Table 2.
Radionuclide | Half-life | Recommended timeframe | Availability | RIT radioisotope counterpart | Residualizing? | Possible accumulation sitesa | Current applicationb | Human studiesc | References |
---|---|---|---|---|---|---|---|---|---|
52Mn | 134.2 h | 1–2 weeks | Cyclotron or reactor |
N/A | Residualizing | Brain, liver, kidney, pancreas |
N/A | No | 16 – 20 |
55Co | 17.5 h | ~ 48 hours | Cyclotron | N/A | Residualizing | Liver, kidney, bone |
Brain ischemia and infarction |
Yes | 21 – 27 |
64Cu | 12.7 h | ~ 48 hours | Cyclotron or reactor, commercially available |
67Cu | Residualizing | Liver, blood, spleen, lung, kidney |
Cancer radiodiagnosis, RIT planning, treatment planning and monitoring |
Yes (immuno -PET) |
28 – 44 |
66Ga | 9.4 h | ~ 36 hours | Cyclotron | 66Ga | Residualizing | Bone, liver, kidney, intestine |
Radiodiagnosis, RIT planning |
Yes | 45 – 50 |
72As | 25.9 h | ~ 72 hours | Cyclotron | 77As | Residualizing | Bone, blood cells |
N/A | Yesd | 51 – 55 |
76Br | 16.2 h | ~ 48 hours | Cyclotron, commercially available |
76Br, 131I | Non- residualizing |
Blood | Radiodiagnosis, RIT planning, brain edema |
Yes | 56 – 70 |
86Y | 14.7 h | ~ 48 hours | Cyclotron or heavy-ion accelerator, limited commercial supplye |
90Y, 177Lu | Residualizing | Bone, blood, liver |
RIT planning and monitoring |
Yes | 71 – 78 |
89Zr | 78.4 h | ~ 1 week | Cyclotron or reactor, limited commercial supply |
90Y, 177Lu | Residualizing | Bone, liver, spleen, kidney |
Radioimmunodiagnosis, RIT planning, treatment planning and monitoring |
Yes (immuno -PET) |
79 – 90 |
124I | 100.2 h | ~ 1 week | Cyclotron, commercially available |
131I, 186Re, 188Re |
Non- residualizing |
Thyroid gland | Pharmacodynamics, Preoperative identification, dosimetry |
Yes (immuno -PET) |
91 – 108 |
Possible accumulation sites refer to the preferable sites for free isotopes.
Current application refers to current studies in both animals and humans.
Human studies include all the radionuclide-involved clinical studies not limited to radiolabeled antibodies.
72As was used in humans to study environmental toxicity associated with high doses of natural arsenic [9].
Limited commercial supply indicates that the radioisotope is limited to a small number of production sites (<5).