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dc.contributor.authorGwak, So-Jung-
dc.contributor.authorKoo, Heebeom-
dc.contributor.authorYun, Yeomin-
dc.contributor.authorYhee, Ji Young-
dc.contributor.authorLee, Hye Yeong-
dc.contributor.authorYoon, Do Heum-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorHa, Yoon-
dc.date.accessioned2024-01-20T05:34:26Z-
dc.date.available2024-01-20T05:34:26Z-
dc.date.created2021-09-05-
dc.date.issued2015-11-
dc.identifier.issn1549-3296-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124805-
dc.description.abstractMethylprednisolone (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.languageEnglish-
dc.publisherWILEY-
dc.subjectNUCLEAR-LOCALIZATION SIGNAL-
dc.subjectIN-VIVO-
dc.subjectFUNCTIONAL RECOVERY-
dc.subjectMETHYLPREDNISOLONE-
dc.subjectCHITOSAN-
dc.subjectTRANSFECTION-
dc.subjectTHERAPY-
dc.subjectCELLS-
dc.subjectCARRIERS-
dc.subjectVECTORS-
dc.titleMultifunctional nanoparticles for gene delivery and spinal cord injury-
dc.typeArticle-
dc.identifier.doi10.1002/jbm.a.35489-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, v.103, no.11, pp.3474 - 3482-
dc.citation.titleJOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A-
dc.citation.volume103-
dc.citation.number11-
dc.citation.startPage3474-
dc.citation.endPage3482-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000362221700006-
dc.identifier.scopusid2-s2.0-84942836354-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusNUCLEAR-LOCALIZATION SIGNAL-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusFUNCTIONAL RECOVERY-
dc.subject.keywordPlusMETHYLPREDNISOLONE-
dc.subject.keywordPlusCHITOSAN-
dc.subject.keywordPlusTRANSFECTION-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusCARRIERS-
dc.subject.keywordPlusVECTORS-
dc.subject.keywordAuthormethylprednisolone-
dc.subject.keywordAuthorchitosan-
dc.subject.keywordAuthorspinal cord injury-
dc.subject.keywordAuthorgene delivery-
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