化学
适体
注意事项
双模
生物传感器
检测点注意事项
对偶(语法数字)
肌钙蛋白I
电化学
电化学发光
纳米技术
检出限
色谱法
电极
心脏病学
生物化学
分子生物学
航空航天工程
物理化学
医学
心肌梗塞
免疫学
材料科学
护理部
艺术
生物
工程类
文学类
作者
Mingxiang Liao,Zhuoliang Hu,Xilin Chen,Mengjie Chen,Zelin Yang,Jianbin Pan,Duanping Sun
标识
DOI:10.1021/acs.analchem.5c02086
摘要
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 Fe3O4/PEI/CdS quantum dots (QDs) (FePQ) functionalized with a Tro6 aptamer as ECL-active capture probes and ferrocene (Fc)-encapsulated UiO-66-NH2 (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-NH2-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.
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