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복잡계자기조립연구단
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Self-Assembled Nanoconstructs Modified with Amplified Aptamers Inhibited Tumor Growth and Retinal Vascular Hyperpermeability via Vascular Endothelial Growth Factor Capturing

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dc.contributor.authorJihyun Lee-
dc.contributor.authorLee B.J.-
dc.contributor.authorYeong Mi Lee-
dc.contributor.authorPark H.-
dc.contributor.authorKim J.H.-
dc.contributor.authorWon Jong Kim-
dc.date.available2017-06-28T07:46:47Z-
dc.date.created2017-05-19-
dc.date.issued2017-05-
dc.identifier.issn1543-8384-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/3628-
dc.description.abstractHere, nanoconstructs consisting of a DNA-amplified aptamer with a biocompatible polymer backbone for capturing target biomolecules are presented. First, the polymer-DNA nanoconstructs were prepared by hybridization of two complementary single-stranded DNAs that were each conjugated to a dextran polymer backbone. The designed polymer-DNA amplified aptamer nanoconstructs (PA-aNCs) were then prepared by utilizing polymer-DNA nanoconstructs conjugated with an aptamer (PA-NCs) using a rolling circle amplification reaction to amplify the aptamer. These PA-aNCs were successfully applied to alleviate tumor growth and vascular endothelial growth factor (VEGF)-induced retinal vascular hyperpermeability in vivo through the highly effective capture of human VEGF as a target molecule. These PA-aNCs could be used as therapeutic agent for anti-VEGF therapy by efficiently capturing human VEGF. © 2017 American Chemical Society-
dc.description.uri1-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.subjectanti-VEGF therapy-
dc.subjectantitumor therapy-
dc.subjectDNA nanoconstructs-
dc.subjectpolymer−DNA conjugates-
dc.subjectretinal vascular hyperpermeability-
dc.titleSelf-Assembled Nanoconstructs Modified with Amplified Aptamers Inhibited Tumor Growth and Retinal Vascular Hyperpermeability via Vascular Endothelial Growth Factor Capturing-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000400633300014-
dc.identifier.scopusid2-s2.0-85018397688-
dc.identifier.rimsid59478ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorJihyun Lee-
dc.contributor.affiliatedAuthorYeong Mi Lee-
dc.contributor.affiliatedAuthorWon Jong Kim-
dc.identifier.doi10.1021/acs.molpharmaceut.6b00949-
dc.identifier.bibliographicCitationMOLECULAR PHARMACEUTICS, v.14, no.5, pp.1460 - 1468-
dc.citation.titleMOLECULAR PHARMACEUTICS-
dc.citation.volume14-
dc.citation.number5-
dc.citation.startPage1460-
dc.citation.endPage1468-
dc.date.scptcdate2018-10-01-
dc.description.wostc2-
dc.description.scptc2-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordAuthoranti-VEGF therapy-
dc.subject.keywordAuthorantitumor therapy-
dc.subject.keywordAuthorDNA nanoconstructs-
dc.subject.keywordAuthorpolymer−DNA conjugates-
dc.subject.keywordAuthorretinal vascular hyperpermeability-
Appears in Collections:
Center for Self-assembly and Complexity(복잡계 자기조립 연구단) > 1. Journal Papers (저널논문)
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