Pet Radiopharmaceuticals

Pet radiopharmaceuticals are positron-emitting, radiolabeled compounds used in positron emission tomography (PET) to visualize physiological processes in living organisms, supporting medical diagnosis and research. After administration, the tracer follows a biologically relevant pathway, and positron decay produces annihilation photons that PET detectors record in coincidence to reconstruct three-dimensional maps of tracer distribution. These images can reveal altered metabolism, receptor expression, perfusion, or other molecular changes before anatomical abnormalities become apparent. In medicine, PET radiopharmaceuticals support cancer detection and staging, neurological and cardiovascular assessment, treatment planning, and monitoring of therapeutic response.

Pet Radiopharmaceuticals - Related Videos

Research

JoVE EoE - Assay Techniques

Controlled Infusion of Radiopharmaceutical Agent Using a Peristaltic Pump

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2025

Source: Léa Rubira1, Hélène Sturer1, Louise Combette1, Sandra Santini1, Stéphane Renaud1, Cyril Fersing1,21Nuclear medicine department, Institut régional du Cancer de Montpellier (ICM), Univ Montpellier, 2IBMM, Univ Montpellier, CNRS, ENSCMThis video demonstrates the safe, controlled infusion of a radiopharmaceutical using a peristaltic pump with a dual-line cassette system. The setup includes connecting saline and infusion lines, positioning the shielded vial, and initiating simultaneous...

Simultaneous PET/MRI Imaging During Mouse Cerebral Hypoxia-ischemia

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Cited by 4 •

2015

The method presented here uses simultaneous positron emission tomography and magnetic resonance imaging. In the cerebral hypoxia-ischemia model, dynamic changes in diffusion and glucose metabolism occur during and after injury. The evolving and irreproducible damage in this model necessitates simultaneous acquisition if meaningful multi-modal imaging data are to be acquired.

Functional Imaging of Brown Fat in Mice with 18F-FDG micro-PET/CT

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Cited by 37 •

2012

A method of functional imaging of mouse brown adipose tissue (BAT) is described in which cold-stimulated uptake of 18F-Fluorodeoxyglucose (FDG) in BAT is non-invasively assessed with a standardized micro-PET/CT protocol. This method is robust and sensitive to detect differences in BAT activities in mouse models.

TSPO-PET/CT Imaging to Detect Infarct Formation in a Mouse Model of Ischemic Stroke

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2025

Source: Chaney, A. M., et.al. PET Imaging of Neuroinflammation Using [11C]DPA-713 in a Mouse Model of Ischemic Stroke. J. Vis. Exp. (2018). This video demonstrates a technique for in vivo imaging of neuroinflammation in a mouse model of ischemic stroke using a TSPO-specific radiotracer. Following injection, the radiotracer binds to TSPO, a protein located on the outer mitochondrial membrane and overexpressed in activated immune cells. A PET/CT scanner detects the radiotracer's distribution and...

Determining Glucose Metabolism Kinetics Using 18F-FDG Micro-PET/CT

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Cited by 15 •

2017

This study describes a protocol that uses 18F-FDG and positron emission tomography/computed tomography (PET/CT) imaging, together with kinetic modelling, to quantify the in vivo, real-time uptake of 18F-FDG into tissues.

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