The hydrogel thiopropyl-sepharose 6B was used as a model matrix system to b
ind the natural cytotoxic sesquiterpene lactones grosheimin 1 and deacylcyn
aropicrin 2. The hydrogel thio groups were bonded to the lactone exomethyle
ne groups and the release of the lactones from the polymer was studied. Sin
ce it is thought that cancer cells have a higher oxidative potential than n
ormal cells, the release was carried out through an oxidative cleavage. Dif
ferent concentrations of hydrogen peroxide solutions were added to the :lac
tone-polymer conjugates, thus, imitating in vivo conditions. The results ob
tained showed that both-the rate and amount of grosheimin and deacylcynarop
icrin release depend linearly on the. H2O2 concentration.