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首页> 外文期刊>Enzyme Research >A Fractional Factorial Design to Study the Effect of Process Variables on the Preparation of Hyaluronidase Loaded PLGA Nanoparticles
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A Fractional Factorial Design to Study the Effect of Process Variables on the Preparation of Hyaluronidase Loaded PLGA Nanoparticles

机译:用于研究工艺变量对透明质酸酶负载PLGA纳米颗粒制备影响的分数阶因子设计

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The present study was initiated to understand the effect of PLGA concentration, PVA concentration, internal-external phase ratio, homogenization speed, and homogenization time on mean particle size, zeta potential, and percentage drug encapsulation using fractional factorial design. Using PLGA (50-50) as the carrier, hyaluronidase loaded PLGA nanoparticles were prepared using double emulsion solvent evaporation technique. The particle size was analyzed by dynamic light scattering technique and protein content by Lowry method. The study showed that homogenization speed as an independent variable had maximum effect on particle size and zeta potential. Internal-external phase volume ratio had maximum effect on drug encapsulation. Mean particle size also had high dependency on the combined effect of PVA concentration and phase volume ratio. Using fractional factorial design particle size of <400 nm, zeta potential of <−30 mV, and percentage encapsulation of 15–18% were achieved.
机译:开始本研究是为了了解PLGA浓度,PVA浓度,内外相比,均质化速度和均质化时间对平均粒径,ζ电位和使用分数因子设计的药物包封百分比的影响。以PLGA(50-50)为载体,采用双乳液溶剂蒸发技术制备了透明质酸酶负载的PLGA纳米颗粒。通过动态光散射技术分析粒度,并通过Lowry方法分析蛋白质含量。研究表明,均质化速度作为独立变量对粒度和Zeta电位影响最大。内外相体积比对药物封装影响最大。平均粒径也高度依赖于PVA浓度和相体积比的综合作用。使用小于400 designnm的分数阶因子设计粒径,<-30 mV的zeta电位以及15%至18%的包封百分比。

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