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211At-Rh(16-S4-diol) as a starting complex for preparing an astatine-labeled radiopharmaceutical

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Abstract

A new procedure for preparing an 211At-labeled radiopharmaceutical is suggested. The 211At anion forms a strong bond with the Rh3+ cation incorporated in the complex with a thiother ligand, 1,5,9,13-tetrathiacyclohexadecane-3,11-diol (16-S4-diol). The reaction conditions are optimized with 131I as astatine analog. The complexes are studied by paper electrophoresis, ion exchange, and thin-layer chromatography. The kinetics of the addition of the 131I anion to Rh(16-S4-diol) and the dependence of the yield of the forming complex 131I-Rh(16-S4-diol) on the temperature, solution acidity, and reactant concentrations are examined. Taking into account the results obtained, the complex 211At-Rh(16-S4-diol) is prepared by adding astatide (211 At) to equivalent amounts of RhCl3 and the tetrathioether (16-S4-diol). the behavior of the astatine complex is studied.

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Original Russian Text © Yu.V. Norseev, A. Bilewicz, M. Pruszynski, 2008, published in Radiokhimiya, 2008, Vol. 50, No. 2, pp. 178–182.

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Norseev, Y.V., Bilewicz, A. & Pruszynski, M. 211At-Rh(16-S4-diol) as a starting complex for preparing an astatine-labeled radiopharmaceutical. Radiochemistry 50, 208–212 (2008). https://doi.org/10.1134/S1066362208020239

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  • DOI: https://doi.org/10.1134/S1066362208020239

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