Gurny R, Doelker E, Peppas N A
Biomaterials. 1982 Jan;3(1):27-32. doi: 10.1016/0142-9612(82)90057-6.
The release behaviour of water-soluble drugs from hydrophobic, porous polymeric matrices is complicated by the dissolution of the drug in the water-filled pores under quiescent conditions. Mathematical models are presented for drug release above and below the solubility limit of the drug in the dissolution medium, for constant void fraction (porosity). Experimental studies of KCl release from the porous ethyl cellulose tablets in water at 37 degrees C are explained in terms of dissolution-controlled and diffusion-controlled steps of the release mechanism.
在静态条件下,水溶性药物从疏水性多孔聚合物基质中的释放行为因药物在充满水的孔隙中的溶解而变得复杂。针对药物在溶解介质中的溶解度极限之上和之下的药物释放情况,给出了在恒定孔隙率(孔隙度)下的数学模型。从释放机制的溶解控制步骤和扩散控制步骤的角度,解释了在37摄氏度下氯化钾从多孔乙基纤维素片剂在水中的释放的实验研究。