A multimodal, β-amyloid-targeted contrast agent was synthesized and studied in vitro. The agent has a higher relaxivity than a clinically approved contrast agent and interacts with β-amyloid aggregates producing changes in relaxation rate and fluorescence emission.
S. M. Vithanarachchi and M. J. Allen, Chem. Commun., 2013, 49, 4148 DOI: 10.1039/C2CC36583A
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