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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

Truc Pham, Ingebjørg N. Hungnes, Charlotte Rivas, Julie Cleaver, George Firth, Philip J. Blower, Jane Sosabowski, Gary Cook, Lefteris Livieratos, Jennifer D. Young, Paul G. Pringle, Michelle Ma

2024Journal of Nuclear Medicine15 citationsDOIOpen Access PDF

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&nbsp;vitro, in prostate cancer cells, and in&nbsp;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.

Topics & Concepts

BiodistributionChemistryGlutamate carboxypeptidase IIProstate cancerRadiochemistryCancerIn vitroMedicineBiochemistryInternal medicineRadiopharmaceutical Chemistry and ApplicationsPeptidase Inhibition and AnalysisProstate Cancer Treatment and Research