A Bis(Aquated) Mn(II)-Based MRI Contrast Agent with a Rigid Hydroquinazoline Unit: Synthesis, Characterization, and in Vivo MR Imaging Study

Since the finding of nephrogenic systemic fibrosis (NFS) in patients with renal impairment and the long-term accumulation of Gd­(III) ions in the central nervous system, the search for nongadolinium ion-based MRI contrast agents made of nutrient metal ions has drawn paramount attention. In this cont...

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Published inACS applied bio materials Vol. 7; no. 3; pp. 1831 - 1841
Main Authors Mallik, Riya, Saha, Muktashree, Sarmah, Amrit, Singh, Vandna, Mohan, Hari, Bhat, Priyanka, Kumaran, S. Senthil, Mukherjee, Chandan
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 18.03.2024
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ISSN2576-6422
2576-6422
DOI10.1021/acsabm.3c01236

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Summary:Since the finding of nephrogenic systemic fibrosis (NFS) in patients with renal impairment and the long-term accumulation of Gd­(III) ions in the central nervous system, the search for nongadolinium ion-based MRI contrast agents made of nutrient metal ions has drawn paramount attention. In this context, the development of Mn­(II)-based MRI contrast agents has been a subject of interest for the last few decades. Herein, we report a pentadentate ligand (Li2[BenzPic2]) composed of two picolinate moieties and a rigid 1,2,3,4-tetrahydroquinazoline unit and the corresponding bis­(aquated) Mn­(II) complex (Complex 1). The complex exhibited high thermodynamic stability (log K cond = 11.62) and kinetic inertness similar to that of the clinically approved Gd­(III)-based contrast agent Magnevist. Complex 1 exerted longitudinal relaxivity (r 1) of 5.32 mM–1 s–1 at 1.41 T, 37 °C, pH 7.4, and it increased by 3.6-fold in the presence of serum albumin protein, confirming a substantial rigidifying interaction (albumin association constant K A = 1.66 × 103 M–1) between the protein and the amphiphilic (log P = −0.45) contrast agent. An intravenous dose of 0.08 mmol/kg in a healthy mouse, excellent MRI signal intensity enhancement in the vasculature of the mouse liver, and brightened images of the gallbladder, kidney, and liver were realized.
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ISSN:2576-6422
2576-6422
DOI:10.1021/acsabm.3c01236