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1.
Nucl Med Biol ; 20(3): 317-24, 1993 Apr.
Article in English | MEDLINE | ID: mdl-8485491

ABSTRACT

New cationic 99Tc/99Tc complexes formed with various symmetrical and asymmetrical vicinal dioximes of different carbon chain length (C5-C8) were synthesized by reduction of pertechnetate with BH4-, separated by HPLC and characterized by i.r./u.v./vis. spectroscopy, FAB mass spectrometry and electrophoresis. All complexes studied are trisdioximes containing boron as a constituent. Their lipophilicity, as assessed by the octanol/saline partition coefficient, ranges over almost four orders of magnitude. The myocardial uptake of the 99mTc complexes in mice proves to be lower than expected. The organ distributions are distinctly affected by the lipophilicity, the position of the dioxime group and the introduction of a terminal methoxy group.


Subject(s)
Heart/diagnostic imaging , Oximes/chemical synthesis , Technetium/chemistry , Animals , Chemical Phenomena , Chemistry, Physical , Chromatography, High Pressure Liquid , Isotope Labeling , Mice , Mice, Inbred Strains , Molecular Structure , Oximes/chemistry , Oximes/pharmacokinetics , Radionuclide Imaging , Spectrometry, Mass, Fast Atom Bombardment , Tissue Distribution
2.
Int J Rad Appl Instrum A ; 43(9): 1079-82, 1992 Sep.
Article in English | MEDLINE | ID: mdl-1330986

ABSTRACT

[99Tc(phen)3]Cl2 was synthesized by reduction of pertechnetate with sodium borohydride in the presence of an excess of 1,10-phenanthroline and characterized by FAB mass spectrometry, magnetic susceptibility measurements, and i.r./vis/u.v. spectrophotometry. For biodistribution evaluation in mice [99mTc(phen)3]Cl2 could be obtained in a radiochemical purity of 92.5% using a similar procedure. The rather hydrophilic chelate was predominantly excreted by the kidneys. Its low blood retention resulted in a heart/blood activity ratio of 4.2 at 100 min post-injection.


Subject(s)
Organotechnetium Compounds/chemical synthesis , Phenanthrolines/chemical synthesis , Animals , Mice , Organotechnetium Compounds/pharmacokinetics , Phenanthrolines/pharmacokinetics , Spectrometry, Mass, Fast Atom Bombardment , Tissue Distribution
3.
Int J Rad Appl Instrum B ; 19(1): 73-8, 1992 Jan.
Article in English | MEDLINE | ID: mdl-1577615

ABSTRACT

New tris(beta-diketonato) complexes of trivalent 99Tc/99mTc with the ligands hexane-2,4-dione, heptane-2,4-dione, heptane-3,5-dione, and octane-3,5-dione were synthesized by reduction of pertechnetate with dithionite in the presence of excess beta-diketone. The complexes were purified by HPLC, identified by elemental analysis and FAB mass spectrometry, and characterized by vis./u.v./i.r. spectrophotometry. The hexane-2,4-dionato complex crystallizes in the monoclinic space group P21/c, isostructurally with pentane-2,4-dionatotechnetium(III). Biodistribution measurements in mice showed the neutral and lipophilic 99mTc-diketonato complexes to penetrate the blood-brain barrier. However, increasing lipophilicity decreased the brain uptake except for the heptane-2,4-dionato complex, which displayed the highest uptake of 0.82% injected dose/g.


Subject(s)
Ketones/chemical synthesis , Organotechnetium Compounds/chemical synthesis , Technetium , Animals , Ligands , Mass Spectrometry , Mice , Octanols , Protein Binding , Serum Albumin, Bovine/metabolism , Solubility , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet , Tissue Distribution , Water , X-Ray Diffraction
4.
Int J Rad Appl Instrum B ; 14(6): 545-53, 1987.
Article in English | MEDLINE | ID: mdl-3429235

ABSTRACT

The synthesis and purification of two new ligands, 15-[bis(3,4-dimethyl arsino)phenyl] pentadecanoic acid (FA-DIARS) and [bis(16,17-dimethyl phosphino)] heptadecanoic acid (FA-DMPE) and the preparation of their corresponding 99Tc/99mTc complexes of the general formula [Tc(III)L2Cl2]+, wherein L is FA-DIARS or FA-DMPE are reported. After careful purification by preparative HPLC, the 99Tc complexes were characterized by spectroscopy, while the 99mTc complexes were used to determine the biodistribution in mice. The results of the organ distribution studies indicated a relatively high uptake in heart (5-7% dose/g). The complexes were, however, found to be very slowly cleared from the blood, probably due to strong binding to serum proteins. Further, the heart to liver and heart to lung ratios were unfavourable. Attempts to improve the efficacy by synthesizing complexes containing one fatty acid per molecule are also described.


Subject(s)
Arsenicals/chemical synthesis , Heart/diagnostic imaging , Liver/metabolism , Lung/metabolism , Myocardium/metabolism , Organometallic Compounds/chemical synthesis , Organophosphorus Compounds/chemical synthesis , Organotechnetium Compounds , Phosphines , Animals , Arsenicals/pharmacokinetics , Indicators and Reagents , Ligands , Mice , Organometallic Compounds/pharmacokinetics , Organophosphorus Compounds/pharmacokinetics , Radionuclide Imaging , Tissue Distribution
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