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dc.contributor.author Acharya, B[Acharya, Bodhraj] ko
dc.contributor.author Chun, SY[Chun, So-Young] ko
dc.contributor.author Kim, SY[Kim, Shin-Yoon] ko
dc.contributor.author Moon, C[Moon, Cheil] ko
dc.contributor.author Shin, HI[Shin, Hong-In] ko
dc.contributor.author Park, EK[Park, Eui Kyun] ko
dc.date.available 2017-07-05T08:59:26Z -
dc.date.created 2017-04-10 -
dc.date.issued 2012-04 -
dc.identifier.citation Journal of Biomedical Materials Research Part B: Applied Biomaterials, v.100B, no.3, pp.841 - 849 -
dc.identifier.issn 1552-4973 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2470 -
dc.description.abstract Calcium phosphate ceramics have been widely used as scaffolds for bone regeneration. Here, to improve the osteogenic potential of hydroxyapatite/ β-tricalcium phosphate (HA/β-TCP) and to apply the bioactive peptide in situ, matrix extracellular phosphoglycoprotein (MEPE) peptide, which has been shown to stimulate osteoblast differentiation, was covalently and directionally immobilized on HA/β-TCP particles. The free-hydroxyl groups on the surface of the HA/β-TCP particles were sequentially conjugated with APTES, PEG-(SS) 2, and the synthetic MEPE peptide. Using FTIR and XPS, immobilization of the MEPE peptide on the HA/β-TCP was confirmed. Implantation of the MEPE peptide-immobilized HA/β-TCP into calvarial defect and subsequent analyses using a micro CT and histology showed significant bone regeneration and increased bone area (9.89-fold) as compared to that of unmodified HA/β-TCP. Moreover, tartrate-resistant acid phosphatase-positive osteoclasts were observed in regenerated bone by the MEPE peptide-immobilized HA/β-TCP, indicating that the bones newly formed by the MEPE peptide-immobilized HA/β-TCP are actively remodeled by osteoclasts. Therefore, our data demonstrate that MEPE peptide immobilization onto the HA/β-TCP surface stimulates bone regeneration associated with physiological bone remodeling. © 2012 WILEY PERIODICALS, INC. -
dc.publisher Wiley Blackwell -
dc.subject Acid Phosphatase Tartrate Resistant Isoenzyme -
dc.subject Animal Experiment -
dc.subject Animal Model -
dc.subject Animals -
dc.subject Bioactive Peptides -
dc.subject Bone -
dc.subject Bone Area -
dc.subject Bone Defect -
dc.subject Bone Mineralization -
dc.subject Bone Regeneration -
dc.subject Bone Remodeling -
dc.subject Calcium Phosphate -
dc.subject Calcium Phosphate Ceramic -
dc.subject Calcium Phosphate Ceramics -
dc.subject Calcium Phosphates -
dc.subject Calvaria -
dc.subject Calvarial Defects -
dc.subject Carboxy Terminal Sequence -
dc.subject Cell Differentiation -
dc.subject Cells, Cultured -
dc.subject Ceramic Particle -
dc.subject Covalent Bond -
dc.subject Disease Models, Animal -
dc.subject Durapatite -
dc.subject Extracellular -
dc.subject Extracellular Matrix Proteins -
dc.subject FT-IR -
dc.subject Glycoproteins -
dc.subject Hematopoietic Stem Cell -
dc.subject Human -
dc.subject Human Cell -
dc.subject Humans -
dc.subject Hydroxyapatite -
dc.subject Immobilized Proteins -
dc.subject In-Situ -
dc.subject Infrared Spectroscopy -
dc.subject Male -
dc.subject Matrix Extracellular Phosphoglycoprotein -
dc.subject MEPE and Bone Marrow Stem Cell -
dc.subject Mice -
dc.subject Mice, Inbred ICR -
dc.subject Micro-Computed Tomography -
dc.subject Micro CT -
dc.subject Mouse -
dc.subject Non-Human -
dc.subject Osteoblast -
dc.subject Osteoblast Differentiation -
dc.subject Osteoblasts -
dc.subject Osteoclast -
dc.subject Osteoclasts -
dc.subject Osteogenic Potential -
dc.subject Peptide Immobilization -
dc.subject Peptides -
dc.subject Phosphatases -
dc.subject Phosphoproteins -
dc.subject Protein Immobilization -
dc.subject Scaffolds (Biology) -
dc.subject Skull Fractures -
dc.subject Stem Cells -
dc.subject Surface Immobilization -
dc.subject Surface Modification -
dc.subject Surface Treatment -
dc.subject Tri-Calcium Phosphates -
dc.subject X Ray Photoelectron Spectroscopy -
dc.title Surface immobilization of MEPE peptide onto HA/ss-TCP ceramic particles enhances bone regeneration and remodeling -
dc.type Article -
dc.identifier.doi 10.1002/jbm.b.32648 -
dc.identifier.wosid 000300983700029 -
dc.identifier.scopusid 2-s2.0-84862815084 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.description.journalClass 1 -
dc.contributor.nonIdAuthor Acharya, B[Acharya, Bodhraj] -
dc.contributor.nonIdAuthor Chun, SY[Chun, So-Young] -
dc.contributor.nonIdAuthor Kim, SY[Kim, Shin-Yoon] -
dc.contributor.nonIdAuthor Shin, HI[Shin, Hong-In] -
dc.contributor.nonIdAuthor Park, EK[Park, Eui Kyun] -
dc.identifier.citationVolume 100B -
dc.identifier.citationNumber 3 -
dc.identifier.citationStartPage 841 -
dc.identifier.citationEndPage 849 -
dc.identifier.citationTitle Journal of Biomedical Materials Research Part B: Applied Biomaterials -
dc.type.journalArticle Article -
dc.contributor.affiliatedAuthor Moon, C[Moon, Cheil] -
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