pH and electrically responsive hydrogels with adhesive property

Applications of sodium alginate (Alg) and polyacrylic acid (PAA) hydrogels in biomedicine are well-known. These are predefined by the strength and weakness of their properties, which in turn depend on the chemical structure and the architecture of their crosslinks. In this work, Alg biopolymer has b...

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Detalles Bibliográficos
Autores: Ramírez Alba, María Dolores, Molins Martinez, Marta, García Torres, José Manuel|||0000-0002-3996-0274, Romanini, Michela|||0000-0002-1685-855X, Macovez, Roberto|||0000-0001-5026-9372, Pérez Madrigal, Maria del Mar|||0000-0002-2498-8485, Alemán Llansó, Carlos|||0000-0003-4462-6075
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/409050
Acceso en línea:https://hdl.handle.net/2117/409050
https://dx.doi.org/10.1016/j.reactfunctpolym.2024.105841
Access Level:acceso abierto
Palabra clave:Biomedical materials
Adhesion properties
Biomedical applications
Bonding energy
Dual network
Conducting hydrogels
Materials biomèdics
Àrees temàtiques de la UPC::Enginyeria biomèdica
Descripción
Sumario:Applications of sodium alginate (Alg) and polyacrylic acid (PAA) hydrogels in biomedicine are well-known. These are predefined by the strength and weakness of their properties, which in turn depend on the chemical structure and the architecture of their crosslinks. In this work, Alg biopolymer has been grafted to synthetic PAA that has been chemically crosslinked using N,N'-methylene-bisacrylamide (MBA) to produce a pH responsive hydrogel with adhesive property. The double crosslinking network, which combines MBA-mediated covalent crosslinks and ionic crosslinks in Alg domains, results in an elastic modulus that resembles that of highly anisotropic and viscoelastic human skin. After addressing the influence of the dual network onto the Alg-g-PAA hydrogel properties, a prospection of its potential as an adhesive has been made considering different surfaces (rubber, paper steel, porcine skin, etc). The bonding energy onto porcine skin, 32.6 ± 4.6 J/m2, revealed that the Alg-g-PAA hydrogel can be proposed in the biomedical field as tissue adhesive for wound healing applications. Finally, the hydrogel has been semi-interpenetrated with poly(hydroxymethyl-3,4-ethylenedioxythiophene) (PEDOT-MeOH) chains through a chemical oxidative polymerization process. The resulting hydrogel, Alg-g-PAA/PEDOT-MeOH, which is even more porous than Alg-g-PAA, in addition to being electro-responsive, maintains adhesive properties.