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Enhanced regeneration of vascularized adipose tissue with dual 3D‐printed elastic polymer/dECM hydrogel complex

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dc.contributor.authorLee, S.-
dc.contributor.authorLee, H.S.-
dc.contributor.authorChung, J.J.-
dc.contributor.authorKim, S.H.-
dc.contributor.authorPark, J.W.-
dc.contributor.authorLee, K.-
dc.contributor.authorJung, Y.-
dc.date.accessioned2021-12-03T11:42:16Z-
dc.date.available2021-12-03T11:42:16Z-
dc.date.created2021-08-31-
dc.date.issued2021-03-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/129113-
dc.description.abstractA 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‐ε‐caprolactone) (PLCL) copolymer, which acted as the main scaffolding, and human adipose tissue derived decel-lularized extracellular matrix (dECM) hydrogels were used as the printing inks to form the scaf-folds. 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 immunofluores-cence 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. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherMDPI AG-
dc.titleEnhanced regeneration of vascularized adipose tissue with dual 3D‐printed elastic polymer/dECM hydrogel complex-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, J.W.-
dc.identifier.doi10.3390/ijms22062886-
dc.identifier.scopusid2-s2.0-85102296226-
dc.identifier.wosid000645698100001-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, v.22, no.6, pp.1 - 22-
dc.relation.isPartOfInternational Journal of Molecular Sciences-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.volume22-
dc.citation.number6-
dc.citation.startPage1-
dc.citation.endPage22-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusSMALL-INTESTINAL SUBMUCOSA-
dc.subject.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusPOROUS SCAFFOLD DESIGN-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusDEGRADATION BEHAVIOR-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusBIOMATERIAL-
dc.subject.keywordPlusBONE-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusANGIOGENESIS-
dc.subject.keywordAuthor3d printing-
dc.subject.keywordAuthorAdipose tissue regeneration-
dc.subject.keywordAuthorAngiogenesis-
dc.subject.keywordAuthorDecellularization-
dc.subject.keywordAuthorDECM hydrogel-
dc.subject.keywordAuthorPLCL-
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