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Treatment of steroid-induced osteonecrosis of the femoral head using porous Se@SiO2 nanocomposites to suppress reactive oxygen species

机译:多孔Se @ SiO2纳米复合材料抑制活性氧治疗类固醇激素引起的股骨头坏死

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摘要

Reducing oxidative stress (ROS) have been demonstrated effective for steroid-induced osteonecrosis of the femoral head (steroid-induced ONFH). Selenium (Se) plays an important role in suppressing oxidative stress and has huge potential in ONFH treatments. However the Se has a narrow margin between beneficial and toxic effects which make it hard for therapy use in vivo. In order to make the deficiency up, a control release of Se (Se@SiO2) were realized by nanotechnology modification. Porous Se@SiO2 nanocomposites have favorable biocompatibility and can reduced the ROS damage effectively. In vitro, the cck-8 analysis, terminal dexynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) stain and flow cytometry analysis showed rare negative influence by porous Se@SiO2 nanocomposites but significantly protective effect against H2O2 by reducing ROS level (detected by DCFH-DA). In vivo, the biosafety of porous Se@SiO2 nanocomposites were confirmed by the serum biochemistry, the ROS level in serum were significantly reduced and the curative effect were confirmed by Micro CT scan, serum Elisa assay (inflammatory factors), Western blotting (quantitative measurement of ONFH) and HE staining. It is expected that the porous Se@SiO2 nanocomposites may prevent steroid-induced ONFH by reducing oxidative stress.
机译:业已证明,降低氧化应激(ROS)对于类固醇激素引起的股骨头坏死(类固醇激素引起的ONFH)有效。硒(Se)在抑制氧化应激中起重要作用,在ONFH治疗中具有巨大潜力。然而,硒在有益作用和毒性作用之间具有狭窄的余量,这使其难以在体内进行治疗。为了弥补这一缺陷,通过纳米技术修饰实现了Se(Se @ SiO2)的控制释放。多孔Se @ SiO2纳米复合材料具有良好的生物相容性,可以有效降低ROS的破坏。在体外,cck-8分析,末端右旋糖核苷酸转移酶(TdT)介导的dUTP缺口末端标记(TUNEL)染色和流式细胞仪分析显示,多孔Se @ SiO2纳米复合材料罕见的负面影响,但通过降低ROS水平可显着保护H2O2(由DCFH-DA检测到)。在体内,通过血清生化证实了多孔Se @ SiO2纳米复合材料的生物安全性,血清中的ROS水平显着降低,并通过Micro CT扫描,血清Elisa测定(炎症因子),Western印迹(定量测量)确认了疗效ONFH)和HE染色。预计多孔Se @ SiO2纳米复合材料可通过降低氧化应激来防止类固醇诱导的ONFH。

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