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

机译:聚乙烯吡咯烷酮-乙酸乙烯酯二元和三元非晶态固体分散体的微注射成型

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摘要

Micro-injection moulding (µIM) 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 µIM 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 µIM, proved to be a successful approach towards a continuous automated manufacturing process to improve the aqueous solubility of poorly water-soluble drugs.
机译:微注射成型(µIM)用于生产聚乙烯吡咯烷酮-醋酸乙烯酯(PVPVA)增塑和未增塑固体分散体的肠溶片,并研究了机械和热处理对分散体性能的影响。系统的物理状态显示出通过µIM步骤不会改变,将药物保持在非晶态。片剂的溶出曲线显示出较慢的溶出速率,这是由于与挤出股相比较低的表面体积比。观察到由于消炎痛(IND)的酸度,剂量在酸性介质中缺乏溶解性。但是,在中性pH值下,药物的溶出速度较慢,且不影响溶出度,显示了开发控释剂量的潜在用途。总体而言,无定形固体分散体(ASD)片剂,热熔挤出(HME)和µIM的生产被证明是一种连续自动化制造工艺的成功方法,可改善水溶性差的药物的水溶性。

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