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[摘要]：Gallium-68 is a generator-produced radionuclide for positron emission tomography (PET) that is being increasingly used for radiolabeling of tumor-targeting peptides. Compounds [Ga-68]3 and [Ga-68]6 are high-affinity urea-based inhibitors of the prostate-specific membrane antigen (PSMA) that were synthesized in decay-uncorrected yields ranging from 60% to 70% and radiochemical purities of more than 99%. Compound [Ga-68]3 demonstrated 3.78 +/- 0.90% injected dose per gram of tissue (%ID/g) within PSMA + PIP tumor at 30 min postinjection, while [Ga-68]6 showed a 2 h PSMA + PIP tumor uptake value of 3.29 +/- 0.77 %ID/g. Target (PSMA + PIP) to nontarget (PSMA - flu) ratios were 4.6 and 18.3, respectively, at those time points. Both compounds delineated tumor clearly by small animal PET. The urea series of imaging agents for PSMA can be radiolabeled with Ga-68, a cyclotron-free isotope useful for clinical PET studies, with maintenance of target specificity. |
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