Related Experiment Video
Updated: Jan 3, 2026

Using Extraordinary Optical Transmission to Quantify Cardiac Biomarkers in Human Serum
Published on: December 13, 2017
Functionalized Graphene Quantum Dot Interfaced Electrochemical Detection of Cardiac Troponin I: An Antibody Free
Muthaiyan Lakshmanakumar1,2, Noel Nesakumar3, Swaminathan Sethuraman1,4
1Centre for Nanotechnology & Advanced Biomaterials (CeNTAB), SASTRA Deemed University, Thanjavur, 613 401, India.
Insights
This study introduces a novel biosensor using functionalized graphene quantum dots for detecting cardiac Troponin I, a key marker for early acute myocardial infarction diagnosis.
Area of Science:
- Biomedical Engineering
- Materials Science
- Analytical Chemistry
Background:
- Cardiovascular disease (CVD) remains a leading global cause of mortality.
- Developing sensitive biosensors for CVD markers is crucial for early diagnosis and treatment.
- Cardiac Troponin I (cTnI) is a critical biomarker for acute myocardial infarction (AMI).
Purpose of the Study:
- To develop an electrochemical biosensor for sensitive and early detection of cardiac Troponin I (cTnI).
- To utilize acetic acid functionalized graphene quantum dots (fGQDs) as an interface for cTnI detection.
- To investigate the diagnostic capacity of the developed biosensor for acute myocardial infarction.
Main Methods:
- Electrochemical detection using cyclic voltammetry (CV) and amperometry.
- Functionalization of graphene quantum dots with acetic acid (fGQDs).
- Carbodiimide conjugation for immobilizing cTnI onto the fGQDs.
- Fourier Transform Infrared Spectrometry (FTIR) for confirming the sensing mechanism.
Main Results:
- The fGQDs modified Au electrode demonstrated sensitive electrocatalytic oxidation of cTnI.
- Achieved a linear detection range of 0.17 to 3 ng/mL for cTnI.
- Obtained a low limit of detection of 0.02 ng/mL for cTnI.
- Bland-Altman plots indicated bias between intra-/inter-cTnI assays and calibrated assays.
Conclusions:
- The developed fGQDs-based electrochemical biosensor offers a promising method for cTnI detection.
- This innovative approach shows potential for the early diagnosis of acute myocardial infarction.
- Further validation with clinical samples is required to confirm applicability in healthcare settings.
Abstract:
According to the World Health Organization (WHO), cardiovascular disease (CVD) is the leading cause of death in the world every year. The design and development of biosensors for the detection of CVD markers could be one of the major contributions of the scientific community to society. In this context, acetic acid functionalized graphene quantum dots (fGQDs) were used as an interface for the electrochemical detection of cardiac Troponin I (cTnI). The interaction of cTnI with fGQDs for the early diagnosis of acute myocardial infarction was investigated using cyclic voltammetry (CV) and amperometry. The carbodiimide conjugation between the N-H group of cTnI and the functionalized COOH group on GQDs enabled the detection of cTnI biomarker. The same sensing mechanism was confirmed using Fourier Transform Infrared Spectrometry (FTIR). The fGQDs modified Au electrode showed remarkable electrocatalytic oxidation of cTnI with good stability and sensitivity over a linear range of 0.17 to 3 ng mL-1 and a low detection limit of 0.02 ng mL-1. Bland-Altman plots substantiate a bias between the intra-/inter-cTnI assay and calibrated cTnI assay with 95% limits of agreement (mean difference ± 1.96 SD). The aim of this study is to describe an innovative method to detect cardiac biomarker cTnI and provide preliminary data on its diagnostic capacity. At the same time, its applicability in clinical setting will have to be validated with a significant number of samples collected from patients.
More Related Videos
07:51Development and Functionalization of Electrolyte-Gated Graphene Field-Effect Transistor for Biomarker Detection
Published on: February 1, 2022
10:12A Sensitive and Specific Quantitation Method for Determination of Serum Cardiac Myosin Binding Protein-C by Electrochemiluminescence Immunoassay
Published on: August 8, 2013