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Core-shell structured Ag@C for direct electrochemistry and hydrogen peroxide biosensor applications

机译:核-壳结构的Ag @ C,用于直接电化学和过氧化氢生物传感器应用

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Ag@C core-shell nano-composites have been prepared by a simple one-step hydrothermal method and are further explored for protein immobilization and bio-sensing. The electrochemical behavior of immobilized horseradish peroxidase (HRP) on Ag@C modified indium-tin-oxide (ITO) electrode and its application as H_2O_2 sensor are investigated. Electrochemical and UV-vis spectroscopic measurements demonstrated that Ag@C nano-composites provide excellent matrixes for the adsorption of HRP and the entrapped HRP retains its bioactivities. It is found that on the HRP-Ag@C/ITO electrode, HRP exhibited a fast electron transfer process and good electrocatalytic reduction toward H_2O_2. Under optimum experimental conditions the biosensor linearly responds to H_2O_2 concentration in the range of 5.0×10~(-7)-1.4×10~(-4)M with a detection limit of 2.0×10~(-7)M (S/N=3). The apparent Michaelis-Menten constant (K _M~(app)) of the biosensor is calculated to be 3.75×10~(-5)M, suggesting high enzymatic activity and affinity toward H_2O_2. In addition, the HRP-Ag@C/ITO bio-electrode shows good reproducibility and long-term stability. Thus, the core-shell structured Ag@C is an attractive material for application in the fabrication of biosensors due to its direct electrochemistry and functionalized surface for efficient immobilization of bio-molecules.
机译:Ag @ C核壳纳米复合材料已通过简单的一步水热法制备,并进一步探索了蛋白质固定化和生物传感的方法。研究了辣根过氧化物酶(HRP)在Ag @ C修饰的氧化铟锡(ITO)电极上的电化学行为及其在H_2O_2传感器中的应用。电化学和紫外可见光谱测量表明,Ag @ C纳米复合材料为HRP的吸附提供了极好的基质,并且被捕获的HRP保留了其生物活性。发现在HRP-Ag @ C / ITO电极上,HRP表现出快速的电子转移过程和对H_2O_2的良好电催化还原。在最佳实验条件下,生物传感器对H_2O_2浓度在5.0×10〜(-7)-1.4×10〜(-4)M范围内线性响应,检出限为2.0×10〜(-7)M(S / N = 3)。该生物传感器的表观米氏(Michaelis-Menten)常数(K_M〜(app))经计算为3.75×10〜(-5)M,表明其高的酶活性和对H_2O_2的亲和力。此外,HRP-Ag @ C / ITO生物电极显示出良好的重现性和长期稳定性。因此,核壳结构的Ag @ C由于具有直接的电化学作用和功能化的表面,可以有效地固定生物分子,因此是用于制造生物传感器的一种有吸引力的材料。

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