• DocumentCode
    2534596
  • Title

    Improved endothelial cell responses on highly controllable nanostructured surface features

  • Author

    Lu, Jing ; Webster, Thomas J.

  • Author_Institution
    Brown Univ., Providence
  • fYear
    2007
  • fDate
    10-11 March 2007
  • Firstpage
    211
  • Lastpage
    212
  • Abstract
    Vascular stenting is the procedure of implanting a thin tube into the site of a narrow or blocked artery due to atherosclerosis. However, conventional metal-made stents cause significant injury to the vascular wall and endothelium, which functions as a protective biocompatible barrier between tissue and circulating blood, resulting in in-stent restenosis and then the development of late thrombosis. These problems can be avoided if formation of the endothelium, which is composed of aligned endothelial cells, is accelerated on metal stents. For this purpose, highly controllable nanostructured surface features on Ti (a popular vascular stent metal) were created to promote endothelialization and to control the direction of endothelial cell function. The objective of this in vitro study was to investigate endothelial cell function on highly controllable nanostructured surface features. In this manner, the present study provides much promise for the use of nanotechnology for improving metals for vascular stent applications.
  • Keywords
    blood vessels; cellular biophysics; nanobiotechnology; nanostructured materials; prosthetics; titanium; Ti; artery; atherosclerosis; endothelial cell responses; endothelialization; endothelium; highly controllable nanostructured surface features; implant; nanotechnology; vascular stenting; Acceleration; Adhesives; Blood; Cells (biology); In vitro; Injuries; Nanopatterning; Nanostructured materials; Surface morphology; Surface topography;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioengineering Conference, 2007. NEBC '07. IEEE 33rd Annual Northeast
  • Conference_Location
    Long Island, NY
  • Print_ISBN
    978-1-4244-1033-0
  • Electronic_ISBN
    978-1-4244-1033-0
  • Type

    conf

  • DOI
    10.1109/NEBC.2007.4413353
  • Filename
    4413353