Fast quantitative labelling of N-isopropyl-para-iodo-amphetamine (IAMP) with 123I in the presence of Cu(I) and ascorbic acid, allowing kit-form preparation
AbstractAbstract
[en] The presence of Cu(II) in the isotopic exchange reaction for the labelling of N-isopropyl-para-iodo-amphetamine with 123I is proven to cause radioiodinated as well as cold side-products. The use of Cu(I) for promoting the nucleophilic isotopic exchange in the presence of an excess of reductant, such as Sn(II) or ascorbic acid, allows an almost quantitative yield to be obtained within 20 minutes. The reaction is assumed to proceed through an organo-copper complex favouring the exchange of the radioiodide. The labelling procedure is suitable to be adapted as a kit-form preparation. (author)
Source
International Atomic Energy Agency, Vienna (Austria); Proceedings series; 581 p; ISBN 92-0-040085-X; ; 1985; p. 303-310; IAEA; Vienna (Austria); International conference on radiopharmaceuticals and labelled compounds; Tokyo (Japan); 22-26 Oct 1984; IAEA-CN--45/1
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Book
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Conference
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Descriptors (DEI)
Descriptors (DEC)
AMINES, AMPHETAMINES, ANALEPTICS, BETA DECAY RADIOISOTOPES, CENTRAL NERVOUS SYSTEM AGENTS, DRUGS, ELECTRON CAPTURE RADIOISOTOPES, ELEMENTS, HOURS LIVING RADIOISOTOPES, INTERMEDIATE MASS NUCLEI, IODINE ISOTOPES, ISOTOPES, LABELLED COMPOUNDS, MATERIALS, METALS, NUCLEI, ODD-EVEN NUCLEI, ORGANIC COMPOUNDS, RADIOACTIVE MATERIALS, RADIOISOTOPES, SYMPATHOMIMETICS, SYNTHESIS, TRANSITION ELEMENTS
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