Glucose Biosensor Based on Dendritic Gold Nanostructures Electrodeposited on Graphite Electrode by Different Electrochemical Methods

In this research, we have demonstrated a one-step electrochemical deposition of dendritic gold nanostructures (DGNs) on a graphite rod (GR) electrode without any template, seeds, surfactants, or stabilizers. Three electrochemical methods, namely, constant potential amperometry (CPA), pulse amperometry, and differential pulse voltammetry, were used for DGN synthesis on GR electrode and further application in enzymatic glucose biosensors. Formed gold nanostructures, including DGNs, were characterized by a field emission scanning electron microscopy. The optimal concentration of HAuCl4 (6.0 mmol L-1), duration of DGNs synthesis (400 s), electrodeposition potential (-0.4 V), and the best electrochemical method (CPA) were determined experimentally. Then the enzyme, glucose oxidase, was adsorbed on the surface of DGNs and covalently cross-linked with glutaraldehyde vapor. The enzymatic glucose biosensor based on DGNs electrodeposited at optimal conditions and modified with glucose oxidase showed a quick response (less than 3 s), a high saturation current (291 mu A), appropriate linear range (up to 9.97 mmol L-1 of glucose, R-2 = 0.9994), good repeatability (RSD 2.4, 2.2 and 1.5% for 2, 30, 97 mmol L-1 of glucose), low limit of detection (0.059 mmol L-1, S/N = 3) and good stability. Additionally, this biosensor could be successfully applied for glucose determination in real samples with good accuracy. These results proved the principle of enzymatic glucose biosensor development based on DGNs as the basis for further investigations.

Automated summary

The research showcased a method for synthesizing dendritic gold nanostructures on a graphite rod electrode for use in enzymatic glucose biosensors. Experimental parameters, including optimal concentration of HAuCl4, synthesis duration, electrodeposition potential, and electrochemical method, were determined to develop a biosensor with quick response, high sensitivity, and stability. These results demonstrate the potential for further investigation and development of enzymatic glucose biosensors based on DGNs.