Hydrophilic thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding

被引:49
|
作者
Verstraete, G. [1 ]
Van Renterghem, J. [2 ]
Van Bockstal, P. J. [2 ]
Kasmi, S. [1 ]
De Geest, B. G. [1 ]
De Beer, T. [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, Lab Pharmaceut Proc Analyt Technol, B-9000 Ghent, Belgium
关键词
Hot melt extrusion; Injection molding; Rheology; Thermoplastic polyurethanes; High drug load; Sustained release; PHARMACEUTICAL APPLICATIONS; DRUG-RELEASE; DELIVERY;
D O I
10.1016/j.ijpharm.2016.04.057
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hydrophilic aliphatic thermoplastic polyurethane (Tecophilic (TM) grades) matrices for high drug loaded oral sustained release dosage forms were formulated via hot melt extrusion/injection molding (HME/IM). Drugs with different aqueous solubility (diprophylline, theophylline and acetaminophen) were processed and their influence on the release kinetics was investigated. Moreover, the effect of Tecophilic (TM) grade, HME/IM process temperature, extrusion speed, drug load, injection pressure and post-injection pressure on in vitro release kinetics was evaluated for all model drugs. H-1 NMR spectroscopy indicated that all grades have different soft segment/hard segment ratios, allowing different water uptake capacities and thus different release kinetics. Processing temperature of the different Tecophilic (TM) grades was successfully predicted by using SEC and rheology. Tecophilic (TM) grades SP60D60, SP93A100 and TG2000 had a lower processing temperature than other grades and were further evaluated for the production of IM tablets. During HME/IM drug loads up to 70% (w/w) were achieved. In addition, Raman mapping and (M)DSC results confirmed the homogenous distribution of mainly crystalline API in all polymer matrices. Besides, hydrophilic TPU based formulations allowed complete and sustained release kinetics without using release modifiers. As release kinetics were mainly affected by drug load and the length of the PEO soft segment, this polymer platform offers a versatile formulation strategy to adjust the release rate of drugs with different aqueous solubility. (c) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:214 / 221
页数:8
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