Drug intelligence / Profile preview

fludeoxyglucose F18

Development stage
Approved
Lead developer
Washington University School of Medicine
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Fludeoxyglucose F18 (18F-FDG) is a positron-emitting radiopharmaceutical and glucose analog used for diagnostic PET imaging. It is transported into cells by glucose transporters (primarily GLUT1 and GLUT3) and subsequently phosphorylated by hexokinase into 18F-FDG-6-phosphate. Because it lacks the 2-hydroxyl group necessary for further glycolysis, the molecule becomes metabolically trapped within the cell, allowing for the visualization of metabolic activity. In the context of abdominal aortic aneurysm (AAA) research at Washington University School of Medicine, 18F-FDG is utilized to visualize and quantify vascular wall inflammation, specifically the metabolic activity of macrophages. This imaging approach, often combined with finite element analysis (FEA), aims to improve the prediction of aneurysm expansion and rupture risk beyond simple diameter measurements.

Brand names
Flucis
Other names
2-deoxy-2-[18F]fluoro-D-glucosefludeoxyglucose (18F)fluorodeoxyglucose F18
02

Targets

GLUT1 (Glucose transporter 1)HK2 (Hexokinase Type II)

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