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Imaging of single human carcinoma cells in vitro using a clinical whole-body magnetic resonance scanner at 3.0 T.

Abstract
The purpose of the present study was to examine whether single human carcinoma cells labeled with iron oxide nanoparticles could be detected by magnetic resonance (MR) imaging on a clinical 3-T scanner using a surface coil only. WiDr human colon carcinoma cells were loaded with two kinds of iron oxide nanoparticles differing by coating and size: aminosilan-coated (MagForce) and carboxy-dextran-coated particles (Resovist). The latter were preferred by the colon carcinoma cell line used here and taken up much faster (12 h) than the smaller carboxydextran-coated Resovist (48 h). Labeled single carcinoma cells, distributed in an agarose gel in a monodisperse layer as controlled by light microscopy, became detectable as punctuate signal extinctions when using a small circularly polarized surface coil in conjunction with a T(2)*-weighted GE sequence at 3 T. The threshold for the detectability of labeled colon carcinoma cells ranged at a load of 4-5 mug iron/10(6) cells. Obviating the need for special hardware additions, this study opens a new lane for single-cell tracking on clinical 3-T MR scanners amenable to patient studies.
AuthorsJens Pinkernelle, Ulf Teichgräber, Fabian Neumann, Lukas Lehmkuhl, Jens Ricke, Regina Scholz, Andreas Jordan, Harald Bruhn
JournalMagnetic resonance in medicine (Magn Reson Med) Vol. 53 Issue 5 Pg. 1187-92 (May 2005) ISSN: 0740-3194 [Print] United States
PMID15844140 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2005 Wiley-Liss, Inc.
Chemical References
  • Contrast Media
  • Dextrans
  • Magnetite Nanoparticles
  • Oxides
  • Iron
  • ferumoxides
  • Ferrosoferric Oxide
Topics
  • Aged
  • Carcinoma (pathology)
  • Colonic Neoplasms (pathology)
  • Contrast Media
  • Dextrans
  • Ferrosoferric Oxide
  • Humans
  • In Vitro Techniques
  • Iron
  • Magnetic Resonance Imaging (methods)
  • Magnetite Nanoparticles
  • Oxides
  • Staining and Labeling
  • Tumor Cells, Cultured

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