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. 2022 Nov 8;50(3):849–858. doi: 10.1007/s00259-022-06016-z

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a Biodistribution of [²¹¹At]PSMA5 and [²¹¹At]PSMA6 in normal ICR mice. b Biodistribution of [²¹¹At]PSMA1, [²¹¹At]PSMA5, and [²¹¹At]PSMA6 in LNCaP xenograft model (NOD/SCID mice). Data are expressed as mean ± standard deviation. Total excretion (%ID) of [²¹¹At]PSMA1 and [²¹¹At]PSMA5 were 0.49 ± 0.37% and 8.26 ± 5.00 % at 3h and 14.7 ± 10.0% and 15.33 ± 6.3% at 24h in the urine, and 14.0 ± 4.8% and 35.2 ± 9.2% at 24h in the feces, respectively. Total excretion (%ID) of [²¹¹At]PSMA6 at 24h were 6.20 ± 1.51% in the urine, and 9.78 ± 0.79% in the feces, respectively