Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Lee, KY | - |
dc.contributor.author | Kwon, IC | - |
dc.contributor.author | Kim, YH | - |
dc.contributor.author | Jo, WH | - |
dc.contributor.author | Jeong, SY | - |
dc.date.accessioned | 2024-01-21T17:16:08Z | - |
dc.date.available | 2024-01-21T17:16:08Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 1998-02-12 | - |
dc.identifier.issn | 0168-3659 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/143237 | - |
dc.description.abstract | Hydrophobically modified chitosan containing 5.1 deoxycholic acid groups per 100 anhydroglucose units was synthesized by an EDC-mediated coupling reaction. Formation and characteristics of self-aggregates of hydrophobically modified chitosan were studied by fluorescence spectroscopy and dynamic light scattering method. The critical aggregation concentration (cac) of the self-aggregate was determined by measuring the fluorescence intensity of pyrene as a fluorescent probe. The cac value in PBS solution (pH 7.2) was 1.7 x 10(-2) mg/ml. Mean diameter of self-aggregates in PBS solution (pH 7.2) was 162 +/- 18 nm with an unimodal size distribution. Charge complex formation between self-aggregates and plasmid DNA was confirmed by electrophoresis on an agarose gel. Migration of DNA on an agarose gel was completely retarded above a charge ratio (+/-) of 4/1 at pH 7.2. The free DNA dissociated from the complexes was observed by electrophoresis above pH 8.0 at a fixed charge ratio of 4/1. An efficient transfection of COS-1 cells was achieved by self-aggregates/DNA complexes. (C) 1998 Elsevier Science B.V. | - |
dc.language | English | - |
dc.publisher | ELSEVIER SCIENCE BV | - |
dc.subject | DRUG CARRIERS | - |
dc.subject | CELLS | - |
dc.subject | THERAPY | - |
dc.title | Preparation of chitosan self-aggregates as a gene delivery system | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/S0168-3659(97)00173-9 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CONTROLLED RELEASE, v.51, no.2-3, pp.213 - 220 | - |
dc.citation.title | JOURNAL OF CONTROLLED RELEASE | - |
dc.citation.volume | 51 | - |
dc.citation.number | 2-3 | - |
dc.citation.startPage | 213 | - |
dc.citation.endPage | 220 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000072419400013 | - |
dc.identifier.scopusid | 2-s2.0-0032509928 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | DRUG CARRIERS | - |
dc.subject.keywordPlus | CELLS | - |
dc.subject.keywordPlus | THERAPY | - |
dc.subject.keywordAuthor | hydrophobic modification | - |
dc.subject.keywordAuthor | chitosan self-aggregate | - |
dc.subject.keywordAuthor | plasmid DNA | - |
dc.subject.keywordAuthor | charge complex | - |
dc.subject.keywordAuthor | cell transfection | - |
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