Electron paramagnetic resonance imaging of tumor pO₂

Radiat Res. 2012 Apr;177(4):376-86. doi: 10.1667/rr2622.1. Epub 2012 Feb 14.

Abstract

Electron paramagnetic resonance imaging (EPRI) can be used to noninvasively and quantitatively obtain three-dimensional maps of tumor pO₂. The paramagnetic tracer triarylmethyl (TAM), a substituted trityl radical moiety, is not toxic to animals and provides narrow isotropic spectra, which is ideal for in vivo EPR imaging experiments. From the oxygen-induced spectral broadening of TAM, pO₂ maps can be derived using EPRI. The instrumentation consists of an EPRI spectrometer and 7T magnetic resonance imaging (MRI) system both operating at a common radiofrequency of 300 MHz. Anatomic images obtained by MRI can be overlaid with pO₂ maps obtained from EPRI. With imaging times of less than 3 min, it was possible to monitor the dynamics of oxygen changes in tumor and distinguish chronically hypoxic regions from acutely hypoxic regions. In this article, the principles of pO₂ imaging with EPR and some relevant examples of tumor imaging are reviewed.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Animals
  • Benzoates / toxicity
  • Cell Hypoxia*
  • Electron Spin Resonance Spectroscopy / instrumentation
  • Electron Spin Resonance Spectroscopy / methods*
  • Glycolysis
  • Heterocyclic Compounds, 3-Ring / toxicity
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / physiology
  • Magnetic Resonance Imaging / instrumentation
  • Magnetic Resonance Imaging / methods
  • Mice
  • Models, Biological
  • Neoplasm Proteins / physiology
  • Neoplasms / blood supply
  • Neoplasms / metabolism
  • Neoplasms / pathology*
  • Neoplasms / radiotherapy
  • Neoplasms, Experimental / blood supply
  • Neoplasms, Experimental / metabolism
  • Neoplasms, Experimental / pathology
  • Neoplasms, Experimental / radiotherapy
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / physiopathology
  • Nuclear Magnetic Resonance, Biomolecular / instrumentation
  • Nuclear Magnetic Resonance, Biomolecular / methods
  • Oxygen / analysis
  • Partial Pressure
  • Radiation Tolerance
  • Spin Labels
  • Trityl Compounds / toxicity
  • Tumor Microenvironment

Substances

  • Benzoates
  • Heterocyclic Compounds, 3-Ring
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Neoplasm Proteins
  • Spin Labels
  • Trityl Compounds
  • Oxygen