Generation of reactive oxygen species during the photolysis of 6-hydroxymethylpterin in alkaline aqueous solutions

F.M. CABRERIZO; A.H. THOMAS; C. LORENTE; M.L. DÁNTOLA; G. PETROSELLI; R. ERRA-BALSELLS; A.L. CAPPARELLI

HELVETICA CHIMICA ACTA

Año: 2004 vol. 87 p. 349 - 365

0018-019X

Photochemical studies of the reactivity of 6-(hydroxymethyl)pterin (2-amino-6-(hydroxymethyl)pteridin-4(1H)-one; HPT) in alkaline aqueous solutions (pH 10.2±10.8) at 350 nm and room temperature were performed. The photochemical reactions were followed by UV/VIS spectrophotometry, thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC), and an enzymatic method for H2O2 determination. In the presence of O2 , 6-formylpterin (2-amino-3,4-dihydro-4-oxopteridine-6-carboxaldehyde; FPT) was the only photoproduct detected. In the absence of O2 , a compound showing an absorbance maximumat 480 nm was observed which was oxidized very fast by O2 in a dark reaction to yield FPT. The quantum yields of substrates disappearance and of photoproducts formation were determined. The formation of H2O2 during the photooxidation was monitored, and the number of mol of H2O2 released per mol of HPT consumed corresponded to a 1:1 stoichiometry. HPT was also investigated for its efficiency of singlet-oxygen (1O2) production and quenching in aqueous solution. The quantum yield of 1O2 production was determined by measurements of the 1O2 luminescence in the near-IR (1270 nm) upon continuous excitation of the sensitizer. The rate constant of 1O2 total quenching by HPTwas determined (kt3.1 ¥ 106 1 s1), indicating that this compound was able to quench 1O2 . However, 1O2 did not participate in the photooxidation of HPT to FPT.