Nitric-oxide generating hydrogels inhibit intimal thickening and promote endothelial cell proliferation

Published

Journal Article

Nitric oxide-generating hydrogels have been shown to inhibit smooth muscle cell proliferation and platelet adhesion, as well as promote endothelial cell proliferation; for this reason these hydrogels should be useful in preventing restenosis, or vessel re-occlusion, following balloon angioplasty. Over 600,000 percutaneous transluminal coronary angioplasty (PTCA) procedures are performed annually in the U.S. [1]; unfortunately, 30-40% of patients treated with PTCA experience failure due to restenosis [2]. We have developed nitric oxide (NO)- generating hydrogels that release NO over a period of days to weeks, depending on material design. They are able to significantly reduce platelet adhesion to collagen and inhibit smooth muscle cell proliferation in vitro. In addition, we have covalently grafted a cell adhesion peptide into the NO-generating hydrogels and assessed the ability of endothelial cells (EC) to proliferate on the surface. ECs showed significantly higher rates of proliferation on the NO-generating hydrogels as compared to controls. The perivascular application of NO-generating hydrogels significantly reduced neointimal formation in an experimental balloon angioplasty model as compared to controls. The combined effects of these NO-generating hydrogels make them well suited for incorporation into blooding-contacting devices and for use as a stent coating or stent replacement to prevent restenosis following balloon angioplasty.

Duke Authors

Cited Authors

  • Lipke, E; Masters, K; Myler, H; Shen, C; West, J

Published Date

  • December 1, 2002

Published In

Volume / Issue

  • 1 /

Start / End Page

  • 475 - 476

International Standard Serial Number (ISSN)

  • 0589-1019

Citation Source

  • Scopus