|
|
||||||||
Center for the Health Sciences and Laboratory of Nuclear Medicine and Radiation Biology, University of California, Los Angeles, California
Correspondence: For reprints contact: Norman Poe, Laboratory of Nuclear Medicine, 900 Veteran Ave., Los Angeles, CA 90024.
ABSTRACT
Progress in myocardial perfusion imaging has been slowed by the lack of radiopharmaceuticals with suitable physical and biologic characteristics. Hexadecenoic acid, terminally labeled with 123I, partially overcomes these limitations by providing a compound that concentrates in the myocardium in proportion to relative regional blood flow and carries a gamma-emitter with desirable detection and imaging qualities. After intravenous injection in experimental animals, the clearance half-times of hexadecenoic acid for blood and myocardium are 1.7 and 20 min, respectively. These values compare favorably with 18-carbon fatty-acid analogs labeled with 11C. In acute and chronic infarction, similar distribution patterns are found for hexadecenoic acid and 43K, which indicates that hexadecenoic acid is a suitable substitute for the potassium analogs now in use for myocardial imaging. Because of the high count rates obtainable with 123I-hexadecenoic acid, good-quality images can be acquired in as little as 23 min per view. Iodine-123-hexadecenoic acid is potentially a useful radiopharmaceutical for clinical application.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| JOURNAL OF NUCLEAR MEDICINE TECHNOLOGY | THE JOURNAL OF NUCLEAR MEDICINE |