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Dexamethasone loaded r3v6 peptide micelles for gene delivery

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dc.contributor.authorLee, Jiyoung-
dc.contributor.authorHyun, Hyesun-
dc.contributor.authorKim, Hyun Ah-
dc.contributor.authorLee, Minhyung-
dc.date.accessioned2022-04-01T10:03:39Z-
dc.date.available2022-04-01T10:03:39Z-
dc.date.created2022-01-24-
dc.date.issued2011-09-14-
dc.identifier.issn0168-3659-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/136548-
dc.description.abstractR3V6 peptides, which were composed of 3 arginines and 6 valines, formed self-assembled micelles in an aqueous solution. To improve the transfection efficiency of the R3V6 peptide micelles, a hydrophobic drug, dexamethasone was loaded into the core of the R3V6 peptide micelles. In vitro transfection assay showed that the dexamethasone-loaded R3V6 peptide micelles deliver DNA more effectively than the R3V6 micelles. In addition, the dexamethasone-loaded R3V6 micelles reduced the IL-6 levels in the lipopolysaccharide (LPS) activated macrophage cells.-
dc.language영어-
dc.language.isoen-
dc.publisherSoochow University Biomedical Polymers Laboratory-
dc.titleDexamethasone loaded r3v6 peptide micelles for gene delivery-
dc.typeConference-
dc.contributor.affiliatedAuthorLee, Minhyung-
dc.identifier.scopusid2-s2.0-84861203851-
dc.identifier.wosid000299125600102-
dc.identifier.bibliographicCitation1st Symposium on Innovative Polymers for Controlled Delivery, pp.E151 - E152-
dc.relation.isPartOf1st Symposium on Innovative Polymers for Controlled Delivery-
dc.relation.isPartOfJOURNAL OF CONTROLLED RELEASE-
dc.citation.title1st Symposium on Innovative Polymers for Controlled Delivery-
dc.citation.startPageE151-
dc.citation.endPageE152-
dc.citation.conferencePlaceCC-
dc.citation.conferencePlaceSuzhou, PEOPLES R CHINA-
dc.citation.conferenceDate2010-09-14-
dc.type.rimsCONF-
dc.description.journalClass1-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0168365911006705?via%3Dihub-
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