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Continuous O-2-Evolving MnFe2O4 Nanoparticle-Anchored Mesoporous Silica Nanoparticles for Efficient Photodynamic Therapy in Hypoxic CancerHighly Cited Paper

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dc.contributor.authorJonghoon Kim-
dc.contributor.authorHye Rim Cho-
dc.contributor.authorHyejin Jeon-
dc.contributor.authorDokyoon Kim-
dc.contributor.authorChangyeong Song-
dc.contributor.authorNohyun Lee-
dc.contributor.authorSeung Hong Choi-
dc.contributor.authorTaeghwan Hyeon-
dc.date.available2018-01-09T07:12:20Z-
dc.date.created2017-09-25-
dc.date.issued2017-08-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/4203-
dc.description.abstractTherapeutic effects of photodynamic therapy (PDT) are limited by cancer hypoxia because the PDT process is dependent on O-2 concentration. Herein, we design biocompatible manganese ferrite nanoparticle-anchored mesoporous silica nanoparticles (MFMSNs) to overcome hypoxia, consequently enhancing the therapeutic efficiency of PDT. By exploiting the continuous O-2-evolving property of MnFe2O4 nanoparticles through the Fenton reaction, MFMSNs relieve hypoxic condition using a small amount of nanoparticles and improve therapeutic outcomes of PDT for tumors in vivo. In addition, MFMSNs exhibit T-2 contrast effect in magnetic resonance imaging (MRI), allowing in vivo tracking of MFMSNs. These findings demonstrate great potential of MFMSNs for theranostic agents in cancer therapy. © 2017 American Chemical Society-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titleContinuous O-2-Evolving MnFe2O4 Nanoparticle-Anchored Mesoporous Silica Nanoparticles for Efficient Photodynamic Therapy in Hypoxic Cancer-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000408074800014-
dc.identifier.scopusid2-s2.0-85027419941-
dc.identifier.rimsid60205ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorJonghoon Kim-
dc.contributor.affiliatedAuthorHye Rim Cho-
dc.contributor.affiliatedAuthorHyejin Jeon-
dc.contributor.affiliatedAuthorDokyoon Kim-
dc.contributor.affiliatedAuthorChangyeong Song-
dc.contributor.affiliatedAuthorSeung Hong Choi-
dc.contributor.affiliatedAuthorTaeghwan Hyeon-
dc.identifier.doi10.1021/jacs.7b05559-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.139, no.32, pp.10992 - 10995-
dc.relation.isPartOfJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume139-
dc.citation.number32-
dc.citation.startPage10992-
dc.citation.endPage10995-
dc.date.scptcdate2018-10-01-
dc.description.wostc37-
dc.description.scptc41-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusMANGANESE FERRITE NANOPARTICLES-
dc.subject.keywordPlusTUMOR OXYGENATION-
dc.subject.keywordPlusFENTON REACTION-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusENHANCE-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusDOTS-
Appears in Collections:
Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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