首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Zein/fucoidan-based composite nanoparticles for the encapsulation of pterostilbene: Preparation, characterization, physicochemical stability, and formation mechanism
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Zein/fucoidan-based composite nanoparticles for the encapsulation of pterostilbene: Preparation, characterization, physicochemical stability, and formation mechanism

机译:基于玉米醇素/岩藻砜的复合纳米颗粒用于封装运动苯丙烯:制备,表征,物理化学稳定性和形成机制

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The objective of this work is to fabricate zein/fucoidan composite nanoparticles for the delivery of pterostilbene, a hydrophobic nutraceuticalwith diverse beneficial biological activities. Pterostilbene-encapsulated zein/fucoidan composite nanoparticles were prepared using an anti-solvent precipitation method. The fucoidan levels affected the physicochemical properties of the composite nanoparticles. When the zein to fucoidan mass ratio was 10:1, 5:1, 2:1, or 1:1, the prepared zein/fucoidan nanoparticles were stable, and these nanoparticles showed higher pterostilbene encapsulation efficiency than did zein nanoparticles. Fucoidan-stabilized zein nanoparticles exhibited globular structure with average diameters of 120-150 nm. Fourier-transform infrared spectroscopy, X-ray diffraction, and fluorescence spectrum analysis confirmed that the formation of composite nanoparticles was mainly driven by electrostatic, hydrogen-bonding, and hydrophobic interactions between pterostilbene, zein, and fucoidan. Furthermore, the photochemical stability of pterostilbene encapsulated in zein/fucoidan nanoparticles was markedly better than that of pterostilbene loaded in zein nanoparticles or unencapsulated pterostilbene. Zein/fucoidan nanoparticles provided a better controlled release of pterostilbene than did zein nanoparticles under simulated gastrointestinal conditions. Moreover, the cytotoxicity assay demonstrated that zein/fucoidan nanoparticleswere nontoxic to Caco-2, HK-2, and L-02 cells. Based on our results, the zein/fucoidan nanoparticles may be a promising delivery carrier for the encapsulation, protection, and release of pterostilbene. (c) 2020 Elsevier B.V. All rights reserved.
机译:这项工作的目的是制造玉米醇溶蛋白/岩藻酮复合纳米粒子用于递送活体苯丙烯,一种疏水性营养素,不同的有益生物活性。使用抗溶剂沉淀法制体制备活体封装的玉米醇溶蛋白/岩藻啉复合纳米粒子。岩藻藻水平影响复合纳米颗粒的物理化学性质。当玉米蛋白抗果环质量比为10:1,5:1,2:1,或1:1时,制备的玉米醇溶蛋白/岩藻酮纳米颗粒是稳定的,并且这些纳米颗粒表现出比玉米蛋白纳米颗粒更高的运动蛋白包封效率。岩藻烷稳定的玉米醇溶蛋白纳米颗粒表现出具有120-150nm的平均直径的球状结构。傅里叶变换红外光谱,X射线衍射和荧光谱分析证实,复合纳米颗粒的形成主要是通过静电,氢键和活骨蛋白,玉米醇蛋白和岩藻糖烷之间的疏水相互作用驱动。此外,在玉米醇溶蛋白/岩藻屈甲烷纳米粒子中包封的活体内的光化学稳定性显着优于玉米醇溶蛋白纳米粒子或未封装的运动苯甲烯中的运动苯丙烯。 Zein / FucoinoNan纳米粒子提供了在模拟胃肠环境下的玉米蛋白纳米颗粒的活体释放的释放。此外,细胞毒性测定证明,玉米醇溶蛋白/骨环烷基纳米颗粒与Caco-2,HK-2和L-02细胞无毒。基于我们的结果,玉米醇溶蛋白/岩藻酮纳米粒子可以是用于包封,保护和释放活体苯丙烯的有前途的输送载体。 (c)2020 Elsevier B.v.保留所有权利。

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