[18F]Atorvastatin: synthesis of a potential molecular imaging tool for the assessment of statin-related mechanisms of action

• Published in: EJNMMI research Vol. 10; no. 1; p. 34
• Main Authors: Clemente, Gonçalo S., Rickmeier, Jens, Antunes, Inês F., Zarganes-Tzitzikas, Tryfon, Dömling, Alexander, Ritter, Tobias, Elsinga, Philip H.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 15.04.2020; Springer Nature B.V; SpringerOpen
• Subjects: 18F-deoxyfluorination; Additives; Aorta; Atherosclerosis; Atorvastatin; Autoradiography; Bioaccumulation; Cardiac Imaging; Cell membranes; Chemical synthesis; Cholesterol; Fluorine-18; HMG-CoA; Imaging; Labelling; Lipids; Medicine; Medicine & Public Health; Nuclear Medicine; Oncology; Optimization; Original Research; Orthopedics; Positron emission tomography; Precursors; Radiology; Reductases; Ruthenium compounds; Statins; Atorvastatin; HMG-CoA; Fluorine-18; Positron emission tomography; Statins; F-deoxyfluorination; 18F-deoxyfluorination
• ISSN: 2191-219X; 2191-219X
• DOI: 10.1186/s13550-020-00622-4

Background Statins are lipid-lowering agents that inhibit cholesterol synthesis and are clinically used in the primary and secondary prevention of cardiovascular diseases. However, a considerable group of patients does not respond to statin treatment, and the reason for this is still not completely understood. [ 18 F]Atorvastatin, the 18 F-labeled version of one of the most widely prescribed statins, may be a useful tool for statin-related research. Results [ 18 F]Atorvastatin was synthesized via an optimized ruthenium-mediated late-stage 18 F-deoxyfluorination. The defluoro-hydroxy precursor was produced via Paal-Knorr pyrrole synthesis and was followed by coordination of the phenol to a ruthenium complex, affording the labeling precursor in approximately 10% overall yield. Optimization and automation of the labeling procedure reliably yielded an injectable solution of [ 18 F]atorvastatin in 19% ± 6% (d.c.) with a molar activity of 65 ± 32 GBq·μmol −1 . Incubation of [ 18 F]atorvastatin in human serum did not lead to decomposition. Furthermore, we have shown the ability of [ 18 F]atorvastatin to cross the hepatic cell membrane to the cytosolic and microsomal fractions where HMG-CoA reductase is known to be highly expressed. Blocking assays using rat liver sections confirmed the specific binding to HMG-CoA reductase. Autoradiography on rat aorta stimulated to develop atherosclerotic plaques revealed that [ 18 F]atorvastatin significantly accumulates in this tissue when compared to the healthy model. Conclusions The improved ruthenium-mediated 18 F-deoxyfluorination procedure overcomes previous hurdles such as the addition of salt additives, the drying steps, or the use of different solvent mixtures at different phases of the process, which increases its practical use, and may allow faster translation to clinical settings. Based on tissue uptake evaluations, [ 18 F]atorvastatin showed the potential to be used as a tool for the understanding of the mechanism of action of statins. Further knowledge of the in vivo biodistribution of [ 18 F]atorvastatin may help to better understand the origin of off-target effects and potentially allow to distinguish between statin-resistant and non-resistant patients.