Ghazy F S, Kimura T, Muranishi S, Sezaki H
J Pharm Pharmacol. 1975 Apr;27(4):268-72. doi: 10.1111/j.2042-7158.1975.tb10697.x.
The influence of the intermediate products of riboflavine photolysis on the absorption of poorly absorbed water-soluble drugs from the rat small intestine has been examined using an in situ recirculation technique. The absorption of phenol red, bromphenol blue (BPB) and their biliary excretion, and lactose isonicotinoyl-hydrazone (lactose-INH) and its plasma concentration were increased in experiments made in the presence of light in contrast to other made in the dark. The absorption of both phenol red and lactose-INH were concentration-dependent. On the other hand, a saturation phenomenon was demonstrated when the concentration of phenol red was kept constant while that of the water-soluble compound flavine mononucleotide (FMN) was changed. The results which were obtained from pretreatment experiments suggest an alteration in the permeability of the intestinal membrane. No enhancement effect could be demonstrated for lumichrome in the presence of absence of light.
采用原位再循环技术,研究了核黄素光解中间产物对大鼠小肠中吸收不良的水溶性药物吸收的影响。与在黑暗中进行的其他实验相比,在有光照的实验中,酚红、溴酚蓝(BPB)及其胆汁排泄,以及乳糖异烟酰腙(乳糖-INH)及其血浆浓度均有所增加。酚红和乳糖-INH的吸收均呈浓度依赖性。另一方面,当酚红浓度保持恒定而水溶性化合物黄素单核苷酸(FMN)浓度改变时,出现了饱和现象。预处理实验结果表明肠膜通透性发生了改变。在有光或无光的情况下,均未显示出光色素的增强作用。