Abstract
Thorium-227 (t1/2 = 18.72 d) is a promising alpha-emitting radiotherapeutic nuclide for treatment of bone metastases. The daughter nuclide 223Ra, which have been used in clinical study for human, also decays via several alpha-emitting nuclides to stable 207Pb. The decay and growth patterns of radioactivity of 227Th and 223Ra after accumulation in bone are specific for each nuclide. We attempt here to evaluate and compare the myelotoxicities of 227Th-EDTMP and 223Ra in rats.
Seven-week-old Sprague-Dawley rats were injected 227Th-EDTMP or 223RaCl2. The body weight and blood cells (RBCs, WBCs, platelets) of each rat were counted before injection and more than 8 weeks after injection.
A rat injected 8 MBq/kg b.w. of 223Ra died 9 day postinjection. The rats injected more than 250 kBq/kg b.w. of 223Ra showed decrease of WBCs and platelets. In the case of 227Th injection, a rat injected 8 MBq/kg b.w. died 8 day postinjection. On the other hand, the rats injected 4 and 2 MBq/kg b.w. died 4 and 6 weeks postinjection, respectively. The rats injected more than 500 kBq/kg b.w. showed weight loss and decrease of RBCs, WBCs, and platelets.
The myelotoxicity of 227Th-EDTMP showed specific pattern and may correlate to the decay and growth pattern of 227Th and its progeny radioactivity.