Abstract
Objective:Phosphorescence quenching has been used successfully to optically measure in vivoblood pO2in the microvasculature. Optical measurements have also been made in some tissues, but it is not clear whether these results accurately reflect tissue pO2. Methods:Recessed pO2microelectrodes and the phosphorescence quenching technique were used simultaneously to measure in vivotissue pO2in hamster skinfold. The optical window for phosphorescence quenching was focused around the tips of microelectrodes that were positioned in tissue regions at least 100 µm from large microvessels. Results:Mean tissue pO2measured by recessed pO2microelectrodes was 18.4 ± 1.7 (SE) Torr, and mean tissue pO2determined from the time course of phosphorescence decay was 18.8 ± 2.0 Torr (no significant difference). The two tissue pO2measurements agreed over a wide range, from 2 to 46 Torr (r = 0.93, 39 paired measurements from six sites in 3 animals). There was no systematic change in the microelectrode tissue pO2during the period of light excitation used for the optical method. Conclusions:Under the conditions of our study, sufficient amounts of porphyrin dye leaked from the vasculature and diffused into tissue, allowing accurate measurements of tissue pO2by the phosphorescence quenching technique. Furthermore, the optical method did not deplete significant amounts of O2from tissue during light excitation.