In Vivo Albumin-Binding of a C-Functionalized Cyclam Platform for 64Cu-PET/CT Imaging in Breast Cancer Model

27 July 2020, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

In the aim to design small molecules capable of binding in vivo to albumin to form bioconjugates, a second generation GluCAB derivative(Glucose-Chelator-Albumin Bioconjugate) has been synthesized and studied for in vivo 64Cu-PET/CT imaging in breast cancer mice models together with its first-generation analogue. This series of radioligands - also capable of complexing therapeutic isotopes and therefore classified as theranostic agents - are working on the principle of tumor targeting through the Enhanced Permeability and Retention (EPR) effect as well as glucose metabolism.

Keywords

macrocyclic chemistry
Radiopharmaceuticals
Copper-64
albumin-binding molecules
Cancer Theranostics
tumor targeting

Supplementary materials

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RT 01SI RTripier final 2020
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RT01 Manuscript RTripier final 2020
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RT 01SI RTripier final 2020
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