| Literature DB >> 28643149 |
Balaram Das1, Satyajit Tripathy1,2, Jaydeep Adhikary3,4, Sourav Chattopadhyay1, Debasis Mandal1, Sandeep Kumar Dash1, Sabyasachi Das1, Aditi Dey1, Sankar Kumar Dey5, Debasis Das3, Somenath Roy6.
Abstract
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.Entities:
Keywords: Apoptosis; Oxidative stress; Silver nanoparticles; Surface functionalization; Toxicity
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Year: 2017 PMID: 28643149 DOI: 10.1007/s00775-017-1468-x
Source DB: PubMed Journal: J Biol Inorg Chem ISSN: 0949-8257 Impact factor: 3.358