The kinetics of Yttrium-90 (Y-90) in bone of mice was investigated in combi
nation with edetate calcium disodium (CaNa(2)EDTA). One group of mice were
intraperitoneally administered 37.5 mg/kg CaNa(2)EDTA or 0.9% NaCl as a con
trol at 1, 22, 34, 46, 58, 70, 82, 94, 154 and 166 h after injection of Y-9
0 acetate (post-administration), and the biodistribution was studied at 3,
24, 72, 120 and 168 h postinjection of Y-90 acetate. No difference between
the post-CaNa(2)EDTA-treated mice and the control was demonstrated in the r
adioactivity in the bone. A decrease in radioactivity in the liver and kidn
eys was accelerated, and the radioactivity was lower than the control at 12
0 h postinjection. The other group of mice were also given the same dose of
chelator at 12 h and 1 h preinjection of Y-90 acetate and at 1, 22, 34, 46
, 58, 70, 82, 94, 154 and 166 h after injection of Y-90 acetate (pre- and p
ost-administration), the radioactivity in bone at 3 h postinjection was sig
nificantly lower than in the control (24.4 +/- 3.92% ID/g vs. 31.7 +/- 2.26
% ID/g, p < 0.05), but the decrease was not sequential. A significant reduc
tion in radioactivity in the blood, kidneys and liver was demonstrated at 3
h, 72 h and 72 h postinjection. In conclusion, the CaNa(2)EDTA with the ad
ministration schedule employed here cannot chelate the Y-90 from bone but t
he free Y-90 before deposition into bone.