Gd‐Aminoethyl‐DO3A Complexes: A Novel Class of pH‐Sensitive MRI Contrast Agents

Abstract

Abstract Molecular imaging relies on the availability of imaging probes designed to modify their efficiency in the presence of a specific parameter, among which pH is one of the most investigated. Introduction of an aminoethyl moiety into the well‐known DO3A platform imparts the desired pH sensitivity to the corresponding Gd 3+ complex. The amine group is accessible and easy to functionalize; in particular, the possibility of tuning its p K AH through N ‐substitution makes it a good pH‐responsive functionality to access a novel class of tailored pH‐sensitive MRI contrast agents. This was demonstrated by a relaxometric study on a functionalized Gd‐DO3A complex bearing a simple primary amine group and comparison with the results of the corresponding N , N ‐dimethyl analogue.