Lu Zhilei, Chen Weiyang, Olivier Eugene, Hamman Josias H
Department of Pharmaceutical Sciences, Tshwane University of Technology, Pretoria, South Africa.
Drug Deliv. 2008 Feb;15(2):87-96. doi: 10.1080/10717540801905009.
The in vitro dissolution, swelling, and erosion behavior of monolithic matrix systems containing the well-known hydrophilic polymer, hydroxypropylmethylcellulose, and a combination of chitosan and polycarbophil in the form of an interpolyelectrolyte complex were compared in this study. The two different types of matrix systems showed both a combination of swelling and erosion as the drug release mechanism. Kinetic analysis of the in vitro release profiles of water-soluble drugs from the matrix tablets illustrated that those containing the chitosan-polycarbophil complex exhibited higher mean dissolution time values and therefore slower drug release compared with the other matrix systems. The analysis also indicated that zero-order release kinetics were approached for some of the formulations containing the chitosan-polycarbophil complex, while this could not be achieved for those containing hydroxypropylmethylcellulose.
在本研究中,比较了含有著名的亲水性聚合物羟丙基甲基纤维素以及呈聚电解质络合物形式的壳聚糖和聚卡波非组合的整体基质系统的体外溶出、溶胀和侵蚀行为。两种不同类型的基质系统均表现出溶胀和侵蚀相结合的药物释放机制。对水溶性药物从基质片剂的体外释放曲线进行动力学分析表明,与其他基质系统相比,含有壳聚糖 - 聚卡波非络合物的系统表现出更高的平均溶出时间值,因此药物释放更慢。分析还表明,一些含有壳聚糖 - 聚卡波非络合物的制剂接近零级释放动力学,而含有羟丙基甲基纤维素的制剂则无法实现这一点。