用分数析因设计研究工艺变量对制备透明质酸酶负载PLGA纳米颗粒的影响。

Q2 Biochemistry, Genetics and Molecular Biology Enzyme Research Pub Date : 2014-01-01 Epub Date: 2014-12-10 DOI:10.1155/2014/162962
K Narayanan, V M Subrahmanyam, J Venkata Rao
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引用次数: 48

摘要

本研究采用分数析因设计,旨在了解PLGA浓度、PVA浓度、内外相比、均质速度和均质时间对平均粒径、zeta电位和药物包封率的影响。以PLGA(50-50)为载体,采用双乳液溶剂蒸发法制备了负载透明质酸酶的PLGA纳米颗粒。用动态光散射技术分析其粒径,用Lowry法分析其蛋白质含量。研究表明,均质速度作为自变量对粒径和zeta电位的影响最大。内、外相体积比对药物包封效果影响最大。平均粒径也高度依赖于PVA浓度和相体积比的综合效应。采用分数因子设计粒径
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Fractional Factorial Design to Study the Effect of Process Variables on the Preparation of Hyaluronidase Loaded PLGA Nanoparticles.

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.

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Enzyme Research
Enzyme Research Biochemistry, Genetics and Molecular Biology-Biochemistry
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