Ch. Vandyck et al., HUMAN BIODISTRIBUTION AND DOSIMETRY OF THE SPECT D-2 DOPAMINE-RECEPTOR RADIOLIGAND [I-123] IBF, Nuclear medicine and biology, 23(1), 1996, pp. 9-16
The research discussed in this article aimed to characterize better th
e biodistribution, excretion and radiation dosimetry of the single pho
ton emission computed tomography (SPECT) D-2 Dopamine receptor radioli
gand [I-123]IBF. Following administration of 111 +/- 12 MBq [I-123]IBF
, seven healthy human subjects were scanned serially with a whole body
imager over a 48-h period. Transmission images were obtained with a s
canning line source for attenuation correction of the emission images.
Urine was collected for 48 h to measure the fraction of activity void
ed by the renal system. Radiation absorbed dose estimates were perform
ed using biokinetic modeling and the Medical Internal Radiation Dose (
MIRD) schema. Highest absorbed doses were to the kidney (0.13 +/- 0.02
mGy/MBq) and urinary bladder wall (0.11 +/- 0.01 mGy/MBq). The effect
ive dose equivalent was 0.041 +/- 0.005 mSv/MBq. Peak brain uptake rep
resented 8% of the injected activity. Rapid urinary excretion minimize
d the absorbed dose to most tissues. The mean cumulative urinary excre
tion fraction was 69%. Thus [I-123]IBF is a promising SPECT agent for
imaging the D-2 dopamine receptor in humans with high brain uptake and
favorable dosimetry.