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含精氨酸基表面活性剂的玉米醇溶蛋白纳米颗粒:理化特性及对生物学性质的影响。

Zein Nanoparticles Containing Arginine-Based Surfactants: Physicochemical Characterization and Effect on the Biological Properties.

机构信息

Department of Surfactants and Nanobiotechnology, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), 08034 Barcelona, Spain.

While was at Biocompatible Surfactant and Liquid Ionic Group, Institut de Química Avançada de Catalunya-CSIC, 08034 Barcelona, Spain.

出版信息

Int J Mol Sci. 2023 Jan 29;24(3):2568. doi: 10.3390/ijms24032568.

Abstract

Cationic surfactants carry antimicrobial activity, based on their interaction and disruption of cell membranes. Nonetheless, their intrinsic toxicity limits their applicability. To overcome this issue, a feasible strategy consists of using solid nanoparticles to improve their delivery. The zein nanoparticles were loaded with four cationic arginine-based surfactants: one single chain Nα-lauroyl-arginine (LAM) and three Gemini surfactants Nα Nω-Bis (Nα-lauroyl-arginine) α, ω-diamide) (C(LA), C(LA) and C(LA)). Blank and loaded zein nanoparticles were characterized in terms of size, polydispersity and zeta potential. Furthermore, the antimicrobial activity against bacteria and yeasts and the hemolytic activity were investigated and compared to the surfactants in a solution. Nanoparticles were found to be monodisperse, presenting a size of between 180-341 nm, a pdI of <0.2 and a positive zeta potential of between +13 and +53 mV, remaining stable over 365 days. The nanoencapsulation maintained the antimicrobial activity as unaltered, while the extensive hemolytic activity found for the surfactants in a solution was reduced drastically. Nuclear Magnetic Ressonance (NMR), molecular docking and monolayer findings indicated that zein entraps the surfactants, interfering in the surfactant-membrane interactions. Accordingly, the nanoepcasulation of arginine surfactants improved their selectivity, while the cationic charges were free to attack and destroy bacteria and fungi; the aliphatic chains were not available to disrupt the cellular membranes.

摘要

阳离子表面活性剂通过与细胞膜相互作用和破坏细胞膜来发挥抗菌活性。然而,其内在毒性限制了其适用性。为了解决这个问题,一种可行的策略是使用固体纳米粒子来改善其传递。玉米醇溶蛋白纳米粒子负载了四种阳离子精氨酸基表面活性剂:一种单链 Nα-月桂酰-精氨酸(LAM)和三种双子表面活性剂 Nα Nω-双(Nα-月桂酰-精氨酸)α,ω-二酰胺)(C(LA)、C(LA)和 C(LA))。空白和负载的玉米醇溶蛋白纳米粒子的粒径、多分散性和zeta 电位进行了表征。此外,还研究了它们对细菌和酵母的抗菌活性和溶血活性,并与溶液中的表面活性剂进行了比较。发现纳米粒子为单分散性,粒径在 180-341nm 之间,pdI<0.2,zeta 电位在+13 到+53mV 之间,在 365 天内保持稳定。纳米封装保持了抗菌活性不变,而在溶液中发现的表面活性剂具有广泛的溶血活性则大大降低。核磁共振(NMR)、分子对接和单层研究表明,玉米醇溶蛋白将表面活性剂包封在内,干扰了表面活性剂与膜的相互作用。因此,精氨酸表面活性剂的纳米封装提高了它们的选择性,同时阳离子电荷可以自由攻击和破坏细菌和真菌;脂肪链不能破坏细胞膜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e4/9917094/ca04afee95a2/ijms-24-02568-g001.jpg

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