The interposition of a cleavable linkage by enzymes on the renal brush border membrane constitutes a promising approach for reducing the renal radioactivity levels of radiolabeled low-molecular-weight antibody fragments and constructs (LMW Abs). Herein, we applied the molecular design to 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)-based reagents for radiotheranostic applications with trivalent radiometals. DOTA or a derivative thereof was conjugated to a Fab through an FGK linkage ([In]In-DO3ABu-Bn-FGK-Fab or [In]In-DOTA-Bn-FGK-Fab). When injected into mice, both generated radiometabolites, [In]In-DO3ABu-Bn-F and [In]In-DOTA-Bn-F, by the angiotensin-converting enzyme at similar rates. Both exhibited significantly lower renal radioactivity levels than a In-labeled Fab prepared by the conventional procedure ([In]In-DOTA-Bn-SCN-Fab). The different elimination rates of each radiometabolite from the kidney significantly affected the renal radioactivity levels. [In]In-DO3ABu-Bn-FGK-Fab preferentially reduced the renal localization without impairing tumor accumulation. These findings would pave the way for developing a DOTA-based radiotheranostic platform for LMW Abs bearing cleavable linkers for renal brush border enzymes.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350918 | PMC |
http://dx.doi.org/10.1021/acs.jmedchem.3c00258 | DOI Listing |
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