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Nanocapsule-coated microparticles prepared in one step: characterization and in vitro drug release profiles evaluation

机译:一步制备纳米胶囊包衣的微粒:表征和体外药物释放曲线评估

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The aim of this work was to prepare and characterize spray-dried nanocapsule-coated microparticles obtained in one step, using indomethacin as a hydrophobic drug model and poly(e-caprolactone) or Eudragit® RS100, as polymers. Nanocapsule-coated microparticles showed micrometric mean sizes (10 - 15 µm) and a reduced surface area (75 - 85 m2g-1) compared to the raw material (214 m2g-1). Microparticles coated with Eudragit® RS100-nanocapsules showed a better control of the drug release. The release profiles fit to the monoexponetial model and to the Power Law. The mechanism of the indomethacin release from the microparticles is non-Fickian and depends on the particles desagglomeration.
机译:这项工作的目的是使用吲哚美辛作为疏水性药物模型,使用聚(e-己内酯)或Eudragit®RS100作为聚合物,制备和表征一步干燥得到的喷雾干燥的纳米胶囊涂层微粒。与原料(214 m2g-1)相比,纳米胶囊包覆的微粒显示出微米级平均尺寸(10-15 µm)和减小的表面积(75-85 m2g-1)。涂有Eudragit®RS100纳米胶囊的微粒显示出更好的药物释放控制。释放配置文件适合单指数模型和幂律。消炎痛从微粒中释放的机理是非菲克式的,并且取决于颗粒的解聚作用。

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