The photocatalytic transformation of buspirone, an analgesic anxiolytic drug, and the formation of intermediates products have been evaluated by adopting titanium dioxide as a photocatalyst. Several molecules resulting from buspirone degradation have been identified and characterized by using HPLC/MS/MS technique. The main intermediates formed in these experimental conditions agree with the major buspirone metabolites found "in vivo" on rats and horses: hydroxy and dihydroxy-buspirone, despyrimidinyl buspirone and 1-pyrimidinyl piperazine. This shows that the photocatalytic system could provide in the present case a useful simulation of the metabolic transformation of dopant substances. Moreover, some more oxidized species have been recognized with the photocatalytic process, and this could offer a suggestion for yet to come metabolism studies.

The photocatalytic process as a tool to identify metabolitic products formed from dopant substances: the case of buspirone

CALZA, Paola;MEDANA, Claudio;PAZZI, Marco;BAIOCCHI, Claudio;PELIZZETTI, Ezio
2004-01-01

Abstract

The photocatalytic transformation of buspirone, an analgesic anxiolytic drug, and the formation of intermediates products have been evaluated by adopting titanium dioxide as a photocatalyst. Several molecules resulting from buspirone degradation have been identified and characterized by using HPLC/MS/MS technique. The main intermediates formed in these experimental conditions agree with the major buspirone metabolites found "in vivo" on rats and horses: hydroxy and dihydroxy-buspirone, despyrimidinyl buspirone and 1-pyrimidinyl piperazine. This shows that the photocatalytic system could provide in the present case a useful simulation of the metabolic transformation of dopant substances. Moreover, some more oxidized species have been recognized with the photocatalytic process, and this could offer a suggestion for yet to come metabolism studies.
2004
35
9
19
buspirone; metabolites; doping control; photocatalysis
P. CALZA; C. MEDANA; M. PAZZI; C. BAIOCCHI; E. PELIZZETTI
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/40834
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