Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility

Detalhes bibliográficos
Autor(a) principal: Mortier, C.
Data de Publicação: 2022
Outros Autores: Costa, D. C. S., Oliveira, M. B., Haugen, H. J., Lyngstadaas, S. P., Blaker, J. J., 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/10773/35278
Resumo: Advances in synthetic routes to chemically modify natural macromolecules such as polysaccharides and proteins have allowed designing functional hydrogels able to tackle current challenges in the biomedical field. Hydrogels are hydrophilic three-dimensional systems able to absorb or retain a large volume of water, prepared from a low percentage of precursor macromolecules. The typical fragile elastic structure of common hydrogel formulations often limits their usage. Three main fabrication strategies involving several compounds or multimodified materials known as double networks, dual-crosslinked networks, and interpenetrating networks have been explored to impart mechanical strength to hydrogels. Widely investigated for synthetic polymers, these approaches allow obtaining added-value hydrogels with a large spectrum of mechanical properties. Advances in the development of such hydrogels with biomacromolecules as main constituent materials have enabled the fabrication of hydrogels with improved key properties for medical use, including biocompatibility, controlled release of active substances and tailored biodegradability, while exploring sustainable sources. This review describes recent advances in the use of proteins, as well as natural and semi-synthetic polymers for the fabrication of hydrogels for biomedical applications. Structures processed via double network, dual-crosslinked, or interpenetrating network strategies are reviewed, and emphasis is given to the type of chemical modifications and reactions, as well as the covalent and non-covalent interactions/bonds involved in those mechanisms.
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spelling Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatilityHydrogelDouble networksDual-crosslinked networksInterpenetrating networksBiomacromoleculesAdvances in synthetic routes to chemically modify natural macromolecules such as polysaccharides and proteins have allowed designing functional hydrogels able to tackle current challenges in the biomedical field. Hydrogels are hydrophilic three-dimensional systems able to absorb or retain a large volume of water, prepared from a low percentage of precursor macromolecules. The typical fragile elastic structure of common hydrogel formulations often limits their usage. Three main fabrication strategies involving several compounds or multimodified materials known as double networks, dual-crosslinked networks, and interpenetrating networks have been explored to impart mechanical strength to hydrogels. Widely investigated for synthetic polymers, these approaches allow obtaining added-value hydrogels with a large spectrum of mechanical properties. Advances in the development of such hydrogels with biomacromolecules as main constituent materials have enabled the fabrication of hydrogels with improved key properties for medical use, including biocompatibility, controlled release of active substances and tailored biodegradability, while exploring sustainable sources. This review describes recent advances in the use of proteins, as well as natural and semi-synthetic polymers for the fabrication of hydrogels for biomedical applications. Structures processed via double network, dual-crosslinked, or interpenetrating network strategies are reviewed, and emphasis is given to the type of chemical modifications and reactions, as well as the covalent and non-covalent interactions/bonds involved in those mechanisms.Elsevier2022-11-24T09:56:00Z2022-09-01T00:00:00Z2022-09info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/35278eng10.1016/j.mtchem.2022.101222Mortier, C.Costa, D. C. S.Oliveira, M. B.Haugen, H. J.Lyngstadaas, S. P.Blaker, J. J.Mano, J. F.info: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:RCAAP2024-02-22T12:07:52Zoai:ria.ua.pt:10773/35278Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:06:18.529017Repositório 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 Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
title Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
spellingShingle Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
Mortier, C.
Hydrogel
Double networks
Dual-crosslinked networks
Interpenetrating networks
Biomacromolecules
title_short Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
title_full Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
title_fullStr Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
title_full_unstemmed Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
title_sort Advanced hydrogels based on natural macromolecules: chemical routes to achieve mechanical versatility
author Mortier, C.
author_facet Mortier, C.
Costa, D. C. S.
Oliveira, M. B.
Haugen, H. J.
Lyngstadaas, S. P.
Blaker, J. J.
Mano, J. F.
author_role author
author2 Costa, D. C. S.
Oliveira, M. B.
Haugen, H. J.
Lyngstadaas, S. P.
Blaker, J. J.
Mano, J. F.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mortier, C.
Costa, D. C. S.
Oliveira, M. B.
Haugen, H. J.
Lyngstadaas, S. P.
Blaker, J. J.
Mano, J. F.
dc.subject.por.fl_str_mv Hydrogel
Double networks
Dual-crosslinked networks
Interpenetrating networks
Biomacromolecules
topic Hydrogel
Double networks
Dual-crosslinked networks
Interpenetrating networks
Biomacromolecules
description Advances in synthetic routes to chemically modify natural macromolecules such as polysaccharides and proteins have allowed designing functional hydrogels able to tackle current challenges in the biomedical field. Hydrogels are hydrophilic three-dimensional systems able to absorb or retain a large volume of water, prepared from a low percentage of precursor macromolecules. The typical fragile elastic structure of common hydrogel formulations often limits their usage. Three main fabrication strategies involving several compounds or multimodified materials known as double networks, dual-crosslinked networks, and interpenetrating networks have been explored to impart mechanical strength to hydrogels. Widely investigated for synthetic polymers, these approaches allow obtaining added-value hydrogels with a large spectrum of mechanical properties. Advances in the development of such hydrogels with biomacromolecules as main constituent materials have enabled the fabrication of hydrogels with improved key properties for medical use, including biocompatibility, controlled release of active substances and tailored biodegradability, while exploring sustainable sources. This review describes recent advances in the use of proteins, as well as natural and semi-synthetic polymers for the fabrication of hydrogels for biomedical applications. Structures processed via double network, dual-crosslinked, or interpenetrating network strategies are reviewed, and emphasis is given to the type of chemical modifications and reactions, as well as the covalent and non-covalent interactions/bonds involved in those mechanisms.
publishDate 2022
dc.date.none.fl_str_mv 2022-11-24T09:56:00Z
2022-09-01T00:00:00Z
2022-09
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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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/35278
url http://hdl.handle.net/10773/35278
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.mtchem.2022.101222
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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