Biosynthesis, characterization of magnetic iron oxide nanoparticles and evaluations of the cytotoxicity and DNA damage of human breast carcinoma cell lines

被引:64
作者
Sulaiman, Ghassan M. [1 ]
Tawfeeq, Amer T. [2 ]
Naji, Amal S. [1 ]
机构
[1] Univ Technol Baghdad, Div Biotechnol, Dept Appl Sci, Baghdad, Iraq
[2] Univ Al Mustansiriyah, Iraqi Ctr Canc & Med Genet Res, Dept Mol Biol, Baghdad, Iraq
关键词
Albizia adianthifolia; biosynthesis; MNPs; AMJ-13; cells; MCF-7; FE3O4; NANOPARTICLES; ALBIZIA-ADIANTHIFOLIA; SILVER NANOPARTICLES; METAL NANOPARTICLES; BIOGENIC SYNTHESIS; LEAF EXTRACT; ANTIBACTERIAL; ANTIOXIDANT; SAPONINS; PLANTS;
D O I
10.1080/21691401.2017.1366335
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Magnetic iron oxide nanoparticles (MNPs) were synthesized using Albizia adianthifolia leaf extract as reducing and protecting agent. Colour changing, UV-Vis spectrum, X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM) confirmed the biosynthesis and characterization of MNPs. The XRD pattern revealed that MNPs are crystalline in nature. FT-IR spectral analysis showed that MNPs was capped with plant constituents. From SEM analysis, the MNPs were generally found to be spherical in shape and the size was ranged 32-100 nm. Free radical scavenging potentials of the MNPs against DPPH were confirmed based on its stable anti-oxidant effects. The synthesized MNPs were used to capture Staphylococcus aureus under the magnetic field effect. Further, it was observed that the MNPs are able to exert cytotoxic effect towards human breast (AMJ-13) and (MCF-7) cancer cells. The anti-proliferative effect of this treatment is due to cell death and inducing apoptosis. Mitochondrial membrane potential, acridine orange-propidium iodide staining assays as well as single cell and DNA gel electrophoresis analyses indicated that MNPs induce cell death only by apoptosis. The findings of present study suggest that the MNPs might be used for medicinal applications particularly for cancer therapeutics.
引用
收藏
页码:1215 / 1229
页数:15
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