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An AC electrokinetics-based electrochemical aptasensor for the rapid detection of microRNA-155
Neil Adrian P Ondevilla1, Tak-Wah Wong2, Nan-Yao Lee3
1Department of Biomedical Engineering, National Cheng Kung University, Tainan, 70101, Taiwan.
Biosensors & Bioelectronics
|December 13, 2021
Summary
This study presents a rapid electrochemical aptasensor using AC electroosmotic flow to detect microRNA-155. It achieves ultra-low detection limits and significantly faster results than traditional methods for early infection detection.
Area of Science:
- Biosensor technology
- Electrochemical analysis
- Biomarker detection
Background:
- Traditional immunosensors suffer from low sensitivity and slow detection due to passive diffusion.
- Alternating current (AC) electrokinetics can enhance analyte transport and binding efficiency.
- MicroRNA-155 (miR-155) is a relevant biomarker for early infection detection.
Purpose of the Study:
- To develop a rapid electrochemical aptasensor for sensitive miR-155 detection.
- To leverage AC electroosmotic (ACEO) flow for enhanced target hybridization.
- To improve upon the speed and sensitivity of existing detection methods.
Main Methods:
- Fabrication of an electrochemical aptasensor.
- Integration of AC electroosmotic (ACEO) flow for analyte preconcentration.
- Optimization of electrokinetic parameters for target collection.
- Detection of miR-155 using the developed aptasensor.
Main Results:
- Achieved a detection limit of 1 aM for miR-155, 100 times lower than conventional methods.
- Detection time reduced to 75 seconds, approximately 50 times faster than traditional methods.
- Demonstrated effective detection in spiked serum samples, confirming real-world applicability.
Conclusions:
- The ACEO-enhanced electrochemical aptasensor offers highly sensitive and rapid detection of miR-155.
- This technology holds promise for real-time sensing of biomarkers for early infection diagnosis.
- The developed method significantly outperforms conventional diffusion-dependent biosensing techniques.

