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用于即时检测心肌肌钙蛋白I的双模式电化学和电化学发光适体生物传感器。

Dual-Mode Electrochemical and Electrochemiluminescent Aptamer Biosensors for Point-of-Care Detection of Cardiac Troponin I.

作者信息

Liao Mingang, Hu Zhuoliang, Chen Xilin, Chen Mengjie, Yang Zelin, Pan Jianbin, Sun Duanping

机构信息

Center for Drug Research and Development, the Second Clinical Medical School (Guangdong Second Provincial General Hospital), Guangdong Pharmaceutical University, Guangzhou, Guangdong 510006, China.

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, Jiangsu 210093, China.

出版信息

Anal Chem. 2025 Aug 12;97(31):16885-16895. doi: 10.1021/acs.analchem.5c02086. Epub 2025 Jul 15.

Abstract

Acute myocardial infarction (AMI), a leading cause of global mortality, requires the rapid and accurate detection of cardiac troponin I (cTnI) for prompt intervention. To address this, we present an innovative dual-mode electrochemiluminescence-electrochemical (ECL-EC) aptasensor for point-of-care detection of cTnI. The platform employs FeO/PEI/CdS quantum dots (QDs) (FePQ) functionalized with a Tro6 aptamer as ECL-active capture probes and ferrocene (Fc)-encapsulated UiO-66-NH (UFc) conjugated with a Tro4 aptamer as dual-functional signal probes. Upon cTnI binding, a sandwich complex forms, enabling dual-signal transduction: ECL signal attenuation is achieved through energy transfer or electron transfer between FePQ and proximal UFc and enhanced square wave voltammetry (SWV) response from accumulated UFc moieties. This ECL-EC mechanism enables self-verification, significantly reducing false signals, while achieving a wide linear range from 0.001 to 100 ng/mL with low detection limits (0.49 and 0.74 pg/mL) for 60 min. Notably, the dual-mode detection system also demonstrates remarkable consistency for cTnI quantification in clinical samples. The integration of magnetic separation, aptamer-based recognition, and UiO-66-NH-enhanced signal amplification ensures clinical practicality. The system demonstrates exceptional specificity, reproducibility, and stability in human serum analysis, not only providing a transformative solution for point-of-care AMI diagnostics but also establishing a versatile framework for developing multimodal biosensors targeting other biomarkers, advancing precision medicine in cardiovascular care.

摘要

急性心肌梗死(AMI)是全球死亡的主要原因,需要快速准确地检测心肌肌钙蛋白I(cTnI)以便及时干预。为解决这一问题,我们提出了一种用于即时检测cTnI的创新型双模式电化学发光-电化学(ECL-EC)适配体传感器。该平台采用用Tro6适配体功能化的FeO/PEI/CdS量子点(QDs)(FePQ)作为ECL活性捕获探针,以及与Tro4适配体共轭的二茂铁(Fc)封装的UiO-66-NH(UFc)作为双功能信号探针。当cTnI结合时,形成夹心复合物,实现双信号转导:通过FePQ和近端UFc之间的能量转移或电子转移实现ECL信号衰减,并通过累积的UFc部分增强方波伏安法(SWV)响应。这种ECL-EC机制能够进行自我验证,显著减少假信号,同时在60分钟内实现0.001至100 ng/mL的宽线性范围和低检测限(0.49和0.74 pg/mL)。值得注意的是,双模式检测系统在临床样本中对cTnI定量也表现出显著的一致性。磁分离、基于适配体的识别和UiO-66-NH增强的信号放大的整合确保了临床实用性。该系统在人血清分析中表现出卓越的特异性、重现性和稳定性,不仅为即时AMI诊断提供了变革性解决方案,还为开发针对其他生物标志物的多模式生物传感器建立了通用框架,推动心血管护理中的精准医学发展。

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