Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications

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Kalot, Ghadir | Godard, Amélie | Busser, Benoît | Pliquett, Jacques | Broekgaarden, Mans | Motto-Ros, Vincent | Wegner, Karl David | Resch-Genger, Ute | Köster, Ulli | Denat, Franck | Coll, Jean-Luc | Bodio, Ewen | Goze, Christine | Sancey, Lucie

Edité par CCSD ; MDPI -

International audience. Boron neutron capture therapy (BNCT) is a radiotherapeutic modality based on the nuclear capture of slow neutrons by stable 10 B atoms followed by charged particle emission that inducing extensive damage on a very localized level (<10 µm). To be efficient, a sufficient amount of 10 B should accumulate in the tumor area while being almost cleared from the normal surroundings. A water-soluble aza-boron-dipyrromethene dyes (BODIPY) fluorophore was reported to strongly accumulate in the tumor area with high and BNCT compatible Tumor/Healthy Tissue ratios. The clinically used 10 B-BSH (sodium borocaptate) was coupled to the water-soluble aza-BODIPY platform for enhanced 10 B-BSH tumor vectorization. We demonstrated a strong uptake of the compound in tumor cells and determined its biodistribution in mice-bearing tumors. A model of chorioallantoic membrane-bearing glioblastoma xenograft was developed to evidence the BNCT potential of such compound, by subjecting it to slow neutrons. We demonstrated the tumor accumulation of the compound in real-time using optical imaging and ex vivo using elemental imaging based on laser-induced breakdown spectroscopy. The tumor growth was significantly reduced as compared to BNCT with 10 B-BSH. Altogether, the fluorescent aza-BODIPY/ 10 B-BSH compound is able to vectorize and image the 10 B-BSH in the tumor area, increasing its theranostic potential for efficient approach of BNCT.

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