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Cerium oxide nanoparticles improve liver regeneration after acetaminophen-induced liver injury and partial hepatectomy in rats

机译:氧化铈纳米颗粒改善对乙酰氨基酚引起的肝损伤和部分肝切除术后大鼠肝脏的再生

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摘要

Characterization of cerium oxide nanoparticles. , Representative TEM images of CeO NPs at different magnifications showing the non-aggregate and spherical shape of the engineered nanoparticles. Inset in is a High Resolution TEM image of single particle showing pure CeO atomic planes; UV–Visible absorption spectrum of the as-synthesized CeO NPs; XRD spectrum of the as-synthesized CeO NPs after being dried under vacuum. Z-Potential distribution and Hydrodynamic diameter measured by DLS of the CeO NPs dispersed in the physiological media (saline solution at pH = 5.5); Cerium concentration in liver, spleen, lung and and kidney from rats treated with CeO NPs for 90 min, 3, 6 and 8 weeks (n = 4 for each group). Oxidative stress was quantified in non-treated and CeO NPs-treated HepG2 cells by measuring DCF fluorescence in basal condition and after inducing oxidative stress with 2 mM H O added to the culture medium ( vs basal and
机译:氧化铈纳米颗粒的表征。 ,CeO NPs在不同放大倍数下的代表性TEM图像,显示了工程纳米颗粒的非聚集和球形形状。插图是显示纯CeO原子平面的单个粒子的高分辨率TEM图像;合成后的CeO NP的紫外可见吸收光谱;真空干燥后的合成CeO NP的XRD光谱。分散在生理介质(pH == 5.5的盐溶液)中的CeO NP的Z-电位分布和通过DLS测量的流体力学直径;用CeO NPs处理90分钟,3、6和8周的大鼠的肝,脾,肺和肾中的铈浓度(每组n = 4)。通过在基础条件下和在培养基中加入2 mM H O诱导氧化应激后,通过测量DCF荧光定量未处理和CeO NPs处理的HepG2细胞中的氧化应激(相对于基础和

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