Compounds, kits and methods for use in medical imaging
A technology of kits and imaging agents, applied in the field of new compounds for medical imaging and treatment, which can solve problems such as blurring
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Embodiment 1
[0066] Example 1: Pretargeted Imaging of Tumors Using Azide-Glucose
[0067] Refer to Figure 2.
[0068] Systemic administration of azide-glucose probe 1. Following optimal accumulation in tissues with high glucose uptake (such as tumors) and optimal clearance from non-target tissues and blood, administration of 18 F labeled imaging probe 2. Construct 2 is intracellularly conjugated to entrapped 1 via a Staudinger ligation. After clearing of unbound 2, PET images can be recorded, delineating tumor location and activity.
Embodiment 2
[0069] Example 2: Pretargeted Imaging of Tumors Using Azide-Amino Acids
[0070] Refer to Figure 3. The E. coli translation apparatus [bertozzi_PNAS2002] recognizes Azidohomoalanine (3) as a methionine substitute, which can serve as a metabolic / proliferation marker. Systemic administration of azidohomoalanine (3). Following optimal accumulation in tissues with high amino acid uptake (such as tumors) and optimal clearance from non-target tissues and blood, administration of 18 F labeled imaging probe 2. Construct 2 is intracellularly conjugated to entrapped 3 via a Staudinger ligation. After clearing of unbound 2, PET images can be recorded, delineating tumor location and activity.
Embodiment 3
[0071] Example 3: Pretargeted Imaging of Tumors Using Azide-Nucleosides
[0072] Refer to Figure 4.
[0073] Cell proliferation is increased in tumors, which leads to increased DNA replication and thus to an increased requirement for nucleosides. Given azide-modified thymidine 4, it is taken up by rapidly dividing cells. After optimal uptake in target cells, inject 18 F-labeled cyclooctyne compound 5, which binds to entrapped 4 via [3+2]azide-alkyne cycloaddition. After clearing of unbound 5, PET images can be recorded, delineating tumor location and activity.
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