. However, current IONP-based liver-specific MRI contrast agents rely on single-phase contrast enhancement of the normal liver, which is not sensitive enough to detect early stage small hepatocellular carcinomas (HCCs). We herein report i-motif DNA-assisted pH-responsive iron oxide nanocluster assemblies (termed RIAs), which provide an inverse contrast enhancemt effect to improve the distinction between normal liver and target HCC tissues. The acidic pH of the tumor microenvironment triggers the disassembly of the RIAs, which leads to a drastic decrease in their relaxivity ratio (r2/r1), thus converting the RIAs from a T2 to T1 contrast agent. This inverse contrast enhancement of normal liver darkening and HCC brightening under T1 imaging mode was validated on an orthotopic HCC model. Our design provides a novel strategy for the exploitation of the next-generation intelligent MRI contrast agents. © 2018 American Chemical Society-
dc.description.uri1-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titleHighly Sensitive Diagnosis of Small Hepatocellular Carcinoma Using pH-Responsive Iron Oxide Nanocluster Assemblies-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000442183700003-
dc.identifier.scopusid2-s2.0-85051657112-
dc.identifier.rimsid65518-
dc.contributor.affiliatedAuthorJianan Liu-
dc.contributor.affiliatedAuthorDokyoon Kim-
dc.contributor.affiliatedAuthorTaeghwan Hyeon-
dc.identifier.doi10.1021/jacs.8b04169-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.140, no.32, pp.10071 - 10074-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume140-
dc.citation.number32-
dc.citation.startPage10071-
dc.citation.endPage10074-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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