Related Experiment Video
Updated: Jul 2, 2026

Fully Automated Centrifugal Microfluidic Device for Ultrasensitive Protein Detection from Whole Blood
Published on: April 16, 2016
A functionalized single-layered titanium carbide MXene based biosensor for selective H2O2 detection using covalently
Devarasu Mohanapriya1, Vadakke Purakkal Sruthi1, Sellappan Senthilkumar1
1Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology (VIT), Vellore-632014, India. senthilkumar.s@vit.ac.in.
None:
Hydrogen peroxide (H2O2) plays a significant role in biological and environmental systems. Therefore, it is crucial to develop an efficient biosensor for H2O2 determination, which is important in environmental monitoring and biomedical diagnostics. In this work, we have synthesized an amine functionalized, single-layered Ti3C2Tx MXene (NH2-S-Ti3C2Tx), which was modified over a glassy carbon electrode (GCE) to construct NH2-S-Ti3C2Tx/GCE. Thus obtained NH2-S-Ti3C2Tx/GCE was utilized as a platform for the covalent cross-linking of water-soluble horseradish peroxidase (HRP) enzyme through a glutaraldehyde coupling reaction to form HRP/NH2-S-Ti3C2Tx/GCE. The fabricated HRP/NH2-S-Ti3C2Tx/GCE biosensor demonstrated a well-defined redox peak with a formal potential of -0.45 V, corresponding to the FeIII/FeII redox center of HRP. Additionally, the designed biosensor has been employed towards the electrocatalytic detection of H2O2 under both static and dynamic conditions. The HRP/NH2-S-Ti3C2Tx/GCE sensor displayed a broad linear range of 20 µM to 1160 µM with a low limit of detection of 5.3 µM and a high sensitivity of 0.078 µA mM-1 cm-2. The reported sensor demonstrated excellent analytical performance due to direct electron transfer through the covalent immobilization of HRP over NH2-S-Ti3C2Tx. Furthermore, the sensor was employed for the real-time detection of H2O2, and it portrayed good recovery results.
