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Article: Development of a three-dimensionally printed scaffold grafted with bone forming peptide-1 for enhanced bone regeneration with in vitro and in vivo evaluations

TitleDevelopment of a three-dimensionally printed scaffold grafted with bone forming peptide-1 for enhanced bone regeneration with in vitro and in vivo evaluations
Authors
Keywords3D printing
Bone forming peptide-1
Bone regeneration
Osteogenesis
Polycaprolactone
Regenerative medicine
Issue Date2019
Citation
Journal of Colloid and Interface Science, 2019, v. 539, p. 468-480 How to Cite?
AbstractDefects in bone are some of the most difficult injuries to treat. Biomimetic scaffolds represent a promising approach for successful bone tissue regeneration. In this study, a three-dimensional (3D) scaffold with osteo-inductive functionality was designed and assayed both in-vitro and in-vivo. Bone formation peptide-1 (BFP1), an osteo-promoting specific peptide, was covalently bound to a 3D printed polycaprolactone (PCL) scaffold using polydopamine (DOPA). The amount of BFP1 immobilized on the surface was found to increase depending on the BFP1 concentration of the loading solution. To observe the biological effects of the 3D scaffolds, human tonsil-derived mesenchymal stem cells (hTMSCs) were isolated. The cells were cultured on the scaffolds and observed to rapidly differentiate into osteoblast-like cells with osteo-promoting capabilities. The scaffolds were implanted in a rabbit calvarial defect model for 8 weeks and successfully stimulated both vessel and bone regeneration. Osteo-promoting 3D scaffolds may provide a safer and more efficient approach for bone repair and remodelling in regenerative medicine.
Persistent Identifierhttp://hdl.handle.net/10722/324070
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 1.760
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLee, Sang Jin-
dc.contributor.authorWon, Jong Eun-
dc.contributor.authorHan, Changhak-
dc.contributor.authorYin, Xiang Yun-
dc.contributor.authorKim, Hyung Keun-
dc.contributor.authorNah, Haram-
dc.contributor.authorKwon, Il Keun-
dc.contributor.authorMin, Byoung Hyun-
dc.contributor.authorKim, Chul Ho-
dc.contributor.authorShin, Yoo Seob-
dc.contributor.authorPark, Su A.-
dc.date.accessioned2023-01-13T03:01:17Z-
dc.date.available2023-01-13T03:01:17Z-
dc.date.issued2019-
dc.identifier.citationJournal of Colloid and Interface Science, 2019, v. 539, p. 468-480-
dc.identifier.issn0021-9797-
dc.identifier.urihttp://hdl.handle.net/10722/324070-
dc.description.abstractDefects in bone are some of the most difficult injuries to treat. Biomimetic scaffolds represent a promising approach for successful bone tissue regeneration. In this study, a three-dimensional (3D) scaffold with osteo-inductive functionality was designed and assayed both in-vitro and in-vivo. Bone formation peptide-1 (BFP1), an osteo-promoting specific peptide, was covalently bound to a 3D printed polycaprolactone (PCL) scaffold using polydopamine (DOPA). The amount of BFP1 immobilized on the surface was found to increase depending on the BFP1 concentration of the loading solution. To observe the biological effects of the 3D scaffolds, human tonsil-derived mesenchymal stem cells (hTMSCs) were isolated. The cells were cultured on the scaffolds and observed to rapidly differentiate into osteoblast-like cells with osteo-promoting capabilities. The scaffolds were implanted in a rabbit calvarial defect model for 8 weeks and successfully stimulated both vessel and bone regeneration. Osteo-promoting 3D scaffolds may provide a safer and more efficient approach for bone repair and remodelling in regenerative medicine.-
dc.languageeng-
dc.relation.ispartofJournal of Colloid and Interface Science-
dc.subject3D printing-
dc.subjectBone forming peptide-1-
dc.subjectBone regeneration-
dc.subjectOsteogenesis-
dc.subjectPolycaprolactone-
dc.subjectRegenerative medicine-
dc.titleDevelopment of a three-dimensionally printed scaffold grafted with bone forming peptide-1 for enhanced bone regeneration with in vitro and in vivo evaluations-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.jcis.2018.12.097-
dc.identifier.pmid30611042-
dc.identifier.scopuseid_2-s2.0-85059325278-
dc.identifier.volume539-
dc.identifier.spage468-
dc.identifier.epage480-
dc.identifier.eissn1095-7103-
dc.identifier.isiWOS:000458343500050-

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