The development of iodine-123-methyl-branched fatty acids and their applications in nuclear cardiology
Conference
·
OSTI ID:6286929
- Oak Ridge National Lab., TN (United States)
- Bonn Univ. (Germany). Inst. fuer Klinische und Experimentelle Nuklearmedizin
- University of Tennessee Medical Center, Knoxville, TN (United States). Dept. of Radiology
- Free Univ. Hospital, Brussels (Belgium). Nuclear Medicine Dept.
- Ulm Univ. (Germany
Continued Interest in the use of iodine-1 23-labeled fatty acids for myocardial Imaging results from observations from a variety of studies that in many types of cardiac disease, regional fatty acid myocardial uptake patterns are often different than regional distribution of flow tracers. These differences may reflect alterations in important parameters of metabolism which can be useful for patient management or therapeutic strategy decision making. In addition, use of iodine-I 23-labeled fatty acid distribution may represent a unique metabolic probe to relate some aspects of the metabolism of these substrates with the regional viability of cardiac tissue. The use of such viability markers could provide important prognostic information on myocardial salvage, helping to identify patients for revascularization or angioplasty. Clinical studies are currently in progress with the iodine-123-labeled 1 5-(p-iodophenyl)-3-R,S-methylpentadecanoic acid (BMIPP) fatty acid analogue at several institutions. The goals of this paper are to discuss development of the concept of metabolic trapping of fatty acids, to briefly review development and evaluation of various radioiodinated methyl-branched fatty acids and to discuss recent patient studies with iodine-123 (BMIPP) using single photon emission computerized tomography (SPECT).
- Research Organization:
- Brookhaven National Lab., Upton, NY (United States)
- Sponsoring Organization:
- DOE; USDOE, Washington, DC (United States)
- DOE Contract Number:
- AC02-76CH00016; AC05-84OR21400
- OSTI ID:
- 6286929
- Report Number(s):
- BNL-48712; CONF-9302119--1; ON: DE93014051; CNN: CRG 900966
- Country of Publication:
- United States
- Language:
- English
Similar Records
The development of iodine-123-methyl-branched fatty acids and their applications in nuclear cardiology
The development of radioiodinated fatty acids for myocardial imaging
The development of radioiodinated fatty acids for myocardial imaging
Conference
·
Tue Jun 01 00:00:00 EDT 1993
·
OSTI ID:10162123
The development of radioiodinated fatty acids for myocardial imaging
Conference
·
Tue Jun 01 00:00:00 EDT 1993
·
OSTI ID:10166649
The development of radioiodinated fatty acids for myocardial imaging
Conference
·
Thu Dec 31 23:00:00 EST 1992
·
OSTI ID:7368496
Related Subjects
38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEAR CHEMISTRY
400703 -- Radiochemistry & Nuclear Chemistry-- Radioisotope Production
550601* -- Medicine-- Unsealed Radionuclides in Diagnostics
62 RADIOLOGY AND NUCLEAR MEDICINE
BETA DECAY RADIOISOTOPES
BODY
CARBOXYLIC ACIDS
CARDIOVASCULAR DISEASES
CARDIOVASCULAR SYSTEM
CHEMICAL PREPARATION
CHEMICAL REACTIONS
COUNTING TECHNIQUES
DISEASES
DRUGS
ELECTRON CAPTURE RADIOISOTOPES
HALOGENATION
HEART
HOURS LIVING RADIOISOTOPES
INTERMEDIATE MASS NUCLEI
IODINATION
IODINE 123
IODINE ISOTOPES
ISOTOPES
LABELLED COMPOUNDS
LABELLING
MONOCARBOXYLIC ACIDS
NUCLEI
ODD-EVEN NUCLEI
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANS
RADIOISOTOPE SCANNING
RADIOISOTOPES
RADIOPHARMACEUTICALS
SYNTHESIS
400703 -- Radiochemistry & Nuclear Chemistry-- Radioisotope Production
550601* -- Medicine-- Unsealed Radionuclides in Diagnostics
62 RADIOLOGY AND NUCLEAR MEDICINE
BETA DECAY RADIOISOTOPES
BODY
CARBOXYLIC ACIDS
CARDIOVASCULAR DISEASES
CARDIOVASCULAR SYSTEM
CHEMICAL PREPARATION
CHEMICAL REACTIONS
COUNTING TECHNIQUES
DISEASES
DRUGS
ELECTRON CAPTURE RADIOISOTOPES
HALOGENATION
HEART
HOURS LIVING RADIOISOTOPES
INTERMEDIATE MASS NUCLEI
IODINATION
IODINE 123
IODINE ISOTOPES
ISOTOPES
LABELLED COMPOUNDS
LABELLING
MONOCARBOXYLIC ACIDS
NUCLEI
ODD-EVEN NUCLEI
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANS
RADIOISOTOPE SCANNING
RADIOISOTOPES
RADIOPHARMACEUTICALS
SYNTHESIS