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Effect of preparation conditions on morphology, drug content and release profiles of poly(hydroxybutyrate) microparticles containing piroxicam

机译:制备条件对含吡罗昔康的聚羟基丁酸酯微粒形态,药物含量和释放曲线的影响

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摘要

In this study, poly(hydroxybutyrate) microparticles containing piroxicam were prepared by the oil-in-water emulsion-solvent evaporation method. The effects of some process conditions on drug content were determined using a 2³ factorial design. The piroxicam loading efficiency varied from 5.5 to 89.8 %. Hollow and irregular microparticles with drug crystals on their surfaces were obtained when 5 mL of chloroform was used as the internal phase. In the release study, all of the piroxicam was released to the dissolution medium (phosphate buffer pH 7.4) after 8 h. Small spherical microspheres with a rough and porous polymeric matrix were obtained when 20 mL of dichloromethane was used as the internal phase and isopropanol was added to the external aqueous phase. These microspheres controlled the piroxicam release for approximately 50 h. The results demonstrated that it is possible to obtain microparticles with specific characteristics by the optimization of the process conditions.
机译:在本研究中,通过水包油乳液-溶剂蒸发法制备了含有吡罗昔康的聚羟基丁酸酯微粒。使用2³析因设计确定某些工艺条件对药物含量的影响。吡罗昔康的装载效率在5.5%至89.8%之间变化。当使用5 mL氯仿作为内相时,可得到表面上有药物晶体的空心和不规则微粒。在释放研究中,所有吡罗昔康都在8小时后释放到溶解介质(磷酸盐缓冲液pH 7.4)中。当将20 mL二氯甲烷用作内相并将异丙醇添加至外部水相中时,获得具有粗糙且多孔的聚合物基质的小球形微球。这些微球控制吡罗昔康的释放约50小时。结果表明,通过优化工艺条件可以获得具有特定特性的微粒。

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