The purpose of the present study is to design and synthesis of novel macrocyclic Mn2+ complex as an alternative to the well-established Gd3+ based chelates for use as an inflammation targeting MR imaging agent. This new complex exhibits higher r1 relaxivity (2.32 mM−1 s−1) than clinically approved Mn-DPDP® (1.6 mM−1 s−1) at 4.7 T. T1-weighted MR coronal images display strong signal enhancement in liver, heart, gallbladder and kidney. In an inflammatory mouse model, it shows greater inflammatory tissues detection with in a clinical dose.
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