首页> 美国卫生研究院文献>Nanoscale Research Letters >Synthesis Characterization and Study of In Vitro Cytotoxicity of ZnO-Fe3O4 Magnetic Composite Nanoparticles in Human Breast Cancer Cell Line (MDA-MB-231) and Mouse Fibroblast (NIH 3T3)
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Synthesis Characterization and Study of In Vitro Cytotoxicity of ZnO-Fe3O4 Magnetic Composite Nanoparticles in Human Breast Cancer Cell Line (MDA-MB-231) and Mouse Fibroblast (NIH 3T3)

机译:ZnO-Fe3O4磁性复合纳米粒子在人乳腺癌细胞系(MDA-MB-231)和小鼠成纤维细胞(NIH 3T3)中的合成表征和体外细胞毒性研究

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摘要

AbstractNovel magnetic composite nanoparticles (MCPs) were successfully synthesized by ex situ conjugation of synthesized ZnO nanoparticles (ZnO NPs) and Fe3O4 NPs using trisodium citrate as linker with an aim to retain key properties of both NPs viz. inherent selectivity towards cancerous cell and superparamagnetic nature, respectively, on a single system. Successful characterization of synthesized nanoparticles was done by XRD, TEM, FTIR, and VSM analyses. VSM analysis showed similar magnetic profile of thus obtained MCPs as that of naked Fe3O4 NPs with reduction in saturation magnetization to 16.63 emu/g. Also, cell viability inferred from MTT assay showed that MCPs have no significant toxicity towards noncancerous NIH 3T3 cells but impart significant toxicity at similar concentration to breast cancer cell MDA-MB-231. The EC50 value of MCPs on MDA-MB-231 is less than that of naked ZnO NPs on MDA-MB-231, but its toxicity on NIH 3T3 was significantly reduced compared to ZnO NPs. Our hypothesis for this prominent difference in cytotoxicity imparted by MCPs is the synergy of selective cytotoxicity of ZnO nanoparticles via reactive oxygen species (ROS) and exhausting scavenging activity of cancerous cells, which further enhance the cytotoxicity of Fe3O4 NPs on cancer cells. This dramatic difference in cytotoxicity shown by the conjugation of magnetic Fe3O4 NPs with ZnO NPs should be further studied that might hold great promise for the development of selective and site-specific nanoparticles.
机译:摘要以柠檬酸三钠为连接基,通过异位共轭合成的ZnO纳米颗粒(ZnO NPs)和Fe3O4 NPs,成功合成了新型磁性复合纳米颗粒(MCPs),目的是保留两个NPs的关键特性。在单个系统上分别具有对癌细胞的固有选择性和超顺磁性。通过XRD,TEM,FTIR和VSM分析成功完成了合成纳米颗粒的表征。 VSM分析显示,由此获得的MCP的磁性与裸Fe3O4 NP相似,但饱和磁化强度降低至16.63emu / g。而且,从MTT测定法推断的细胞生存力表明,MCP对非癌性NIH 3T3细胞没有明显的毒性,但是以与乳腺癌细胞MDA-MB-231相似的浓度赋予明显的毒性。 MDA-MB-231上的MCP的EC50值小于MDA-MB-231上裸露的ZnO NP的EC50值,但与ZnO NP相比,其对NIH 3T3的毒性显着降低。我们对MCP所赋予的细胞毒性显着差异的假设是ZnO纳米粒子通过活性氧(ROS)选择性发挥细胞毒性和耗尽癌细胞的清除活性的协同作用,从而进一步增强了Fe3O4 NP对癌细胞的细胞毒性。磁性Fe3O4 NPs与ZnO NPs结合所显示的这种细胞毒性的显着差异应进一步研究,这可能对开发选择性和位点特异性纳米粒子具有广阔的前景。

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