Ultrasmall Mn-doped Iron Oxide Nanoparticles with Dual Hepatobiliary and Renal Clearances for T1 MR Liver Imaging

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dc.contributor.authorLee, Sanghoonko
dc.contributor.authorLim, Mi Heeko
dc.contributor.authorByun, Arimko
dc.contributor.authorJo, Juheeko
dc.contributor.authorSuh, Jong-Minko
dc.contributor.authorYoo, Jeasangko
dc.contributor.authorKim, Ji-wookko
dc.contributor.authorShin, Tae-Hyunko
dc.contributor.authorChoi, Jin-silko
dc.date.accessioned2024-04-25T06:00:16Z-
dc.date.available2024-04-25T06:00:16Z-
dc.date.created2024-04-25-
dc.date.created2024-04-25-
dc.date.issued2024-04-
dc.identifier.citationNanoscale Advance, v.6, no.8, pp.2177 - 2184-
dc.identifier.issn2516-0230-
dc.identifier.urihttp://hdl.handle.net/10203/319226-
dc.description.abstractAlthough magnetic nanoparticles demonstrate significant potential as magnetic resonance imaging (MRI) contrast agents, their negative contrasts, liver accumulation, and limited excretion hinder their application. Herein, we developed ultrasmall Mn-doped iron oxide nanoparticles (UMIOs) with distinct advantages as T-1 MRI contrast agents. Exceptionally small particle sizes (ca. 2 nm) and magnetization values (5 emu g(Mn+Fe)(-1)) of UMIOs provided optimal T-1 contrast effects with an ideally low r(2)/r(1) value of similar to 1. Furthermore, the use of Mn as a dopant facilitated hepatocyte uptake of the particles, allowing liver imaging. In animal studies, UMIOs exhibited significantly enhanced contrasts for sequential T-1 imaging of blood vessels and the liver, distinguishing them from conventional magnetic nanoparticles. UMIOs were systematically cleared via dual hepatobiliary and renal excretion pathways, highlighting their safety profile. These characteristics imply substantial potential of UMIOs as T-1 contrast agents for the accurate diagnosis of liver diseases.-
dc.languageEnglish-
dc.publisherRoyal Society of Chemistry-
dc.titleUltrasmall Mn-doped Iron Oxide Nanoparticles with Dual Hepatobiliary and Renal Clearances for T1 MR Liver Imaging-
dc.typeArticle-
dc.identifier.wosid001190783200001-
dc.type.rimsART-
dc.citation.volume6-
dc.citation.issue8-
dc.citation.beginningpage2177-
dc.citation.endingpage2184-
dc.citation.publicationnameNanoscale Advance-
dc.identifier.doi10.1039/d3na00933e-
dc.contributor.localauthorLim, Mi Hee-
dc.contributor.nonIdAuthorLee, Sanghoon-
dc.contributor.nonIdAuthorByun, Arim-
dc.contributor.nonIdAuthorJo, Juhee-
dc.contributor.nonIdAuthorSuh, Jong-Min-
dc.contributor.nonIdAuthorKim, Ji-wook-
dc.contributor.nonIdAuthorShin, Tae-Hyun-
dc.contributor.nonIdAuthorChoi, Jin-sil-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCONTRAST-ENHANCED MRI-
dc.subject.keywordPlusFE3O4 NANOPARTICLES-
dc.subject.keywordPlusHEPATIC-UPTAKE-
dc.subject.keywordPlusAGENTS-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordPlusCOPRECIPITATION-
dc.subject.keywordPlusMAGNETIZATION-
dc.subject.keywordPlusNANOCRYSTALS-
dc.subject.keywordPlusDELIVERY-
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CH-Journal Papers(저널논문)
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