Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair

Detalhes bibliográficos
Autor(a) principal: Neves, Sara Carvalheira
Data de Publicação: 2011
Outros Autores: Teixeira, L. S. Moreira, Moroni, L., Reis, R. L., Blitterswijk, C. A. van, Alves, N. M., Karperien, M., Mano, J. F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/12913
Resumo: Chitosan (CHT)/poly(ε-caprolactone) (PCL) blend 3D fiber-mesh scaffolds were studied as possible support structures for articular cartilage tissue (ACT) repair. Micro-fibers were obtained by wet-spinning of three different polymeric solutions: 100:0 (100CHT), 75:25 (75CHT) and 50:50 (50CHT) wt.% CHT/PCL, using a common solvent solution of 100 vol.% of formic acid. Scanning electron microscopy (SEM) analysis showed a homogeneous surface distribution of PCL. PCL was well dispersed throughout the CHT phase as analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. The fibers were folded into cylindrical moulds and underwent a thermal treatment to obtain the scaffolds. μCT analysis revealed an adequate porosity, pore size and interconnectivity for tissue engineering applications. The PCL component led to a higher fiber surface roughness, decreased the scaffolds swelling ratio and increased their compressive mechanical properties. Biological assays were performed after culturing bovine articular chondrocytes up to 21 days. SEM analysis, live-dead and metabolic activity assays showed that cells attached, proliferated, and were metabolically active over all scaffolds formulations. Cartilaginous extracellular matrix (ECM) formation was observed in all formulations. The 75CHT scaffolds supported the most neo-cartilage formation, as demonstrated by an increase in glycosaminoglycan production. In contrast to 100CHT scaffolds, ECM was homogenously deposited on the 75CHT and 50CHT scaffolds. Although mechanical properties of the 50CHT scaffold were better, the 75CHT scaffold facilitated better neo-cartilage formation.
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spelling Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repairChitosanPolycaprolactoneScaffoldCartilage tissue engineeringScience & TechnologyChitosan (CHT)/poly(ε-caprolactone) (PCL) blend 3D fiber-mesh scaffolds were studied as possible support structures for articular cartilage tissue (ACT) repair. Micro-fibers were obtained by wet-spinning of three different polymeric solutions: 100:0 (100CHT), 75:25 (75CHT) and 50:50 (50CHT) wt.% CHT/PCL, using a common solvent solution of 100 vol.% of formic acid. Scanning electron microscopy (SEM) analysis showed a homogeneous surface distribution of PCL. PCL was well dispersed throughout the CHT phase as analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. The fibers were folded into cylindrical moulds and underwent a thermal treatment to obtain the scaffolds. μCT analysis revealed an adequate porosity, pore size and interconnectivity for tissue engineering applications. The PCL component led to a higher fiber surface roughness, decreased the scaffolds swelling ratio and increased their compressive mechanical properties. Biological assays were performed after culturing bovine articular chondrocytes up to 21 days. SEM analysis, live-dead and metabolic activity assays showed that cells attached, proliferated, and were metabolically active over all scaffolds formulations. Cartilaginous extracellular matrix (ECM) formation was observed in all formulations. The 75CHT scaffolds supported the most neo-cartilage formation, as demonstrated by an increase in glycosaminoglycan production. In contrast to 100CHT scaffolds, ECM was homogenously deposited on the 75CHT and 50CHT scaffolds. Although mechanical properties of the 50CHT scaffold were better, the 75CHT scaffold facilitated better neo-cartilage formation.The research leading to these results has received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under grant agreement number NMP4-SL-2009-229292 and it was also supported in part by a grant from the Dutch Program for Tissue Engineering (DPTE) to Liliana S. Moreira-Teixeira and Marcel Karperien.ElsevierUniversidade do MinhoNeves, Sara CarvalheiraTeixeira, L. S. MoreiraMoroni, L.Reis, R. L.Blitterswijk, C. A. vanAlves, N. M.Karperien, M.Mano, J. F.20112011-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/12913eng0142-961210.1016/j.biomaterials.2010.09.07320980050http://www.sciencedirect.com/science/article/pii/S014296121001286Xinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T11:55:38Zoai:repositorium.sdum.uminho.pt:1822/12913Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:45:11.376982Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
title Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
spellingShingle Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
Neves, Sara Carvalheira
Chitosan
Polycaprolactone
Scaffold
Cartilage tissue engineering
Science & Technology
title_short Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
title_full Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
title_fullStr Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
title_full_unstemmed Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
title_sort Chitosan/Poly(ε-caprolactone) blend scaffolds for cartilage repair
author Neves, Sara Carvalheira
author_facet Neves, Sara Carvalheira
Teixeira, L. S. Moreira
Moroni, L.
Reis, R. L.
Blitterswijk, C. A. van
Alves, N. M.
Karperien, M.
Mano, J. F.
author_role author
author2 Teixeira, L. S. Moreira
Moroni, L.
Reis, R. L.
Blitterswijk, C. A. van
Alves, N. M.
Karperien, M.
Mano, J. F.
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Neves, Sara Carvalheira
Teixeira, L. S. Moreira
Moroni, L.
Reis, R. L.
Blitterswijk, C. A. van
Alves, N. M.
Karperien, M.
Mano, J. F.
dc.subject.por.fl_str_mv Chitosan
Polycaprolactone
Scaffold
Cartilage tissue engineering
Science & Technology
topic Chitosan
Polycaprolactone
Scaffold
Cartilage tissue engineering
Science & Technology
description Chitosan (CHT)/poly(ε-caprolactone) (PCL) blend 3D fiber-mesh scaffolds were studied as possible support structures for articular cartilage tissue (ACT) repair. Micro-fibers were obtained by wet-spinning of three different polymeric solutions: 100:0 (100CHT), 75:25 (75CHT) and 50:50 (50CHT) wt.% CHT/PCL, using a common solvent solution of 100 vol.% of formic acid. Scanning electron microscopy (SEM) analysis showed a homogeneous surface distribution of PCL. PCL was well dispersed throughout the CHT phase as analyzed by differential scanning calorimetry and Fourier transform infrared spectroscopy. The fibers were folded into cylindrical moulds and underwent a thermal treatment to obtain the scaffolds. μCT analysis revealed an adequate porosity, pore size and interconnectivity for tissue engineering applications. The PCL component led to a higher fiber surface roughness, decreased the scaffolds swelling ratio and increased their compressive mechanical properties. Biological assays were performed after culturing bovine articular chondrocytes up to 21 days. SEM analysis, live-dead and metabolic activity assays showed that cells attached, proliferated, and were metabolically active over all scaffolds formulations. Cartilaginous extracellular matrix (ECM) formation was observed in all formulations. The 75CHT scaffolds supported the most neo-cartilage formation, as demonstrated by an increase in glycosaminoglycan production. In contrast to 100CHT scaffolds, ECM was homogenously deposited on the 75CHT and 50CHT scaffolds. Although mechanical properties of the 50CHT scaffold were better, the 75CHT scaffold facilitated better neo-cartilage formation.
publishDate 2011
dc.date.none.fl_str_mv 2011
2011-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/12913
url http://hdl.handle.net/1822/12913
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0142-9612
10.1016/j.biomaterials.2010.09.073
20980050
http://www.sciencedirect.com/science/article/pii/S014296121001286X
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eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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