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A systematic review on silver nanoparticles-induced cytotoxicity: Physicochemical properties and perspectives.银纳米颗粒诱导细胞毒性的系统综述:物理化学性质与展望
J Adv Res. 2017 Nov 2;9:1-16. doi: 10.1016/j.jare.2017.10.008. eCollection 2018 Jan.
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Regulation of apoptosis through bcl-2/bax proteins expression and DNA damage by nano-sized gadolinium oxide.通过纳米氧化钆调控bcl-2/bax蛋白表达及DNA损伤诱导的细胞凋亡
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Behaviour of silver nanoparticles in simulated saliva and gastrointestinal fluids.银纳米颗粒在模拟唾液和胃肠液中的行为。
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Biocompatible lutein-polymer-lipid nanocapsules: Acute and subacute toxicity and bioavailability in mice.生物相容性叶黄素-聚合物-脂质纳米胶囊:小鼠急性和亚急性毒性及生物利用度
Mater Sci Eng C Mater Biol Appl. 2016 Dec 1;69:1318-27. doi: 10.1016/j.msec.2016.08.029. Epub 2016 Aug 15.
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The immunomodulatory effects of titanium dioxide and silver nanoparticles.二氧化钛和银纳米颗粒的免疫调节作用。
Food Chem Toxicol. 2015 Nov;85:78-83. doi: 10.1016/j.fct.2015.05.015. Epub 2015 Jun 4.
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Thermal co-reduction approach to vary size of silver nanoparticle: its microbial and cellular toxicology.热共还原法改变银纳米粒子的尺寸:其微生物和细胞毒理学。
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Immunomodulatory properties of silver nanoparticles contribute to anticancer strategy for murine fibrosarcoma.银纳米颗粒的免疫调节特性有助于制定针对小鼠纤维肉瘤的抗癌策略。
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Comparative toxicity of silicon dioxide, silver and iron oxide nanoparticles after repeated oral administration to rats.二氧化硅、银和氧化铁纳米颗粒对大鼠重复口服给药后的比较毒性
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Nanotoxicity of silver nanoparticles to red blood cells: size dependent adsorption, uptake, and hemolytic activity.银纳米颗粒对红细胞的纳米毒性:尺寸依赖性吸附、摄取及溶血活性
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10
Silver nanoparticles: their potential toxic effects after oral exposure and underlying mechanisms--a review.银纳米颗粒:口服暴露后的潜在毒性作用及其潜在机制——综述
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热共还原法制备的银纳米颗粒对Wistar大鼠肝脏造成损伤:急性和亚慢性毒性分析

Silver nanoparticles engineered by thermal co-reduction approach induces liver damage in Wistar rats: acute and sub-chronic toxicity analysis.

作者信息

Dasgupta Nandita, Ranjan Shivendu, Ramalingam Chidambaram, Gandhi Mansi

机构信息

1Nano-food Research Group, Instrumental and Food Analysis Laboratory, Industrial Biotechnology Division, School of BioSciences and Technology, Vellore Institute of Technology, Vellore, Tamil Nadu India.

2Department of Biotechnology, Institute of Engineering and Technology, Dr. APJ Abdul Kalam Technical University (Formerly Uttar Pradesh Technical University), Lucknow, Uttar Pradesh 226021 India.

出版信息

3 Biotech. 2019 Apr;9(4):125. doi: 10.1007/s13205-019-1651-6. Epub 2019 Mar 6.

DOI:10.1007/s13205-019-1651-6
PMID:30863704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6403278/
Abstract

Recently, nanotechnology applications have increased tremendously in consumer products. However, it has been observed that these nanoparticles can cause a potential risk to the environment as well as human health. In the present manuscript, we have analyzed acute and sub-chronic toxicity of engineered silver nanoparticles (AgNPs) by assessing the impact on Wistar rats. AgNPs were synthesized by a novel approach-thermal co-reduction-with spherical shape and a uniform size distribution of 60 nm. The estimated LD value was observed to be more than 2000 mg/kg bw in acute toxicity studies. Sub-chronic toxicity indicated impairment of liver and kidney enzymes and various hematological and biochemical parameters. Tissue distribution studies indicated the target organ for accumulation is liver after treatment with AgNP. Particle deposition and congestion was observed in major organs-though, and heart and pancreatic tissues were not affected even by the higher doses. On the basis of the observations of this study, it is concluded that up to 40 mg/kgbw is a safer dose of AgNPs (60 nm, engineered by thermal co-reduction approach) and further research will be required to validate the long-term accumulation in body. In addition, it can also be considered by policymakers for the safer use of AgNPs.

摘要

近年来,纳米技术在消费品中的应用急剧增加。然而,人们观察到这些纳米颗粒可能对环境以及人类健康造成潜在风险。在本论文中,我们通过评估对Wistar大鼠的影响,分析了工程化银纳米颗粒(AgNPs)的急性和亚慢性毒性。AgNPs采用一种新颖的方法——热共还原法合成,呈球形,尺寸分布均匀,为60纳米。在急性毒性研究中,估计的半数致死量值超过2000毫克/千克体重。亚慢性毒性表明肝脏和肾脏酶以及各种血液学和生化参数受损。组织分布研究表明,用AgNP处理后,积累的靶器官是肝脏。不过,在主要器官中观察到了颗粒沉积和充血现象,即使是高剂量也未影响心脏和胰腺组织。基于本研究的观察结果,得出结论:高达40毫克/千克体重是AgNPs(60纳米,通过热共还原法工程化)的安全剂量,需要进一步研究来验证其在体内的长期积累情况。此外,政策制定者在安全使用AgNPs时也可予以考虑。