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dc.contributor.authorYI SUN WOO-
dc.contributor.authorYune, TY-
dc.contributor.authorKim, TW-
dc.contributor.authorChung, H-
dc.contributor.authorChoi, YW-
dc.contributor.authorKwon, IC-
dc.contributor.authorLee, EB-
dc.contributor.author정서영-
dc.date.accessioned2024-01-21T14:14:09Z-
dc.date.available2024-01-21T14:14:09Z-
dc.date.created2021-09-05-
dc.date.issued2000-03-
dc.identifier.issn0724-8741-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141542-
dc.description.abstractPurpose. To develop a non-viral gene delivery system in the form of an oil-in-water (o/w) lipid emulsion. Method. Cationic lipid emulsions were formulated with soybean oil, 1,2-dioleoyl-sn-glycero-3-trimethylammonium-propane (DOTAP) as a cationic emulsifier and other co-emulsifiers. The physical characteristics of the lipid emulsion and the emulsion/DNA complex were determined. The in vitro transfection efficiency of the emulsion/DNA complex was determined in the presence of up to 90% serum. Results. The average droplet size and zeta potential of emulsions were cn. 180 nm and ca. +50 mV, respectively. Among the emulsions, a stable formulation was selected to form a complex with a plasmid DNA encoding chloramphenicol acetyltransferase. By increasing the ratio of emulsion to DNA, zeta-potential of the emulsion/DNA complex increased monotonously from negative to positive without any changes in the complex size. The complex was stable against DNase I digestion and an anionic poly-L-aspartic acid (PLAA). The complex delivered DNA into the cells successfully, and the transfection efficiency was not affected by complex formation time from 20 min to 2 h. More importantly, the cationic lipid emulsion facilitated the transfer of DNA in the presence of up to 90% serum. Conclusions. The cationic lipid emulsion/DNA complex has physical stability and serum resistant properties for gene transfer.-
dc.languageEnglish-
dc.publisherKLUWER ACADEMIC/PLENUM PUBL-
dc.titleA cationic lipid emulsion/DNA complex as a physically stable and serum-resistant gene delivery system-
dc.typeArticle-
dc.identifier.doi10.1023/A:1007553106681-
dc.description.journalClass1-
dc.identifier.bibliographicCitationPHARMACEUTICAL RESEARCH, v.17, no.3, pp.314 - 320-
dc.citation.titlePHARMACEUTICAL RESEARCH-
dc.citation.volume17-
dc.citation.number3-
dc.citation.startPage314-
dc.citation.endPage320-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000086595000010-
dc.identifier.scopusid2-s2.0-0033998938-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusDRUG CARRIERS-
dc.subject.keywordPlusPLASMID DNA-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusTRANSFECTION-
dc.subject.keywordPlusFORMULATIONS-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusLIPOFECTION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusCELLS-
dc.subject.keywordAuthorgene transfer-
dc.subject.keywordAuthorlipid emulsions-
dc.subject.keywordAuthorpoly(ethylene glycol)-
dc.subject.keywordAuthortransfection-
dc.subject.keywordAuthorcationic lipids-
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KIST Article > 2000
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