• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

不同尺寸二氧化硅纳米颗粒对角膜的毒性及蛋白质冠层作为一种治疗策略

Toxicity of silicon dioxide nanoparticles with varying sizes on the cornea and protein corona as a strategy for therapy.

作者信息

Sun Dayu, Gong Linji, Xie Jing, Gu Xianliang, Li Yijian, Cao Qinglin, Li Qiyou, A Luodan, Gu Zhanjun, Xu Haiwei

机构信息

Department of Physiology, Third Military Medical University (Army Medical University), Chongqing 400038, China; Southwest Hospital/Southwest Eye Hospital, Third Military Medical University (Army Medical University), Chongqing 400038, China; Key Laboratory of Visual Damage and Regeneration & Restoration of Chongqing, Chongqing 400038, China.

Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.; University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Sci Bull (Beijing). 2018 Jul 30;63(14):907-916. doi: 10.1016/j.scib.2018.05.037. Epub 2018 Jun 8.

DOI:10.1016/j.scib.2018.05.037
PMID:36658972
Abstract

The human cornea is exposed directly to particulate matter (PM) in polluted air. This exposure can cause eye discomfort and corneal injury. Ultrafine PM (diameter <100 nm) is thought to be particularly harmful to health, but there is limited research investigating its toxicity to the eye. In this study, we evaluated toxicity differences among 30-, 40-, 100- and 150-nm silicon dioxide nanoparticles (SiO NPs) on the cornea. A 24-hour in vitro exposure of primary human corneal epithelial cells (hCECs) to ultrafine (30 and 40 nm) SiO NPs produced toxicity, as evidenced by cell membrane damage, reduced cell viability, increased cell death and mitochondrial dysfunction. In vivo exposure to the same nanoparticles produced observable corneal injury. These effects were more severe with ultrafine than with fine (100 and 150 nm) SiO NPs. Common antioxidant compounds, e.g., glutathione, did not protect the cornea from SiO NP-induced damage. However, foetal bovine serum (FBS) did significantly reduce toxicity, likely by forming a protective protein corona around the nanoparticles. This finding suggests that FBS (or its derivatives) may be a useful clinical therapy for corneal toxicity caused by ultrafine particulates.

摘要

人角膜直接暴露于污染空气中的颗粒物(PM)。这种暴露会导致眼部不适和角膜损伤。超细颗粒物(直径<100纳米)被认为对健康特别有害,但研究其对眼睛毒性的研究有限。在本研究中,我们评估了30纳米、40纳米、100纳米和150纳米二氧化硅纳米颗粒(SiO NPs)对角膜的毒性差异。原代人角膜上皮细胞(hCECs)体外暴露于超细(30和40纳米)SiO NPs 24小时产生了毒性,表现为细胞膜损伤、细胞活力降低、细胞死亡增加和线粒体功能障碍。体内暴露于相同的纳米颗粒会导致可观察到的角膜损伤。超细SiO NPs的这些影响比细颗粒(100和150纳米)更严重。常见的抗氧化化合物,如谷胱甘肽,并不能保护角膜免受SiO NP诱导的损伤。然而,胎牛血清(FBS)确实显著降低了毒性,可能是通过在纳米颗粒周围形成保护性蛋白质冠层。这一发现表明,FBS(或其衍生物)可能是治疗超细颗粒物引起的角膜毒性的一种有用的临床疗法。

相似文献

1
Toxicity of silicon dioxide nanoparticles with varying sizes on the cornea and protein corona as a strategy for therapy.不同尺寸二氧化硅纳米颗粒对角膜的毒性及蛋白质冠层作为一种治疗策略
Sci Bull (Beijing). 2018 Jul 30;63(14):907-916. doi: 10.1016/j.scib.2018.05.037. Epub 2018 Jun 8.
2
Combined exposure to nano-silica and lead induced potentiation of oxidative stress and DNA damage in human lung epithelial cells.纳米二氧化硅和铅联合暴露致肺上皮细胞氧化应激和 DNA 损伤增强。
Ecotoxicol Environ Saf. 2015 Dec;122:537-44. doi: 10.1016/j.ecoenv.2015.09.030. Epub 2015 Sep 29.
3
Dynamic development of the protein corona on silica nanoparticles: composition and role in toxicity.硅纳米颗粒上蛋白质冠的动态发展:组成与毒性作用
Nanoscale. 2013 Jul 21;5(14):6372-80. doi: 10.1039/c3nr33280b. Epub 2013 Jun 4.
4
Comparative Toxic Effects of Manufactured Nanoparticles and Atmospheric Particulate Matter in Human Lung Epithelial Cells.纳米颗粒与大气颗粒物对人肺上皮细胞的比较毒理效应。
Int J Environ Res Public Health. 2020 Dec 22;18(1):22. doi: 10.3390/ijerph18010022.
5
Silica dioxide nanoparticles combined with cold exposure induce stronger systemic inflammatory response.二氧化硅纳米颗粒与冷暴露相结合会引发更强的全身炎症反应。
Environ Sci Pollut Res Int. 2017 Jan;24(1):291-298. doi: 10.1007/s11356-016-7649-2. Epub 2016 Oct 6.
6
An assessment of the impact of SiO2 nanoparticles of different sizes on the rest/wake behavior and the developmental profile of zebrafish larvae.评估不同大小的 SiO2 纳米颗粒对斑马鱼幼体的休息/醒来行为和发育情况的影响。
Small. 2013 Sep 23;9(18):3161-8. doi: 10.1002/smll.201300430. Epub 2013 Mar 7.
7
Immunotoxicity of silicon dioxide nanoparticles with different sizes and electrostatic charge.不同尺寸和静电荷的二氧化硅纳米颗粒的免疫毒性
Int J Nanomedicine. 2014 Dec 15;9 Suppl 2(Suppl 2):183-93. doi: 10.2147/IJN.S57934. eCollection 2014.
8
Toxicity of engineered nanomaterials with different physicochemical properties and the role of protein corona on cellular uptake and intrinsic ROS production.具有不同物理化学性质的工程纳米材料的毒性以及蛋白质冠层对细胞摄取和内源性活性氧产生的作用。
Toxicology. 2020 Sep;442:152545. doi: 10.1016/j.tox.2020.152545. Epub 2020 Aug 2.
9
Mechanistic study of silica nanoparticles on the size-dependent retinal toxicity in vitro and in vivo.关于体外和体内二氧化硅纳米颗粒的大小依赖性视网膜毒性的机制研究。
J Nanobiotechnology. 2022 Mar 19;20(1):146. doi: 10.1186/s12951-022-01326-8.
10
Silicon dioxide nanoparticles induce insulin resistance through endoplasmic reticulum stress and generation of reactive oxygen species.二氧化硅纳米颗粒通过内质网应激和活性氧的产生诱导胰岛素抵抗。
Part Fibre Toxicol. 2019 Nov 7;16(1):41. doi: 10.1186/s12989-019-0327-z.

引用本文的文献

1
Circadian disruption and ROS-NLRP3 signaling mediate sleep deprivation-enhanced silica nanoparticle toxicity in lacrimal glands.昼夜节律紊乱和ROS-NLRP3信号传导介导睡眠剥夺增强泪腺中二氧化硅纳米颗粒的毒性。
J Nanobiotechnology. 2025 Sep 2;23(1):600. doi: 10.1186/s12951-025-03630-5.
2
Microplastics and nanoplastics in the ocular environment: Pathways, toxic effects, and future challenges.眼部环境中的微塑料和纳米塑料:途径、毒性作用及未来挑战。
Curr Res Toxicol. 2025 Aug 7;9:100251. doi: 10.1016/j.crtox.2025.100251. eCollection 2025.
3
The impact of cell density variations on nanoparticle uptake across bioprinted A549 gradients.
细胞密度变化对生物打印A549梯度上纳米颗粒摄取的影响。
Front Bioeng Biotechnol. 2025 Apr 30;13:1584635. doi: 10.3389/fbioe.2025.1584635. eCollection 2025.
4
Corneal Vascularization Associated With a Novel PDGFRB Variant.角膜血管化与新型 PDGFRB 变异有关。
Invest Ophthalmol Vis Sci. 2023 Nov 1;64(14):9. doi: 10.1167/iovs.64.14.9.
5
Biodegradable polymeric nanoparticles increase risk of cardiovascular diseases by inducing endothelium dysfunction and inflammation.可生物降解聚合物纳米颗粒通过诱导内皮功能障碍和炎症增加心血管疾病的风险。
J Nanobiotechnology. 2023 Feb 24;21(1):65. doi: 10.1186/s12951-023-01808-3.
6
High-Capacity Mesoporous Silica Nanocarriers of siRNA for Applications in Retinal Delivery.用于视网膜递药的高载量介孔硅纳米载体的 siRNA
Int J Mol Sci. 2023 Feb 1;24(3):2753. doi: 10.3390/ijms24032753.
7
Cell membrane-coated nanoparticles: a novel multifunctional biomimetic drug delivery system.细胞膜包覆的纳米颗粒:一种新型多功能仿生药物传递系统。
Drug Deliv Transl Res. 2023 Mar;13(3):716-737. doi: 10.1007/s13346-022-01252-0. Epub 2022 Nov 22.
8
SIRT1 Protects Against Particulate Matter-Induced Oxidative Stress in Human Corneal and Conjunctival Epithelial Cells.SIRT1 可预防人眼角膜和结膜上皮细胞内的颗粒物质诱导的氧化应激。
Invest Ophthalmol Vis Sci. 2022 Sep 1;63(10):19. doi: 10.1167/iovs.63.10.19.
9
Fullerenol protects cornea from ultraviolet B exposure.富勒醇可保护眼角膜免受紫外线 B 的伤害。
Redox Biol. 2022 Aug;54:102360. doi: 10.1016/j.redox.2022.102360. Epub 2022 Jun 3.
10
Comparison of cytotoxicity effects induced by four different types of nanoparticles in human corneal and conjunctival epithelial cells.四种不同类型纳米颗粒对人眼角膜和结膜上皮细胞诱导的细胞毒性作用比较。
Sci Rep. 2022 Jan 7;12(1):155. doi: 10.1038/s41598-021-04199-3.