Answers are grounded in this paper and cite their sources.
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 Gd3+ complex. The amine group is accessible and easy to functionalize; in particular, the possibility of tuning its pKAH 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.
No takes yet. Share an insight, caveat, or question.
Giovenzana et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: