Dual-Crosslinked Degradable Elastomeric Networks With Self-Healing Properties: Bringing Multi(catechol) Star-Block Copolymers into Play.

catechol degradable network dual cross-linking elastomers polyester self-healing

Journal

ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991

Informations de publication

Date de publication:
11 Jan 2023
Historique:
pubmed: 25 12 2022
medline: 14 1 2023
entrez: 24 12 2022
Statut: ppublish

Résumé

In the biomedical field, degradable chemically crosslinked elastomers are interesting materials for tissue engineering applications, since they present rubber-like mechanical properties matching those of soft tissues and are able to preserve their three-dimensional (3D) structure over degradation. Their use in biomedical applications requires surgical handling and implantation that can be a source of accidental damages responsible for the loss of properties. Therefore, their inability to be healed after damage or breaking can be a major drawback. In this work, biodegradable dual-crosslinked networks that exhibit fast and efficient self-healing properties at 37 °C are designed. Self-healable dual-crosslinked (chemically and physically) elastomeric networks are prepared by two methods. The first approach is based on the mix of hydrophobic poly(ethylene glycol)-poly(lactic acid) (PEG-PLA) star-shaped copolymers functionalized with either catechol or methacrylate moieties. In the second approach, hydrophobic bifunctional PEG-PLA star-shaped copolymers with both catechol and methacrylate on their structure are used. In the two systems, the supramolecular network is responsible for the self-healing properties, thanks to the dynamic dissociation/reassociation of the numerous hydrogen bonds between the catechol groups, whereas the covalent network ensures mechanical properties similar to pure methacrylate networks. The self-healable materials display mechanical properties that are compatible with soft tissues and exhibit linear degradation because of the chemical cross-links. The performances of networks from mixed copolymers versus bifunctional copolymers are compared and demonstrate the superiority of the latter. The biocompatibility of the materials is also demonstrated, confirming the potential of these degradable and self-healable elastomeric networks to be used for the design of temporary medical devices.

Identifiants

pubmed: 36565284
doi: 10.1021/acsami.2c17515
doi:

Substances chimiques

monomethoxypolyethyleneglycol-polylactide block copolymer 0
Polymers 0
Polyethylene Glycols 3WJQ0SDW1A
Methacrylates 0
Catechols 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2077-2091

Auteurs

Mathilde Grosjean (M)

Polymers for Health and Biomaterials, IBMM, Univ Montpellier, CNRS, ENSCM, 34090Montpellier, France.

Louis Gangolphe (L)

Polymers for Health and Biomaterials, IBMM, Univ Montpellier, CNRS, ENSCM, 34090Montpellier, France.
LRP, Univ Grenoble Alpes, CNRS, Grenoble INP, 38000Grenoble, France.

Stéphane Déjean (S)

Polymers for Health and Biomaterials, IBMM, Univ Montpellier, CNRS, ENSCM, 34090Montpellier, France.

Sylvie Hunger (S)

Polymers for Health and Biomaterials, IBMM, Univ Montpellier, CNRS, ENSCM, 34090Montpellier, France.

Audrey Bethry (A)

Polymers for Health and Biomaterials, IBMM, Univ Montpellier, CNRS, ENSCM, 34090Montpellier, France.

Frédéric Bossard (F)

LRP, Univ Grenoble Alpes, CNRS, Grenoble INP, 38000Grenoble, France.

Xavier Garric (X)

Polymers for Health and Biomaterials, IBMM, Univ Montpellier, CNRS, ENSCM, 34090Montpellier, France.
Department of Pharmacy, Nîmes University Hospital, 30900Nîmes, France.

Benjamin Nottelet (B)

Polymers for Health and Biomaterials, IBMM, Univ Montpellier, CNRS, ENSCM, 34090Montpellier, France.

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Classifications MeSH