H. Herzog et al., PHARMACOKINETICS AND RADIATION-DOSE OF O-15 LABELED BUTANOL IN RCBF STUDIES IN HUMANS, European journal of nuclear medicine, 21(2), 1994, pp. 138-143
In this positron emission tomography (PET) study in humans we determin
ed the pharmacokinetics and radiation dose of oxygen-15 labelled butan
ol, a recently introduced tracer for regional cerebral blood flow (rCB
F). This report includes a description of the automated preparation of
O-15-butanol which allows repetitive activation studies, each 15 min
apart. Dynamic rCBF studies were extended by prolonged measurements up
to 15 min after injection over different organs such as brain, liver,
kidneys and bladder. All measurements were done with a whole-body PET
camera PC4096-15WB. Based on the pharmacokinetic data in 13 subjects
the radiation doses to single organs were calculated according to MIRD
pamphlet No. 11 and the effective dose defined by ICRP 60 as an indic
ator of radiation dose to the total body. The liver received the highe
st radiation dose of about 2.2 mGy per 1500 MBq of injected O-15-butan
ol, which is the typical amount of administered tracer in one rCBF mea
surement. The dose to the kidneys was 1.6 mGy, to the stomach 0.8 mGy,
and to the brain 0.16 mGy. The effective dose was 0.54 mGy, which was
similar to that of (H2O)-O-15, but lower than the effective dose from
(CO2)-O-15 in amounts typically applied in human rCBF studies.