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首页> 外文期刊>Revista Ion >Detección electroquímica de peróxido de hidrógeno usando peroxidasa de pasto Guinea (Panicum maximum) inmovilizada sobre electrodos serigrafiados de puntos cuánticos
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Detección electroquímica de peróxido de hidrógeno usando peroxidasa de pasto Guinea (Panicum maximum) inmovilizada sobre electrodos serigrafiados de puntos cuánticos

机译:用对量子点筛分电极固定的草过氧化物酶几内亚豚(Panicum最大)的电化学检测

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摘要

Electrochemical biosensors are analytical tools of fast and reliable response that have acquired interest in the last years due to the possibility of integrating biomolecules and electrodes made of nanometric materials. In this study, an electrochemical biosensor to detect hydrogen peroxide (H2O2) based on Guinea Grass peroxidase (GGP) immobilized on screen-printed quantum dots electrodes (SPQDE) was developed. GGP was partially purified from Guinea grass leaves having a specific activity of 602 U mg-1.Then, GGP was immobilized by physical adsorption on the surface on SPQDE and the electrochemical behavior was carried out through cyclic voltammetry and chronoamperometry techniques. GGP revealed a well-defined pair of redox signals at 17mV/-141mV corresponding to the redox process of the heme group (Fe2+/Fe3+) of peroxidases. The bioelectrocatalytic reduction of H2O2 has a redox potential of -645 mV vs Ag. This process was controlled by the diffusion of the species on the electrode surface using a scan rate range of 50-500 mV s. Chronoamperometry studies allow us the construction of calibration curves of reduction current vs H2O2 concentration for the determination of analytical parameters such as sensitivity, linear range and minimum detection level. The development of this amperometric biosensor becomes a preliminary step for the construction of a portable and rapid response device for the analysis of H2O2 in samples of environmental and biomedical interest.
机译:电化学生物传感器是由于可能集成了由纳米材料制成的生物分子和电极而在过去几年中获得了兴趣的快速可靠响应的分析工具。在该研究中,开发了一种基于固定在丝网印刷的量子点电极(SPQDE)上固定的豚草过氧化物酶(GGP)的电化学生物传感器。 GGP部分从具有602u Mg-1.Th的特定活性的豚草叶部分纯化,通过物理吸附在SPQDE上的表面上固定GGP,通过循环伏安法和计时法进行电化学行为。 GGP在17mV / -141mV下显示出对应于过氧化物酶的氧化铈(Fe2 + / Fe3 +)的氧化还原方法的17mV / -141mV的明确定义的氧化还原信号。 H 2 O 2的生物电催化还原具有-645mV Vs Ag的氧化还原电位。该过程由物种在电极表面上的扩散来控制,使用50-500mV S的扫描速率范围。计时率研究允许我们构建减少电流Vs H2O2浓度的校准曲线,用于测定分析参数,如灵敏度,线性范围和最小检测水平。该功率化生物传感器的发展成为用于在环境和生物医学兴趣的样本中分析H2O2的便携式和快速响应装置的初步步骤。

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