以肠道聚合物为载体的蛋白质纳米包封。

D Dupeyrón, M González, V Sáez, J Ramón, J Rieumont
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引用次数: 21

摘要

在这项初步工作中,一种肠道聚合物被用于包封牛血清白蛋白(BSA)作为模型蛋白药物。聚(丙交酯-共乙二醇酯)通常作为聚合物基质用于口服给药,但在这种情况下,肠道聚合物被有效地用于保护胃环境中的蛋白质。采用改进的水/油/水技术减小纳米颗粒的直径,透射电镜实验表明,得到的纳米颗粒的平均直径在100 nm以下。颗粒的球形性质及其直径在很大程度上取决于工艺参数的控制。样品B4的包封效率为77%,样品B3和样品B4的蛋白质释放谱表明该体系具有控释特性。最后,电泳(SDS-PAGE)结果表明,在包封条件下,BSA没有受到化学反应的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nano-encapsulation of protein using an enteric polymer as carrier.

In this preliminary work, an enteric polymer has been used for encapsulating bovine serum albumine (BSA) as a model protein drug. Poly (lactide-co- glycolide) has been commonly used for oral administration purposes as a polymer matrix, but in this case an enteric polymer was used effectively to protect the protein in a gastric environment. A modified water/oil/water technique was used to decrease the particle diameter, and transmission electron microscopy experiments showed that the average diameter of the nanoparticles obtained was below 100 nm. The spherical nature of the particles and their diameters strongly depend on the control of the process parameters. The encapsulation efficiency was 77% for sample B4, and protein release profiles for both samples B3 and B4 indicate that these systems possess controlled-release characteristics. Finally, as a result of electrophoresis (SDS-PAGE), the BSA was not chemically affected under encapsulation conditions.

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