Abstract
Typically, the synthesis of radiometal-based radiopharmaceuticals is performed in buffered aqueous solutions. We found that the presence of organic solvents like ethanol increased the radiolabeling yields of [(68)Ga]Ga-DOTA (DOTA = 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacatic acid). In the present study, the effect of organic cosolvents [ethanol (EtOH), isopropyl alcohol, and acetonitrile] on the radiolabeling yields of the macrocyclic chelator DOTA with several trivalent radiometals (gallium-68, scandium-44, and lutetium-177) was systematically investigated. Various binary water (H(2)O)/organic solvent mixtures allowed the radiolabeling of DOTA at a significantly lower temperature than 95 °C, which is relevant for the labeling of sensitive biological molecules. Simultaneously, much lower amounts of the chelators were required. This strategy may have a fundamental impact on the formulation of trivalent radiometal-based radiopharmaceuticals. The equilibrium properties and formation kinetics of [M(DOTA)](-) (M(III)= Ga(III), Ce(III), Eu(III), Y(III), and Lu(III)) complexes were investigated in H(2)O/EtOH mixtures (up to 70 vol % EtOH). The protonation constants of DOTA were determined by pH potentiometry in H(2)O/EtOH mixtures (0-70 vol % EtOH, 0.15 M NaCl, 25 °C). The log K(1)(H) and log K(2)(H) values associated with protonation of the ring N atoms decreased with an increase of the EtOH content. The formation rates of [M(DOTA)](-) complexes increase with an increase of the pH and [EtOH]. Complexation occurs through rapid formation of the diprotonated [M(H(2)DOTA)](+) intermediates, which are in equilibrium with the kinetically active monoprotonated [M(HDOTA)] intermediates. The rate-controlling step is deprotonation (and rearrangement) of the monoprotonated intermediate, which occurs through H(2)O ((*M(HL)) k(H(2)O)) and OH(-) ((*M(HL)) k(OH)) assisted reaction pathways. The rate constants are essentially independent of the EtOH concentration, but the (M(HL)) k(H2O) values increase from Ce(III) to Lu(III). However, the log K(M(HL))(H) protonation constants, analogous to the log K(H)(2) value, decrease with increasing [EtOH], which increases the concentration of the monoprotonated M(HDOTA) intermediate and accelerates formation of the final complexes. The overall rates of complex formation calculated by the obtained rate constants at different EtOH concentrations show a trend similar to that of the complexation rates determined with the use of radioactive isotopes.