Preparation of No-Carrier-Added Technetium-99m Complexes via Metal-Assisted Cleavage from a Solid Phase

A novel method for the preparation of no-carrier-added (nca) complexes [99mTc(CO)3L] (L = diethylenetriamine or picolylamine-N-acetic acid) is described. The ligands were covalently bound to a solid support of organic polymers via formation of a tertiary amine from the chelating unit. This C−N bond...

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Veröffentlicht in:Bioconjugate chemistry 2004-01, Vol.15 (1), p.195-202
Hauptverfasser: Mundwiler, Stefan, Candreia, Lukas, Häfliger, Pascal, Ortner, Kirstin, Alberto, Roger
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Sprache:eng
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Zusammenfassung:A novel method for the preparation of no-carrier-added (nca) complexes [99mTc(CO)3L] (L = diethylenetriamine or picolylamine-N-acetic acid) is described. The ligands were covalently bound to a solid support of organic polymers via formation of a tertiary amine from the chelating unit. This C−N bond to the solid phase is selectively cleaved during the formation of the technetium complexes by intramolecular nucleophilic attack of a remaining hydroxy ligand to the α-carbon. The complex [99mTc(CO)3L] is released into solution while uncomplexed ligand and uncleaved complex remain solid-phase bound. High specific activity technetium complexes can then be isolated by simple filtration. Cleavage yield depends on temperature, pH, and ligand. Up to 50% release from the solid phase could be achieved under optimized conditions. Corresponding to the 99mTc concentration, free ligand is present in concentrations lower than 10-7 M. If a targeting vector is conjugated to these ligands, no-carrier-added radiopharmaceuticals can be prepared in that way.
ISSN:1043-1802
1520-4812
DOI:10.1021/bc034171f