Synthesis of 99mTc-Radiolabeled Uridine as a Potential Tumor Imaging Agent

被引:1
作者
Talaat H.M. [1 ]
Ibrahim I.T. [1 ]
Bayomy N.A. [1 ]
Farouk N. [1 ]
机构
[1] Hot Laboratories Centre, Atomic Energy Authority, P.O. Box 13759, Cairo
关键词
radiopharmaceuticals; technetium-99m; tumor imaging; uridine;
D O I
10.1134/S1066362218010095
中图分类号
学科分类号
摘要
Uridine, a pyrimidine nucleoside essential for the synthesis of RNA and biomembranes, was radiolabeled with 99mTc to obtain a potential tumor imaging agent. The maximal radiochemical yield of about 96.5%, as determined by paper chromatography and instant thin-layer chromatography, was reached under the following optimum conditions: 1 mg of uridine, 20 μg of SnCl2·2H2O as reducing agent, 20 mg of mannitol as a stabilizer, and pH 8. 99mTc-uridine is stable in vitro at room temperature for up to 6 h post labeling. The biodistrbution study in tumor-bearing mice shows high target-to-nontarget ratio. These results match with the high docking score of the complex on uridine phosphorylase enzyme. 99mTc-uridine shows promise as a tumor imaging agent. © 2018, Pleiades Publishing, Inc.
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页码:51 / 57
页数:6
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