DC Field | Value | Language |
---|---|---|
dc.contributor.author | G Jiang | - |
dc.contributor.author | Sang-Hyun Min | - |
dc.contributor.author | Mi-Na Kim | - |
dc.contributor.author | Dong Chul Lee | - |
dc.contributor.author | Mi-Jung Lim | - |
dc.contributor.author | Young Il Yeom | - |
dc.date.accessioned | 2017-08-29 | - |
dc.date.available | 2017-08-29 | - |
dc.date.issued | 2006 | - |
dc.identifier.issn | 1671-4083 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/16990 | - |
dc.description.abstract | Aim: 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.publisher | Springer-Nature Pub Group | - |
dc.title | Alginate/PEI/DNA polyplexes: a new gene delivery system | - |
dc.title.alternative | Alginate/PEI/DNA polyplexes: a new gene delivery system | - |
dc.type | Article | - |
dc.citation.title | Acta Pharmacologica Sinica | - |
dc.citation.number | 5 | - |
dc.citation.endPage | 445 | - |
dc.citation.startPage | 439 | - |
dc.citation.volume | 41 | - |
dc.contributor.affiliatedAuthor | Sang-Hyun Min | - |
dc.contributor.affiliatedAuthor | Mi-Na Kim | - |
dc.contributor.affiliatedAuthor | Dong Chul Lee | - |
dc.contributor.affiliatedAuthor | Mi-Jung Lim | - |
dc.contributor.affiliatedAuthor | Young Il Yeom | - |
dc.contributor.alternativeName | Jiang | - |
dc.contributor.alternativeName | 민상현 | - |
dc.contributor.alternativeName | 김미나 | - |
dc.contributor.alternativeName | 이동철 | - |
dc.contributor.alternativeName | 임미정 | - |
dc.contributor.alternativeName | 염영일 | - |
dc.identifier.bibliographicCitation | Acta Pharmacologica Sinica, vol. 41, no. 5, pp. 439-445 | - |
dc.subject.keyword | Alginate | - |
dc.subject.keyword | Gene delivery | - |
dc.subject.keyword | Polyethylenimine | - |
dc.subject.keyword | Polyplex | - |
dc.subject.local | Alginate | - |
dc.subject.local | gene delivery | - |
dc.subject.local | Gene delivery | - |
dc.subject.local | Polyethylenimine (PEI) | - |
dc.subject.local | Polyethylenimine | - |
dc.subject.local | polyethylenimine | - |
dc.subject.local | Polyplex | - |
dc.subject.local | polyplex | - |
dc.description.journalClass | Y | - |
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