Alginate/PEI/DNA polyplexes: a new gene delivery system

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dc.contributor.authorG Jiang-
dc.contributor.authorSang-Hyun Min-
dc.contributor.authorMi-Na Kim-
dc.contributor.authorDong Chul Lee-
dc.contributor.authorMi-Jung Lim-
dc.contributor.authorYoung Il Yeom-
dc.date.accessioned2017-08-29-
dc.date.available2017-08-29-
dc.date.issued2006-
dc.identifier.issn1671-4083-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/16990-
dc.description.abstractAim: To avoid the limitation of the use of cationic polyethlenimine (PEI)-complexed plasmid DNA use for in vitro or in vivo gene delivery due to its cytotoxicity and lower efficiency in the presence of serum. Methods: A polyplex with decreased positive charge on the complex surface was designed. The PEI/DNA (PD) complexes coated with an anionic biodegradable polymer, alginate were prepared and their gene delivery behavior with PD was compared. Results: The alginate-coated PD polyplex, where alginate: PEI: DNA [alginate: DNA, 0.15 (w/w); PEI: DNA, N:P = 10] showed about 10-30 fold-increased transfection efficiency compared to corresponding non-coated complexes to C3 cells in the presence of 50% serum. The surface charge of the alginate-coated complex was approximately half of that of the alginate-lacking complex. The size of alginate-coated complex was slightly smaller than that of the corresponding complex without alginate. The former complex also showed a reduced erythrocyte aggregation activity and decreased cytotoxicities to C3 cells in comparison with PD complex. Conclusion: The alginate-coated PD polyplexes as a new gene delivery system can improve transfection efficiency in high serum concentration with low cytotoxicity to C3 cells.-
dc.publisherSpringer-Nature Pub Group-
dc.titleAlginate/PEI/DNA polyplexes: a new gene delivery system-
dc.title.alternativeAlginate/PEI/DNA polyplexes: a new gene delivery system-
dc.typeArticle-
dc.citation.titleActa Pharmacologica Sinica-
dc.citation.number5-
dc.citation.endPage445-
dc.citation.startPage439-
dc.citation.volume41-
dc.contributor.affiliatedAuthorSang-Hyun Min-
dc.contributor.affiliatedAuthorMi-Na Kim-
dc.contributor.affiliatedAuthorDong Chul Lee-
dc.contributor.affiliatedAuthorMi-Jung Lim-
dc.contributor.affiliatedAuthorYoung Il Yeom-
dc.contributor.alternativeNameJiang-
dc.contributor.alternativeName민상현-
dc.contributor.alternativeName김미나-
dc.contributor.alternativeName이동철-
dc.contributor.alternativeName임미정-
dc.contributor.alternativeName염영일-
dc.identifier.bibliographicCitationActa Pharmacologica Sinica, vol. 41, no. 5, pp. 439-445-
dc.subject.keywordAlginate-
dc.subject.keywordGene delivery-
dc.subject.keywordPolyethylenimine-
dc.subject.keywordPolyplex-
dc.subject.localAlginate-
dc.subject.localgene delivery-
dc.subject.localGene delivery-
dc.subject.localPolyethylenimine (PEI)-
dc.subject.localPolyethylenimine-
dc.subject.localpolyethylenimine-
dc.subject.localPolyplex-
dc.subject.localpolyplex-
dc.description.journalClassY-
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Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
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