PFKFB3, a glycolysis-related enzyme upregulated in inflammatory conditions and angiogenesis, is an emerging target for diagnosis and therapy of atherosclerosis. The fluorinated phenoxindazole [F] was synthesized, radiolabeled in 17 ± 5% radiochemical yield and >99% radiochemical purity, and formulated for preclinical PET/CT imaging in mice. stability analysis showed no significant metabolite formation. Biodistribution studies showed high blood pool activity and slow hepatobiliary clearance. Significant activity was detected in the lung 2 h postinjection (pi) (11.0 ± 1.5%ID/g), while at 6 h pi no pulmonary background was observed. autoradiography at 6 h pi showed significant high uptake of [F] in the arch region and brachiocephalic artery of atherosclerotic mice, and no uptake in control mice, matching plaques distribution seen by lipid staining along with PFKFB3 expression seen by immunofluorescent staining. PET scans showed higher aortic region uptake of [F] in atherosclerotic ApoEFbn1 than in control mice (0.78 ± 0.05 vs 0.44 ± 0.09%ID/g). [F] was detected in aortic arch and brachiocephalic artery of ApoE (with moderate atherosclerosis) and ApoEFbn1 (with severe, advanced atherosclerosis) mice, suggesting this tracer may be useful for the noninvasive detection of atherosclerotic plaques .

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236280PMC
http://dx.doi.org/10.1021/acsmedchemlett.9b00677DOI Listing

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