A MoS@TiCT MXene hybrid-based electrochemical aptasensor (MEA) for sensitive and rapid detection of Thyroxine.

Bioelectrochemistry

School of Integrative Engineering, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul 06974, Republic of Korea.

Published: February 2021

AI Article Synopsis

  • This study introduces a novel electrochemical aptasensor (MEA) that utilizes a hybrid of MoS and TiCT MXene for the sensitive and rapid detection of the hormone Thyroxine (T4), which is essential for various bodily functions.
  • The aptasensor is constructed using a nano-hybrid on a carbon electrode, with gold nanostructures enhancing the surface, allowing for improved signal amplification and a limit of detection of 0.39 pg/mL within 10 minutes.
  • The aptasensor demonstrates effective T4 detection in human serum samples, yielding results that align well with the traditional ELISA method, indicating its reliability.

Article Abstract

In the present study, a MoS@TiCT MXene hybrid-based electrochemical aptasensor (MEA) was introduced for sensitive and rapid quantification of Thyroxine (T4). T4 is a crucial hormone and plays a key role in various body functions. Therefore, there is high demand for an accurate, sensitive, and rapid method for the detection of T4. To construct the aptasensor, a nano-hybrid (NH) consisting of TiCT MXene and MoS nanosheets (NS) was synthesized, and applied to a carbon electrode surface, followed by the electroplating of gold nanostructures (GN). The smart combination of TiCT MXene and MoSNS enhanced the physiochemical properties of the electrode surface, as well as provided a building block to form 3D GN. The 3D architecture of the GN offered a unique substrate to capture numerous T4 aptamer molecules, which consequently amplified the signal by nearly 6-fold. The MEA quantified thyroxine with a limit of detection (LOD) of 0.39 pg/mL over a dynamic range ((7.8 × 10) to (7.8 × 10)) pg/mL within 10 min. Moreover, the MEA successfully detected T4 in human serum samples. Lastly, the results obtained from the aptasensor were compared with those from the ELISA standard method. The comparative analysis showed good agreement between the two methods.

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Source
http://dx.doi.org/10.1016/j.bioelechem.2020.107674DOI Listing

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