Qin Sai-Nan, Nong Yun-Chuan, Cao Chuan-Liang, Chen Li-Yang, Cao Yi-Jie, Wan Ting, Feng Lei, Salminen Kalle, Sun Jian-Jun, Li Ju
Ministry of Education Key Laboratory for Analytical Science of Food Safety and Biology, College of Chemistry, Fuzhou University, Fuzhou, 350116, China.
Zhecheng Hospital of Traditional Chinese Medicine, Shangqiu, Henan Province, 476200, China.
Talanta. 2025 Mar 1;284:127250. doi: 10.1016/j.talanta.2024.127250. Epub 2024 Nov 19.
Acute myocardial infarction (AMI) is one of the top contributors to global disease mortality. AMI biomarkers, such as cardiac troponin I (cTnI), are often detected with enzyme-linked immunosorbent assay (ELISA) that suffers from several well-known drawbacks such as poor stability and slow and cumbersome operation. Therefore, it is necessary to develop a new analytical technique that can rapidly analyse and detect cTnI for early screening of AMI. In this work, a nanoporous electrochemical aptamer-based (E-AB) sensor for rapid and sensitivite detect of cTnI was designed. Firstly, the aptamer was truncated, and then molecular docking simulation and circular dichroism (CD) were used to screen for aptamers with significant conformational changes when binding to the target, in order to enhance the sensitivity of E-AB sensors. Subsequently, nanoporous electrodes with active area 20 times higher than that of smooth electrodes were fabricated by electrochemical alloying/dealloying, which enabled E-AB sensors to obtain higher signal-to-noise ratios, providing favorable assurance for the detection results. Under optimal conditions, E-AB sensors could specifically detect cTnI in serum and blood with a detection limit of 1 pg/mL. At the same time, the sensor and enzyme-linked immunoassay (ELISA) had identical detection results when measuring target levels from real clinical samples. Furthermore, the sensor exhibited good reproducibility, stability, providing a simple and low-cost method for detecting cTnI, which is expected to help early AMI patients obtain accurate diagnosis.
急性心肌梗死(AMI)是全球疾病死亡的主要原因之一。AMI生物标志物,如心肌肌钙蛋白I(cTnI),通常采用酶联免疫吸附测定(ELISA)进行检测,但该方法存在一些众所周知的缺点,如稳定性差、操作缓慢且繁琐。因此,有必要开发一种新的分析技术,能够快速分析和检测cTnI,用于AMI的早期筛查。在这项工作中,设计了一种基于纳米多孔电化学适配体(E-AB)的传感器,用于快速、灵敏地检测cTnI。首先,对适配体进行截短,然后利用分子对接模拟和圆二色性(CD)筛选与靶标结合时具有显著构象变化的适配体,以提高E-AB传感器的灵敏度。随后,通过电化学合金化/脱合金制备了活性面积比光滑电极高20倍的纳米多孔电极,使E-AB传感器能够获得更高的信噪比,为检测结果提供了良好的保证。在最佳条件下,E-AB传感器能够特异性检测血清和血液中的cTnI,检测限为1 pg/mL。同时,在检测实际临床样本中的靶标水平时,该传感器与酶联免疫吸附测定(ELISA)的检测结果相同。此外,该传感器具有良好的重现性和稳定性,为检测cTnI提供了一种简单、低成本的方法,有望帮助早期AMI患者获得准确诊断。