Dual-mode of electrochemical-colorimetric imprinted sensing strategy based on self-sacrifice beacon for diversified determination of cardiac troponin I in serum

适体 肌钙蛋白I 电化学 检出限 线性范围 分子印迹聚合物 化学 亚甲蓝 肌钙蛋白复合物 色谱法 核化学 材料科学 选择性 心肌梗塞 有机化学 电极 医学 光催化 生物 精神科 遗传学 物理化学 催化作用
作者
Guihua Zhang,Li Zhang,Ying Yu,Bixia Lin,Yumin Wang,Manli Guo,Yujuan Cao
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:167: 112502-112502 被引量:36
标识
DOI:10.1016/j.bios.2020.112502
摘要

Diversified determination of cardiac troponin I (cTnI) in serum is of great significance for the clinical diagnose and daily monitoring of acute myocardial infarction. Herein, an electrochemical-colorimetric dual-mode imprinted sensing strategy was proposed. Firstly, the aptamer-functionalized Fe3+-polydopamine ([email protected]3+-PDA) was constructed as the self-sacrifice beacon. Furthermore, an epitope magnetic molecularly imprinted polymer was prepared to recognize cTnI. Once the cTnI was captured, the beacon was then bound to it through the aptamer, which formed a sandwich-like complex. Under acidic condition, the [email protected]3+-PDA was disintegrated to release large amount of Fe3+, and further converted to Prussian blue (PB). On one hand, the electrochemical response of the PB was sensitive to the cTnI amount. On the other hand, the addition of the yellow K3[Fe(CN)6] into different amounts of the produced PB was able to result in different colors, which enabled the visual detection of cTnI. Under the optimal condition, the sensing strategy exhibited a linear range from 1.0 × 10−2 to 1.0 × 103 ng mL−1, and the detection limits were 3.2 and 7.4 pg mL−1 for the electrochemical and colorimetric modes, respectively. Besides, It is demonstrated that the dual-mode strategy shows favorable selectivity and stability in the assays, indicating a diversified application prospect in both clinic analysis and daily care.
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