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The hemolysis of human red blood cells was initiated by a water soluble free radical initiator, 2,2′ azobis (2 amidinopropane hydrochloride)(AAPH), at 37 ℃ in phosphate buffered saline(pH=7.4). The respective addition of 1 [ N (o hydroxybenzylidene)amino]tetradecane(TDCA), 1,2 di[ N (o hydroxybenzylidene)amino]cyclohexane(DACH), 4 [ N (o hydroxybenzylidene)amino]benzoic acid(PABA), 4 nitro[ N (o hydroxybenzylidene)]aniline(APNA) or N (o hydroxybenzylidene)aniline(APA) can all prolong the inhibition period of hemolysis, indicating that the above Schiff bases play an antioxidative role in free radical induced hemolysis. It can be concluded that Schiff base with an alkyl group or a conjugated system in the molecule protect red blood cells against free radical induced hemolysis efficiently. This information may be useful for antioxidant drug design.
The hemolysis of human red blood cells was initiated by a water soluble free radical initiator, 2,2 ’azobis (2 amidinopropane hydrochloride) (AAPH) at 37 ° C in phosphate buffered saline (pH = 7.4) N (o hydroxybenzylidene) amino] tetradecane (TDCA), 1,2 di [N (o hydroxybenzylidene) amino] cyclohexane hydroxybenzylidene] aniline (APNA) or N (o hydroxybenzylidene) aniline (APA) can all prolong the inhibition period of hemolysis, indicating that the above Schiff bases play an antioxidant role in free radical induced hemolysis. It can be concluded that Schiff base with an alkyl group or a conjugated system in the molecule protect red blood cells against free radical induced hemolysis efficiently. This information may be useful for antioxidant drug design.