Hanzhu Zhao, Aiping Song, Liyan Wang, Xiaolu Hou, Dongmei Cui, Xiaotong Sun, Lingzhi Niu, Lin Jin, Haoyuan An, Wei Li
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There's less study on corneal wound healing effects. and the previous research hasn't compared ZnO and GO corneal toxicity.</p><p><strong>Methods: </strong>We systematically established a complete chain study of in vitro and in vivo experiments and mouse corneal injury model, and comprehensively evaluated the ocular safety and toxicity of ZnO and GO.</p><p><strong>Results: </strong>We found that 50 ug/mL GO and 0.5 ug/mL ZnO can reduce human corneal epithelial cells (HCEpiC) viability in a concentration-dependent manner. Short-term repeated exposure to ZnO can cause sterile inflammation of the cornea with concentration-dependence, while GO have not been significantly altered. 50 ug/mL ZnO could significantly delay the healing of corneal wounds, while GO did not change wound healing.</p><p><strong>Conclusion: </strong>The toxic effect of ZnO is higher than that of GO. Inflammatory signal transduction, oxidative stress and apopnano zitosis are involved in the ocular toxicity injury process of nanoparticles. 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引用次数: 0
摘要
目的:氧化锌(ZnO)因其独特的化学特性被广泛应用于化妆品领域。氧化石墨烯(GO)作为一种新兴的纳米材料,在滴眼液领域的应用也逐渐兴起。目前,有关氧化锌和 GO 暴露于眼睛的研究主要集中在对视神经细胞的应用或毒性方面。方法:我们系统地建立了一个完整的研究链条,研究了氧化锌和氧化亚铜对角膜伤口愈合的影响:方法:我们系统地建立了一个完整的体内外实验链研究和小鼠角膜损伤模型,全面评价了氧化锌和 GO 的眼部安全性和毒性:结果:我们发现,50微克/毫升的GO和0.5微克/毫升的氧化锌能以浓度依赖的方式降低人角膜上皮细胞(HCEpiC)的活力。短期反复接触氧化锌可导致角膜无菌性炎症,且与浓度有关,而 GO 则没有明显改变。50 微克/毫升的氧化锌可明显延迟角膜伤口的愈合,而 GO 则不会改变伤口的愈合:结论:ZnO 的毒性效应高于 GO。结论:ZnO 的毒性作用高于 GO,炎症信号转导、氧化应激和凋亡参与了纳米颗粒的眼毒性损伤过程。相关研究可为人们的眼健康和眼保护风险控制提供判断依据。
Research on the damage and wound repair of cornea by GO and ZnO.
Objective: The widespread use of nanoparticles in recent years has increased the risk of ocular exposure. zinc oxide (ZnO) is widely used in the field of cosmetics because of its unique chemical properties. The application of graphene oxide (GO) as an emerging nanomaterial in the field of eye drops is also gradually emerging. Currently, research on ZnO and GO eye exposure mainly focuses on application or toxicity to optic nerve cells. There's less study on corneal wound healing effects. and the previous research hasn't compared ZnO and GO corneal toxicity.
Methods: We systematically established a complete chain study of in vitro and in vivo experiments and mouse corneal injury model, and comprehensively evaluated the ocular safety and toxicity of ZnO and GO.
Results: We found that 50 ug/mL GO and 0.5 ug/mL ZnO can reduce human corneal epithelial cells (HCEpiC) viability in a concentration-dependent manner. Short-term repeated exposure to ZnO can cause sterile inflammation of the cornea with concentration-dependence, while GO have not been significantly altered. 50 ug/mL ZnO could significantly delay the healing of corneal wounds, while GO did not change wound healing.
Conclusion: The toxic effect of ZnO is higher than that of GO. Inflammatory signal transduction, oxidative stress and apopnano zitosis are involved in the ocular toxicity injury process of nanoparticles. Research can provide a judgement basis for people's eye health and eye protection risk control.
期刊介绍:
Cutaneous and Ocular Toxicology is an international, peer-reviewed journal that covers all types of harm to cutaneous and ocular systems. Areas of particular interest include pharmaceutical and medical products; consumer, personal care, and household products; and issues in environmental and occupational exposures.
In addition to original research papers, reviews and short communications are invited, as well as concise, relevant, and critical reviews of topics of contemporary significance.