Related Experiment Video
Updated: Aug 25, 2026

Chemiluminescence-based Assays for Detection of Nitric Oxide and its Derivatives from Autoxidation and Nitrosated Compounds
Published on: February 16, 2022
Flow-injection analysis and voltammetric detection of NADH with a poly-Toluidine Blue modified electrode
Yanling Chen1, Junhua Yuan, Chunxiang Tian
1Faculty of Material Science and Chemistry Engineering, China University of Geosciences, Wuhan 430074, P R China. ylchen@cug.edu.cn
Abstract:
Poly-Toluidine Blue film was prepared by electrooxidative polymerization at a glassy carbon electrode in a phosphate buffer solution. The resulting chemically modified electrode (CME) exhibited excellent electrocatalysis toward the oxidation of reduced nicotinamide coenzyme (NADH) with over a 450 mV decrease of the overpotential compared with that at a bare glassy carbon electrode. Two electrochemical determinations of NADH, cyclic voltammetry and flow injection analysis, were established based on the electrocatalytical performance of the resulting modified electrode. Under an identical determinate condition, the voltammetric detection for NADH gave a detection limit of 3.3 micromol L(-1) with a linear concentration range of 9.1 micromol L(-1) to 1.8 mmol L(-1). As a detector in a flow-injection system, the CME gave a detection limit of 0.1 micromol L(-1) for NADH with a linear concentration range of 1.0 micromol L(-1) to 3.2 mmol L(-1). Obviously, flow-injection analysis is superior to voltammetric detection in NADH determination for its lower detection limit and wider detectable linear range.
Related Concept Videos
Voltammetric Techniques: Pulse Voltammetry
Voltammetric Techniques: Linear-Scan (E vs Time)
Electrodeposition
Electrodeposition can...
Voltammetric Techniques: Cyclic Voltammetry
Precipitation Titration: Endpoint Detection Methods
In the Volhard method, a standard excess of AgNO3 is first added to the...
Effects of EDTA on End-Point Detection Methods
In the visual method, metal-ion indicators (metallochromic dyes), which have distinct colors in their free and complex forms, are added to the mixture to signal the titration's end point. They form stable complexes with metal ions, but these complexes are weaker than the corresponding metal–EDTA complexes. As a result, EDTA...

