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Title: Nuclear medicine progress report for quarter ending December 31, 1983

Technical Report ·
OSTI ID:7007714

In this report a multi-step synthesis of 19-iodo-3-(R,S)-methyl-18-nonadecenoic acid is described. In this new agent, the iodine is stabilized as a trans vinyliodide and the methyl group in position-3 was introduced to inhibit ..beta..-oxidation. The /sup 125/I-labeled agent was evaluated in unfasted rats and showed essentially no loss from the myocardium over the initial 30 min period. Three new (/sup 125/I)-labeled iodopentenyl-substituted cation analogues have also been prepared and evaluated in rats to determine the relation between structure and relative heart and hepatobiliary uptake. The triphenylarsonium and dihexylphenylphosphonium analogues showed tissue distribution properties very similar to the parent -triphenylphosphonium agent. The -dimethyl-n-octylphosphonium analogue, however, showed lower heart uptake and much greater hepatobiliary clearance. Carrier-free /sup 103/ /sup 106/RuCl/sub 3/ by utilizing ruthenocenylmethyltrimethylammonium iodide as the key synthetic intermediate. The amino acid analog was evaluated as a pancreatic imaging agent but no selective uptake in the pancreas was observed. The High Flux Isotope Reactor (HFIR) resumed operation in January after replacement of the beryllium reflector shield. For the July-December 1983 period, several shipments of radiolabeled agents were made to Medical Cooperative investigators. 9 references, 3 figures, 4 tables.

Research Organization:
Oak Ridge National Lab., TN (USA)
DOE Contract Number:
AC05-84OR21400
OSTI ID:
7007714
Report Number(s):
ORNL/TM-9037; ON: DE84012037
Country of Publication:
United States
Language:
English