TECHNETIUM-LABELED HEPARIN - PRELIMINARY-REPORT OF A NEW RADIOPHARMACEUTICAL WITH POTENTIAL FOR IMAGING DAMAGED CORONARY-ARTERIES AND MYOCARDIUM
- 1 January 1978
- journal article
- research article
- Vol. 19 (7) , 810-815
Abstract
Heparin was labeled with [99mTc] pertechnetate and its ability to image damaged coronary vessels and myocardium during and following myocardial ischemia was studied in experimental animals. 99mTc heparin localizes in damaged myocardium and coronary vessels in canine models of temporary myocardial ischemia and reperfusion and in damaged myocardium during fixed coronary occlusion. Scintigraphic detection of damaged myocardium was possible in both models, but the highest levels of 99mTc heparin in damaged myocardial tissue were found in those dogs with temporary coronary occlusion and reflow. 99mTc heparin may be of value as a positive imaging agent when coronary arteries or myocardium are injured and either reperfusion is allowed and/or significant blood flow persists in the damaged area.This publication has 7 references indexed in Scilit:
- Sites and Mechanisms of Localization of Technetium-99m Phosphorus Radiopharmaceuticals in Acute Myocardial Infarcts and other TissuesJournal of Clinical Investigation, 1977
- Variation among Commercial Activated Partial Thromboplastin Time Reagents in Response to HeparinAmerican Journal of Clinical Pathology, 1977
- Pathophysiology of technetium-99m stannous pyrophosphate and thallium-201 scintigraphy of acute anterior myocardial infarcts in dogs.Journal of Clinical Investigation, 1976
- Intracellular Plasma Protein : a Manifestation of Cell Injury in Myocardial IschaemiaNature, 1966
- IRREVERSIBLE ELECTROCHEMICAL PRECIPITATION OF MAMMALIAN PLATELETS AND INTRAVASCULAR THROMBOSISProceedings of the National Academy of Sciences, 1965
- The Elimination from Plasma of Intravenous Heparin An Experimental Study on Dogs and HumansActa Medica Scandinavica, 1963
- Electrical Potential Differences Across the Normal Aorta and Aortic Grafts of DogsAmerican Journal of Physiology-Legacy Content, 1953