Formation of self-assembled polyelectrolyte complex derived from BSA and nanogels: a study to optimize processing parameters and preserve protein integrity.

IF 2.4 4区 医学 Q3 CHEMISTRY, MEDICINAL
Jahanzeb Mudassir, Aamir Jalil, Khizar Abbas, Yusrida Darwis
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引用次数: 0

Abstract

Objective: The aim of this work was to identify, optimize, and use nondestructive process to develop nano-formulation using polyelectrolyte complexation (PEC) between polymeric nanocarrier and bovine serum albumin.

Significance: Proteins are mostly degraded during preparation and loading into nano-carriers which hinders success in protein delivery.

Method: Herein, novel PEC consisting of model protein BSA and nanogels (NGs), were prepared to form self-assembled polyelectrolyte nanocomplexes (BSA/NGs-PEC). The BSA/NGs-PEC were obtained by mixing BSA and nanogels at various weight ratios (1:2, 1:4, 1:5, 1:6, 1:8, 1:10), pH values of solution (1.2, 4.0, 6.0), incubation time (2, 4, 6, 8 h), and stirring rate (without, 100, 200 rpm). The prepared PEC were evaluated for particle size (PS), polydispersity index (PDI), zeta potential (ZP), and percentage of complexation efficiency (%CE). To study insights into structural integrity and biological activity, the SDS-PAGE and esterase activity assay was performed on BSA released from final optimized formulation.

Results: The optimized parameters were BSA/nanogels mixing ratios at 1:8, pH of complex-forming medium at 4.0, incubation time of 6 h, and stirring rate at 100 rpm. The SDS-PAGE and esterase activity assay revealed that the primary structure and bioactivity, respectively, of BSA was still intact.

Conclusion: The results suggest that current scheme for optimization has considerable potential for creating protein-based delivery system by using PEC via electrostatic interaction.

由牛血清白蛋白和纳米凝胶衍生的自组装聚电解质复合物的形成:优化加工参数和保持蛋白质完整性的研究。
目的:利用聚合纳米载体与牛血清白蛋白的聚电解质络合(PEC)制备纳米制剂。意义:蛋白质在制备和装载纳米载体的过程中大多被降解,这阻碍了蛋白质的成功递送。方法:制备由模型蛋白BSA和纳米凝胶(NGs)组成的新型聚电解质纳米复合物(BSA/NGs-PEC)。分别以不同的质量比(1:2、1:4、1:5、1:6、1:8、1:10)、溶液pH(1.2、4.0、6.0)、孵育时间(2、4、6、8小时)和搅拌速率(无、100、200 rpm)混合BSA/NGs-PEC。对制备的PEC进行了粒径(PS)、多分散性指数(PDI)、zeta电位(ZP)和络合效率百分比(%CE)的评价。为了研究其结构完整性和生物活性,对最终优化配方释放的牛血清白蛋白进行了SDS-PAGE和酯酶活性测定。结果:优化后的工艺参数为:BSA/Nanogels的混合比为1:8,复合成型介质pH为4.0,培养时间为6 h,搅拌速度为100 rpm。SDS-PAGE和酯酶活性分析表明,牛血清白蛋白的初级结构和生物活性均未改变。结论:目前的优化方案具有很大的潜力,可以通过静电相互作用建立基于蛋白质的PEC传递系统。
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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来源期刊
CiteScore
6.80
自引率
0.00%
发文量
82
审稿时长
4.5 months
期刊介绍: The aim of Drug Development and Industrial Pharmacy is to publish novel, original, peer-reviewed research manuscripts within relevant topics and research methods related to pharmaceutical research and development, and industrial pharmacy. Research papers must be hypothesis driven and emphasize innovative breakthrough topics in pharmaceutics and drug delivery. The journal will also consider timely critical review papers.
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