Optimization of the preparation conditions of radioiodoepidepride: A dopamine D2receptor antagonist radioligand |
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| Authors: | N. Farouk M. A. Motaleb H. A. Shweeta K. Farah M. T. Kolaly |
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| Affiliation: | (1) Labeled Compounds Department,,Hot Labs Centre, Atomic Energy Authority, P.O. Box 13759, Cairo, Egypt;(2) Labeled Compounds Department,,Hot Labs Centre, Atomic Energy Authority, P.O. Box 13759, Cairo, Egypt;(3) Labeled Compounds Department,,Hot Labs Centre, Atomic Energy Authority, P.O. Box 13759, Cairo, Egypt;(4) Labeled Compounds Department,,Hot Labs Centre, Atomic Energy Authority, P.O. Box 13759, Cairo, Egypt;(5) Labeled Compounds Department,,Hot Labs Centre, Atomic Energy Authority, P.O. Box 13759, Cairo, Egypt |
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| Abstract: | Summary [125I]iodepidepride, (s)-(-)-[(1-ethyl-2-pyrrolidinyl)methyl]-5-[125I]-iodo-2,3-dimethoxybenzamide is the iodine substituted analogue of isoremoxipride, both of which are very potent dopamine D2-antagonists. Epidepride was radioiodinated using different oxidizing agents such as chloramine-T, iodogen, iodogen glass frit and hydrogen peroxide. Chloramine-T is a powerful oxidizing agent compared to both iodogen and hydrogen peroxide so that the side products, especially the chlorinated epidepride, decreases the radiochemical yield. This chlorinated epidepride is minimized in the case of iodogen and iodogen glass frit and are not observed in case of the non-chlorinated oxidizing agent hydrogen peroxide. TLC and HPLC were used to analyze the reaction components and to estimate both the radiochemical yield and purity. The reaction parameters such as reaction time, pH, epidepride and oxidizing agent concentrations and the stabilty of the final product were studied to optimize the radiochemical yield and purity. The optimized radiochemical yield was about 90% and the radiochemical purity of the final product was 99.9%. |
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