Sr. Thomas et al., QUANTITATIVE PO2 IMAGING IN-VIVO WITH PERFLUOROCARBON F-19 NMR - TRACKING OXYGEN FROM THE AIRWAY THROUGH THE BLOOD TO ORGAN-TISSUES, Artificial cells, blood substitutes, and immobilization biotechnology, 22(4), 1994, pp. 1029-1042
The physiological redistribution of perfluorocarbon (PFC) compounds to
liver, spleen, bone marrow, and lung after intravenous (IV) or intrap
eritoneal CIP) administration of PFC emulsions affords the unique oppo
rtunity for non-invasive monitoring of oxygenation status of these org
ans and tissues utilizing fluorine (F-19) nuclear magnetic resonance (
NMR) imaging techniques. PFCs also may be introduced directly into the
pulmonary airways by procedures such as liquid ventilation, intratrac
heal instillation, or aerosol inhalation. Considerations of importance
when establishing methodology for accurate quantitation of oxygen par
tial pressure (pO(2)) in vivo using F-19 NMR include: 1.) error analys
is of the calibration curves which relate pO(2) to the measured PFC F-
19 relaxation rate, 2.) optimization of the NMR pulse sequence for eff
icient oxygen sensitive data acquisition and, 3.) fluorine signal inde
pendence from emulsion aqueous phase bioconstituents. The porcine mode
l was investigated at 0.14T following IV or IP administration of the P
FC emulsion containing perfluorotributylamine (FC-43) to demonstate th
e capability for tracking oxygen with F-19 NMR from the lung through t
he blood to selected organ tissues. Quantitative pO(2) projection imag
es and isobaric contour graphs were derived for the liver, spleen, and
lungs as a function of inspired oxygen. Blood pO(2) levels in aorta,
pulmonary artery, and hepatic vein were monitored simultaneously with
NMR imaging for correlative analysis.