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16-Cyclopentadienyl tricarbonyl 99mTc 16-oxo-hexadecanoic acid: synthesis and evaluation of fatty acid metabolism in mouse myocardium.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2008 Jun 26; Vol. 51 (12), pp. 3630-4. Date of Electronic Publication: 2008 May 27. - Publication Year :
- 2008
-
Abstract
- We synthesized 16-cyclopentadienyl tricarbonyl 99mTc 16-oxo-hexadecanoic acid (99mTc-CpTT-16-oxo-HDA, 1) and investigated its potential as a radiotracer for evaluating fatty acid metabolism in myocardium. Radiotracer 1 was synthesized in 22.6 +/- 6.3% decay-corrected yield by a double ligand transfer reaction between the ferrocene adduct of methyl hexadecanoate ( 2) and Na99mTcO 4 in the presence of Cr(CO)6 and CrCl3, followed by hydrolysis of the methyl ester group. Radiotracer 1 was found to be chemically stable (99% at 6 h) when incubated in human serum. A tissue distribution study in mice showed that high radioactivity accumulated in heart (9.03%ID/g at 1 min and 5.41%ID/g at 5 min postinjection) with rapid clearance and that heart to blood uptake ratios increased with time (2.13 at 5 min and 3.76 at 30 min postinjection). Metabolite analysis of the heart tissues using a simple extraction method showed that 99mTc-CpTT-4-oxo-butyric acid was detected as the major radioactive metabolite by HPLC, suggesting that 1 is metabolized to 99mTc-CpTT-4-oxo-butyric acid via beta-oxidation in myocardium.
- Subjects :
- Animals
Heart diagnostic imaging
Humans
In Vitro Techniques
Male
Mice
Mice, Inbred ICR
Organotechnetium Compounds chemistry
Organotechnetium Compounds pharmacokinetics
Radionuclide Imaging
Radiopharmaceuticals chemistry
Radiopharmaceuticals pharmacokinetics
Tissue Distribution
Fatty Acids metabolism
Myocardium metabolism
Organotechnetium Compounds chemical synthesis
Radiopharmaceuticals chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 0022-2623
- Volume :
- 51
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 18503263
- Full Text :
- https://doi.org/10.1021/jm800049h