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Updated: Apr 28, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
Published on: October 7, 2025
Localized Dual-Cycle Amplification Integrating Entropy-Driven Reaction and Catalytic Hairpin Assembly for miRNA
Liuting Mo1, Shiya Tang1, Runhong Qin1
1Institute of Optical Materials and Chemical Biology, Guangxi Key Laboratory of Electrochemical Energy Materials, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, P. R. China.
None:
Intracellular microRNA (miRNA) detection plays a crucial role in cancer diagnosis and treatment monitoring. However, current methods face challenges in sensitivity, specificity, and cellular application. Here, we present a novel localized dual-cycle amplification (LDA) system integrating localized entropy-driven DNA circuit reaction (LEDR) and localized catalytic hairpin assembly (LCHA) for sensitive miRNA imaging in living cells. This approach employs a dual-nanosphere platform functionalized with EDR and CHA units. The presence of target miR-155 initiates a cascade reaction of LEDR-LCHA process. The LDA system demonstrates several advantages: (1) enhanced sensitivity with a detection limit of 1.42 pM for miR-155; (2) enhanced reaction kinetics due to localized strategy, reaching signal plateau within 15 min under in vitro conditions; (3) efficient cellular uptake without transfection reagents and improved stability in biological fluids. The system successfully monitored intracellular miR-155 levels and discriminated between cancer and normal samples in both living cells and clinical tissues. This LDA system achieves a synergistic integration of sensitivity, rapid response, and practical applicability for intracellular miRNA detection, offering a robust platform for cancer diagnostics.
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