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Harnessing the Bioorthogonal Inverse Electron Demand Diels-Alder Cycloaddition for Pretargeted PET Imaging
Published on: February 3, 2015
Advances in GPCR-Targeted PET Radiotracer Patents (2020-2025).
Rebecca Ferrisi1, Clara Mocchetti1, Alessia Cazzaniga1
1Department of Pharmaceutical Sciences, Medicinal Chemistry Section "Pietro Pratesi", University of Milan, Via L. Mangiagalli 25, 20133 Milan, Italy.
Patent analysis reveals G protein-coupled receptor (GPCR)-targeted positron emission tomography (PET) radiotracers are advancing diagnostics. Innovations focus on oncology and central nervous system disorders, expanding theranostic potential.
Area of Science:
- Molecular Imaging
- Radiochemistry
- Pharmacology
Background:
- Positron emission tomography (PET) enables non-invasive in vivo imaging of biological processes.
- G protein-coupled receptors (GPCRs) are key targets for PET radiotracers due to their disease relevance.
- Radiotracers must exhibit high affinity and selectivity for their molecular targets.
Purpose of the Study:
- To review patents (2020-2025) on GPCR-targeted PET radiotracers.
- To analyze design strategies, radionuclide choices, and translational applications.
- To cover oncology, CNS disorders, and inflammatory diseases.
Main Methods:
- Patent literature analysis (2020-2025).
- Focus on GPCR-targeted PET radiotracers.
- Categorization by disease area and design approach.
Main Results:
- Most tracers adapt existing ligands for imaging.
- Oncology patents favor peptide/metal-chelator platforms for theranostics.
- CNS tracers use small molecules optimized for blood-brain barrier penetration.
- Emerging strategies target GPCR signaling states, not just binding sites.
Conclusions:
- GPCR-targeted PET tracers are established diagnostic tools.
- Patent trends show expanding clinical utility and translational research applications.
- Theranostic strategies incorporating GPCR tracers are developing across diseases.
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