Development of Non-Cell Adhesive Vascular Grafts Using Supramolecular Building Blocks

Macromol Biosci. 2016 Mar;16(3):350-62. doi: 10.1002/mabi.201500278. Epub 2015 Nov 27.

Abstract

Cell-free approaches to in situ tissue engineering require materials that are mechanically stable and are able to control cell-adhesive behavior upon implantation. Here, the development of mechanically stable grafts with non-cell adhesive properties via a mix-and-match approach using ureido-pyrimidinone (UPy)-modified supramolecular polymers is reported. Cell adhesion is prevented in vitro through mixing of end-functionalized or chain-extended UPy-polycaprolactone (UPy-PCL or CE-UPy-PCL, respectively) with end-functionalized UPy-poly(ethylene glycol) (UPy-PEG) at a ratio of 90:10. Further characterization reveals intimate mixing behavior of UPy-PCL with UPy-PEG, but poor mechanical properties, whereas CE-UPy-PCL scaffolds are mechanically stable. As a proof-of-concept for the use of non-cell adhesive supramolecular materials in vivo, electrospun vascular scaffolds are applied in an aortic interposition rat model, showing reduced cell infiltration in the presence of only 10% of UPy-PEG. Together, these results provide the first steps toward advanced supramolecular biomaterials for in situ vascular tissue engineering with control over selective cell capturing.

Keywords: biomaterials; non-cell adhesive behavior; supramolecular polymers; vascular grafts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bioprosthesis*
  • Blood Vessel Prosthesis*
  • Cell Adhesion
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Mice
  • NIH 3T3 Cells
  • Polyesters / chemistry*
  • Polyethylene Glycols / chemistry*
  • Pyrimidinones / chemistry*
  • Rats
  • Tissue Scaffolds / chemistry*

Substances

  • Polyesters
  • Pyrimidinones
  • polycaprolactone
  • Polyethylene Glycols
  • polyethylene glycol 1000