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Updated: Jun 12, 2026

Aptamer-Based Target Detection Facilitated by a 3-Stage G-Quadruplex Isothermal Exponential Amplification Reaction
Published on: October 6, 2022
An ultrasensitive aptamer-based fluorescent biosensor for luteinizing hormone with mutually orthogonal DNAzyme and
Yuhao Li1, Yanni Wang1, Linwei Pan1
1College of Pharmacy and Biological Engineering, Chongqing University of Technology, Chongqing, 400054, PR China.
We developed a novel sensing platform for ultrasensitive detection of luteinizing hormone (LH). This method uses DNAzyme and self-replicating catalytical hairpin assembly (SR-CHA) for highly sensitive and specific LH detection.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Molecular Diagnostics
Background:
- Sensitive detection of luteinizing hormone (LH) is crucial for disease diagnosis and managing physiological functions.
- Existing methods may lack the required sensitivity or specificity for early disease detection.
Purpose of the Study:
- To develop a novel sensing platform for ultrasensitive luteinizing hormone (LH) detection.
- To harness a synergistic amplification strategy for enhanced analytical performance.
Main Methods:
- Developed a sensing platform utilizing DNAzyme and self-replicating catalytical hairpin assembly (SR-CHA).
- The platform employs an aptamer-based approach for LH recognition.
- Employs a cascade amplification strategy involving DNAzyme and SR-CHA for signal enhancement.
Main Results:
- Achieved an ultrasensitive detection limit for LH as low as 0.00038 mIU/mL in buffer and 0.0006 mIU/mL in real samples.
- Demonstrated a broad dynamic range for LH detection (0.001 to 100 mIU/mL).
- Exhibited excellent selectivity and strong correlation with the ELISA method.
Conclusions:
- The developed platform offers a simple, sensitive, and specific method for LH detection.
- Shows significant potential for constructing various aptamer-based biosensors.
- Provides a promising tool for early disease diagnosis and monitoring physiological functions.
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