The mixing of xenon between the blood and the
saline solution. By using short rf pulses of small tipping angle,
129Xe NMR spectra were acquired as a function of time after
injection of the xenon/saline solution into the blood. The main
figure shows the time dependence of the xenon signal in the RBC and in
the saline/plasma, normalized by the total signal. Within the first
second, the rise of the RBC signal and the reduction of the
saline/plasma signal describe the dynamic process of xenon entering
the RBC from the saline/plasma during mixing. From the exponential
fits (shown as solid lines), the time scale for this process is
estimated to be about 200 ms. (Inset) The time
dependence of the integrated xenon signal from both peaks in the
spectra. From the decay starting after 2 s, the
T1 of the two components is found to be
5.0 s. The initial rise in the total xenon signal intensity during
the first second, following the vigorous injection and mixing of the
xenon/saline solution, is most likely caused by xenon-containing
blood/saline mixture descending from the walls of the sample tube
into the region of the detection coil. NMR experiments were performed
on a Bruker AM-400 spectrometer.