Ernst Moritz Arndt University, Department of Pharmacy, Institute of Biopharmaceutics and Pharmaceutical Technology, Center of Drug Absorption and Transport, 3 Felix Hausdorff Street, Greifswald 17489, Germany.
Ernst Moritz Arndt University, Department of Pharmacy, Institute of Biopharmaceutics and Pharmaceutical Technology, Center of Drug Absorption and Transport, 3 Felix Hausdorff Street, Greifswald 17489, Germany.
Int J Pharm. 2018 May 30;543(1-2):368-375. doi: 10.1016/j.ijpharm.2018.04.005. Epub 2018 Apr 6.
Robust in vitro drug release behavior is an important feature of extended release (ER) hydrophilic matrix formulations for accurate prediction of in vivo drug release. In this study, ER hydrophilic matrix tablets of metoprolol tartrate were formulated using a high viscosity grade of hypromellose as a rate-limiting polymer. Expectedly, this formulation showed an undesirable initial burst release followed by controlled drug release. Application of a barrier membrane (BM) coating of ethylcellulose with a pore former (hypromellose) resulted in the elimination of the burst effect. The aim of this study was to investigate the robustness of in vitro metoprolol release from BM-coated hydrophilic matrix tablets by simulating the physicochemical properties of gastrointestinal fluids and mechanical stress in the fasted- and fed state human gastrointestinal (GI) tract. Uncoated and BM-coated matrices were subjected to various dissolution studies simulating the varying pH conditions and additional physicochemical parameters, and the mechanical stress that can be caused by GI motility during both fasted and fed state GI passage. The BM-coated formulation showed robust drug release without an initial burst in all test scenarios. BM-coated matrix formulations thus represent a very promising approach for obtaining a highly controlled and robust drug release from oral ER formulations.
体外药物释放行为稳健是延长释放(ER)亲水基质制剂的一个重要特征,可准确预测体内药物释放。在这项研究中,采用高粘度等级的羟丙甲纤维素作为限速聚合物,对酒石酸美托洛尔的 ER 亲水基质片进行了配方设计。预期该配方会出现不理想的初始突释,随后是控制药物释放。应用乙基纤维素的屏障膜(BM)包衣和致孔剂(羟丙甲纤维素),消除了突释效应。本研究旨在通过模拟空腹和进食状态下人体胃肠道(GI)的理化性质和机械应力,考察 BM 包衣亲水基质片从体外释放美托洛尔的稳健性。未包衣和 BM 包衣的基质都进行了各种溶解研究,模拟不同的 pH 值条件和其他理化参数,以及 GI 运动在空腹和进食状态下通过 GI 道时可能引起的机械应力。在所有测试情况下,BM 包衣制剂均表现出稳定的药物释放,无初始突释。因此,BM 包衣基质制剂为获得口服 ER 制剂高度控制和稳健的药物释放提供了一种很有前途的方法。