Das Balaram, Tripathy Satyajit, Adhikary Jaydeep, Chattopadhyay Sourav, Mandal Debasis, Dash Sandeep Kumar, Das Sabyasachi, Dey Aditi, Dey Sankar Kumar, Das Debasis, Roy Somenath
Immunology and Microbiology Laboratory, Department of Human Physiology with Community Health, Vidyasagar University, Midnapore, West Bengal, 721 102, India.
Department of Physiology, Michigan State University, East Lansing, MI, 48824, USA.
J Biol Inorg Chem. 2017 Aug;22(6):893-918. doi: 10.1007/s00775-017-1468-x. Epub 2017 Jun 22.
Currently toxicological research in Silver nanoparticle is a leading issue in medical science. The surface chemistry and physical dimensions of silver nanoparticles (Ag-NPs) play an important role in toxicity. The aim of this present study was to evaluate the in vitro and in vivo toxicity of Ag-NPs as well as the alteration of toxicity profile due to surface functionalization (PEG and BSA) and the intracellular signaling pathways involved in nanoparticles mediated oxidative stress and apoptosis in vitro and in vivo system. Ag-NPs released excess Ag ions leads to activation of NADPH oxidase and helps in generating the reactive oxygen species (ROS). Silver nanoparticles elicit the production of excess amount of ROS results activation of TNF-α. Ag-NPs activates caspase-3 and 9 which are the signature of mitochondrial pathway. Ag-NPs are responsible to decrease the antioxidant enzymes and imbalance the oxidative status into the cells but functionalization with BSA and PEG helps to protect the adverse effect of Ag-NPs on the cells. This study suggested that Ag-NPs are toxic to normal cells which directly lead with human health. Surface functionalization may open the gateway for further use of Ag-NPs in different area such as antimicrobial and anticancer therapy, industrial use or in biomedical sciences.
目前,银纳米颗粒的毒理学研究是医学领域的一个前沿问题。银纳米颗粒(Ag-NPs)的表面化学性质和物理尺寸在毒性方面起着重要作用。本研究的目的是评估Ag-NPs的体外和体内毒性,以及由于表面功能化(聚乙二醇和牛血清白蛋白)导致的毒性特征变化,以及体外和体内系统中纳米颗粒介导的氧化应激和细胞凋亡所涉及的细胞内信号通路。释放过量银离子的Ag-NPs会导致NADPH氧化酶的激活,并有助于产生活性氧(ROS)。银纳米颗粒引发过量ROS的产生,导致肿瘤坏死因子-α(TNF-α)的激活。Ag-NPs激活半胱天冬酶-3和9,这是线粒体途径的标志。Ag-NPs会导致抗氧化酶减少,并使细胞内的氧化状态失衡,但用牛血清白蛋白和聚乙二醇进行功能化有助于保护细胞免受Ag-NPs的不利影响。这项研究表明,Ag-NPs对正常细胞有毒性,这直接关系到人类健康。表面功能化可能为Ag-NPs在抗菌和抗癌治疗、工业用途或生物医学科学等不同领域的进一步应用打开大门。