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dc.contributor.author최한곤-
dc.date.accessioned2018-02-21T23:58:38Z-
dc.date.available2018-02-21T23:58:38Z-
dc.date.issued2015-09-
dc.identifier.citationBIOMATERIALS, v. 62, Page. 155-163en_US
dc.identifier.issn0142-9612-
dc.identifier.issn1878-5905-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0142961215004123-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/39268-
dc.description.abstractHere, we designed biomimetic DNA nanoballs for delivery of multiple antisense oligonucleotides (ASOs). DNA templates with ASOs-complementary sequences were amplified by rolling circle amplification (RCA). RCA products were loaded with two types of ASOs by hybridization, condensed using adenovirus-derived Mu peptide, and coated with hyaluronic acid (HA) for delivery into CD44-overexpressing tumor cells. HA-coated, Mu peptide-condensed, dual ASO-loaded DNA nanoballs (HMA nanoballs) showed considerable cellular entry of Cy5-incorporated RCA product DNA and fluorescent ASOs, whereas Mu peptide-condensed, dual ASO-loaded DNA nanoballs (MA nanoballs) revealed limited uptake. Dual ASOs, Dz13 and OGX-427, delivered by HMA nanoballs could reduce the levels of protein targets and exert anticancer effects. Enhanced tumor distribution was observed for fluorescent HMA nanoballs than the corresponding MA nanoballs. Upon intravenous co-administration with doxorubicin, HMA nanoballs exerted the greatest anti-tumor effects among the groups. These results suggest HMA nanoballs as a nanoplatform for sequence-specific delivery of multiple ASOs and other functional oligonucleotides. (c) 2015 Elsevier Ltd. All rights reserved.en_US
dc.description.sponsorshipThis work was supported by research grants from the Ministry of Science, ICT and Future Planning (NRF-2014K2A2A4001156, NRF-2015R1A2A1A01005674), and from the Ministry of Trade, Industry & Energy (Technology Innovation Program, Grant No. 10050648), Republic of Korea.en_US
dc.language.isoen_USen_US
dc.publisherELSEVIER SCI LTDen_US
dc.subjectDNA nanoballsen_US
dc.subjectRolling circle amplificationen_US
dc.subjectBiomimetic condensationen_US
dc.subjectAntisense oligonucleotidesen_US
dc.subjectSequence-specific loadingen_US
dc.subjectC-JUNen_US
dc.subjectCANCER CELLSen_US
dc.subjectANTISENSE OLIGONUCLEOTIDESen_US
dc.subjectRNA INTERFERENCEen_US
dc.subjectDRUG-DELIVERYen_US
dc.subjectDOXORUBICINen_US
dc.subjectTHERAPEUTICSen_US
dc.subjectSTABILITYen_US
dc.subjectMOLECULEen_US
dc.subjectSYSTEMen_US
dc.titleBiomimetic DNA nanoballs for oligonucleotide deliveryen_US
dc.typeArticleen_US
dc.relation.volume62-
dc.identifier.doi10.1016/j.biomaterials.2015.04.037-
dc.relation.page155-163-
dc.relation.journalBIOMATERIALS-
dc.contributor.googleauthorKim, MG-
dc.contributor.googleauthorPark, JY-
dc.contributor.googleauthorShim, GY-
dc.contributor.googleauthorChoi, HG-
dc.contributor.googleauthorOh, YK-
dc.relation.code2015001659-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF PHARMACY[E]-
dc.sector.departmentDEPARTMENT OF PHARMACY-
dc.identifier.pidhangon-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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