Abstract
Radioarsenic labelled radiopharmaceuticals could be a valuable asset to Positron Emission Tomography (PET). In particular, the long half-lives of 72As (T1/2=26 h) and 74As (T1/2=17.8 d) allow to investigate slow physiological or metabolical processes, like the enrichment and distribution of antibodies in tumor tissue. This work describes the direct production of no-carrier-added (nca) arsenic isotopes*As, with*=71, 72, 73, 74 or 77, the reaction to [*As]AsI3 and its radiochemical separation from the irradiated solid germanium oxide via polystyrene-based solid-phase extraction. The germanium oxide target, irradiated at a cyclotron or a nuclear reactor, is dissolved in concentrated HF and Ge is separated almost quantitatively (99.97%) as [GeF6]2-. [*As]AsI3 is formed by addition of potassium iodide. The radiochemical separation yield for arsenic is >90%. [*As]AsI 3 is a versatile radioarsenic labelling synthon.
Original language | English (US) |
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Pages (from-to) | 343-351 |
Number of pages | 9 |
Journal | Applied Radiation and Isotopes |
Volume | 63 |
Issue number | 3 |
DOIs | |
State | Published - Sep 2005 |
Keywords
- As-71
- As-72
- As-73
- As-74
- As-77
- Radiochemical separation
- Solid-phase extraction
ASJC Scopus subject areas
- Radiation