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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
An electrochemical sensor based on AuPd@FeO nanozymes for a sensitive and in situ quantitative detection of hydrogen
Mengjiao Dai1,2, Qunyan Zhu1, Dongxue Han3
1State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, Jilin, China. wangzx@ciac.ac.cn.
Abstract:
The hydrogen peroxide (H2O2) levels in living organisms and environment have strong effects on many biological processes inducing cell apoptosis/cell necrosis and wound disinfection. Therefore, it is important to have an accurate and in situ detection of H2O2. Herein, an AuPd@FeO nanozyme-based electrochemical (EC) sensor (termed as AuPd@FeO NPs/GCE) with good stability and anti-interference ability has been prepared for the detection of H2O2 by differential pulse voltammetry (DPV) and chronoamperometry dual-measurement modes. The AuPd@FeO NPs/GCE exhibits good linear relationships in the ranges from 13.0 to 6.0 × 103 μM (DPV measurement) and 50 to 1.0 × 103 μM (chronoamperometry measurement), low detection limits (LODs) of 1.6 μM (DPV measurement) and 3.0 μM (chronoamperometry measurement) and high sensitivities of 83.8 nA μM-1 cm-2 (DPV measurement) and 120.7 nA μM-1 cm-2 (chronoamperometry measurement). The practicability of the as-prepared AuPd@FeO NPs/GCE has been demonstrated by an in situ real-time detection of H2O2 released from adherent living MCF-7 cells triggered by varying amounts of N-formyl-L-methionyl-L-leucyl-L-phenylalanine (FMLP) from 0.5 to 3.0 μM and the quantitative determination of H2O2 in commercial disinfectants.
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