Gupta V K, Assmus M W, Beckert T E, Price J C
Department of Pharmaceutical and Biomedical Sciences, University of Georgia, College of Pharmacy, Athens, GA 30602, USA.
Int J Pharm. 2001 Feb 1;213(1-2):93-102. doi: 10.1016/s0378-5173(00)00650-5.
The objective of this work was to optimize a novel potential colonic drug delivery system by using a statistical procedure. Pellets were prepared by powder layering of 5-aminosalicylic acid (5-ASA) on nonpareils (0.5--0.6 mm) in a coating pan. Drug-layered pellets were coated with an inner layer of a combination of Eudragit RL and RS and an outer layer of Eudragit FS in a fluidized-bed apparatus. Central composite design was used to study the effect of three independent variables. The proportion of the more hydrophilic polymer Eudragit RL had the most significant effect on drug release--higher proportion gave faster release; the amount of inner and outer coat did not have a significant effect on the rate of drug release at either 6 or 12 h in the range studied. A second order polynomial equation was fitted to the data, and the resulting equation was used to predict the responses in the optimal region. An optimized formulation was prepared and evaluated for individual responses. The experimental values of the response variables highly agreed with the predicted values. The results demonstrated the reliability of the model in the preparation of coated pellets having predictable drug release for colonic delivery of 5-ASA.
本研究的目的是通过统计学方法优化一种新型的潜在结肠给药系统。采用包衣锅将5-氨基水杨酸(5-ASA)粉末分层包裹在非那西汀(0.5-0.6mm)上制备微丸。在流化床设备中,将药物层微丸用Eudragit RL和RS的组合内层以及Eudragit FS外层进行包衣。采用中心复合设计研究三个自变量的影响。亲水性更强的聚合物Eudragit RL的比例对药物释放影响最为显著——比例越高,释放越快;在所研究的范围内,内层和外层包衣量在6小时或12小时时对药物释放速率均无显著影响。将二阶多项式方程拟合到数据上,并使用所得方程预测最佳区域内的响应。制备了优化配方并对各个响应进行评估。响应变量的实验值与预测值高度一致。结果证明了该模型在制备具有可预测药物释放的包衣微丸用于5-ASA结肠给药方面的可靠性。