Continuous O-2-Evolving MnFe2O4 Nanoparticle-Anchored Mesoporous Silica Nanoparticles for Efficient Photodynamic Therapy in Hypoxic CancerHighly Cited Paper
DC Field | Value | Language |
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dc.contributor.author | Jonghoon Kim | - |
dc.contributor.author | Hye Rim Cho | - |
dc.contributor.author | Hyejin Jeon | - |
dc.contributor.author | Dokyoon Kim | - |
dc.contributor.author | Changyeong Song | - |
dc.contributor.author | Nohyun Lee | - |
dc.contributor.author | Seung Hong Choi | - |
dc.contributor.author | Taeghwan Hyeon | - |
dc.date.available | 2018-01-09T07:12:20Z | - |
dc.date.created | 2017-09-25 | - |
dc.date.issued | 2017-08 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/4203 | - |
dc.description.abstract | Therapeutic 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.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | Continuous O-2-Evolving MnFe2O4 Nanoparticle-Anchored Mesoporous Silica Nanoparticles for Efficient Photodynamic Therapy in Hypoxic Cancer | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000408074800014 | - |
dc.identifier.scopusid | 2-s2.0-85027419941 | - |
dc.identifier.rimsid | 60205 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Jonghoon Kim | - |
dc.contributor.affiliatedAuthor | Hye Rim Cho | - |
dc.contributor.affiliatedAuthor | Hyejin Jeon | - |
dc.contributor.affiliatedAuthor | Dokyoon Kim | - |
dc.contributor.affiliatedAuthor | Changyeong Song | - |
dc.contributor.affiliatedAuthor | Seung Hong Choi | - |
dc.contributor.affiliatedAuthor | Taeghwan Hyeon | - |
dc.identifier.doi | 10.1021/jacs.7b05559 | - |
dc.identifier.bibliographicCitation | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.139, no.32, pp.10992 - 10995 | - |
dc.relation.isPartOf | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | - |
dc.citation.title | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | - |
dc.citation.volume | 139 | - |
dc.citation.number | 32 | - |
dc.citation.startPage | 10992 | - |
dc.citation.endPage | 10995 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 37 | - |
dc.description.scptc | 41 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.subject.keywordPlus | MANGANESE FERRITE NANOPARTICLES | - |
dc.subject.keywordPlus | TUMOR OXYGENATION | - |
dc.subject.keywordPlus | FENTON REACTION | - |
dc.subject.keywordPlus | IN-VIVO | - |
dc.subject.keywordPlus | CELLS | - |
dc.subject.keywordPlus | CHEMOTHERAPY | - |
dc.subject.keywordPlus | ENHANCE | - |
dc.subject.keywordPlus | RESISTANCE | - |
dc.subject.keywordPlus | DOTS | - |