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Ceria–Zirconia Nanoparticles as an Enhanced Multi-Antioxidant for Sepsis Treatment

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dc.contributor.authorMin Soh-
dc.contributor.authorKang D.-W.-
dc.contributor.authorJeong H.-G.-
dc.contributor.authorDokyoon Kim-
dc.contributor.authorKim D.Y.-
dc.contributor.authorYang W.-
dc.contributor.authorChangyeong Song-
dc.contributor.authorSeungmin Baik-
dc.contributor.authorChoi I.-Y.-
dc.contributor.authorKi S.-K.-
dc.contributor.authorHyek Jin Kwon-
dc.contributor.authorTaeho Kim-
dc.contributor.authorKim C.K.-
dc.contributor.authorLee S.-H.-
dc.contributor.authorTaeghwan Hyeon-
dc.date.available2018-07-18T02:08:29Z-
dc.date.created2018-03-16-
dc.date.issued2017-09-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/4783-
dc.description.abstractThe two oxidation states of ceria nanoparticles, Ce3+ and Ce4+, play a pivotal role in scavenging reactive oxygen species (ROS). In particular, Ce3+ is largely responsible for removing O2− and .OH that are associated with inflammatory response and cell death. The synthesis is reported of 2 nm ceria–zirconia nanoparticles (CZ NPs) that possess a higher Ce3+/Ce4+ ratio and faster conversion from Ce4+ to Ce3+ than those exhibited by ceria nanoparticles. The obtained Ce0.7Zr0.3O2 (7CZ) NPs greatly improve ROS scavenging performance, thus regulating inflammatory cells in a very low dose. Moreover, 7CZ NPs are demonstrated to be effective in reducing mortality and systemic inflammation in two representative sepsis models. These findings suggest that 7CZ NPs have the potential as a therapeutic nanomedicine for treating ROS-related inflammatory diseases. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinhei-
dc.description.uri1-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectceria–zirconia nanoparticles-
dc.subjectinflammation-
dc.subjectreactive oxygen species-
dc.subjectsepsis-
dc.subjecttherapeutic nanomedicine-
dc.titleCeria–Zirconia Nanoparticles as an Enhanced Multi-Antioxidant for Sepsis Treatment-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000409410700015-
dc.identifier.scopusid2-s2.0-85021846361-
dc.identifier.rimsid62824ko
dc.contributor.affiliatedAuthorMin Soh-
dc.contributor.affiliatedAuthorDokyoon Kim-
dc.contributor.affiliatedAuthorChangyeong Song-
dc.contributor.affiliatedAuthorSeungmin Baik-
dc.contributor.affiliatedAuthorHyek Jin Kwon-
dc.contributor.affiliatedAuthorTaeho Kim-
dc.contributor.affiliatedAuthorTaeghwan Hyeon-
dc.identifier.doi10.1002/anie.201704904-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.38, pp.11399 - 11403-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume56-
dc.citation.number38-
dc.citation.startPage11399-
dc.citation.endPage11403-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordAuthorceria–zirconia nanoparticles-
dc.subject.keywordAuthorinflammation-
dc.subject.keywordAuthorreactive oxygen species-
dc.subject.keywordAuthorsepsis-
dc.subject.keywordAuthortherapeutic nanomedicine-
Appears in Collections:
Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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