Synthesis and preclinical evaluation of BOLD-100 radiolabeled with ruthenium-97 and ruthenium-103

• Published in: Dalton transactions : an international journal of inorganic chemistry Vol. 53; no. 13; pp. 631 - 64
• Main Authors: Happl, B, Balber, T, Heffeter, P, Denk, C, Welch, J. M, Köster, U, Alliot, C, Bonraisin, A.-C, Brandt, M, Haddad, F, Sterba, J. H, Kandioller, W, Mitterhauser, M, Hacker, M, Keppler, B. K, Mindt, T. L
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 26.03.2024
• Subjects: Autoradiography; Computed tomography; Medical imaging; Photon emission; Ruthenium isotopes; Transportation systems; Tumors
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/d4dt00118d

BOLD-100 (formerly IT-139, KP1339), a well-established chemotherapeutic agent, is currently being investigated in clinical trials for the treatment of gastric, pancreatic, colorectal, and bile duct cancer. Despite numerous studies, the exact mode of action is still the subject of discussions. Radiolabeled BOLD-100 could be a powerful tool to clarify pharmacokinetic pathways of the compound and to predict therapy responses in patients using nuclear molecular imaging prior to the therapy. In this study, the radiosyntheses of carrier-added (c.a.) [ 97/103 Ru]BOLD-100 were performed with the two ruthenium isotopes ruthenium-103 ( 103 Ru; β − , γ) and ruthenium-97 ( 97 Ru; EC, γ), of which in particular the latter isotope is suitable for imaging by single-photon emission computed tomography (SPECT). To identify the best tumor-to-background ratio for diagnostic imaging, biodistribution studies were performed with two different injected doses of c.a. [ 103 Ru]BOLD-100 (3 and 30 mg kg −1 ) in Balb/c mice bearing CT26 allografts over a time period of 72 h. Additionally, ex vivo autoradiography of the tumors (24 h p.i.) was conducted. Our results indicate that the higher injected dose (30 mg kg −1 ) leads to more unspecific accumulation of the compound in non-targeted tissue, which is likely due to an overload of the albumin transport system. It was also shown that lower amounts of injected c.a. [ 103 Ru]BOLD-100 resulted in a relatively higher tumor uptake and, therefore, a better tumor-to-background ratio, which are encouraging results for future imaging studies using c.a. [ 97 Ru]BOLD-100. Radiolabeling of the chemotherapeutic agent BOLD-100 with ruthenium-103 enables animal experiments with lower amounts of injected drug. This leads to a relatively higher tumor uptake and promising tumor-to-background ratio for future imaging studies.