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dc.contributor.authorPark, Mi Ran-
dc.contributor.authorKim, Hyon Woo-
dc.contributor.authorHwang, Chang Sun-
dc.contributor.authorHan, Ki Ok-
dc.contributor.authorChoi, Yun Jaie-
dc.contributor.authorSong, Soo Chang-
dc.contributor.authorCho, Myung Haing-
dc.contributor.authorCho, Chong Su-
dc.date.accessioned2024-01-21T00:01:06Z-
dc.date.available2024-01-21T00:01:06Z-
dc.date.created2021-09-03-
dc.date.issued2008-02-
dc.identifier.issn1099-498X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/133793-
dc.description.abstractBackground Polyethylenimine (PEI) is toxic although it is one of the most successful and widely used gene delivery polymers with the aid of the proton sponge effect. Therefore, development of new novel gene delivery carriers having high efficiency with less toxicity is necessary. Methods In this study, a degradable poly(ester amine) carrier based on poly(ethylene glycol) diacrylate (PEGDA) and low molecular weight linear PEI was prepared. Furthermore, we compared the gene expression of the polymer/DNA complexes using two delivery methods: intravenous administration as an invasive method and aerosol as a non-invasive method. Results The synthesized polymer had a relatively small molecular weight (MW = 7980) with 25 h half-life in vitro. The polymer/DNA complexes were formed at an N/P ratio of 9. The particle sizes and zeta-potentials of the complexes were dependent on N/P ratio. Compared to PEI 25K, the newly synthesized polymer exhibited high transfection efficiency with low toxicity. Poly(ester amine)-mediated gene expression in the lung and liver was higher than that of the conventional PEI carrier. Interestingly, non-invasive aerosol delivery induced higher gene expression in all organs compared to intravenous method in an in vivo mice study. Such an expressed gene via a single aerosol administration in the lung and liver remained unchanged for 7 days. Conclusions Our study demonstrates that poly(ester amine) may be applied as an useful gene carrier. Copyright (C) 2007 John Wiley & Sons, Ltd.-
dc.languageEnglish-
dc.publisherJOHN WILEY & SONS LTD-
dc.subjectLOW-MOLECULAR-WEIGHT-
dc.subjectPLASMID DNA-
dc.subjectPOLY(ETHYLENE IMINE)-
dc.subjectAEROSOL DELIVERY-
dc.subjectPOLYETHYLENIMINE-
dc.subjectCOMPLEXES-
dc.subjectVECTOR-
dc.subjectMOUSE-
dc.subjectCELLS-
dc.subjectLUNG-
dc.titleHighty efficient gene transfer with degradabte poty(ester arnine) based on poty(ethytene gtycol) diacrytate and potyethytenimine in vitro and in vivo-
dc.typeArticle-
dc.identifier.doi10.1002/jgm.1139-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF GENE MEDICINE, v.10, no.2, pp.198 - 207-
dc.citation.titleJOURNAL OF GENE MEDICINE-
dc.citation.volume10-
dc.citation.number2-
dc.citation.startPage198-
dc.citation.endPage207-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000253430100009-
dc.identifier.scopusid2-s2.0-39449116343-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.type.docTypeArticle-
dc.subject.keywordPlusLOW-MOLECULAR-WEIGHT-
dc.subject.keywordPlusPLASMID DNA-
dc.subject.keywordPlusPOLY(ETHYLENE IMINE)-
dc.subject.keywordPlusAEROSOL DELIVERY-
dc.subject.keywordPlusPOLYETHYLENIMINE-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusVECTOR-
dc.subject.keywordPlusMOUSE-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusLUNG-
dc.subject.keywordAuthorpolyethylenimine-
dc.subject.keywordAuthorpoly(ethylene glycol)-
dc.subject.keywordAuthorpoly(ester amine)-
dc.subject.keywordAuthornonviral gene delivery-
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