TY - JOUR
T1 - Noninvasive in vivo oximetric imaging by radiofrequency FT EPR
AU - Subramanian, Sankaran
AU - Yamada, Ken Ichi
AU - Irie, Akira
AU - Murugesan, Ramachandran
AU - Cook, John A.
AU - Devasahayam, Nallathamby
AU - Van Dam, Gootzian M.
AU - Mitchell, James B.
AU - Krishna, Murali C.
PY - 2002
Y1 - 2002
N2 - A novel method, called relaxo-oximetry, for rapid spatially resolved in vivo measurements of oxygen concentration using time-domain radiofrequency (RF) electron paramagnetic resonance (EPR) is described. Time-domain data from triaryl methyl (TAM)-based single-electron contrast agents were processed by systematic deletion of the initial time points to arrive at T2*-weighted discrimination of signal amplitudes. In experiments involving phantoms, the line widths [∼ (T2*)-1] increased as a function of oxygen, and the slope (line width/pO2) was the same for both absorption- and magnitude-mode line shapes. Line widths derived from T2* weighting and the computed pO2 values agreed favorably with the measured ones from phantoms of known oxygen tension. In vivo relaxo-oximetry was performed on C3H mice, and it was found that the liver was more hypoxic than the kidneys. For tumors, 2D oxygen maps were generated while the animal breathed room air or Carbogen® (95% O2/5% CO2). Carbogen® enhanced oxygen concentration within the tumor, and the pO2 histograms showed considerable heterogeneity. Clark electrode oxygen measurements on organs and tumors were in good agreement with tissue oxygen measurements done by relaxo-oximetry. Thus, from a single spatial image data set, pO2 measurements can be done noninvasively by relaxo-oximetry, and 3D imaging can be performed in less than 3 min.
AB - A novel method, called relaxo-oximetry, for rapid spatially resolved in vivo measurements of oxygen concentration using time-domain radiofrequency (RF) electron paramagnetic resonance (EPR) is described. Time-domain data from triaryl methyl (TAM)-based single-electron contrast agents were processed by systematic deletion of the initial time points to arrive at T2*-weighted discrimination of signal amplitudes. In experiments involving phantoms, the line widths [∼ (T2*)-1] increased as a function of oxygen, and the slope (line width/pO2) was the same for both absorption- and magnitude-mode line shapes. Line widths derived from T2* weighting and the computed pO2 values agreed favorably with the measured ones from phantoms of known oxygen tension. In vivo relaxo-oximetry was performed on C3H mice, and it was found that the liver was more hypoxic than the kidneys. For tumors, 2D oxygen maps were generated while the animal breathed room air or Carbogen® (95% O2/5% CO2). Carbogen® enhanced oxygen concentration within the tumor, and the pO2 histograms showed considerable heterogeneity. Clark electrode oxygen measurements on organs and tumors were in good agreement with tissue oxygen measurements done by relaxo-oximetry. Thus, from a single spatial image data set, pO2 measurements can be done noninvasively by relaxo-oximetry, and 3D imaging can be performed in less than 3 min.
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U2 - 10.1002/mrm.10133
DO - 10.1002/mrm.10133
M3 - Article
C2 - 11979580
AN - SCOPUS:0036234635
SN - 0740-3194
VL - 47
SP - 1001
EP - 1008
JO - Magnetic Resonance in Medicine
JF - Magnetic Resonance in Medicine
IS - 5
ER -