Abstract
Samarium-153 is a promising radionuclide for targeted radionuclide therapy (TRNT) because of its highly favorable decay characteristics. 153Sm has a half-life of 1.93 days and emits Beta- particles (705 keV, 635 keV) which are suitable for therapy. 153Sm also emits Y photons (103 keV) with characteristics that allow SPECT imaging, making 153Sm a high-potential theranostic radioisotope.
The full potential of 153Sm is currently not being exploited because of the limited specific activity available as a result of its carrier-added production route (152Sm(n,Y)153Sm). In our previous work, we tried to remedy this by applying mass separation after the neutron activation to produce 153Sm with a much higher specific activity [1]. In this study, we use high specific activity (HSA) samarium-153 for the radiolabeling of the somatostatin analogue DOTA-TATE. This study
reports the radiolabeling and early biological evaluation of [153Sm] Sm-DOTA-TATE.
The full potential of 153Sm is currently not being exploited because of the limited specific activity available as a result of its carrier-added production route (152Sm(n,Y)153Sm). In our previous work, we tried to remedy this by applying mass separation after the neutron activation to produce 153Sm with a much higher specific activity [1]. In this study, we use high specific activity (HSA) samarium-153 for the radiolabeling of the somatostatin analogue DOTA-TATE. This study
reports the radiolabeling and early biological evaluation of [153Sm] Sm-DOTA-TATE.
| Original language | English |
|---|---|
| Pages (from-to) | S20 |
| Number of pages | 1 |
| Journal | Nuclear Medicine and Biology |
| Volume | 108-109 |
| Issue number | Supplement |
| DOIs | |
| State | Published - May 2022 |
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