A comparative study between melt granulation/compression and hot melt extrusion/injection molding for the manufacturing of oral sustained release thermoplastic polyurethane matrices

被引:28
|
作者
Verstraete, G. [1 ]
Mertens, P. [1 ]
Grymonpre, W. [1 ]
Van Bockstal, P. J. [2 ]
De Beer, T. [2 ]
Boone, M. N. [3 ]
Van Hoorebeke, L. [3 ]
Remon, J. P. [1 ]
Vervaet, C. [1 ]
机构
[1] Univ Ghent, Lab Pharmaceut Technol, Ottergemsesteenweg 460, B-9000 Ghent, Belgium
[2] Univ Ghent, Lab Pharmaceut Proc Analyt Technol, Ghent, Belgium
[3] Univ Ghent, Dept Phys & Astron, Radiat Phys Ctr Xray Tomog, Ghent, Belgium
基金
比利时弗兰德研究基金会;
关键词
Hot melt extrusion; Twin screw melt granulation; Matrices; High drug load; Sustained release; Thermoplastic polyurethanes; Metformin hydrochloride; METFORMIN; TABLETS; PHARMACOKINETICS; HPMC; EXTRUSION; PHASE; IMAGE; FOOD;
D O I
10.1016/j.ijpharm.2016.09.072
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
During this project 3 techniques (twin screw melt granulation/compression (TSMG), hot melt extrusion (HME) and injection molding (IM)) were evaluated for the manufacturing of thermoplastic polyurethane (TPU)-based oral sustained release matrices, containing a high dose of the highly soluble metformin hydrochloride. Whereas formulations with a drug load between 0 and 70% (w/w) could be processed via HME/(IM), the drug content of granules prepared via melt granulation could only be varied between 85 and 90% (w/w) as these formulations contained the proper concentration of binder (i.e. TPU) to obtain a good size distribution of the granules. While release from HME matrices and IM tablets could be sustained over 24 h, release from the TPU-based TSMG tablets was too fast (complete release within about 6 h) linked to their higher drug load and porosity. By mixing hydrophilic and hydrophobic TPUs the in vitro release kinetics of both formulations could be adjusted: a higher content of hydrophobic TPU was correlated with a slower release rate. Although mini-matrices showed faster release kinetics than IM tablets, this observation was successfully countered by changing the hydrophobic/hydrophilic TPU ratio. In vivo experiments via oral administration to dogs confirmed the versatile potential of the TPU platform as intermediate-strong and low-intermediate sustained characteristics were obtained for the IM tablets and HME mini-matrices, respectively. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:602 / 611
页数:10
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