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Study on Preparation and Property of Drug Loading of AZM-PCL Nanoparticels

机译:AZM-PCL纳米粒子的制备及载药性能研究

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This study was to prepare polycaprolactone (PCL) nanoparticles.The biodegradable PCL was used as the carrier,and Azithromycin (AZM) was used as the model drug.AZM-PCL nanoparticles (AZM-PCL-NPS) were prepared by desolvation method.The effect of preparation condition:concentration of PCL,molecular weight of PCL,organic solvents,dosage ratio and so on,were specially noted and compared.A homogeneous size distribution and good dispersion were observed,the average diameter was around 70~400 nm,and the distribution index was 0.036~0.136.The drug loading reached 27.69 %,and the efficiency of encapsulation reached as high as 93.25%.The results were better than the other similar researches,this preparation way was successful.
机译:本研究的目的是制备聚己内酯(PCL)纳米粒子,以可生物降解的PCL为载体,以阿奇霉素(AZM)为模型药物,通过去溶剂化法制备AZM-PCL纳米粒子(AZM-PCL-NPS)。制备条件的影响:特别注意和比较了PCL的浓度,PCL的分子量,有机溶剂,剂量比等。观察到粒径分布均匀,分散性好,平均直径在70〜400 nm左右,且分布指数为0.036〜0.136,载药量达到27.69%,包封率高达93.25%,效果优于其他同类研究,该制备方法是成功的。

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