Abstract

The rapid increase in applications of scandium isotopes in nuclear medicine requires new efficient production routes for these radioisotopes. Recently, irradiations of calcium in cyclotrons by α, deuteron, and proton beams have been used. Therefore, effective post-irradiation separation and preconcentration of the radioactive scandium from the calcium matrix are important to obtain the pure final product in a relatively small volume. Nobias resin was used as a sorbent for effective separation of 44Sc from calcium targets. Separation was performed at pH 3 using a column containing 10 mg of resin. Scandium was eluted with 100 μL of 2 mol L−1 HCl. Particular attention was paid to the reduction of calcium concentration, presence of metallic impurities, robustness and simple automation. 44Sc was separated with 94.9 ± 2.8% yield, with results in the range of 91.7–99.0%. Purity of the eluate was confirmed with ICP-OES determination of metallic impurities and >99% chelation efficiency with DOTATATE, followed by >36 h radiochemical stability of the complex. A wide range of optimal conditions and robustness to target variability and suspended matter facilitates the proposed method in automatic systems for scandium isotope separation and synthesis of scandium-labeled radiopharmaceuticals.

Highlights

  • Due to their specific properties, interest in the positron-emitting scandium isotopes as supplementary Positron Emission Tomography (PET) isotopes has recently been observed. Sc (t1/2 = 3.89 h, branching ratio β+ : 88%)and Sc (t1/2 = 3.97 h, branching ratio β+ : 94.3%) are good alternatives to 68 Ga, as they use similar complexing mechanisms

  • DOTA-octapeptides are a group of PET tracers that bind to somatostatin receptors (SST) that are over-expressed on the neuroendocrine tumor (NET) cells

  • 44 Sc was produced in reactions induced by 15 MeV protons

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Summary

Introduction

44 Sc (t1/2 = 3.97 h, branching ratio β+ : 94.3%) are good alternatives to 68 Ga, as they use similar complexing mechanisms. Their half-lives are almost four times longer, which promotes applications for imaging processes, having slower pharmacokinetcs profiles. DOTA-octapeptides are a group of PET tracers that bind to somatostatin receptors (SST) that are over-expressed on the neuroendocrine tumor (NET) cells. Imaging of neuroendocrine tumors [1,2] exhibiting overexpression of somatostatin receptor type 2 (SSTR2) was promisingly demonstrated in some clinical and preclinical studies with somatostatine analogues [3,4,5].

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