sup 67/68^Ga-Labeling Agent That Liberates ^sup 67/68^Ga-NOTA-Methionine by Lysosomal Proteolysis of Parental Low Molecular Weight Polypeptides to Reduce Renal Radioactivity Levels

The renal localization of gallium-67 or gallium-68 (67/68Ga)-labeled low molecular weight (LMW) probes such as peptides and antibody fragments constitutes a problem in targeted imaging. Wu et al. previously showed that 67Ga-labeled S-2-(4-isothiocyanatobenzyl)-1,4,7-triazacyclononane-1,4,7-triacetic acid (SCN-Bz-NOTA)-conjugated methionine (67Ga-NOTA-Met) was rapidly excreted from the kidney in urine following lysosomal proteolysis of the parental 67Ga-NOTA-Bz-SCN-disulfide-stabilized Fv fragment (Bioconjugate Chem., (1997) 8, 365-369). In the present study, a new 67/68Ga-labeling reagent for LMW probes that liberates 67/68Ga-NOTA-Met was designed, synthesized, and evaluated using longer-lived 67Ga in order to reduce renal radioactivity levels. We employed a methionine-isoleucine (MI) dipeptide bond as the cleavable linkage. The amine residue of MI was coupled with SCN-Bz-NOTA for 67Ga-labeling, while the carboxylic acid residue of MI was derivatized to maleimide for antibody conjugation in order to synthesize NOTA-MI-Mal. A Fab fragment of the anti-Her2 antibody was thiolated with iminothiolane, and NOTA-MI-Mal was conjugated with the antibody fragment by maleimide-thiol chemistry. The Fab fragment was also conjugated with SCN-Bz-NOTA (NOTA-Fab) for comparison. 67Ga-NOTA-MI-Fab was obtained at radiochemical yields of over 95% and was stable in murine serum for 24 h. In the biodistribution study using normal mice, 67Ga-NOTA-MI-Fab registered significantly lower renal radioactivity levels from 1 to 6 h postinjection than those of 67Ga-NOTA-Fab. An analysis of urine samples obtained 6 h after the injection of 67Ga-NOTA-MI-Fab showed that the majority of radioactivity was excreted as 67Ga-NOTA-Met. In the biodistribution study using tumor-bearing mice, the tumor to kidney ratios of 67Ga-NOTA-MI-Fab were 4 times higher (6 h postinjection) than those of 67Ga-NOTA-Fab. Although further studies including the structure of radiometabolites and/or cleavable linkages are required, the results of the present study indicate that the current chemical design is applicable to the development of 67Ga-labeled Fabs for low renal radioactivity levels.