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Cited 109 time in webofscience Cited 116 time in scopus
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dc.contributor.authorGeun Ho Im-
dc.contributor.authorSoo Min Kim-
dc.contributor.authorDong-Gyu Lee-
dc.contributor.authorWon Jae Lee-
dc.contributor.authorJung Hee Lee-
dc.contributor.authorLee, IS-
dc.date.accessioned2016-04-01T08:12:29Z-
dc.date.available2016-04-01T08:12:29Z-
dc.date.created2013-02-27-
dc.date.issued2013-03-
dc.identifier.issn0142-9612-
dc.identifier.other2013-OAK-0000026585-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/27468-
dc.description.abstractTo investigate whether it is possible to develop a dual magnetic resonance (MR) contrast agent, Fe3O4/MnO hybrid nanocrystals were modified to integrate the T-1 and T-2 contrast-enhancing abilities of each compound, and their characteristics as MR contrast agents were investigated. In vitro and in vivo investigations revealed that the Fe3O4/MnO dumbbell-shaped nanocrystal exerted a negative T-2 contrast effect in its intact form and also gave rise to a positive contrast effect in T-1-weighted MR imaging by releasing Mn2+ ions in a low pH environment. This induced organ-specific contrast enhancement for both T-1- and T-2-weighted in vivo MR imaging. The usefulness of the Fe3O4/MnO hybrid nanocrystals as dual contrast agents was evaluated by in vivo MR imaging of an orthotopic xenograft model of human hepatocellular carcinoma (HCC). After injection of the Fe3O4/MnO hybrid nanocrystals, dual contrast-enhanced MR images that synergistically combined the T-2 and T-1 contrast effects from the Fe3O4 grain and released Mn2+ ions were obtained by a single acquisition of MR imaging. This facilitated the detection of HCC with a high degree of conspicuity that could not be achieved with any single contrast agent. (C) 2012 Elsevier Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfBIOMATERIALS-
dc.titleFe3O4/MnO hybrid nanocrystals as a dual contrast agent for both T-1- and T-2-weighted liver MRI-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1016/J.BIOMATERIALS.2012.11.054-
dc.author.googleIm G.H., Kim S.M., Lee D.-G., Lee W.J., Lee J.H., Lee I.S.-
dc.relation.volume34-
dc.relation.issue8-
dc.relation.startpage2069-
dc.relation.lastpage2076-
dc.contributor.id10179922-
dc.relation.journalBIOMATERIALS-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOMATERIALS, v.34, no.8, pp.2069 - 2076-
dc.identifier.wosid000315003500020-
dc.date.tcdate2019-02-01-
dc.citation.endPage2076-
dc.citation.number8-
dc.citation.startPage2069-
dc.citation.titleBIOMATERIALS-
dc.citation.volume34-
dc.contributor.affiliatedAuthorDong-Gyu Lee-
dc.contributor.affiliatedAuthorLee, IS-
dc.identifier.scopusid2-s2.0-84871522844-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc55-
dc.description.scptc50*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusIRON-OXIDE NANOPARTICLES-
dc.subject.keywordPlusMAGNETIC-RESONANCE-
dc.subject.keywordPlusMANGAFODIPIR TRISODIUM-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusMNO NANOPARTICLES-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusRELAXIVITY-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusSIZE-
dc.subject.keywordPlusCELLS-
dc.subject.keywordAuthorNanoparticle-
dc.subject.keywordAuthorMRI (magnetic resonance imaging)-
dc.subject.keywordAuthorContrast agent-
dc.subject.keywordAuthorLiver-
dc.subject.keywordAuthorDual contrast agent-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-

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