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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Real-time amperometric monitoring of cellular hydrogen peroxide based on electrodeposited reduced graphene oxide incorporating adsorption of electroactive methylene blue hybrid composites
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Real-time amperometric monitoring of cellular hydrogen peroxide based on electrodeposited reduced graphene oxide incorporating adsorption of electroactive methylene blue hybrid composites

机译:基于电沉积还原氧化石墨烯并结合电活性亚甲基蓝杂化复合材料吸附的细胞过氧化氢的实时安培监测

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摘要

This paper demonstrates a novel strategy for real-time monitoring of cellular small biomolecules based on graphene hybrid composites film, which was fabricated by one step electrodeposited reduced graphene oxide (ERGO) incorporating adsorption of electroactive methylene blue (MB) onto glassy carbon electrode (GCE). UV-visible spectroscopy, FT-IR spectroscopy, electrochemistry and scanning electron microscopy were employed for systematical characterization of GO-MB adsorptive nanostructure. The ERGO-MB/GCE shows more favorable electron transfer kinetics for potassium ferricyanide and potassium ferrocyanide probe molecules, which are important electroactive compounds, compared with bare GCE, MB/GCE and ERGO/GCE. The electrochemical behaviors of dissolved oxygen and hydrogen peroxide (H2O2) at ERGO-MB/GCE were investigated by cyclic voltammetry, suggesting that the modified electrode exhibits enhanced electrocatalytic activity toward H2O2. Under physiological condition, the ERGO-MB/GCE showed a linear amperometric response from 0.5 mu M to 11.68 mM for H2O2, with the detection limit of 60 nM (S/N = 3), and also showed high sensitivity (102 A mu M-1- cm(-2)) and short response time within 2 s for H2O2 detection. Besides, the reproducibility, stability and anti-interference ability of the proposed nonenzymatic H2O2 biosensor were also proved. The developed method has been successfully applied to determination of H2O2 released from living cells, which could be clearly distinguished cancer cells including Hep3B, HepG2 and HeLa cells from normal cells HEK 293. This assay shows great potential for nonenzymatic determination of H2O2 in physiological and pathological investigations. (C) 2016 Elsevier B.V. All rights reserved.
机译:本文展示了一种基于石墨烯杂化复合膜的细胞小生物分子实时监测的新策略,该方法是通过一步电沉积还原氧化石墨烯(ERGO)并将电活性亚甲基蓝(MB)吸附到玻璃碳电极(GCE)上制成的)。紫外可见光谱,傅立叶变换红外光谱,电化学和扫描电子显微镜用于GO-MB吸附纳米结构的系统表征。与裸露的GCE,MB / GCE和ERGO / GCE相比,ERGO-MB / GCE对重要的电活性化合物铁氰化钾和亚铁氰化钾探针分子显示出更有利的电子转移动力学。通过循环伏安法研究了溶解氧和过氧化氢(H2O2)在ERGO-MB / GCE上的电化学行为,表明改性电极对H2O2的电催化活性增强。在生理条件下,ERGO-MB / GCE对H2O2的线性安培响应为0.5μM至11.68 mM,检出限为60 nM(S / N = 3),并且还显示出高灵敏度(102 AμM -1- cm(-2))和2 s内的H2O2检测响应时间短。此外,还证明了所提出的非酶过氧化氢生物传感器的重现性,稳定性和抗干扰能力。所开发的方法已成功应用于活细胞中释放的H2O2的测定,可以清楚地区分正常细胞HEK 293中的Hep3B,HepG2和HeLa细胞。调查。 (C)2016 Elsevier B.V.保留所有权利。

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