Novel bifunctional DATA chelator for quick access to site-directed PET Ga-radiotracers: preclinical proof-of-principle with [Tyr]octreotide.

Molecular imaging of tumors with the PET radionuclide Ga has gained momentum in clinical oncology due to the expanding availability of commercial Ge/Ga-generators in combination with state-of-the-art PET/CT and PET/MRI hybrid imaging systems. Concurrently, interesting peptide-based or small-size vectors have been developed for theranostic use in cancer patients. Owing to the short half-life of Ga (t = 67.7 min) and the sensitivity of many targeting biomolecules, labeling and kit reconstitution in mild conditions allowing for quick access to ready-for-injection PET-tracers are highly desirable. The novel DATA ((6-pentanoic acid)-6-(amino)methy-1,4-diazepinetriacetate) chelator previously showing promising qualities for kit type labeling, was coupled to TOC ([Tyr]octreotide). We herein report results from a first proof-of-principle study directly comparing Ga-DATA-TOC with the well-established Ga-DOTA-TOC in a series of preclinical models. Both analogs were shown to be sst-preferring and specifically internalized in AR42J and HEK293-hsst cells, with Ga-DOTA-TOC internalizing faster in both cell lines. Similarly, after injection in mice bearing either AR42J or HEK293-hsst tumors, both tracers efficiently and specifically localized in the implants. Whereas Ga-DOTA-TOC exhibited higher tumor values, Ga-DATA-TOC cleared faster from background tissues. These findings support the suitability of the newly introduced bifunctional chelator DATA as a reliable, quick and convenient means for labeling medically relevant vectors with the PET radiometal Ga.