Exponential amplification reaction and triplex DNA mediated aggregation of gold nanoparticles for sensitive colorimetric detection of microRNA
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Updated: Oct 13, 2026

Rapid Nanoprobe Signal Enhancement by In Situ Gold Nanoparticle Synthesis
Published on: March 7, 2018
Shuangqin Wei1, Guifang Chen2, Xingqing Jia1
1Department of Hepatology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Abstract:
Abnormal expression of specific microRNAs (miRNAs) is associated with the occurrence, development and prognosis of many diseases. In this study, a miRNA detection method based on exponential amplification reaction (EXPAR) and triplex DNA mediated aggregation of gold nanoparticles (AuNPs) was established. Specifically, one class of AuNPs is conjugated with an EXPAR probe, on which there is a complementary sequence of the target miRNA. The EXPAR reaction is triggered and duplex DNA is formed on the surface of AuNPs when the target miRNA exists. Then, single DNA probe on another class of AuNPs interacts with the duplex DNA to form triplex DNA, leading to the aggregation of the two classes of AuNPs, which could be quantified by UV-vis. The proposed method is highly selective and can afford a detection limit of 0.23 fM. Notably, all the ingredients needed for the analysis can pre-add to a tube and only 30 min is needed for the whole detection process. The method is simple, fast and with considerable selectivity and accuracy, so a great potential for this method is expected to meet the need of point-of-care testing of miRNA.
Insights
A novel method detects microRNAs (miRNAs) using gold nanoparticles and exponential amplification. This simple, fast assay offers high selectivity and accuracy for disease diagnostics.
Area of Science:
- Biomedical Engineering
- Molecular Diagnostics
- Nanotechnology
Background:
- Aberrant microRNA (miRNA) expression is linked to various disease states.
- Accurate and rapid miRNA detection is crucial for disease diagnosis and prognosis.
- Existing detection methods can be complex and time-consuming.
Purpose of the Study:
- To develop a sensitive and selective miRNA detection method.
- To utilize exponential amplification reaction (EXPAR) and gold nanoparticle (AuNP) aggregation.
- To enable rapid, point-of-care miRNA analysis.
Main Methods:
- Conjugating AuNPs with EXPAR probes complementary to target miRNAs.
- Utilizing EXPAR to form duplex DNA on AuNPs in the presence of target miRNA.
- Inducing AuNP aggregation via triplex DNA formation for UV-vis quantification.
Main Results:
- Achieved a detection limit of 0.23 µM for target miRNAs.
- Demonstrated high selectivity and accuracy in miRNA detection.
- Developed a one-tube assay completed in 30 minutes.
Conclusions:
- The EXPAR and AuNP aggregation method provides a simple, fast, and accurate approach for miRNA detection.
- This technique shows significant potential for point-of-care diagnostic applications.
- The method addresses the need for efficient miRNA analysis in clinical settings.
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