Reactions of methyl, hydroxyl and peroxyl radicals with the DOTA chelating agent used in medical imaging.

The mechanism of reaction of DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) with ·CH, CHO· and ·OH radicals were studied. The radicals were formed in situ radiolytically. The methyl radicals react orders of magnitude slower with DOTA and with M(DOTA) than the hydroxyl radicals. The various final products were identified and mechanisms for their formation are proposed. CHO· radicals do not react, or react too slowly to be observed, with DOTA and with M(DOTA) as long as the central cation is not oxidized by the peroxyl radical. The results imply that synthesis of the M(DOTA)(M = radioisotope) complexes in a water-organic solvent (ethanol or 2-propanol or acetonitrile) mixture is not only kinetically desired but the so formed complex also decreases the radiolytic decomposition of DOTA.