Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)

Detalhes bibliográficos
Autor(a) principal: Nijst, Christiaan L. E.
Data de Publicação: 2007
Outros Autores: Bruggeman, Joost P., Karp, Jeffrey M., Ferreira, Lino, Zumbuehl, Andreas, Bettinger, Christopher J., Langer, Robert
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10524
https://doi.org/10.1021/bm070423u
Resumo: Elastomeric networks are increasingly being investigated for a variety of biomedical applications including drug delivery and tissue engineering. However, in some cases, their preparation requires the use of harsh processing conditions (e.g., high temperature), which limits their biomedical application. Herein, we demonstrate the ability to form elastomeric networks from poly(glycerol-co-sebacate) acrylate (PGSA) under mild conditions while preserving a wide range of physical properties. These networks presented a Young's modulus between 0.05 and 1.38 MPa, an ultimate strength from 0.05 to 0.50 Mpa, and elongation at break between 42% and 189% strain, by varying the degree of acrylation (DA) of PGSA. The in vitro enzymatic and hydrolytic degradation of the polymer networks was dependent on the DA. The copolymerization of poly(ethylene glycol) diacrylate with PGSA allowed for an additional control of mechanical properties and swelling ratios in an aqueous environment, as well as enzymatic and hydrolytic degradation. Photocured PGSA networks demonstrated in vitro biocompatibility as judged by sufficient human primary cell adherence and subsequent proliferation into a confluent monolayer. These photocurable degradable elastomers could have potential application for the encapsulation of temperature-sensitive factors and cells for tissue engineering.
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spelling Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)Elastomeric networks are increasingly being investigated for a variety of biomedical applications including drug delivery and tissue engineering. However, in some cases, their preparation requires the use of harsh processing conditions (e.g., high temperature), which limits their biomedical application. Herein, we demonstrate the ability to form elastomeric networks from poly(glycerol-co-sebacate) acrylate (PGSA) under mild conditions while preserving a wide range of physical properties. These networks presented a Young's modulus between 0.05 and 1.38 MPa, an ultimate strength from 0.05 to 0.50 Mpa, and elongation at break between 42% and 189% strain, by varying the degree of acrylation (DA) of PGSA. The in vitro enzymatic and hydrolytic degradation of the polymer networks was dependent on the DA. The copolymerization of poly(ethylene glycol) diacrylate with PGSA allowed for an additional control of mechanical properties and swelling ratios in an aqueous environment, as well as enzymatic and hydrolytic degradation. Photocured PGSA networks demonstrated in vitro biocompatibility as judged by sufficient human primary cell adherence and subsequent proliferation into a confluent monolayer. These photocurable degradable elastomers could have potential application for the encapsulation of temperature-sensitive factors and cells for tissue engineering.American Chemical Society2007-10-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10524http://hdl.handle.net/10316/10524https://doi.org/10.1021/bm070423uengBiomacromolecules. 8:10 (2007) 3067-30731525-7797Nijst, Christiaan L. E.Bruggeman, Joost P.Karp, Jeffrey M.Ferreira, LinoZumbuehl, AndreasBettinger, Christopher J.Langer, Robertinfo: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:RCAAP2020-05-29T09:41:55Zoai:estudogeral.uc.pt:10316/10524Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:37.870397Repositório 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 Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
title Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
spellingShingle Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
Nijst, Christiaan L. E.
title_short Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
title_full Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
title_fullStr Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
title_full_unstemmed Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
title_sort Synthesis and Characterization of Photocurable Elastomers from Poly(glycerol-co-sebacate)
author Nijst, Christiaan L. E.
author_facet Nijst, Christiaan L. E.
Bruggeman, Joost P.
Karp, Jeffrey M.
Ferreira, Lino
Zumbuehl, Andreas
Bettinger, Christopher J.
Langer, Robert
author_role author
author2 Bruggeman, Joost P.
Karp, Jeffrey M.
Ferreira, Lino
Zumbuehl, Andreas
Bettinger, Christopher J.
Langer, Robert
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Nijst, Christiaan L. E.
Bruggeman, Joost P.
Karp, Jeffrey M.
Ferreira, Lino
Zumbuehl, Andreas
Bettinger, Christopher J.
Langer, Robert
description Elastomeric networks are increasingly being investigated for a variety of biomedical applications including drug delivery and tissue engineering. However, in some cases, their preparation requires the use of harsh processing conditions (e.g., high temperature), which limits their biomedical application. Herein, we demonstrate the ability to form elastomeric networks from poly(glycerol-co-sebacate) acrylate (PGSA) under mild conditions while preserving a wide range of physical properties. These networks presented a Young's modulus between 0.05 and 1.38 MPa, an ultimate strength from 0.05 to 0.50 Mpa, and elongation at break between 42% and 189% strain, by varying the degree of acrylation (DA) of PGSA. The in vitro enzymatic and hydrolytic degradation of the polymer networks was dependent on the DA. The copolymerization of poly(ethylene glycol) diacrylate with PGSA allowed for an additional control of mechanical properties and swelling ratios in an aqueous environment, as well as enzymatic and hydrolytic degradation. Photocured PGSA networks demonstrated in vitro biocompatibility as judged by sufficient human primary cell adherence and subsequent proliferation into a confluent monolayer. These photocurable degradable elastomers could have potential application for the encapsulation of temperature-sensitive factors and cells for tissue engineering.
publishDate 2007
dc.date.none.fl_str_mv 2007-10-08
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10524
http://hdl.handle.net/10316/10524
https://doi.org/10.1021/bm070423u
url http://hdl.handle.net/10316/10524
https://doi.org/10.1021/bm070423u
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biomacromolecules. 8:10 (2007) 3067-3073
1525-7797
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dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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