Key result
Novel click chemistry-based 68Ga PET selectively targets atherosclerotic plaques in preclinical models.
Why the study?
Does a click chemistry-based PET imaging strategy using 68Ga improve the specific detection of LDL accumulation in atherosclerotic plaques in LDLr-/- mice?
Does a click chemistry-based PET imaging strategy using 68Ga improve the specific detection of LDL accumulation in atherosclerotic plaques in LDLr-/- mice?
A novel click chemistry-based 68Ga PET imaging strategy enables highly specific and sensitive noninvasive detection of LDL accumulation in atherosclerotic plaques in a preclinical model.
Low-density lipoprotein (LDL) plays a central role in the development of atherosclerosis, making its detection critical for cardiovascular disease management. Radionuclide imaging of LDL offers distinct advantages over other modalities but remains limited by poor specificity and the need for long-lived isotopes. We present a click chemistry-based PET imaging strategy using gallium-68 (68Ga), a short-lived radionuclide, for the specific detection of LDL accumulation in atherosclerotic plaques. The approach relies on a two-step inverse electron-demand Diels–Alder reaction between trans-cyclooctene (TCO)-modified LDL and tetrazine-functionalized iron oxide nanoparticles radiolabeled with 68Ga. In vivo PET/CT imaging in LDL receptor-deficient (LDLr–/–) mice showed selective uptake of the nanoparticles in atherosclerotic lesions, with minimal signal in wild-type controls. This method demonstrated high specificity and sensitivity, while reducing background signal and radiation exposure. Our results support the potential of this approach as a noninvasive and translatable platform for early diagnosis and risk assessment in cardiovascular disease.
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Nogales et al. (2025) studied Atherosclerosis. Click chemistry-based PET imaging strategy using gallium-68 (68Ga) vs. Wild-type controls was evaluated on Selective uptake of nanoparticles in atherosclerotic lesions. A click chemistry-based PET imaging strategy using 68Ga demonstrated selective uptake of nanoparticles in atherosclerotic lesions of LDLr–/– mice with minimal signal in wild-type controls.
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