3D printing of high drug loaded dosage forms using thermoplastic polyurethanes

被引:168
|
作者
Verstraete, G. [1 ]
Samaro, A. [1 ]
Grymonpre, W. [1 ]
Vanhoorne, V. [1 ]
Van Snick, B. [1 ]
Boone, M. N. [2 ]
Hellemans, T. [3 ]
Van Hoorebeke, L. [2 ]
Remon, J. P. [1 ]
Vervaet, C. [1 ]
机构
[1] Univ Ghent, Lab Pharmaceut Technol, Ottergemsesteenweg 460, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Phys & Astron, Radiat Phys Ctr Xray Tomog, Ghent, Belgium
[3] Univ Ghent, Fac Biosci Engn, Dept Food Technol Safety & Hlth, Ghent, Belgium
关键词
Personalized medicine; 3D printing; Fused deposition modelling; Thermoplastic polyurethanes; Sustained release; High drug load; HOT-MELT EXTRUSION; RELEASE CHARACTERISTICS; TABLETS; FABRICATION; FORMULATION; IMMEDIATE; MATRICES; DEVICES; PHASE;
D O I
10.1016/j.ijpharm.2017.12.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It was the aim of this study to develop high drug loaded (> 30%, w/w), thermoplastic polyurethane (TPU)-based dosage forms via fused deposition modelling (FDM). Model drugs with different particle size and aqueous solubility were pre-processed in combination with diverse TPU grades via hot melt extrusion (HME) into filaments with a diameter of 1.75 +/- 0.05 mm. Subsequently, TPU-based filaments which featured acceptable quality attributes (i.e. consistent filament diameter, smooth surface morphology and good mechanical properties) were printed into tablets. The sustained release potential of the 3D printed dosage forms was tested in vitro. Moreover, the impact of printing parameters on the in vitro drug release was investigated. TPU-based filaments could be loaded with 60% (w/w) fine drug powder without observing severe shark skinning or inconsistent filament diameter. During 3D printing experiments, HME filaments based on hard TPU grades were successfully converted into personalized dosage forms containing a high concentration of crystalline drug (up to 60%, w/w). In vitro release kinetics were mainly affected by the matrix composition and tablet infill degree. Therefore, this study clearly demonstrated that TPU-based FDM feedstock material offers a lot of formulation freedom for the development of personalized dosage forms.
引用
收藏
页码:318 / 325
页数:8
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