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U.S. Department of Energy
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Nuclear medicine progress report for quarter ending March 31, 1987

Technical Report ·
DOI:https://doi.org/10.2172/5977304· OSTI ID:5977304
Studies using Langendorff-perfused rat hearts have shown for the first time the formation of a polar metabolite from the methyl-branched fatty acid, BMIPP. Evaluation of the radioactive components in the outflow tract of hearts after administration of the straight-chain analogue (I-131)IPPA and (I-125)BMIPP were pursued. Analysis of lipid extracts by thin-layer chromatography illustrated the presence of a product considerably more polar than BMIPP. These results suggest for the first time that the slow myocardial clearance observed with BMIPP in clinical studies may be associated with the wash-out of an unidentified metabolite. As a continuation of an evaluation of the effects of tellurium (Te) heteroatom position and the position of alkenyliodide substitution on myocardial uptake and retention properties, several new Te fatty acids have been synthesized and studied in rats. The new agents were prepared by coupling of internal alkenyl iodides prepared from the corresponding boronic acid analogues with sodium alkoxycarbonyl tellurols. Evaluation of the four new analogues demonstrated an unexpected relationship between chain length, and the position of the Te heteroatom and alkenyliodide moiety. 5 figs., 1 tab.
Research Organization:
Oak Ridge National Lab., TN (USA)
DOE Contract Number:
AC05-84OR21400
OSTI ID:
5977304
Report Number(s):
ORNL/TM-10441; ON: DE88000024
Country of Publication:
United States
Language:
English

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