Drug intelligence / Profile preview

18F-FDG-University of California, Davis

Development stage
Unknown
Lead developer
University of California, Davis
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

18F-FDG-University of California, Davis refers to the specific application and research protocols involving 18F-fluorodeoxyglucose (18F-FDG) conducted at the University of California, Davis. 18F-FDG is a radiolabeled glucose analog used as a positron emission tomography (PET) tracer. It is transported into cells by glucose transporters (GLUT) and subsequently phosphorylated by the enzyme hexokinase into 18F-FDG-6-phosphate. Because this molecule cannot undergo further glycolysis, it becomes metabolically trapped within cells, allowing for the visualization and quantification of glucose metabolism. Researchers at UC Davis are utilizing the EXPLORER total-body PET/CT system to develop single-tracer multiparametric imaging solutions. This methodology aims to extract both quantitative blood flow (perfusion) and glucose metabolic rates from a single dynamic 18F-FDG PET scan using advanced tracer kinetic modeling, primarily for investigating cardiovascular diseases and myofascial pain.

Other names
18F-fluorodeoxyglucosefludeoxyglucose F 182-deoxy-2-[18F]fluoro-D-glucoseFluorodeoxyglucose F18
02

Targets

GLUT1 (Glucose transporter 1)HK2 (Hexokinase Type II)SLC2A3 (Glucose transporter type 3)

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