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Receptor-Targeted Peptide Conjugates Based on Diphosphines Enable Preparation of<sup>99m</sup>Tc and<sup>188</sup>Re Theranostic Agents for Prostate Cancer

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2024

Year

Abstract

Benchtop <sup>99</sup>Mo/<sup>99m</sup>Tc and <sup>188</sup>W/<sup>188</sup>Re generators enable economical production of molecular theranostic <sup>99m</sup>Tc and <sup>188</sup>Re radiopharmaceuticals, provided that simple, kit-based chemistry exists to radiolabel targeting vectors with these radionuclides. We have previously described a diphosphine platform that efficiently incorporates <sup>99m</sup>Tc into receptor-targeted peptides. Here, we report its application to label a prostate-specific membrane antigen (PSMA)-targeted peptide with <sup>99m</sup>Tc and <sup>188</sup>Re for diagnostic imaging and systemic radiotherapy of prostate cancer. <b>Methods:</b> Two diphosphine-dipeptide bioconjugates, DP1-PSMAt and DP2-PSMAt, were formulated into kits for radiolabeling with <sup>99m</sup>Tc and <sup>188</sup>Re. The resulting radiotracers were studied in vitro, in prostate cancer cells, and in vivo in mouse xenograft models, to assess similarity of uptake and biodistribution for each <sup>99m</sup>Tc/<sup>188</sup>Re pair of agents. <b>Results:</b> Both DP1-PSMAt and DP2-PSMAt could be efficiently radiolabeled with <sup>99m</sup>Tc and <sup>188</sup>Re using kit-based methods to furnish the isostructural compounds M-DP1-PSMAt and M-DP2-PSMAt (M = [<sup>99m</sup>Tc]Tc, [<sup>188</sup>Re]Re). All <sup>99m</sup>Tc/<sup>188</sup>Re radiotracers demonstrated specific uptake in PSMA-expressing prostate cancer cells, with negligible uptake in prostate cancer cells that did not express PSMA or in which PSMA uptake was blocked. M-DP1-PSMAt and M-DP2-PSMAt also exhibited high tumor uptake (18-30 percentage injected dose per gram at 2 h after injection), low retention in nontarget organs, fast blood clearance, and excretion predominantly via a renal pathway. Importantly, each pair of <sup>99m</sup>Tc/<sup>188</sup>Re radiotracers showed near-identical biologic behavior in these experiments. <b>Conclusion:</b> We have prepared and developed novel pairs of isostructural PSMA-targeting <sup>99m</sup>Tc/<sup>188</sup>Re theranostic agents. These generator-based theranostic agents have potential to provide access to the benefits of PSMA-targeted diagnostic imaging and systemic radiotherapy in health care settings that do not routinely have access to either reactor-produced <sup>177</sup>Lu radiopharmaceuticals or PET/CT infrastructure.

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