In vitro studies of heparin-coated magnetic nanoparticles for use in the treatment of neointimal hyperplasia

Nanomedicine. 2018 Jun;14(4):1191-1200. doi: 10.1016/j.nano.2018.02.011. Epub 2018 Mar 8.

Abstract

Restenosis by neointimal hyperplasia is still an ongoing concern in endovascular surgery. Slowing vascular smooth muscle cell (VSMC) proliferation by reversing the phenotype change, would allow vessel healing and re-endotheliazation. To accomplish this, we have developed heparin-coated magnetic nanoparticles for targeted drug therapy of neointimal hyperplasia. Iron oxide nanoparticles were modified with a poly (ethylene oxide) based coating and then further functionalized with heparin. In vitro experiments were conducted to observe changes in phenotype, metabolic activity, and viability of three relevant cell lines including VSMC, endothelial cells and fibroblasts. Inhibition of proliferation of VSMCs was observed with doses as low as 1 μg/mL Fe of heparin loaded nanoparticle where endothelial cells showed an increase in proliferation in response to treatment. Fibroblasts showed relatively low response. Results suggest proliferation suppression of VSMCs due to phenotype coupled with the increase in endothelial cell proliferation at low doses of heparin coated nanoparticles.

Keywords: Endothelial cells; Heparin; Magnetic nanoparticles; Neointimal hyperplasia; Vascular cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Cell Proliferation / drug effects
  • Endothelial Cells / drug effects
  • Female
  • Heparin / chemistry*
  • Heparin / therapeutic use*
  • Hyperplasia / drug therapy*
  • Magnetite Nanoparticles / chemistry*
  • Magnetite Nanoparticles / therapeutic use*
  • Mice
  • Mice, Nude
  • Neointima / drug therapy*
  • Rats
  • Swine

Substances

  • Magnetite Nanoparticles
  • Heparin