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Microscale radiosynthesis, preclinical imaging and dosimetry study of [ 18 F]AMBF 3 -TATE: A potential PET tracer for clinical imaging of somatostatin receptors.

BACKGROUND: Peptides labeled with positron-emitting isotopes are emerging as a versatile class of compounds for the development of highly specific, targeted imaging agents for diagnostic imaging via positron-emission tomography (PET) and for precision medicine via theranostic applications. Despite the success of peptides labeled with gallium-68 (for imaging) or lutetium-177 (for therapy) in the clinical management of patients with neuroendocrine tumors or prostate cancer, there are significant advantages of using fluorine-18 for imaging. Recent developments have greatly simplified such labeling: in particular, labeling of organotrifluoroborates via isotopic exchange can readily be performed in a single-step under aqueous conditions and without the need for HPLC purification. Though an automated synthesis has not yet been explored, microfluidic approaches have emerged for 18 F-labeling with high speed, minimal reagents, and high molar activity compared to conventional approaches. As a proof-of-concept, we performed microfluidic labeling of an octreotate analog ([18 F]AMBF3 -TATE), a promising 18 F-labeled analog that could compete with [68 Ga]Ga-DOTATATE with the advantage of providing a greater number of patient doses per batch produced.

METHODS: Both [18 F]AMBF3 -TATE and [68 Ga]Ga-DOTATATE were labeled, the former by microscale methods adapted from manual labeling, and were imaged in mice bearing human SSTR2-overexpressing, rat SSTR2 wildtype, and SSTR2-negative xenografts. Furthermore, a dosimetry analysis was performed for [18 F]AMBF3 -TATE.

RESULTS: The micro-synthesis exhibited highly-repeatable performance with radiochemical conversion of 50 ± 6% (n = 15), overall decay-corrected radiochemical yield of 16 ± 1% (n = 5) in ~40 min, radiochemical purity >99%, and high molar activity. Preclinical imaging with [18 F]AMBF3 -TATE in SSTR2 tumor models correlated well with [68 Ga]Ga-DOTATATE. The favorable biodistribution, with the highest tracer accumulation in the bladder followed distantly by gastrointestinal tissues, resulted in 1.26 × 10-2  mSv/MBq maximal estimated effective dose in human, a value lower than that reported for current clinical 18 F- and 68 Ga-labeled compounds.

CONCLUSIONS: The combination of novel chemical approaches to 18 F-labeling and microdroplet radiochemistry have the potential to serve as a platform for greatly simplified development and production of 18 F-labeled peptide tracers. Favorable preclinical imaging and dosimetry of [18 F]AMBF3 -TATE, combined with a convenient synthesis, validate this assertion and suggest strong potential for clinical translation.

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