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Cited 14 time in webofscience Cited 14 time in scopus
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dc.contributor.authorLee, J.-
dc.contributor.authorLee, B.J.-
dc.contributor.authorLee, Y.M.-
dc.contributor.authorPark, H.-
dc.contributor.authorKim, J.H.-
dc.contributor.authorKim, W.J.-
dc.date.accessioned2018-07-17T10:46:09Z-
dc.date.available2018-07-17T10:46:09Z-
dc.date.created2017-12-21-
dc.date.issued2017-05-
dc.identifier.issn1543-8384-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/92108-
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.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfMOLECULAR PHARMACEUTICS-
dc.subjectaptamer-
dc.subjectcomplementary DNA-
dc.subjectdextran-
dc.subjectDNA-
dc.subjectpolymer-
dc.subjectsingle stranded DNA-
dc.subjectvasculotropin-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectArticle-
dc.subjectbiocompatibility-
dc.subjectblood vessel permeability-
dc.subjectconjugation-
dc.subjectcontrolled study-
dc.subjectDNA hybridization-
dc.subjectgene amplification-
dc.subjectgrowth inhibition-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectretina blood vessel-
dc.subjectsynthesis-
dc.subjecttumor growth-
dc.titleSelf-Assembled Nanoconstructs Modified with Amplified Aptamers Inhibited Tumor Growth and Retinal Vascular Hyperpermeability via Vascular Endothelial Growth Factor Capturing-
dc.typeArticle-
dc.identifier.doi10.1021/acs.molpharmaceut.6b00949-
dc.type.rimsART-
dc.identifier.bibliographicCitationMOLECULAR PHARMACEUTICS, v.14, no.5, pp.1460 - 1468-
dc.identifier.wosid000400633300014-
dc.date.tcdate2019-02-01-
dc.citation.endPage1468-
dc.citation.number5-
dc.citation.startPage1460-
dc.citation.titleMOLECULAR PHARMACEUTICS-
dc.citation.volume14-
dc.contributor.affiliatedAuthorKim, W.J.-
dc.identifier.scopusid2-s2.0-85018397688-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc4-
dc.type.docTypeArticle-
dc.subject.keywordPlusANTI-ANGIOGENIC THERAPY-
dc.subject.keywordPlusDIABETIC-RETINOPATHY-
dc.subject.keywordPlusMACULAR DEGENERATION-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordPlusPEGAPTANIB-
dc.subject.keywordPlusTARGET-
dc.subject.keywordAuthoranti-VEGF therapy-
dc.subject.keywordAuthorDNA nanoconstructs-
dc.subject.keywordAuthorpolymer-DNA conjugates-
dc.subject.keywordAuthorantitumor therapy-
dc.subject.keywordAuthorretinal vascular hyperpermeability-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-

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김원종KIM, WON JONG
Dept of Chemistry
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