The kinetics of hydrolysis and photolysis of N-1-retinoyl-5-fluorouracil (d
esignated Re-5-Fu) in buffer solution and in biological media were studied
to assess its feasibility as a prodrug for 5-fluorouracil (designated 5-Fu)
. The mechanism of the hydrolysis is also discussed. Hydrolysis of Re-5-Fu
yields 5-Fu in quantitative amounts. The pH-rate profile obtained revealed
the occurrence of acid and base catalysed as well as a spontaneous or water
-catalysed hydrolysis. The rates of hydrolysis were remarkably accelerated
in the presence of biological media. The study of photolysis kinetics showe
d that Re-5-Fu is a photosensitive compound. The Re-5-Fu is more lipophilic
than 5-Fu as shown by the partition coefficient in a 1-octanol-aqueous buf
fer system.