DNA binding and cytotoxicity studies of magnetic nanofluid containing antiviral drug oseltamivir |
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| Authors: | Nahid Shahabadi Maryam Shadkam Kamran Mansouri |
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| Institution: | 1. Faculty of Chemistry, Department of Inorganic Chemistry, Razi University, Kermanshah, Iran;2. Medical Biology Research Center (MBRC), Kermanshah University of Medical Sciences, Kermanshah, Iran;3. Medical Biology Research Center (MBRC), Kermanshah University of Medical Sciences, Kermanshah, Iran;4. Faculty of Advanced Medical Technologies, Department of Molecular Medicine, Tehran University of Medical Sciences, Tehran, Iran |
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| 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 |
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| Keywords: | nanofluids oseltamivir antiproliferative effect human breast adenocarcinoma cell line |
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