• DocumentCode
    1184813
  • Title

    The influence of elastin-coated 520-nm- and 20-nm-diameter nanoparticles on human fibroblasts in vitro

  • Author

    Berry, Catherine C. ; Rudershausen, Sandra ; Teller, Joachim ; Curtis, Adam S G

  • Author_Institution
    Inst. of Biomed. & Life Sci., Glasgow Univ., UK
  • Volume
    1
  • Issue
    3
  • fYear
    2002
  • Firstpage
    105
  • Lastpage
    109
  • Abstract
    Magnetic nanoparticles have been used for biomedical purposes for several years. In recent years, nanotechnology has developed to a stage that makes it possible to engineer particles to provide opportunities for the site-specific delivery of drugs. To this end, a variety of iron oxide particles have been synthesized. The size and surface of the particles are crucial factors in the application of the particles. Therefore, this study involves the use of two types of magnetic nanoparticles derivatized with elastin and synthesized with differing diameters, compared with identical underivatized plain particles. This influence in vitro was assessed using human dermal fibroblasts and various techniques to observe cell-particle interaction, including light and fluorescence microscopy and scanning electron microscopy. The results indicate that derivatized particles induce alterations in cell behavior and morphology distinct from the plain particles, suggesting that cell response can be directed via specifically engineered particle surfaces. However, little difference was observed between the different diameters.
  • Keywords
    biomagnetism; cellular biophysics; drug delivery systems; magnetic particles; nanoparticles; nanotechnology; optical microscopy; proteins; scanning electron microscopy; superparamagnetism; 20 nm; 520 nm; FeO; cell behavior; cell morphology; cell response; cell-particle interaction; derivatized particles; diameters; elastin-coated nanoparticles; fluorescence microscopy; human dermal fibroblasts; human fibroblasts; in vitro; iron oxide particles; light microscopy; magnetic nanoparticles; nanotechnology; particle size; particle surface; scanning electron microscopy; site-specific drug delivery; specifically engineered particle surfaces; superparamagnetic particles; underivatized plain particles; Biomedical engineering; Drugs; Fibroblasts; Humans; In vitro; Iron; Nanoparticles; Nanotechnology; Scanning electron microscopy; Surface morphology;
  • fLanguage
    English
  • Journal_Title
    NanoBioscience, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    1536-1241
  • Type

    jour

  • DOI
    10.1109/TNB.2003.809467
  • Filename
    1195397