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大小效应和黏液在 E551 食品添加剂和工程化二氧化硅纳米颗粒的肠道毒性中的作用。

Size effect and mucus role on the intestinal toxicity of the E551 food additive and engineered silica nanoparticles.

机构信息

PEPITE EA4267, Univ. Bourgogne Franche-Comté, Besançon, France.

Laboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303, CNRS/Université Bourgogne Franche-Comté, Dijon, France.

出版信息

Nanotoxicology. 2022 Mar;16(2):165-182. doi: 10.1080/17435390.2022.2063084. Epub 2022 May 17.

Abstract

The E551 food additive is composed of synthetic amorphous silica particles. The current regulation does not mention any specifications regarding their size and granulometric distribution, thus allowing the presence of silica nanoparticles despite their potential toxicity. The digestion process could modify their physicochemical properties and then influence their toxicological profile. After physicochemical characterization, subacute toxicity of engineered silica nanoparticles from 20 to 200 nm, native and digested E551 additives were evaluated from models of the intestinal barrier. Single cultures and a co-culture of enterocytes and mucus-secreting cells were established to investigate the mucus role. Toxicological endpoints including cytotoxicity, ROS production, intestinal permeability increase, and actin filament disruption were addressed after a 7-day exposure. The results showed a size-dependent effect of silica nanoparticles on cytotoxicity and intestinal permeability. A time-dependent disruption of actin filaments was observed in Caco-2 cells. The mucus layer spread on the HT29-MTX single culture acted as an efficient protective barrier while in the co-culture, small nanoparticles were able to cross it to reach the cells. From a hydrodynamic diameter of 70 nm, nanoparticles were not internalized in the intestinal cells, even in mucus-free models. Digestion did not affect the physicochemical properties of the additive. Due to a mean hydrodynamic diameter close to 200 nm, both native and digested E551 additives did not induce any toxic effect in intestinal barrier models. This study emphasized a cutoff size of 70 nm from which the interactions of the E551 additive with intestinal cells would be limited.

摘要

E551 食品添加剂由合成无定形二氧化硅颗粒组成。目前的法规没有提到其大小和粒度分布的任何规格,因此尽管存在潜在毒性,但仍允许存在纳米二氧化硅。消化过程可能会改变它们的物理化学性质,然后影响它们的毒理学特征。经过物理化学特性分析后,从小肠屏障模型中评估了粒径为 20 至 200nm 的工程化二氧化硅纳米颗粒、天然和消化后的 E551 添加剂的亚急性毒性。建立了单层培养物和肠细胞与黏液分泌细胞的共培养物,以研究黏液的作用。在 7 天的暴露后,研究了包括细胞毒性、ROS 产生、肠道通透性增加和肌动蛋白丝破坏在内的毒理学终点。结果表明,二氧化硅纳米颗粒的细胞毒性和肠道通透性具有尺寸依赖性。在 Caco-2 细胞中观察到肌动蛋白丝的时间依赖性破坏。在 HT29-MTX 单层培养物上扩散的黏液层起到了有效的保护屏障作用,而在共培养物中,小纳米颗粒能够穿过黏液层到达细胞。由于水动力学直径为 70nm,纳米颗粒甚至在无黏液模型中也不会被肠细胞内化。消化不会影响添加剂的物理化学性质。由于天然和消化后的 E551 添加剂的平均水动力学直径接近 200nm,因此它们都不会在肠道屏障模型中引起任何毒性作用。本研究强调了 70nm 的截止尺寸,在此尺寸下,E551 添加剂与肠道细胞的相互作用将受到限制。

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