Endothelialization and Anticoagulation Potential of Surface-Modified PET Intended for Vascular Applications

Macromol Biosci. 2018 Jul;18(7):e1800125. doi: 10.1002/mabi.201800125. Epub 2018 Jun 13.

Abstract

In vascular tissue engineering, great attention is paid to the immobilization of biomolecules onto synthetic grafts to increase bio- and hemocompatibility-two critical milestones in the field. The surface modification field of poly(ethylene terephthalate) (PET), a well-known vascular-graft material, is matured and oversaturated. Nevertheless, most developed methods are laborious multistep procedures generally accompanied by coating instability or toxicity issues. Herein, a straightforward surface modification procedure is presented engineered to simultaneously promote surface endothelialization and anticoagulation properties via the covalent immobilization of gelatin through a photoactivated azide derivative. A complete physicochemical characterization and biological study including cytotoxicity and endotoxin testing are performed. In addition, biocompatibility toward small (diameter ≤ 6 mm) and/or large caliber (diameter ≥ 6 mm) vessels is assessed by micro- and macrovascular endothelial cell assays. Superior bio- and hemocompatibility properties are seen for the gelatin-covalently modified PET surfaces compared to the conventional surface-modification procedures based on physisorption.

Keywords: azide photografting; endothelialization; endotoxin content; hemocompatibility; poly(ethylene terephthalate).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticoagulants / chemistry*
  • Anticoagulants / pharmacology
  • Azides / chemistry
  • Biocompatible Materials / chemistry*
  • Biocompatible Materials / pharmacology
  • Biomarkers / metabolism
  • Blood Vessel Prosthesis
  • Blood Vessels / cytology
  • Blood Vessels / drug effects
  • Blood Vessels / metabolism
  • Cell Survival / drug effects
  • E-Selectin / genetics
  • E-Selectin / metabolism
  • Gelatin / chemistry*
  • Gene Expression
  • Human Umbilical Vein Endothelial Cells / cytology
  • Human Umbilical Vein Endothelial Cells / drug effects*
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Lipopolysaccharides / pharmacology
  • Platelet Endothelial Cell Adhesion Molecule-1 / genetics
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism
  • Polyethylene Terephthalates / chemistry*
  • Polyethylene Terephthalates / pharmacology
  • Surface Properties
  • Tissue Engineering / methods
  • von Willebrand Factor / genetics
  • von Willebrand Factor / metabolism

Substances

  • Anticoagulants
  • Azides
  • Biocompatible Materials
  • Biomarkers
  • E-Selectin
  • Lipopolysaccharides
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Polyethylene Terephthalates
  • SELE protein, human
  • Von Willebrand antigen
  • von Willebrand Factor
  • Gelatin