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Automated Production of [<sup>68</sup>Ga]Ga-Desferrioxamine B on Two Different Synthesis Platforms
oleh: Martin Kraihammer, Miloš Petřík, Christine Rangger, Michael Gabriel, Hubertus Haas, Bernhard Nilica, Irene Virgolini, Clemens Decristoforo
Format: | Article |
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Diterbitkan: | MDPI AG 2024-09-01 |
Deskripsi
<b>Background/Objectives:</b> PET imaging of bacterial infection could potentially provide added benefits for patient care through non-invasive means. [<sup>68</sup>Ga]Ga-desferrioxamine B—a radiolabelled siderophore—shows specific uptake by human-pathogenic bacteria like <i>Staphylococcus aureus</i> or <i>Pseudomonas aeruginosa</i> and sufficient serum stability for clinical application. In this report, we present data for automated production of [<sup>68</sup>Ga]Ga-desferrioxamine B on two different cassette-based synthesis modules (Modular-Lab PharmTracer and GRP 3V) utilising commercially obtainable cassettes together with a licensed <sup>68</sup>Ge/<sup>68</sup>Ga radionuclide generator. <b>Methods:</b> Quality control, including the determination of radiochemical purity, as well as a system suitability test, was set up via RP-HPLC on a C18 column. The two described production processes use an acetic acid/acetate buffer system with ascorbic acid as a radical scavenger for radiolabelling, yielding ready-to-use formulations with sufficient activity yield. <b>Results:</b> Batch data analysis demonstrated radiochemical purity of >95% by RP-HPLC combined with ITLC and excellent stability up to 2 h after synthesis. Specifications for routine production were set up and validated with four masterbatches for each synthesis module. <b>Conclusions:</b> Based on this study, an academic clinical trial for imaging of bacterial infection was initiated. Both described synthesis methods enable automated production of [<sup>68</sup>Ga]Ga-desferrioxamine B in-house with high reproducibility for clinical application.