MOLECULAR MECHANISM OF DRUG PHOTOSENSITIZATION .4. PHOTOHEMOLYSIS SENSITIZED BY CARPROFEN

被引:21
作者
DEGUIDI, G
CHILLEMI, R
COSTANZO, LL
GIUFFRIDA, S
CONDORELLI, G
机构
[1] Dipartimento di Scienze Chimiche, Università di Catania, 95125 Catania
关键词
PHOTOSENSITIZATION; PHOTOHEMOLYSIS; CARPROFEN PHOTOLYSIS;
D O I
10.1016/1011-1344(93)80021-Z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Red blood cell lysis photosensitized by carprofen (CPF) was investigated. The photohemolysis process was observed in both aerobic and anaerobic conditions. Irradiation (310-390 nm) of buffered CPF solutions at pH 7.4 in deaerated conditions leads to a dehalogenation process via intermediate radicals with formation of the compound 2-(2-carbazolyl)propanoic acid (I) in the presence of hydrogen donors. Irradiation of I produces decarboxylation via free radicals and the formation of a stable decarboxylated compound, 2-ethylcarbazole (II). The photodegradation products I and II do not show lytic activity. The dechlorinated product I shows photosensitizing ability which was studied in the presence of the red blood cells in both aerated and deaerated solution. When carried out in the presence of additives, the observed photohemolysis suggests the involvement of free radicals and singlet oxygen in the membrane damage induced by both CPF and photoproduct I irradiation, whereas there is no evidence of any role for hydroxyl radicals. Superoxide anion is involved only in the photosensitization process induced by photoproduct I.
引用
收藏
页码:239 / 246
页数:8
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