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.
Supplementary materials
Title
RT 01SI RTripier final 2020
Description
Actions
Title
RT01 Manuscript RTripier final 2020
Description
Actions
Title
RT 01SI RTripier final 2020
Description
Actions