Carbon-11 labeled radiotracers, such as 11C-acetate and
11C-palmitate are widely used in positron
emission tomography (PET) for noninvasive evaluation of myocardial metabolism under varied
physiological conditions.These tracers are attractive probes of tissue physiology, because they are
simply radiolabled versions of the native biochemical substrates. One of the major metabolites
generated by these tracers upon the administration is 11CO2 produced via the citric acid cycle. In
quantitative modeling of
11C-acetate and
11C-palmitate PET data, the fraction of blood
11C
radioactivity present as
11CO2 needs to be measured to obtain a correct radiotracer arterial
input function. Accordingly, the literature describes a method whereby the total blood
11C-activity
is counted in blood samples treated with base solution, while the fraction of
1 1CO2 is measured
after the blood is treated with acid followed by a 10 minutes gas-purge. However, a detailed
description of the experimental validation of this method was not provided. The goal of this study
was to test the reliability of a 10 minute gas purging method used to assay
11CO2 radioactivity in
blood