The photolysis of α-tocopherol ( I ) in olive oil (O) and in some model systems ( n -hexane = H; anhydrous n -hexane = HA, and triolein = T) was studied under sunlight and under artificial light (λ > 290 nm) by HPLC and GC/MS. In O and T, I disappeared linearly to 50% of the starting concentration, reached a constant value, and finally disappeared rapidly from the medium. In the model system, photolysis followed a pseudo-first-order kinetics. Although no peaks attributable to photoproducts were found in O, a main product identified by 1 H and 13 C NMR and GC/MS as 5-formyltocopherol ( II ) was found in the model systems. Irradiation of compound II led to species undetectable by HPLC in agreement with a slower consecutive kinetic process than that of I . In the HA and T systems, the formation of II occurred at lower levels than in H. The possible behavior of photodegradation is discussed.
No takes yet. Share an insight, caveat, or question.
Pirisi et al. (1998) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: