Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! By
Dna Binding and Cytotoxicity Studies of Magnetic Nanofluid Containing Antiviral Drug Oseltamivir Publisher Pubmed



Shahabadi N1, 2 ; Shadkam M1 ; Mansouri K2, 3
Authors

Source: Journal of Biomolecular Structure and Dynamics Published:2019


Abstract

In this work, the possibility of preparing a nanoparticle with improved treatment properties was investigated. In this regard, synthesis, characterization, in vitro cytotoxicity and DNA binding of Fe3O4@oleate/oseltamivir magnetic nanoparticles (MNPs) were investigated. Fe3O4 nanoparticles were synthesized via chemical co-precipitation and coated by oleate bilayers. Then, Fe3O4@OA MNPs were functionalized with an antiviral drug (oseltamivir), for better biological applications. The MNPs were subsequently characterized by zeta sizer and Zeta potential measurements, Fourier transform infrared (FT-IR) spectroscopy, vibrating sample magnetometer (VSM) and transmission electron microscopy (TEM) analyses. The TEM image demonstrated that average sizes of Fe3O4@OA/oseltamivir MNPs were about 8 nm. The in vitro cytotoxicity of Fe3O4@OA/oseltamivir MNPs was studied against cancer cell lines (MCF-7 and MDA-MB-231) and compared with oseltamivir drug. The results illustrated that Fe3O4@OA/oseltamivir magnetic nanoparticles have better antiproliferative effects on the mentioned cell lines as compared with oseltamivir. Also, in vitro DNA binding studies were done by UV–Vis, circular dichroism, and Fluorescence spectroscopy. The results indicated that Fe3O4@OA/oseltamivir MNPs bound to DNA via groove binding. Moreover, this magnetic nanofluid has potential for magnetic hyperthermia therapy due to magnetic core of its nanoparticles. Communicated by Ramaswamy H. Sarma. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
Other Related Docs
10. Ph-Responsive Polymer in a Core–Shell Magnetic Structure As an Efficient Carrier for Delivery of Doxorubicin to Tumor Cells, International Journal of Polymeric Materials and Polymeric Biomaterials (2018)
12. Increasing Dna Binding Affinity of Doxorubicin by Loading on Fe3o4 Nanoparticles: A Multi-Spectroscopic Study, Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy (2020)
16. Magnetic Metal–Organic Framework Based on Zinc and 5-Aminolevulinic Acid: Mr Imaging and Brain Tumor Therapy, Journal of Inorganic and Organometallic Polymers and Materials (2021)