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Long-term hydrolytic degradation study of polycaprolactone films and fibers grafted with poly(sodium styrene sulfonate): Mechanism study and cell response.
Leroux, Amélie; Ngoc Nguyen, Tuan; Rangel, André; Cacciapuoti, Isabelle; Duprez, Delphine; Castner, David G; Migonney, Véronique.
Afiliação
  • Leroux A; Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.
  • Ngoc Nguyen T; Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.
  • Rangel A; Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.
  • Cacciapuoti I; Inovarion, Paris 75005, France.
  • Duprez D; Laboratoire de Biologie du Développement, Sorbonne Université, Institut Biologie Paris Seine, CNRS, UMR 7622, INSERM U1156, F75005 Paris, France.
  • 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.
  • Migonney V; Laboratory of Biomaterials and Polymers of Specialty, Institut Galilée, Université Sorbonne Paris Nord, CSPBAT UMR CNRS 7244, Villetaneuse 93430, France.
Biointerphases ; 15(6): 061006, 2020 11 17.
Article em En | MEDLINE | ID: mdl-33203213
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poliésteres / Polímeros / Ácidos Sulfônicos Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poliésteres / Polímeros / Ácidos Sulfônicos Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article