Kawashima Y, Niwa T, Takeuchi H, Hino T, Itoh Y
Gifu Pharmaceutical University, Japan.
J Pharm Sci. 1992 Feb;81(2):135-40. doi: 10.1002/jps.2600810207.
Hollow microspheres (microballoons), loaded with drug in their outer polymer shells, were prepared by a novel emulsion-solvent diffusion method. The ethanol:dichloromethane solution of drug (tranilast or ibuprofen) and an enteric acrylic polymer were poured into an agitated aqueous solution of polyvinyl alcohol that was thermally controlled at 40 degrees C. The gas phase generated in the dispersed polymer droplet by the evaporation of dichloromethane formed an internal cavity in the microsphere of the polymer with the drug. The drugs incorporated in the solidified shell of the polymer were found to be partially or completely amorphous. The flowability and packability of the resultant microballoons were much improved compared with the raw crystals of drug. The microballoons floated continuously over the surface of acidic dissolution media containing surfactant for greater than 12 h in vitro. The drug release behavior of the microballoons was characterized as an enteric property, and drug release rates were drastically reduced depending on the polymer concentration at pH 6.8.
通过一种新型的乳液-溶剂扩散法制备了在其外部聚合物壳中负载药物的中空微球(微球囊)。将药物(曲尼司特或布洛芬)和肠溶丙烯酸聚合物的乙醇:二氯甲烷溶液倒入在40℃下进行温度控制的搅拌聚乙烯醇水溶液中。二氯甲烷蒸发在分散的聚合物液滴中产生的气相在含有药物的聚合物微球中形成一个内腔。发现掺入聚合物固化壳中的药物部分或完全为无定形。与药物的原始晶体相比,所得微球囊的流动性和可填充性有了很大提高。在体外,微球囊在含有表面活性剂的酸性溶解介质表面连续漂浮超过12小时。微球囊的药物释放行为表现出肠溶特性,并且在pH 6.8时,药物释放速率根据聚合物浓度而急剧降低。