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Multifunctional tumor pH-sensitive self-assembled nanoparticles for bimodal imaging and treatment of resistant heterogeneous tumorsHighly Cited Paper

DC Field Value Language
dc.contributor.authorDaishun Ling-
dc.contributor.authorPark W.-
dc.contributor.authorPark S.-J.-
dc.contributor.authorYang Lu-
dc.contributor.authorKyoung Sub Kim-
dc.contributor.authorMichael J. Hackett-
dc.contributor.authorByung Hyo Kim-
dc.contributor.authorYim H.-
dc.contributor.authorJeon Y.S.-
dc.contributor.authorNa K.-
dc.contributor.authorTaeg Hwan Hyeon-
dc.date.available2015-04-20T06:01:06Z-
dc.date.created2014-08-11-
dc.date.issued2014-04-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/1056-
dc.description.abstractNanoparticle-based diagnosis-therapy integrative systems represent an emerging approach to cancer treatment. However, the diagnostic sensitivity, treatment efficacy, and bioavailability of nanoparticles as well as the heterogeneity and drug resistance of tumors pose tremendous challenges for clinical implementation. We herein report on the fabrication of tumor pH-sensitive magnetic nanogrenades (termed PMNs) composed of self-assembled iron oxide nanoparticles and pH-responsive ligands. These PMNs can readily target tumors via surface-charge switching triggered by the acidic tumor microenvironment, and are further disassembled into a highly active state in acidic subcellular compartments that ""turns on"" MR contrast, fluorescence and photodynamic therapeutic activity. We successfully visualized small tumors implanted in mice via unique pH-responsive T1MR contrast and fluorescence, demonstrating early stage diagnosis of tumors without using any targeting agents. Furthermore, pH-triggered generation of singlet oxygen enabled pH-dependent photodynamic therapy to selectively kill cancer cells. In particular, we demonstrated the superior therapeutic efficacy of PMNs in highly heterogeneous drug-resistant tumors, showing a great potential for clinical applications. © 2014 American Chemical Society.-
dc.description.uri1-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.subjectBiochemistry-
dc.subjectFluorescence-
dc.subjectNanoparticles-
dc.subjectPhotodynamic therapy-
dc.subjectTumors-
dc.subjectClinical application-
dc.subjectEarly-stage diagnosis-
dc.subjectIron oxide nanoparticle-
dc.subjectSelf assembled nanoparticles-
dc.subjectSubcellular compartments-
dc.subjectTherapeutic activity-
dc.subjectTherapeutic efficacy-
dc.subjectTumor microenvironment-
dc.subjectDiagnosis-
dc.titleMultifunctional tumor pH-sensitive self-assembled nanoparticles for bimodal imaging and treatment of resistant heterogeneous tumors-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000334657600029-
dc.identifier.scopusid2-s2.0-84898956458-
dc.identifier.rimsid315ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorDaishun Ling-
dc.contributor.affiliatedAuthorYang Lu-
dc.contributor.affiliatedAuthorMichael J. Hackett-
dc.contributor.affiliatedAuthorByung Hyo Kim-
dc.contributor.affiliatedAuthorTaeg Hwan Hyeon-
dc.identifier.doi10.1021/ja4108287-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.136, no.15, pp.5647 - 5655-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume136-
dc.citation.number15-
dc.citation.startPage5647-
dc.citation.endPage5655-
dc.date.scptcdate2018-10-01-
dc.description.wostc190-
dc.description.scptc198-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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