Abstract
The radionuclide-generator based access to radiopharmaceutical isotopes represents a valuable alternative to directly produced isotopes at particle accelerators or nuclear reactors. The 44Ti based generator is of increasing interest for the delivery of PET-radiopharmaceutical isotopes used for imaging. The product of this generator 44Sc represents with its 3.97 h half-life and 94.3% positron branching [1] a very promising candidate for labeling PET radiopharmaceuticals. The long half-life of 58.9±0.3 y [2] of the 44Ti assures a constant and long lasting production of the daughter nuclide. Here we present a gas phase separation method of scandium from titanium via thermal release in vacuum. Titanium foils were irradiated with 40Ar to produce scandium in multinucleon transfer reactions. Another production reaction used was the irradiation of titanium by neutrons from the SINQ neutron source at the Paul Scherrer Institute PSI. The titanium metal foils containing 44mSc and 46Sc were heated up for time periods of 15 and 60 min to temperatures between 900 and 1500 °C in vacuum. Thus release properties of scandium from titanium under these conditions were studied. The released scandiumwas collected on tantalum foils and could be rinsed of with concentrated nitric acid resulting in carrier free scandium nitrate solutions. From the experimental results optimum release conditions are suggested.
| Original language | English |
|---|---|
| Pages (from-to) | 193-196 |
| Number of pages | 4 |
| Journal | Radiochimica Acta |
| Volume | 99 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 2011 |
| Externally published | Yes |
Funding
Acknowledgment. This work was supported by the Swiss National Science Foundation (grant: 200020-117671/1). The authors thank the staff of the PSI Philips Cyclotron for providing stable and intense beams of argon.
Keywords
- Diffusion
- Scandium
- Thermal release
- Titanium