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Departments of 1 Radiation Oncology and of 2 Biochemistry and Biophysics, Medical School, University of Pennsylvania, Philadelphia, Pennsylvania 19104; and 3 Medical Systems Corporation, Greenvale, New York 11548
Received 12 June 1995; accepted in final form 23 January 1997.
Cerniglia, George J., David F. Wilson, Marek Pawlowski,
Sergei Vinogradov, and John Biaglow. Intravascular oxygen
distribution in subcutaneous 9L tumors and radiation sensitivity.
J. Appl. Physiol. 82(6):
1939-1945, 1997.
Phosphorescence quenching was evaluated as a
technique for measuring PO2 in tumors and for determining the effect of increased
PO2 on sensitivity of the tumors to
radiation. Suspensions of cultured 9L cells or small pieces of solid
tumors from 9L cells were injected subcutaneously on the hindquarter of
rats, and tumors were grown to between 0.2 and 1.0 cm in diameter.
Oxygen-dependent quenching of the phosphorescence of intravenously
injected Pd-meso-tetra-(4-carboxyphenyl) porphine was used to image the
in vivo distribution of PO2 in the
vasculature of small tumors and surrounding tissue. Maps (512 × 480 pixels) of tissue oxygen distribution showed that the
PO2 within 9L tumors was low
(2-12 Torr) relative to the surrounding muscle tissue (20-40
Torr). When the rats were given 100% oxygen or carbogen (95%
O2-5%
CO2) to breathe, the
PO2 in the tumors increased
significantly. This increase was variable among tumors and was greater
with carbogen compared with 100% oxygen. Based on irradiation and
regrowth studies, carbogen breathing increased the sensitivity of the
tumors to radiation. This is consistent with the measured increase in
PO2 in the tumor vasculature. It is
concluded that phosphorescence quenching can be used for noninvasive
determination of the oxygenation of tumors. This method for oxygen
measurements has great potential for clinical application in tumor
identification and therapy.
phosphorescence; imaging; glioma
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