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即时 SPR 传感器用于急性心肌梗死诊断的研究进展

Development of a Point-of-Care SPR Sensor for the Diagnosis of Acute Myocardial Infarction.

机构信息

Institute of Chemistry, Faculty of Maths and Natural Sciences, Technical University of Berlin, Straße des 17. Juni 124, 10623 Berlin, Germany.

Institute of Materials Science, Faculty of Engineering, Kiel University, 24143 Kiel, Germany.

出版信息

Biosensors (Basel). 2023 Feb 5;13(2):229. doi: 10.3390/bios13020229.

Abstract

A novel point-of-care surface plasmon resonance (SPR) sensor was developed for the sensitive and real-time detection of cardiac troponin I (cTnI) using epitope-imprinted molecular receptors. The surface coverage of a nano-molecularly imprinted polymer (nanoMIP)-functionalized SPR sensor chip and the size of nanoMIPs (155.7 nm) were characterized using fluorescence microscopy and dynamic light scattering techniques, respectively. Atomic force microscopy, electrochemical impedance spectroscopy, square wave voltammetry and cyclic voltammetry techniques confirmed the successful implementation of each step of the sensor fabrication. The SPR bio-detection assay was initially established by targeting the cTnI peptide template, and the sensor allowed the detection of the peptide in the concentration range of 100-1000 nM with a correlation coefficient (R) of 0.96 and limit of detection (LOD) of 76.47 nM. The optimum assay conditions for protein recognition were subsequently determined, and the cTnI biomarker could be detected in a wide concentration range (0.78-50 ng mL) with high reproducibility (R = 0.91) and sensitivity (LOD: 0.52 ng mL). The overall sensor results were subjected to three binding isotherm models, where nanoMIP-cTnI interaction followed the Langmuir binding isotherm with the dissociation constant of 2.99 × 10 M, indicating a very strong affinity between the cTnI biomarker and epitope-imprinted synthetic receptor. Furthermore, the selectivity of the sensor was confirmed through studying with a control nanoMIP that was prepared by imprinting a non-specific peptide template. Based on the cross-reactivity tests with non-specific molecules (i.e., glucose, p53 protein, transferrin and bovine serum albumin), the nanoMIP-SPR sensor is highly specific for the target biomarker. The developed biomimetic sensor, relying on the direct assay strategy, holds great potential not only for the early and point-of-care testing of acute myocardial infarction but also for other life-threatening diseases that can be diagnosed by determining the elevated levels of certain biomarkers.

摘要

一种新型的即时护理表面等离子体共振(SPR)传感器,使用表位印迹分子受体,用于灵敏、实时地检测心肌肌钙蛋白 I(cTnI)。使用荧光显微镜和动态光散射技术分别对纳米分子印迹聚合物(nanoMIP)功能化 SPR 传感器芯片的表面覆盖率和 nanoMIP 的大小(155.7nm)进行了表征。原子力显微镜、电化学阻抗谱、方波伏安法和循环伏安法技术证实了传感器制造各个步骤的成功实施。SPR 生物检测分析首先通过靶向 cTnI 肽模板进行建立,传感器允许在 100-1000nM 的浓度范围内检测到肽,相关系数(R)为 0.96,检测限(LOD)为 76.47nM。随后确定了蛋白质识别的最佳分析条件,并且可以在较宽的浓度范围内(0.78-50ng mL)检测到 cTnI 生物标志物,具有较高的重现性(R=0.91)和灵敏度(LOD:0.52ng mL)。总体传感器结果符合三种结合等温线模型,其中 nanoMIP-cTnI 相互作用遵循 Langmuir 结合等温线,解离常数为 2.99×10-6M,表明 cTnI 生物标志物和表位印迹合成受体之间具有很强的亲和力。此外,通过研究用印迹非特异性肽模板制备的对照 nanoMIP,证实了传感器的选择性。基于与非特异性分子(即葡萄糖、p53 蛋白、转铁蛋白和牛血清白蛋白)的交叉反应测试,nanoMIP-SPR 传感器对目标生物标志物具有高度特异性。该开发的仿生传感器,基于直接分析策略,不仅对急性心肌梗死的早期和即时护理测试具有巨大潜力,而且对其他可以通过确定某些生物标志物的升高水平来诊断的危及生命的疾病也具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f04/9953663/74d46706ee21/biosensors-13-00229-sch001.jpg

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