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PLGA Docetaxel Nanoparticles: Preparation and In Vitro Evaluation

机译:PLGA多西他赛纳米颗粒:制备和体外评估

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摘要

In this study PLGA nanoparticles containing docetaxel have been developed. The effect of different formulation parameters such as drug/polymer ratios, oil phase combination, volume and surfactant amount were evaluated. The size and size distribution and surface morphology of the nanoparticles were then investigated by laser light scattering and scanning electron microscopy. The drug encapsulation efficiency and in vitro release profiles were measured by HPLC. It was shown that the polymeric nanoparticles could provide a suitable release profile and exerts an adequate control on the drag diffusion rate.
机译:在这项研究中,已开发出包含多西紫杉醇的PLGA纳米颗粒。评估了不同配方参数(如药物/聚合物的比例,油相组合,体积和表面活性剂的量)的影响。然后通过激光散射和扫描电子显微镜研究纳米颗粒的尺寸和尺寸分布以及表面形态。通过HPLC测量药物包封效率和体外释放曲线。结果表明,聚合物纳米颗粒可以提供合适的释放曲线,并可以对药物的扩散速率进行适当的控制。

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