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Effect of supercritical fluid density on nanoencapsulated drug particle size using the supercritical antisolvent method

机译:使用超临界反溶剂法的超临界流体密度对纳米胶囊药物粒径的影响

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摘要

The reported work demonstrates and discusses the effect of supercritical fluid density (pressure and temperature of supercritical fluid carbon dioxide) on particle size and distribution using the supercritical antisolvent (SAS) method in the purpose of drug encapsulation. In this study, paracetamol was encapsulated inside L-polylactic acid, a semicrystalline polymer, with different process parameters, including pressure and temperature, using the SAS process. The morphology and particle size of the prepared nanoparticles were determined by scanning electron microscopy and transmission electron microscopy. The results revealed that increasing temperature enhanced mean particle size due to the plasticizing effect. Furthermore, increasing pressure enhanced molecular interaction and solubility; thus, particle size was reduced. Transmission electron microscopy images defined the internal structure of nanoparticles. Thermal characteristics of nanoparticles were also investigated via differential scanning calorimetry. Furthermore, X-ray diffraction pattern revealed the changes in crystallinity structure during the SAS process. In vitro drug release analysis determined the sustained release of paracetamol in over 4 weeks.
机译:报道的工作使用超临界抗溶剂(SAS)方法演示和讨论了超临界流体密度(超临界流体二氧化碳的压力和温度)对粒径和分布的影响,目的是进行药物封装。在这项研究中,扑热息痛使用SAS工艺封装在具有不同工艺参数(包括压力和温度)的半结晶聚合物L-聚乳酸内。通过扫描电子显微镜和透射电子显微镜确定所制备的纳米颗粒的形态和粒径。结果表明,由于增塑作用,温度升高提高了平均粒径。此外,增加压力可增强分子相互作用和溶解性;因此,减小了粒径。透射电子显微镜图像定义了纳米颗粒的内部结构。还通过差示扫描量热法研究了纳米颗粒的热特性。此外,X射线衍射图揭示了SAS过程中结晶结构的变化。体外药物释放分析确定了扑热息痛在4周内的持续释放。

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