Robustness of barrier membrane coated metoprolol tartrate matrix tablets: Drug release evaluation under physiologically relevant in vitro conditions

被引:13
作者
Klein, Sandra [1 ]
Seeger, Nicole [1 ]
Mehta, Raxit [2 ]
Missaghi, Shahrzad [2 ]
Grybos, Relindis [1 ]
Rajabi-Siahboomi, Ali [2 ]
机构
[1] Ernst Moritz Arndt Univ Greifswald, Dept Pharm, Inst Biopharmaceut & Pharmaceut Technol, Ctr Drug Absorpt & Transport, 3 Felix Hausdorff St, D-17489 Greifswald, Germany
[2] Colorcon Inc, Global Headquarters, 275 Ruth Rd, Harleysville, PA 19438 USA
关键词
Barrier membrane coating; Hydrophilic matrix tablets; Matrices; Extended release; Sustained release; Surelease; Pore former; FOOD-INDUCED CHANGES; DOSAGE FORMS; THEOPHYLLINE ABSORPTION; GASTROINTESTINAL-TRACT; NIFEDIPINE; FORMULATIONS; PROFILES; HUMANS; MEAL; BIOAVAILABILITY;
D O I
10.1016/j.ijpharm.2018.04.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:368 / 375
页数:8
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