Giannola L I, Di Stefano V, De Caro V
Dipartimento di Chimica e Tecnologie Farmaceutiche, Universitá di Palermo, Italy.
Pharmazie. 1993 Feb;48(2):123-6.
White beeswax microspheres were investigated as a vehicle for the controlled release of anticancer agents. The in vitro diffusion of fluorouracil (1) and its prodrug ftorafur (2) was studied. The transfer rate constants from simulated gastro-intestinal juices to simulated plasma, throughout artificial wall lipid membranes, were defined. The constant's values suggested that the two drugs are poorly absorbed from stomach and main absorption occurred in the intestinal tract. Microspheres of 1 and 2 were prepared by a meltable dispersion of white beeswax and a wetting agent. The method is simple, inexpensive, rapid and reproducible. The drug release from the prepared microspheres was evaluated in vitro. More than 95% of the isolated microspheres were of particle size range 100-425 microns. The average drug content was 4%. Drug dissolution was greatly retarded as a result of microsphere formation.
研究了白色蜂蜡微球作为抗癌药物控释载体的情况。研究了氟尿嘧啶(1)及其前药呋氟尿嘧啶(2)的体外扩散。确定了药物从模拟胃肠液通过人工壁脂质膜向模拟血浆的转运速率常数。该常数的值表明这两种药物在胃中的吸收较差,主要吸收发生在肠道。通过白色蜂蜡和一种湿润剂的可熔分散体制备了1和2的微球。该方法简单、廉价、快速且可重复。对制备的微球进行了体外药物释放评估。超过95%的分离微球粒径范围为100-425微米。平均药物含量为4%。微球的形成大大延缓了药物的溶解。