Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Tae Hee | - |
dc.contributor.author | Jung, Youngmee | - |
dc.contributor.author | Kim, Soo Hyun | - |
dc.date.accessioned | 2024-01-19T23:01:00Z | - |
dc.date.available | 2024-01-19T23:01:00Z | - |
dc.date.created | 2021-09-03 | - |
dc.date.issued | 2018-05 | - |
dc.identifier.issn | 1937-3341 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/121440 | - |
dc.description.abstract | Produced through electrospinning, poly(l-lactide-co-caprolactone) (PLCL) membranes, which have a porous structure and are biodegradable, are of interest in various medical fields. The porous-structured electrospun membrane is particularly interesting because of several favorable properties as follows: it exudes fluid from the wound, does not build up under the wound covering, and does not cause wound desiccation. Moreover, extracellular matrix (ECM)-based structures derived by tissue decellularization have application as engineered tissue scaffolds and as supports for cellular regeneration. In particular, heart decellularized ECM (hdECM) has various pro-angiogenic factors that can induce angiogenesis for wound healing. In this regard, a nanofibrous electrospun hdECM-based hybrid scaffold (NEhdHS), which is a PLCL membrane, including hdECM as an active agent, was tested as a wound dressing to assess its fundamental biochemical and physical features in wound healing. Use of NEhdHS with its porous structure and pro-angiogenic factors is expected to provide an effective wound dressing and reduced scarring. We first demonstrate the effectiveness of a proposed decellularization protocol through analysis of dECM components and describe the mechanical properties of the fabricated NEhdHS. Next, we present an in vitro angiogenesis analysis of the NEhdHS, using a coculture system with human dermal fibroblasts and human umbilical vein endothelial cells; the results of which confirm its biocompatibility and show that the NEhdHS can significantly enhance angiogenesis over that obtained from PLCL or gelatin-containing PLCL scaffolds. We also studied the effectiveness of the NEhdHS in vivo. Using a rat excisional wound-splinting model, we show that covering the upper part of the wound with NEhdHS significantly reduces scarring in the wound healing process compared to that with PLCL or gelatin-containing PLCL scaffolds. Based upon its properties, we conclude that the NEhdHS has potential for application in wound dressing. | - |
dc.language | English | - |
dc.publisher | MARY ANN LIEBERT, INC | - |
dc.subject | MACROPHAGE PHENOTYPES | - |
dc.subject | BACTERIAL CELLULOSE | - |
dc.subject | IN-VITRO | - |
dc.subject | TISSUE | - |
dc.subject | CHITOSAN | - |
dc.subject | ANGIOGENESIS | - |
dc.subject | MECHANISMS | - |
dc.subject | GROWTH | - |
dc.subject | SKIN | - |
dc.subject | NANOPARTICLES | - |
dc.title | Nanofibrous Electrospun Heart Decellularized Extracellular Matrix-Based Hybrid Scaffold as Wound Dressing for Reducing Scarring in Wound Healing | - |
dc.type | Article | - |
dc.identifier.doi | 10.1089/ten.tea.2017.0318 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | TISSUE ENGINEERING PART A, v.24, no.9-10, pp.830 - 848 | - |
dc.citation.title | TISSUE ENGINEERING PART A | - |
dc.citation.volume | 24 | - |
dc.citation.number | 9-10 | - |
dc.citation.startPage | 830 | - |
dc.citation.endPage | 848 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000419555000001 | - |
dc.identifier.scopusid | 2-s2.0-85047205968 | - |
dc.relation.journalWebOfScienceCategory | Cell & Tissue Engineering | - |
dc.relation.journalWebOfScienceCategory | Cell Biology | - |
dc.relation.journalWebOfScienceCategory | Engineering, Biomedical | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Biomaterials | - |
dc.relation.journalResearchArea | Cell Biology | - |
dc.relation.journalResearchArea | Engineering | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | MACROPHAGE PHENOTYPES | - |
dc.subject.keywordPlus | BACTERIAL CELLULOSE | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | TISSUE | - |
dc.subject.keywordPlus | CHITOSAN | - |
dc.subject.keywordPlus | ANGIOGENESIS | - |
dc.subject.keywordPlus | MECHANISMS | - |
dc.subject.keywordPlus | GROWTH | - |
dc.subject.keywordPlus | SKIN | - |
dc.subject.keywordPlus | NANOPARTICLES | - |
dc.subject.keywordAuthor | heart decellularized extracellular matrix | - |
dc.subject.keywordAuthor | angiogenesis | - |
dc.subject.keywordAuthor | wound healing | - |
dc.subject.keywordAuthor | scarless wound dressing | - |
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