Gallium-68 is a versatile radionuclide widely used in PET imaging for its short half-life and high-resolution capabilities, enabling applications in oncology, cardiology, and inflammatory disease research. Alfa Cytology provides comprehensive preclinical services, from 68Ga radiopharmaceutical development to in vivo imaging studies, supporting the advancement of innovative diagnostics and therapeutics.
Gallium-68 is a positron-emitting radionuclide widely valued in PET imaging due to its short half-life of approximately 68 minutes, which balances imaging time with patient safety by minimizing radiation exposure. This short half-life enables efficient imaging workflows, allowing for rapid data acquisition and minimizing delay between synthesis and imaging. Additionally, 68Ga provides high-resolution images due to its optimal positron emission energy, enhancing the clarity and sensitivity needed for precise disease localization. In recent years, the development of 68Ga-labeled drugs and imaging agents has expanded significantly, targeting a range of conditions in oncology, cardiology, and inflammatory diseases, among others.
Fig.1 The four main steps of the 68Ga-radiolabeling procedure. (Nelson BJB, et al., 2022)
More and more 68Ga-labeled compounds have been entering clinical trials, while clinical applications have already extended from oncology to cardiovascular diseases and inflammatory conditions. 68Ga also has an important role in the new discipline of theragnostic, which utilizes diagnostic and therapeutic functions and furthers precision medicine. Its capability for targeting specific molecular pathways has placed it as a key tool in future drug development.
Our services make provision in all aspects of development by various clients of 68Ga-labeled radiopharmaceuticals, imaging agents, and tracers. We provide specific solutions starting from early design to preclinical evaluation, including but not limited to the following.
We design 68Ga-labeled imaging agents and tracers to advance the development of diagnostics related to cancer, cardiovascular, neurodegenerative and inflammatory diseases. Our service encompasses ligand and tracer design, optimization up to radiolabeling.
Target Discovery for 68Ga-Radiopharmaceutical
Our extensive experience enables us to focus on a range of specific targets, such as PSMA, somatostatin receptors, HER2, dopamine receptors, amyloid beta plaques, TSPO, infection markers, angiotensin II receptors, and cardiac function markers.
Design and Optimization of 68Ga-Labeled Compounds
We design and synthesize efficient 68Ga-labeled compounds and ligands, focusing on the optimization of chelators toward enhanced stability and bioavailability.
Radiolabeling and Quality Control
Offering efficient68Ga radiolabeling services with comprehensive quality control, we ensure radiochemical purity, chemical purity, and radiolabel stability, adhering to the highest quality standards.
In Vitro/In Vivo Efficacy Evaluation
We provide binding studies, cellular uptake assays, biodistribution, and pharmacokinetic studies using small animal models. Our animal PET/SPECT imaging platform offers real-time visualization of tracer or drug biodistribution.
68Ga exhibits excellent coordination properties, allowing it to effectively bind with a variety of molecules to form stable complexes.
Utilizing high-resolution PET imaging, we deliver actionable data on in vivo targeting of 68Ga-labeled compounds, aiding drug discovery and disease research applications.
Alfa Cytology specialize in the development of state-of-the-art 68Ga radiopharmaceuticals, integrating efforts from radiochemistry laboratories to advanced imaging techniques. Leveraging our expertise in radiochemistry and nuclear medicine, we ensure seamless transitions from early research to preclinical development stages. For more information about our 68Ga radiopharmaceutical development services or to discuss your project, please contact us.
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Alfa Cytology offers efficient, customized, and professional R&D services related to radionuclide drug conjugates.