Copper-Based MOF Derivative with Enhanced Electrocatalytic Activity for Highly Sensitive and Ultrafast Detection of Salivary Glucose

Currently, invasive blood-testing methods that are widely employed for diabetes monitoring present issues including discomfort, infection risks, and delayed wound healing, which lead to poor patient compliance, creating a demand for noninvasive testing methods, including saliva-based testing. However, the implementation of saliva glucose monitoring is hindered by the necessity of achieving high sensitivity, accuracy, and rapid response times. Precise atom regulation in metal-organic frameworks (MOFs) is poised to create fast, highly sensitive, and specific electronic interfaces, enabling ultrafast sensing methods, based on which a noninvasive glucose MOF derived Cu-CuO/C sensor is proposed. The sensor employs Cu-CuO/C composites, utilizing the properties of oxygen vacancies to enhance the catalytic oxidation activity of glucose, enabling high sensitivity and rapid response. Finite element simulations revealed that the synergy between the carbon substrate and Cu-CuO heterojunction optimized charge transfer and mass transport pathways, significantly improving sensor performance. Additionally, theoretical calculations demonstrated that the Cu-CuO/C electrode effectively lowers the Gibbs free energy barrier, facilitating glucose oxidation by promoting the desorption of intermediates and enhancing electrocatalytic activity. Experimental validation of the sensor performance revealed an extremely fast response time (0.3 s) and high sensitivity (919.86 μA·mM<sup>-1</sup>·cm<sup>-2</sup>), with a detection range from 0.001 to 7.33 mM (<i>R</i><sup>2</sup> = 0.997). Selectivity tests and real sample tests in artificial and human saliva further confirmed the sensor's reliability in practical applications. Finally, Cu-CuO/C was immobilized onto screen-printed electrodes, resulting in a portable biosensor that was validated for rapid glucose detection in portable instruments, paving the way for wearable real-time continuous monitoring devices.

Authors

Institutions

Publication Details

Journal
Analytical Chemistry
Published
2026-03-04
DOI
https://doi.org/10.1021/acs.analchem.5c06883
Primary Topic
Electrochemical sensors and biosensors
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Copper-Based MOF Derivative with Enhanced Electrocatalytic Activity for Highly Sensitive and Ultrafast Detection of Salivary Glucose

Weizhi Wang, Shixiang Lu, Jieling Qin, Xi Hao
Analytical Chemistry
Electrochemical sensors and biosensors
article

Copper-Based MOF Derivative with Enhanced Electrocatalytic Activity for Highly Sensitive and Ultrafast Detection of Salivary Glucose

Weizhi Wang, Shixiang Lu, Jieling Qin, Xi Hao
article en

Abstract

Currently, invasive blood-testing methods that are widely employed for diabetes monitoring present issues including discomfort, infection risks, and delayed wound healing, which lead to poor patient compliance, creating a demand for noninvasive testing methods, including saliva-based testing. However, the implementation of saliva glucose monitoring is hindered by the necessity of achieving high sensitivity, accuracy, and rapid response times. Precise atom regulation in metal-organic frameworks (MOFs) is poised to create fast, highly sensitive, and specific electronic interfaces, enabling ultrafast sensing methods, based on which a noninvasive glucose MOF derived Cu-CuO/C sensor is proposed. The sensor employs Cu-CuO/C composites, utilizing the properties of oxygen vacancies to enhance the catalytic oxidation activity of glucose, enabling high sensitivity and rapid response. Finite element simulations revealed that the synergy between the carbon substrate and Cu-CuO heterojunction optimized charge transfer and mass transport pathways, significantly improving sensor performance. Additionally, theoretical calculations demonstrated that the Cu-CuO/C electrode effectively lowers the Gibbs free energy barrier, facilitating glucose oxidation by promoting the desorption of intermediates and enhancing electrocatalytic activity. Experimental validation of the sensor performance revealed an extremely fast response time (0.3 s) and high sensitivity (919.86 μA·mM<sup>-1</sup>·cm<sup>-2</sup>), with a detection range from 0.001 to 7.33 mM (<i>R</i><sup>2</sup> = 0.997). Selectivity tests and real sample tests in artificial and human saliva further confirmed the sensor's reliability in practical applications. Finally, Cu-CuO/C was immobilized onto screen-printed electrodes, resulting in a portable biosensor that was validated for rapid glucose detection in portable instruments, paving the way for wearable real-time continuous monitoring devices.

Analytical ChemistryVol. 98(10)
Beijing Institute of Technology (CN)
Zero hunger
Openalex Percentile: Top 36%
Electrochemical sensors and biosensors
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.