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Synthesis of novel CoC_x@C nanoparticles

机译:新型CoC_x @ C纳米粒子的合成

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CoC_x nanoparticles encapsulated in carbon shells were synthesized using a pulsed plasma in liquid ethanol. This is the first time that monolithic cubic phase cobalt carbide nanoparticles have been obtained. X-ray diffraction refinement of the nanoparticles showed that the lattice parameter of prepared cubic phase cobalt carbide is larger than that of CoC_x (44-0962) and cubic phase Co (15-0806 and 01-1259). The x-ray absorption fine structure spectra near the Co K-edge of the synthesized sample indicated differences from commercial metallic cobalt and cobalt oxide samples. High resolution transmission electron microscopy revealed that a thin carbon coating covered the surface of the nanoparticles. These carbon layers might isolate core CoC_x material from the outside environment, and allow functionalization by carboxyl groups for the further purpose of targeted drug delivery. The obtained CoC_x@C particles, with a crystallite size of about 10 nm confirmed by the electron microscope, aggregate into 20-40 nm secondary particles in distilled water as shown by dynamic light scattering, and possess high saturation magnetization of about 120 emu g~(-1). The sodium 3′-[1-(phenylaminocarbonyl)-3,4-tetrazolium]-bis(4-methoxy-6-nitro) benzene sulfonic acid hydrate assay and defragmentation of deoxyribonucleic acid on MCF-7 cells after incubation with particles indicate relatively low cytotoxicity of CoC_x@C nanoparticles, compared with micro-sized and nano-sized metallic cobalt particles and commonly used iron oxides. For the small sized CoC_x@C particles, the release of cobalt ions was checked by a chelation method with ethylenediaminetetraacetic acid solution to be at a very low level compared with other reference materials.
机译:使用脉冲等离子体在液体乙醇中合成了封装在碳壳中的CoC_x纳米颗粒。这是第一次获得整体立方相碳化钴纳米颗粒。纳米粒子的X射线衍射分析表明,所制备的立方相碳化钴的晶格参数大于CoC_x(44-0962)和立方相Co(15-0806和01-1259)的晶格参数。合成样品的Co K边缘附近的X射线吸收精细结构光谱表明与商业金属钴和氧化钴样品有所不同。高分辨率透射电子显微镜显示,薄的碳涂层覆盖了纳米颗粒的表面。这些碳层可将核心CoC_x材料与外部环境隔离,并允许通过羧基官能化,以实现靶向药物输送的进一步目的。如通过动态光散射所示,所获得的CoC_x @ C颗粒具有由电子显微镜确认的约10nm的微晶尺寸,聚集在蒸馏水中的20-40nm的次级颗粒中,并且具有约120emu g的高饱和磁化强度。 (-1)。与颗粒孵育后,MCF-7细胞上的3'-[1-(苯基氨基羰基)-3,4-四唑]-双(4-甲氧基-6-硝基)苯磺酸钠水合物测定和脱氧核糖核酸的碎片整理表明相对与微米级和纳米级的金属钴颗粒以及常用的氧化铁相比,CoC_x @ C纳米颗粒具有较低的细胞毒性。对于小尺寸的CoC_x @ C颗粒,通过乙二胺四乙酸溶液的螯合方法检测到钴离子的释放与其他参考材料相比处于非常低的水平。

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