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Background Astatine-211 is currently considered as one of the most promising alpha particle emit- ters for application in targeted alpha therapy (TA T) of cancers (Eychenne et al. 2021),
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The isotope astatine-211 (211 At) is of considerable interest for the emerging cancer treatment modality of Targeted Alpha Therapy (TAT) [1, 2]. Astatine-211 shows a 100 % alpha
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The α-emitter astatine-211 (211 At) has experienced increased interest due to its favorable decay properties. As a result, various 211 At-astatination strategies have been developed to address
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Even though most research groups are merely adapting 211 At to existing 177 Lu or 225 Ac analogs, some newcomers and startups are genuinely considering the advantages of 211 At over
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Astatine-211 can be produced in medium energy cyclotrons by alpha particle bombardment of natural bismuth. The produced astatine is then commonly recovered from the
Abstract 211 At is a promising nuclide among various α-emitters for targeted α therapy. In order to expand its accessibility, we''re creating a 211 Rn– 211 At generator. Using N
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This document provides a comprehensive overview of the history of Astatine-211''s discovery, its primary synthesis route via the 209Bi(α, 2n)211At nuclear reaction, and detailed experimental protocols for its
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