Ouyang Ruizhuo, Ma Yuanhui, Jiang Lan, Zhang Xiaoqing, Liu Xi, Wang Ying, Huang Ying, Zhao Yuefeng, Jiang Yuqin, Miao Yuqing, Liu Baolin
Institute of Bismuth and Rhenium Science, University of Shanghai for Science and Technology, Shanghai, 200093, China.
USST-UH International Joint Laboratory for Tumor Diagnosis and Energy Treatment, University of Shanghai for Science and Technology, Shanghai, 200093, China.
Mikrochim Acta. 2025 Jan 31;192(2):115. doi: 10.1007/s00604-025-06977-6.
Ternary heterojunction BiS/MoS/BiMoO was designed as a signal probe to develop a dual signal amplification strategy empowered electrochemical biosensor for sensitive miRNA-21 detection by combining with catalytic hairpin assembly (CHA). The combination of the BiS/MoS/BiMoO heterojunction as a tracer indication probe and the CHA amplification strategy not only took fully use of the highly dense nanowire interwoven structure and superior active region of the probe, but also endowed the ability to improve the molecular hybridization efficiency by collision, which significantly avoided the cumbersome chain design and greatly simplified the step-by-step construction of the electrode surface. Hairpin H1 was first added dropwise to the gold nanoparticle-decorated electrode surface, and then opened by the introduced miRNA-21 to initiate the specific hybridization. Once the H2-MB/BiS/MoS/BiMoO heterojunction was added, more sensitive and rapid detection of miRNA-21 would be achieved through the introduction of methylene blue since the cocatalysis of hairpin assembly and ternary heterojunction BiS@MoS@BiMoO. Finally, the constructed biosensor demonstrated effective performance in the detection of miRNA-21 within the linear range of 1 fM to 100 pM with a detection limit of 0.31 fM. The satisfactory analysis of human blood samples further validated the preferable reliability and practicability of this new strategy for the ultrasensitive detection of miRNA.
三元异质结BiS/MoS/BiMoO被设计为一种信号探针,通过与催化发夹组装(CHA)相结合,开发一种具有双信号放大策略的电化学生物传感器,用于灵敏检测miRNA-21。将BiS/MoS/BiMoO异质结作为示踪指示探针与CHA放大策略相结合,不仅充分利用了探针高度密集的纳米线交织结构和优异的活性区域,还赋予了通过碰撞提高分子杂交效率的能力,显著避免了繁琐的链设计,大大简化了电极表面的逐步构建。首先将发夹H1滴加到金纳米颗粒修饰的电极表面,然后通过引入的miRNA-21使其打开以启动特异性杂交。一旦加入H2-MB/BiS/MoS/BiMoO异质结,由于发夹组装和三元异质结BiS@MoS@BiMoO的协同催化作用,通过引入亚甲基蓝将实现对miRNA-21更灵敏、快速的检测。最终,构建的生物传感器在1 fM至100 pM的线性范围内检测miRNA-21时表现出有效性能,检测限为0.31 fM。对人体血液样本的满意分析进一步验证了这种用于超灵敏检测miRNA的新策略具有较好的可靠性和实用性。