Nagareya N, Uchida T, Matsuyama K
Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya City, Japan.
Chem Pharm Bull (Tokyo). 1998 Oct;46(10):1613-7. doi: 10.1248/cpb.46.1613.
The objective of this study was to produce enteric microspheres containing bovine insulin as a model drug using a water-in-oil-in-water (w/o/w) emulsion solvent evaporation method, and the preparative conditions were optimized. When hydroxypropylmethylcellulose acetate succinate (AS-HG type; high content of succinyl group) was employed as an enteric wall material, optimized microspheres showed almost 90% of the loading efficiency of insulin and 30.8 microns of mean volume diameter. The mixture of methylene chloride and acetone (4:1) as an oleaginous phase, 400 microliters of bovine insulin solution (dissolved in 30% of acetic acid) as an internal aqueous phase, and 1.0% of polyvinylalcohol dissolved in pH 3.0 citrate buffer as an external aqueous phase, were employed in the experiment. In relation to other enteric cellulose derivatives (AS-MG type, AS-LG type; medium and low content of succinyl group, respectively), the microencapsulation using a simultaneous preparation method also resulted in quite high loading efficiencies, whereas the choice of poly(methyl methacrylate) as a wall material caused aggregation or flocculation in the preparative process of every batch. The AS-HG microspheres showed very fast release profile in pH 6.8 buffer, but no released fraction was observed in pH 1.2 buffer. This phenomenon suggested enteric characteristics of prepared microspheres. Finally AS-HG microspheres containing 4% lauric acid and 9% insulin were prepared, suspended in 0.1% of carboxymethyl cellulose solution, and administered to the rat rectum (corresponding to 50 I.U./kg insulin). The plasma glucose level reached minimum level at 0.5 h after administration then gradually rose to normal.
本研究的目的是采用水包油包水(w/o/w)乳液溶剂蒸发法制备含有牛胰岛素作为模型药物的肠溶微球,并对制备条件进行优化。当使用醋酸琥珀酸羟丙基甲基纤维素(AS-HG型;琥珀酰基含量高)作为肠溶壁材时,优化后的微球显示胰岛素的负载效率接近90%,平均体积直径为30.8微米。实验采用二氯甲烷和丙酮(4:1)的混合物作为油相,400微升牛胰岛素溶液(溶解于30%的乙酸中)作为内水相,以及1.0%溶解于pH 3.0柠檬酸盐缓冲液中的聚乙烯醇作为外水相。与其他肠溶纤维素衍生物(AS-MG型、AS-LG型;分别为琥珀酰基含量中等和低)相比,采用同时制备法进行微囊化也能获得相当高的负载效率,而选择聚甲基丙烯酸甲酯作为壁材会导致每一批次的制备过程中出现聚集或絮凝现象。AS-HG微球在pH 6.8缓冲液中显示出非常快速的释放曲线,但在pH 1.2缓冲液中未观察到释放部分。这种现象表明所制备的微球具有肠溶特性。最后制备了含有4%月桂酸和9%胰岛素的AS-HG微球,将其悬浮于0.1%的羧甲基纤维素溶液中,并经大鼠直肠给药(相当于50国际单位/千克胰岛素)。给药后0.5小时血浆葡萄糖水平达到最低水平,然后逐渐升至正常水平。