Oxidation of egg phosphatidylcholine and catechols (L-3,4-dihydroxyphe
nylalanine or dopamine) in liposome dispersions was studied. These cat
echols, encapsulated in liposomes, were shown to decrease the rate of
phosphatidylcholine oxidation by factors of 4.9 and 2.6, respectively,
at storage in darkness at 4 degrees C. After 40 min of Fe(II)-ascorba
te-induced oxidation, the level of malonaldehyde in such liposomes rem
ained constant, while in the empty liposomes, it increased 3.4-fold. E
gg phosphatidylcholine protected catechols encapsulated into liposomes
from oxidation, and the rate of this oxidation was shown to be substa
ntially lower than that in micellar solutions under the same condition
s. Evidently, this can be due to the barrier function of a lipid bilay
er.