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用海藻酸钠-壳聚糖包封的硒纳米颗粒的配方用于霍乱弧菌 LPS 的控制释放:一种新型纳米疫苗的候选递药系统。

Formulation of selenium nanoparticles encapsulated by alginate-chitosan for controlled delivery of Vibrio Cholerae LPS: A novel delivery system candidate for nanovaccine.

机构信息

Department of Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Department of Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Int J Biol Macromol. 2022 May 31;208:494-508. doi: 10.1016/j.ijbiomac.2022.03.087. Epub 2022 Mar 23.

DOI:10.1016/j.ijbiomac.2022.03.087
PMID:35337913
Abstract

The lipopolysaccharide (LPS) of Vibrio cholerae plays a significant role in stimulating primary protection and immune responses. LPS delivery has been limited by the stimulation of inflammatory cytokines. This work aimed to report the synthesis and performance of this formulation in modulating immune responses and protecting LPS against acidic gastric medium. Alg-Cs-LPS-SeNPs composite was fabricated by an ionic cross-linking/in situ reduction method. Cytokines TNF-α, IL-6, IL-10, and TGF-β were assessed after cells were incubated with different compounds of the system. The main outcomes revealed that encapsulation of LPS-loaded SeNPs in the alginate-chitosan complex was associated with a high entrapment efficiency and could effectively protect LPS against acidic GIT medium. Kinetic profiling revealed that LPS was more slowly released from LPS-loaded Alg-Cs-LPS-SeNPs at pH 1.2, 7.4, and 6.8. These results indicated that Alg-Cs-LPS-SeNPs composite was able to significantly increase anti-inflammatory cytokines and reduce the release of pro-inflammatory cytokines. Thus, these findings show that this system for LPS delivery could be easily biosynthesized and encapsulated for use in the pharmaceutical industry. This study provides proof of the potential for future use of oral LPS vaccines, concomitantly inducing immunomodulatory effects.

摘要

霍乱弧菌的脂多糖 (LPS) 在刺激初级保护和免疫反应方面起着重要作用。LPS 的递送受到炎症细胞因子刺激的限制。本工作旨在报告该制剂在调节免疫反应和保护 LPS 免受酸性胃介质方面的合成和性能。通过离子交联/原位还原法制备 Alg-Cs-LPS-SeNPs 复合材料。用不同的系统化合物孵育细胞后,评估细胞因子 TNF-α、IL-6、IL-10 和 TGF-β。主要结果表明,将负载 LPS 的 SeNPs 包封在藻酸盐-壳聚糖复合物中与高包封效率相关,并能有效保护 LPS 免受酸性 GIT 介质的影响。动力学分析表明,在 pH 1.2、7.4 和 6.8 时,负载 LPS 的 Alg-Cs-LPS-SeNPs 中 LPS 的释放速度更慢。这些结果表明,Alg-Cs-LPS-SeNPs 复合材料能够显著增加抗炎细胞因子的释放,减少促炎细胞因子的释放。因此,这些发现表明,这种 LPS 递送系统可以很容易地进行生物合成和封装,用于制药工业。本研究为口服 LPS 疫苗的未来应用提供了证据,同时诱导免疫调节作用。

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