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Effect of RGDS and KRSR Peptides Immobilized on Silk Fibroin Nanofibrous Mats for Cell Adhesion and Proliferation

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dc.contributor.authorKim, Jong Wook-
dc.contributor.authorKi, Chang Seok-
dc.contributor.authorPark, Young Hwan-
dc.contributor.authorKim, Hyun Jeong-
dc.contributor.authorUm, In Chul-
dc.date.accessioned2013-01-23T02:15:55Z-
dc.date.available2013-01-23T02:15:55Z-
dc.date.issued2010-05-
dc.identifier.citationMACROMOLECULAR RESEARCH, Vol.18, No.5, pp.442-448ko_KR
dc.identifier.issn1598-5032-
dc.identifier.urihttps://hdl.handle.net/10371/81015-
dc.description.abstractIn this study, RGDS and KRSR peptides were immobilized onto electrospun silk fibroin (SF) nanofibrous mats by imide bond formation, and the cell affinities were evaluated as an immobilized SF scaffold. The MTT assay showed that cell adhesion and spreading of normal human dermal fibroblast (NHDF) occurs on SF nanofibrous mat with immobilized RGDS peptide in the early culture time (within 2-4 h after seeding). On the other hand, the KRSR peptide was more effective on normal human osteoblasts (NHOst). Therefore, the cell adhesion peptides RGDS and KRSR are effective in improving cell adhesion, spreading and proliferation of specific cell types. Moreover, these effects depend on the peptide density. The performance of the SF nanofibrous mats with immobilized peptides may be enhanced as a scaffold for specific uses.ko_KR
dc.language.isoenko_KR
dc.publisherSpringer Verlagko_KR
dc.subjectsilk fibroinko_KR
dc.subjectpeptide immobilizationko_KR
dc.subjectcell affinityko_KR
dc.subjectnanofiberko_KR
dc.subjectscaffoldko_KR
dc.titleEffect of RGDS and KRSR Peptides Immobilized on Silk Fibroin Nanofibrous Mats for Cell Adhesion and Proliferationko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor김종욱-
dc.contributor.AlternativeAuthor기창석-
dc.contributor.AlternativeAuthor박영환-
dc.contributor.AlternativeAuthor김현정-
dc.contributor.AlternativeAuthor엄인철-
dc.identifier.doi10.1007/s13233-010-0514-0-
dc.citation.journaltitleMACROMOLECULAR RESEARCH-
dc.description.tc0-
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