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Study on different preparation methods of pirarubicin liposomes

机译:吡菌蛋白脂质体的不同制剂方法研究

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To explore the promising industrialized technique for the preparations of pirarubicin liposomes, pirarubicin was encapsulated into the liposomes using three different preparing techniques, modified transmembrane ammonium sulfate gradient, thin film evaporation and micro-fluidic technique. Therefore the preliminary study of the morphology, particle size distribution, entrapment efficiency and drug loading amount of liposomes were investigated. TEM showed the THP liposomes were small spherical and sphere-like vesicles. Particle size determination showed that the average particle size were about 400(nm), and the micro-fluidic technique of liposomes had mono-disperse size distribution. And the entrapment efficiency of the three techniques were 96.0.%, 79.3% and 86.4% respectively, accordingly the drug loading amount were 4.8%, 4.0% and 4.3%.
机译:为了探讨对吡喃素脂质体脂质体的制剂的有前途的工业化技术,使用三种不同的制备技术将吡咯花素包封在脂质体中,改性跨膜硫酸铵梯度,薄膜蒸发和微流体技术。因此,研究了对脂质体的形态,粒度分布,夹带效率和药物负载量的初步研究。 TEM显示THP脂质体是小球形和球形囊泡。粒度测定表明,平均粒度为约400(nm),并且脂质体的微流体技术具有单分散尺寸分布。并且三种技术的夹带效率分别为96.0.0%。%,79.3%和86.4%,因此药物负载量为4.8%,4.0%和4.3%。

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