Vascularization and cellular isolation potential of a novel electrospun cell delivery vehicle

J Biomed Mater Res A. 2014 Jul;102(7):2208-19. doi: 10.1002/jbm.a.34900. Epub 2013 Aug 10.

Abstract

A clinical need exists for a cell delivery device that supports long-term cell viability, cell retention within the device and retrieval of delivered cells if necessary. Previously, cell isolation devices have been based on hollow fiber membranes, porous polymer scaffolds, alginate systems, or micro-machined membranes. We present the development and characterization of a novel dual porosity electrospun membrane based device, which supports cellular infiltration and vascularization of its outer porous layer and maintains cellular isolation within a lumen bounded by an inner low porosity layer. Electrospinning conditions were initially established to support electrospun fiber deposition onto nonconductive silicone surfaces. With these parameters established, devices for in vivo evaluations were produced using nylon as a nonconductive scaffold for deposition of dual porosity electrospun fibers. The outer porous layer supported the development of a penetrating microcirculation and the membrane supported the transfer of insulin from encapsulated sustained release pellets for 4 weeks. Viable cells implanted within the device could be identified after 2 weeks of implantation. Through the successful demonstration of survival and cellular isolation of human epithelial cells within the implanted devices and the ability to use the device to deliver insulin, we have established the utility of this device toward localized cell transplantation. The cell delivery device establishes a platform to test the feasibility of approaches to cell dose control and cell localization at the site of implantation in the clinical use of modified autologous or allogeneic cells.

Keywords: cellular isolation; electrospinning; neovascularization; porosity; vascularized cell delivery.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biocompatible Materials
  • Blood Vessels / growth & development*
  • Cell Separation*
  • Diffusion
  • Insulin / administration & dosage*
  • Microscopy, Electron, Scanning
  • Porosity
  • Tissue Scaffolds*

Substances

  • Biocompatible Materials
  • Insulin