Biodistribution of 99mTc‐sunitinib as a potential radiotracer for tumor hypoxia imaging |
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Authors: | T. M. Sakr D. M. El‐Safoury Gehanne A. S. Awad M. A. Motaleb |
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Affiliation: | 1. Radioactive Isotopes and Generator Department, Hot Labs Center, Atomic Energy Authority, , Cairo, Egypt;2. Labeled Compounds Department, Hot Labs Center, Atomic Energy Authority, , Cairo, Egypt;3. Pharmaceutics and Industrial Pharmacy Department, Faculty of Pharmacy, Ain Shams University, , Cairo, Egypt |
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Abstract: | Tyrosine kinases are groups of enzymes, which are over‐expressed in solid tumor cells, representing good targets for different drugs such as sunitinib (N‐[2‐(diethylamino)ethyl]‐5‐{[(3Z)‐5‐fluoro‐2‐oxo‐2,3‐dihydro‐1H‐indol‐3‐ylidene]methyl}‐2,4‐dimethyl‐1H‐pyrrole‐3‐carboxamide). The aim of this work was to design and synthesize 99mTc‐sunitinib radiotracer and to study its tumor binding specificity as a novel selective radiopharmaceutical for tumor hypoxia imaging. The in vivo biodistribution of 99mTc‐sunitinib in tumor bearing mice showed high target/non‐target (T/NT) ratio (T/NT ~ 3 at 60 min post injection). This preclinical high biological accumulation in tumor cells suggests that 99mTc‐sunitinib is ready to go through the clinical trials as a potential selective radiotracer able to image tumor hypoxia. |
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Keywords: | sunitinib technetium‐99 m SPECT Tumor imaging hypoxia |
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