Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Gwak, So-Jung | - |
dc.contributor.author | Koo, Heebeom | - |
dc.contributor.author | Yun, Yeomin | - |
dc.contributor.author | Yhee, Ji Young | - |
dc.contributor.author | Lee, Hye Yeong | - |
dc.contributor.author | Yoon, Do Heum | - |
dc.contributor.author | Kim, Kwangmeyung | - |
dc.contributor.author | Ha, Yoon | - |
dc.date.accessioned | 2024-01-20T05:34:26Z | - |
dc.date.available | 2024-01-20T05:34:26Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 2015-11 | - |
dc.identifier.issn | 1549-3296 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/124805 | - |
dc.description.abstract | Methylprednisolone (MP) is a glucocorticoid that is used as an anti-inflammatory agent to the treat spinal cord injury (SCI). A low molecular weight chitosan was used to synthesize chitosan-MP conjugate, which was used to evaluate the gene therapy, anti-inflammatory and anti-apoptotic effects of MP. The cytotoxicity of chitosan-MP nanoparticles and the transfection efficiency of plasmid DNA were evaluated by MTT and luciferase assays. A chitosan-MP/pDNA complexes was injected into injured spinal cord to evaluate the anti-inflammatory and anti-apoptotic effects of these complexes using terminal deoxynucleotide transferase dUTP nick end labeling (TUNEL) and ED1 staining, respectively. In addition, to evaluate the distribution of chitosan-MP/pDNA complexes, p-gal encapsulated chitosan-MP was injected into the injected site. Cell survival was similar in cells treated with chitosan-MP conjugate and untreated cells. Luciferase expression was higher in cells treated with the chitosan-MP/pDNA than cells treated with the chitosan/pDNA. The chitosan-MP/pDNA complexes also reduced apoptosis and inflammation at the injury site. These results suggest that chitosan-MP conjugation is an effective gene delivery system to treat SCI. (c) 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3474-3482, 2015. | - |
dc.language | English | - |
dc.publisher | WILEY | - |
dc.subject | NUCLEAR-LOCALIZATION SIGNAL | - |
dc.subject | IN-VIVO | - |
dc.subject | FUNCTIONAL RECOVERY | - |
dc.subject | METHYLPREDNISOLONE | - |
dc.subject | CHITOSAN | - |
dc.subject | TRANSFECTION | - |
dc.subject | THERAPY | - |
dc.subject | CELLS | - |
dc.subject | CARRIERS | - |
dc.subject | VECTORS | - |
dc.title | Multifunctional nanoparticles for gene delivery and spinal cord injury | - |
dc.type | Article | - |
dc.identifier.doi | 10.1002/jbm.a.35489 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, v.103, no.11, pp.3474 - 3482 | - |
dc.citation.title | JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A | - |
dc.citation.volume | 103 | - |
dc.citation.number | 11 | - |
dc.citation.startPage | 3474 | - |
dc.citation.endPage | 3482 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000362221700006 | - |
dc.identifier.scopusid | 2-s2.0-84942836354 | - |
dc.relation.journalWebOfScienceCategory | Engineering, Biomedical | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Biomaterials | - |
dc.relation.journalResearchArea | Engineering | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | NUCLEAR-LOCALIZATION SIGNAL | - |
dc.subject.keywordPlus | IN-VIVO | - |
dc.subject.keywordPlus | FUNCTIONAL RECOVERY | - |
dc.subject.keywordPlus | METHYLPREDNISOLONE | - |
dc.subject.keywordPlus | CHITOSAN | - |
dc.subject.keywordPlus | TRANSFECTION | - |
dc.subject.keywordPlus | THERAPY | - |
dc.subject.keywordPlus | CELLS | - |
dc.subject.keywordPlus | CARRIERS | - |
dc.subject.keywordPlus | VECTORS | - |
dc.subject.keywordAuthor | methylprednisolone | - |
dc.subject.keywordAuthor | chitosan | - |
dc.subject.keywordAuthor | spinal cord injury | - |
dc.subject.keywordAuthor | gene delivery | - |
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