Cristallini C, Enriquez De Grassi G, Guardines L, Gaussmann R
Appl Biochem Biotechnol. 1984;10:267-72. doi: 10.1007/BF02783761.
A procedure to obtain a controlled-release microencapsulated anti-inflammatory drug based on a solvent evaporation method is described. The present method makes use of ethylcellulose as the polymer and methylene chloride as solvent. The evaporation of solvent is controlled by means of an air stream. Variations in the preparative procedure and their effects on capsule dimensions and permeabilities were studied. The release behavior of the drug is determined, and two different diffusion constants are also determined: 7.0 X 10(-10) cm2/s and 1.2 X 10(-10) cm2/s, corresponding to low and high release time. Based on these results it is proposed that these microcapsules have a nonhomogeneous polymeric wall, and are more porous in the outer surface. This model might be applicable to the microcapsules obtained by means of the solvent evaporation method.
描述了一种基于溶剂蒸发法制备控释微囊化抗炎药物的方法。本方法使用乙基纤维素作为聚合物,二氯甲烷作为溶剂。通过气流控制溶剂的蒸发。研究了制备过程中的变化及其对胶囊尺寸和渗透率的影响。测定了药物的释放行为,还确定了两个不同的扩散常数:7.0×10⁻¹⁰ cm²/s和1.2×10⁻¹⁰ cm²/s,分别对应低释放时间和高释放时间。基于这些结果,提出这些微囊具有不均匀的聚合物壁,且外表面孔隙率更高。该模型可能适用于通过溶剂蒸发法获得的微囊。