INHIBITORY EFFECTS OF CATECHOL DERIVATIVES ON OXIDATION OF SOYBEAN PHOSPHATIDYLCHOLINE LIPOSOMES INDUCED BY HYDROPHILIC AND HYDROPHOBIC FREE-RADICAL INITIATORS
S. Kitagawa et al., INHIBITORY EFFECTS OF CATECHOL DERIVATIVES ON OXIDATION OF SOYBEAN PHOSPHATIDYLCHOLINE LIPOSOMES INDUCED BY HYDROPHILIC AND HYDROPHOBIC FREE-RADICAL INITIATORS, Chemical and Pharmaceutical Bulletin, 43(8), 1995, pp. 1263-1266
Effects of pyrocatechol and six of its monosubstituents on oxidation o
f soybean phosphatidylcholine liposome induced by hydophilic free radi
cal initiator, 2,2'-azobis(2-amidinopropane)dihydrochloride (AAPH), an
d hydrophobic free radical initiator, 2,2'-azobis(2,4-dimethylvaleroni
trile) (AMVN), were determined and relationships with their redox pote
ntials and hydrophobic parameters were studied for their inhibitory ef
fects by regression analysis, Inhibitory potencies of the catechol com
pounds on hydrophilic AAPH-induced oxidation clearly correlated with t
heir redox potentials, whereas no significant effects of the hydrophob
icities of the compounds were found, These results indicated that scav
enging activities of these compounds on AAPH-initiated radical chain r
eactions were controlled by their electron donor activities. Inhibitor
y potencies of these compounds on hydrophobic AMVN-induced oxidation o
f liposome, in contrast, were significantly correlated with their hydr
ophobicity, although regression analysis revealed that their electron
donor activities were also important,