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Chitosan-coated C-phycocyanin Liposome for Extending the Neuroprotective Time Window Against Ischemic Brain Stroke

Cited 7 time in wos
Cited 9 time in scopus

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dc.contributor.authorGoo, Yong Chung-
dc.contributor.authorShim, Kyou Hee-
dc.contributor.authorKim, Hye Jin-
dc.contributor.authorMin, Seul Ki-
dc.contributor.authorShin, Hwa Sung-
dc.date.accessioned2020-10-20T01:56:18Z-
dc.date.available2020-10-20T01:56:18Z-
dc.date.issued2018-10-
dc.identifier.urihttps://repository.kopri.re.kr/handle/201206/10874-
dc.description.abstractThe time window for neuroprotection during ischemic brain stroke is short, and hence, development of neuroprotectants is critical to extend this time window. This study sought to verify if muco-adhesive chitosan coating improves the neuroprotective potential of the pre-proven C-Phycocyanin-pertaining liposome (C-Pc liposome). The use of chitosan-coated liposomes extended the neuroprotective time window by 6 h after occlusion, and further improved the neuroprotection efficiency of the C-Pc liposome in a rat Middle Cerebral Artery Occlusion (MCAO) model. Beneficial changes in mRNA expressions of antioxidants, inflammatory cytokines and glia scar proteoglycans were evident in the C-Pc liposomes. In addition, in the cultured astrocytes, the chitosan- coated C-Pc liposome expressed anti-oxidative activity without cytotoxicity.en_US
dc.languageEnglishen_US
dc.subjectPharmacology & Pharmacyen_US
dc.subject.classification해당사항없음en_US
dc.titleChitosan-coated C-phycocyanin Liposome for Extending the Neuroprotective Time Window Against Ischemic Brain Strokeen_US
dc.title.alternative허혈성 뇌졸중의 치료가능시간을 증가시키기 위한 키토산 코팅 C-Pc 리포좀 개발en_US
dc.typeArticleen_US
dc.identifier.bibliographicCitationGoo, Yong Chung, et al. 2018. "Chitosan-coated C-phycocyanin Liposome for Extending the Neuroprotective Time Window Against Ischemic Brain Stroke". <em>CURRENT PHARMACEUTICAL DESIGN</em>, 24(17): 1859-1864.-
dc.citation.titleCURRENT PHARMACEUTICAL DESIGNen_US
dc.citation.volume24en_US
dc.citation.number17en_US
dc.identifier.doi10.2174/1381612824666180515123543-
dc.citation.startPage1859en_US
dc.citation.endPage1864en_US
dc.description.articleClassificationSCI-
dc.description.jcrRateJCR 2016:45.5252918287938en_US
dc.subject.keywordBrain strokeen_US
dc.subject.keywordC-phycocyaninen_US
dc.subject.keywordChitosanen_US
dc.subject.keywordIschemia and reperfusionen_US
dc.subject.keywordLiposomeen_US
dc.subject.keywordNeuroprotectionen_US
dc.identifier.localId2018-0221-
dc.identifier.scopusid2-s2.0-85053594261-
dc.identifier.wosid000441084200006-
Appears in Collections  
2018-2019, Development of in vitro 3D cell culture and in vivo zebrafish model for studying pathogenesis and drug target of schizophrenia (18-19) / Min, Seul Ki (PN18120)
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