DNA Transfection Using Linear Poly(ethylenimine) Prepared by Controlled Acid Hydrolysis of Poly(2-ethyl-2-oxazoline)

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dc.contributor.authorJeong, JHko
dc.contributor.authorSong, SHko
dc.contributor.authorLim, DWko
dc.contributor.authorLee, Hko
dc.contributor.authorPark, Tae Gwanko
dc.date.accessioned2009-11-10-
dc.date.available2009-11-10-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-06-
dc.identifier.citationJ. CONTROLLED RELEASE, v.73, no.2-3, pp.391 - 399-
dc.identifier.issn0168-3659-
dc.identifier.urihttp://hdl.handle.net/10203/12302-
dc.description.abstractA series of linear poly(ethylenimine) (L-PEI) containing varying amounts of cationic charge density in its backbone was produced by controlled hydrolysis of poly(2-ethyl-2-oxazoline) (PEtOz) for using as a nonviral DNA transfection agent. The effects of cationic charge density and molecular weight of the L-PEI on the cytotoxicity and transfection efficiency were studied. The efficiency of transfection was monitored by using a luciferase reporter gene system. Gel retardation assay and dynamic light scattering (DLS) showed that the condensation capacity of L-PEI was suitable for transfection. Highly compacted L-PEI/DNA complex (similar to 150 nm) was obtained with a surface charge value of around +28.4 mV. Cell cytotoxicity was affected to a great extent by the hydrolysis percent of L-PEI as well as by the molecular weight. Transfection efficiency of luciferase plasmid DNA against NIH 3T3 fibroblast was largely dependent upon the hydrolysis percent (charge density) in the polymer backbone and the molecular weight of the L-PEI, but independent of the total amount of cationic charges used for DNA condensation. L-PEI with a hydrolysis percent of 88.0% exhibited comparable transfection efficiency to that of commonly used branched PEI. (C) 2001 Elsevier Science B.V. All rights reserved.-
dc.description.sponsorshipthe grants (HMP-99-B-02-0002) from the Ministry of Health and Welfare,Republic of Korea.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherELSEVIER SCIENCE BV-
dc.subjectGENE DELIVERY-
dc.subjectIN-VIVO-
dc.subjectMOLECULAR-WEIGHT-
dc.subjectNONVIRAL VECTOR-
dc.subjectPOLYETHYLENIMINE-
dc.subjectCOMPLEXES-
dc.subjectCELLS-
dc.subjectEFFICIENCY-
dc.subjectPOLYMERS-
dc.subjectCULTURE-
dc.titleDNA Transfection Using Linear Poly(ethylenimine) Prepared by Controlled Acid Hydrolysis of Poly(2-ethyl-2-oxazoline)-
dc.typeArticle-
dc.identifier.wosid000169454900022-
dc.identifier.scopusid2-s2.0-0035850217-
dc.type.rimsART-
dc.citation.volume73-
dc.citation.issue2-3-
dc.citation.beginningpage391-
dc.citation.endingpage399-
dc.citation.publicationnameJ. CONTROLLED RELEASE-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorPark, Tae Gwan-
dc.contributor.nonIdAuthorJeong, JH-
dc.contributor.nonIdAuthorSong, SH-
dc.contributor.nonIdAuthorLim, DW-
dc.contributor.nonIdAuthorLee, H-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorpoly( 2-ethyl-2-oxazoline)-
dc.subject.keywordAuthorcontrolled hydrolysis-
dc.subject.keywordAuthorlinear poly(ethylenimine)-
dc.subject.keywordAuthorgene transfection-
dc.subject.keywordAuthorcharge density-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusMOLECULAR-WEIGHT-
dc.subject.keywordPlusNONVIRAL VECTOR-
dc.subject.keywordPlusPOLYETHYLENIMINE-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusPOLYMERS-
dc.subject.keywordPlusCULTURE-
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