A sensitive electrochemiluminescent biosensor based on AuNP-functionalized ITO for a label-free immunoassay of
Xiang Liu1, Chen Fang2, Jilin Yan1
1Institute of Analytical Chemistry, Dushu Lake Campus, Soochow University, Industrial Park, Suzhou 215123, PR China.
Insights
This study presents a novel, label-free electrochemiluminescent immunosensor for detecting C-peptide, a key diabetes biomarker. The developed assay offers high sensitivity and specificity for improved diabetes diagnosis and research.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Clinical Diagnostics
Background:
- C-peptide is a co-product of insulin secretion by pancreatic β-cells.
- C-peptide levels in body fluids are closely linked to diabetes mellitus.
- Accurate and sensitive C-peptide detection is crucial for diabetes management.
Purpose of the Study:
- To develop a simple, sensitive, and specific label-free electrochemiluminescent (ECL) immunosensor for C-peptide quantification.
- To establish a versatile platform for diabetes clinical diagnosis, classification, and research.
Main Methods:
- Fabrication of an indium tin oxide (ITO) electrode decorated with gold nanoparticles (AuNPs) using (3-aminopropyl)trimethoxysilane.
- Immobilization of anti-C-peptide antibodies onto the AuNP-modified electrode.
- Quantification of C-peptide via label-free ECL signaling using luminol as the probe, measuring ECL inhibition.
Main Results:
- The fabricated electrode's characteristics were confirmed using electron microscopy, cyclic voltammetry, and electrochemical impedance spectroscopy.
- The immunosensor achieved a wide linear detection range for C-peptide from 0.05 ng/mL to 100 ng/mL.
- A low detection limit of 0.0142 ng/mL was achieved, demonstrating high sensitivity.
Conclusions:
- The developed label-free ECL immunosensor provides a sensitive and specific method for C-peptide detection.
- This strategy represents a promising and versatile platform for diabetes-related clinical applications and research.
- The assay's simplicity and effectiveness support its potential for widespread adoption in diagnostics.
Abstract:
The C-peptide is a co-product of pancreatic β-cells during insulin secretion; its content in body fluid is closely related to diabetes. This paper reports an immune-sensing strategy for a simple and effective assay of C-peptide based on label-free electrochemiluminescent (ECL) signaling, with high sensitivity and specificity. The basal electrode was constructed of an indium tin oxide (ITO) glass as a conductive substrate, which was decorated by Au nanoparticles (AuNPs) with hydrolysed (3-aminopropyl)trimethoxysilane as the linker. The characteristics of the fabricated electrode were investigated by electron microscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. After immobilizing the C-peptide antibody, which takes great advantage of AuNPs' binding capacity, this immunosensor can quantify C-peptide using luminol as the ECL probe. By measuring ECL inhibition, calibration can be established to report the C-peptide concentration between 0.05 ng mL-1 and 100 ng mL-1 with a detection limit of 0.0142 ng mL-1. As a proof of concept, the proposed strategy is a promising and versatile platform for the clinical diagnosis, classification, and research of diabetes.
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