Harland R S, Gazzaniga A, Sangalli M E, Colombo P, Peppas N A
School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907.
Pharm Res. 1988 Aug;5(8):488-94. doi: 10.1023/a:1015913207052.
The swelling and dissolution behavior of pharmaceutical systems containing a drug and a polymer can be analyzed by a mathematical model which predicts the drug released and the gel layer thickness as a function of time. It is possible to approximate the values of several of the physicochemical parameters of this model in order to obtain an order-of-magnitude analysis of the tablet dissolution process. Selected experimental results of tablet dissolution and drug release are analyzed and conclusions are made about the importance of the drug and polymer content and solubility in the release behavior.
含有药物和聚合物的药物系统的溶胀和溶解行为可以通过一个数学模型进行分析,该模型可预测药物释放量和凝胶层厚度随时间的变化。为了对片剂溶解过程进行量级分析,可以对该模型的几个物理化学参数值进行近似估算。分析了片剂溶解和药物释放的选定实验结果,并就药物和聚合物含量以及溶解度对释放行为的重要性得出了结论。