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Title: Nuclear medicine: Progress report for quarter ending September 30, 1986

Technical Report ·
DOI:https://doi.org/10.2172/6941915· OSTI ID:6941915

The synthesis of two new dimethyl-branched analogues of 15-(p-iodophenyl)-3,3'-dimethylpentadecanoic acid (DMIPP) is described. Methyl-branching was introduced into the 6- and 9-positions to determine the effect of the position of dimethyl-branching on myocardial uptake and clearance kinetics in rats. The goal of these studies is to maximize heart uptake and retention and minimize blood and liver uptake. The 6,6'-dimethyl- (6,6'-DMIPP) and 9.9'-dimethyl- (9,9'-DMIPP) analogues were prepared by multi-step sequences involving successive Friedel-Crafts/Wolf Kishner reactions on thiophene. Regiospecific para-iodination using thallation and treatment with iodide provided the two new analogues. The 9,9'-(I-125)DMIPP was evaluated in rats and showed somewhat lower uptake than 3,3'-DMIPP (3.13 dose/gm at 5 min versus 4.18) and more rapid clearance (approx.30% at 1 h). In addition the heart:blood ratios were lower for the 9,9'-dimethyl isomer. These studies have demonstrated the effects of the position of dimethyl substitution on uptake and retention. 1 ref., 3 figs., 2 tabs.

Research Organization:
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
DOE Contract Number:
AC05-84OR21400
OSTI ID:
6941915
Report Number(s):
ORNL/TM-10294; ON: DE87005288
Resource Relation:
Other Information: Portions of this document are illegible in microfiche products. Original copy available until stock is exhausted
Country of Publication:
United States
Language:
English

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