Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Park, Kwang-Sook | - |
dc.contributor.author | Kim, Byoung-Ju | - |
dc.contributor.author | Lih, Eugene | - |
dc.contributor.author | Park, Wooram | - |
dc.contributor.author | Lee, Soo-Hong | - |
dc.contributor.author | Joung, Yoon Ki | - |
dc.contributor.author | Han, Dong Keun | - |
dc.date.accessioned | 2024-01-19T22:33:03Z | - |
dc.date.available | 2024-01-19T22:33:03Z | - |
dc.date.created | 2021-09-03 | - |
dc.date.issued | 2018-06 | - |
dc.identifier.issn | 1742-7061 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/121300 | - |
dc.description.abstract | Artificial scaffolds made up of various synthetic biodegradable polymers have been reported to have many advantages including cheap manufacturing, easy scale up, high mechanical strength, convenient manipulation, and molding into an unlimited variety of shapes. However, the synthetic biodegradable polymers still have the insufficiency for cartilage regeneration owing to their acidic degradation products. To reduce acidification by degradation of synthetic polymers, we incorporated magnesium hydroxide (MH) nanoparticles into porous polymer scaffold not only to effectively neutralize the acidic hydrolysate but also to minimize the structural disturbance of scaffolds. The neutralization effect of poly(D,L-lactic-co-glycolic acid; PLGA)/MH scaffold was confirmed with the maintenance of neutral pH, contrary to a PLGA scaffold with low pH. Further, the scaffolds were applied to evaluate the chondrogenic differentiation of the human bone marrow mesenchymal stem cells. In in vitro study, the PLGA/MH scaffold enhanced the chondrogenesis markers and reduced the calcification, compared to the PLGA scaffold. Additionally, the PLGA/MH scaffold reduced the release of inflammatory cytokines, compared to the PLGA scaffold, as the cell death decreased. Moreover, the addition of MH reduced necrotic cell death at the early stage of chondrogenic differentiation. Further, the necrotic cell death by the PLGA scaffold was mediated by cleavage of caspase-1, the so-called interleukin 1-converting enzyme, and MH alleviated it as well as nuclear factor kappa B expression. Furthermore, the PLGA/MH scaffold highly supported chondrogenic healing of rat osteochondral defect sites in in vivo study. Therefore, it was suggested that a synthetic polymer scaffold containing MH could be a novel healing tool to support cartilage regeneration and further treatment of orthopedic patients. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved. | - |
dc.language | English | - |
dc.publisher | ELSEVIER SCI LTD | - |
dc.subject | MESENCHYMAL STEM-CELLS | - |
dc.subject | ARTICULAR CHONDROCYTES | - |
dc.subject | EXTRACELLULAR PH | - |
dc.subject | MATRIX SYNTHESIS | - |
dc.subject | TNF-ALPHA | - |
dc.subject | CARTILAGE | - |
dc.subject | CALCIFICATION | - |
dc.subject | STABILITY | - |
dc.subject | ACID | - |
dc.subject | DIFFERENTIATION | - |
dc.title | Versatile effects of magnesium hydroxide nanoparticles in PLGA scaffold-mediated chondrogenesis | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.actbio.2018.04.022 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | ACTA BIOMATERIALIA, v.73, pp.204 - 216 | - |
dc.citation.title | ACTA BIOMATERIALIA | - |
dc.citation.volume | 73 | - |
dc.citation.startPage | 204 | - |
dc.citation.endPage | 216 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000436222600016 | - |
dc.identifier.scopusid | 2-s2.0-85046148459 | - |
dc.relation.journalWebOfScienceCategory | Engineering, Biomedical | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Biomaterials | - |
dc.relation.journalResearchArea | Engineering | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | MESENCHYMAL STEM-CELLS | - |
dc.subject.keywordPlus | ARTICULAR CHONDROCYTES | - |
dc.subject.keywordPlus | EXTRACELLULAR PH | - |
dc.subject.keywordPlus | MATRIX SYNTHESIS | - |
dc.subject.keywordPlus | TNF-ALPHA | - |
dc.subject.keywordPlus | CARTILAGE | - |
dc.subject.keywordPlus | CALCIFICATION | - |
dc.subject.keywordPlus | STABILITY | - |
dc.subject.keywordPlus | ACID | - |
dc.subject.keywordPlus | DIFFERENTIATION | - |
dc.subject.keywordAuthor | Magnesium hydroxide | - |
dc.subject.keywordAuthor | Chondrogenesis | - |
dc.subject.keywordAuthor | Calcification | - |
dc.subject.keywordAuthor | Cell death | - |
dc.subject.keywordAuthor | Inflammation | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.