Micro-Injection Moulding of Poly(vinylpyrrolidone-vinyl acetate) Binary and Ternary Amorphous Solid Dispersions

被引:3
作者
Pezzoli, Romina [1 ,2 ]
Hopkins, Michael, Jr. [1 ]
Direur, Guillaume [3 ]
Gately, Noel [1 ]
Lyons, John G. [4 ]
Higginbotham, Clement L. [2 ,3 ]
机构
[1] Athlone Inst Technol, Appl Polymer Technol, Dublin Rd, Athlone N37 HD68, Co Westmeath, Ireland
[2] Synth & Solid State Pharmaceut Ctr SSPC, Dublin Rd, Athlone N37 HD68, Co Westmeath, Ireland
[3] Athlone Inst Technol, Mat Res Inst, Dublin Rd, Athlone N37 HD68, Co Westmeath, Ireland
[4] Athlone Inst Technol, Fac Engn & Informat, Dublin Rd, Athlone N37 HD68, Co Westmeath, Ireland
来源
PHARMACEUTICS | 2019年 / 11卷 / 05期
基金
爱尔兰科学基金会;
关键词
amorphous solid dispersions; class II drugs; continuous processing; micro-injection moulding; indomethacin; poly(vinylpyrrolidone-vinyl acetate); HOT-MELT EXTRUSION; PHARMACEUTICAL APPLICATIONS; INDOMETHACIN; RELEASE; PARAMETERS; SYSTEMS;
D O I
10.3390/pharmaceutics11050240
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Micro-injection moulding (mu IM) was used for the production of enteric tablets of plasticised and unplasticised solid dispersions of poly(vinylpyrrolidone-vinyl acetate) (PVPVA), and the effect of the mechanical and thermal treatment on the properties of the dispersions was investigated. The physical state of the systems showed to be unaltered by the mu IM step, maintaining the drug in the amorphous state. The dissolution profile of the tablets showed a slower dissolution rate due to the lower surface to volume ratio compared to the extruded strands. The lack of solubility of the doses in the acidic medium as a consequence of the acidity of indomethacin (IND) was observed. However, in neutral pH the drug dissolution showed slower rates without affecting the dissolution extent, showing a potential application for the development of controlled release doses. Overall, the production of tablets of amorphous solid dispersions (ASD), coupling hot-melt extrusion (HME) and mu IM, proved to be a successful approach towards a continuous automated manufacturing process to improve the aqueous solubility of poorly water-soluble drugs.
引用
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页数:15
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