Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Lee, Soojin | - |
dc.contributor.author | Lee, Hyun Su | - |
dc.contributor.author | Chung, Justin J. | - |
dc.contributor.author | Kim, Soo Hyun | - |
dc.contributor.author | Park, Jong Woong | - |
dc.contributor.author | Lee, Kangwon | - |
dc.contributor.author | Jung, Youngmee | - |
dc.date.accessioned | 2024-01-19T15:05:25Z | - |
dc.date.available | 2024-01-19T15:05:25Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 2021-03 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/117328 | - |
dc.description.abstract | A flexible and bioactive scaffold for adipose tissue engineering was fabricated and evaluated by dual nozzle three-dimensional printing. A highly elastic poly (L-lactide-co-epsilon-caprolactone) (PLCL) copolymer, which acted as the main scaffolding, and human adipose tissue derived decellularized extracellular matrix (dECM) hydrogels were used as the printing inks to form the scaffolds. To prepare the three-dimensional (3D) scaffolds, the PLCL co-polymer was printed with a hot melting extruder system while retaining its physical character, similar to adipose tissue, which is beneficial for regeneration. Moreover, to promote adipogenic differentiation and angiogenesis, adipose tissue-derived dECM was used. To optimize the printability of the hydrogel inks, a mixture of collagen type I and dECM hydrogels was used. Furthermore, we examined the adipose tissue formation and angiogenesis of the PLCL/dECM complex scaffold. From in vivo experiments, it was observed that the matured adipose-like tissue structures were abundant, and the number of matured capillaries was remarkably higher in the hydrogel-PLCL group than in the PLCL-only group. Moreover, a higher expression of M2 macrophages, which are known to be involved in the remodeling and regeneration of tissues, was detected in the hydrogel-PLCL group by immunofluorescence analysis. Based on these results, we suggest that our PLCL/dECM fabricated by a dual 3D printing system will be useful for the treatment of large volume fat tissue regeneration. | - |
dc.language | English | - |
dc.publisher | MDPI | - |
dc.subject | SMALL-INTESTINAL SUBMUCOSA | - |
dc.subject | MESENCHYMAL STEM-CELLS | - |
dc.subject | POROUS SCAFFOLD DESIGN | - |
dc.subject | EXTRACELLULAR-MATRIX | - |
dc.subject | DEGRADATION BEHAVIOR | - |
dc.subject | IN-VITRO | - |
dc.subject | BIOMATERIAL | - |
dc.subject | BONE | - |
dc.subject | INFLAMMATION | - |
dc.subject | ANGIOGENESIS | - |
dc.title | Enhanced Regeneration of Vascularized Adipose Tissue with Dual 3D-Printed Elastic Polymer/dECM Hydrogel Complex | - |
dc.type | Article | - |
dc.identifier.doi | 10.3390/ijms22062886 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.22, no.6, pp.1 - 22 | - |
dc.citation.title | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - |
dc.citation.volume | 22 | - |
dc.citation.number | 6 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 22 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000645698100001 | - |
dc.identifier.scopusid | 2-s2.0-85102296226 | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | SMALL-INTESTINAL SUBMUCOSA | - |
dc.subject.keywordPlus | MESENCHYMAL STEM-CELLS | - |
dc.subject.keywordPlus | POROUS SCAFFOLD DESIGN | - |
dc.subject.keywordPlus | EXTRACELLULAR-MATRIX | - |
dc.subject.keywordPlus | DEGRADATION BEHAVIOR | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | BIOMATERIAL | - |
dc.subject.keywordPlus | BONE | - |
dc.subject.keywordPlus | INFLAMMATION | - |
dc.subject.keywordPlus | ANGIOGENESIS | - |
dc.subject.keywordAuthor | 3d printing | - |
dc.subject.keywordAuthor | PLCL | - |
dc.subject.keywordAuthor | decellularization | - |
dc.subject.keywordAuthor | angiogenesis | - |
dc.subject.keywordAuthor | dECM hydrogel | - |
dc.subject.keywordAuthor | adipose tissue regeneration | - |
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