Vargas F, Canudas N
Centro de Quimica, Instituto Venezolano de Investigationes Cientificas (IVIC), Caracas.
Pharmazie. 1993 Dec;48(12):900-4.
Fenofibrate (1), gemfibrozil (2), clofibric acid (3), benzafibrate (4) and clofibrate (5) were found to be photolabile by UV-B (290-320 nm) light under aerobic conditions. The drugs 1, 2, 3 and 4 were phototoxic in vitro when examined by the photohemolysis test both under oxygen and argon atmosphere, although the photohemolysis rate was markedly lower under anaerobic conditions. Based on the inhibition of this process upon addition of butylated hydroxyanisole (BHA) and reduced glutathione (GSH), a radical chain (type I) mechanism appears to operate. Inhibition was seen in the presence of sodium azide (NaN3) and 1,4-diazabicyclo[2.2.2]octane (DABCO) as also in D2O induced-photohemolysis. No photohemolysis was evident for clofibrate (5) under these conditions. In summary, fenofibrate, gemfibrozil, clofibric acid and bezafribrate are phototoxic in vitro. This behavior can be explained through the involvement of free radicals, singlet oxygen and stable photoproducts.
在有氧条件下,非诺贝特(1)、吉非贝齐(2)、氯贝酸(3)、苯扎贝特(4)和氯贝特(5)被发现对UV-B(290 - 320纳米)光不稳定。在氧气和氩气气氛下通过光溶血试验检测时,药物1、2、3和4在体外具有光毒性,尽管在厌氧条件下光溶血率明显较低。基于添加丁基化羟基茴香醚(BHA)和还原型谷胱甘肽(GSH)后对该过程的抑制作用,似乎存在自由基链(I型)机制。在叠氮化钠(NaN₃)和1,4 - 二氮杂双环[2.2.2]辛烷(DABCO)存在的情况下以及在重水诱导的光溶血中均观察到抑制作用。在这些条件下,氯贝特(5)未出现明显的光溶血现象。总之,非诺贝特、吉非贝齐、氯贝酸和苯扎贝特在体外具有光毒性。这种行为可以通过自由基、单线态氧和稳定光产物的参与来解释。