Long-term hydrolytic degradation study of polycaprolactone films and fibers grafted with poly(sodium styrene sulfonate): Mechanism study and cell response.


Journal

Biointerphases
ISSN: 1559-4106
Titre abrégé: Biointerphases
Pays: United States
ID NLM: 101275679

Informations de publication

Date de publication:
17 11 2020
Historique:
entrez: 18 11 2020
pubmed: 19 11 2020
medline: 30 9 2021
Statut: epublish

Résumé

Polycaprolactone (PCL) is a widely used biodegradable polyester for tissue engineering applications when long-term degradation is preferred. In this article, we focused on the analysis of the hydrolytic degradation of virgin and bioactive poly(sodium styrene sulfonate) (pNaSS) functionalized PCL surfaces under simulated physiological conditions (phosphate buffer saline at 25 and 37 °C) for up to 120 weeks with the aim of applying bioactive PCL for ligament tissue engineering. Techniques used to characterize the bulk and surface degradation indicated that PCL was hydrolyzed by a bulk degradation mode with an accelerated degradation-three times increased rate constant-for pNaSS grafted PCL at 37 °C when compared to virgin PCL at 25 °C. The observed degradation mechanism is due to the pNaSS grafting process (oxidation and radical polymerization), which accelerated the degradation until 48 weeks, when a steady state is reached. The PCL surface was altered by pNaSS grafting, introducing hydrophilic sulfonate groups that increase the swelling and smoothing of the surface, which facilitated the degradation. After 48 weeks, pNaSS was largely removed from the surface, and the degradation of virgin and pNaSS grafted surfaces was similar. The cell response of primary fibroblast cells from sheep ligament was consistent with the surface analysis results: a better initial spreading of cells on pNaSS surfaces when compared to virgin surfaces and a tendency to become similar with degradation time. It is worthy to note that during the extended degradation process the surfaces were able to continue inducing better cell spreading and preserve their cell phenotype as shown by collagen gene expressions.

Identifiants

pubmed: 33203213
doi: 10.1116/6.0000429
pmc: PMC7673838
doi:

Substances chimiques

Buffers 0
Polyesters 0
Polymers 0
Sulfonic Acids 0
polycaprolactone 24980-41-4
Collagen 9007-34-5
styrenesulfonic acid polymer ZSL2FB6GXN

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

061006

Subventions

Organisme : NIBIB NIH HHS
ID : P41 EB002027
Pays : United States

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Auteurs

Amélie Leroux (A)

Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.

Tuan Ngoc Nguyen (T)

Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.

André Rangel (A)

Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.

Isabelle Cacciapuoti (I)

Inovarion, Paris 75005, France.

Delphine Duprez (D)

Laboratoire de Biologie du Développement, Sorbonne Université, Institut Biologie Paris Seine, CNRS, UMR 7622, INSERM U1156, F75005 Paris, France.

David G Castner (DG)

National ESCA and Surface Analysis Center for Biomedical Problems (NESAC/Bio), Departments of Bioengineering and Chemical Engineering, University of Washington, Box 351653, Seattle 98195, Washington.

Véronique Migonney (V)

Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.

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Classifications MeSH