A Molecularly Imprinted Polymer-Based Electrochemical Sensor for Heart Failure Detection

P. Longsompurana, R. P. Pooarporn
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Abstract

The number of Heart Failure (HF) patients is increasing every year, which suggests that early BNP detection is necessary. It is highly desired to look for a new sensor because the Brain Natriuretic Peptide (BNP) has the potential to be a cardiac biomarker for the diagnosis of HF. Due to this, the goal of this study was to create and develop a novel electrochemical sensor for BNP detection based on Molecularly Imprinted Polymer (MIP) rather than an antibody. The modification of carbon Screen Printed Electrode (SPCE) using functionalized-multiwall carbon nanotube/tris (bipyridine) ruthenium (II) chloride (f-MWCNTs/Ru) composites has the advantage of improving the electrode's electron transfer process, as effectively shown by the Cyclic Voltammogram (CV). Pyrrole (Py) and pyrrole-3-carboxylic acid (Py3C) were used as a copolymeric matrix to create the BNP recognition sites. BNP and two monomers were electropolymerized together in a single step by CV method. Differential Pulse Voltammetry (DPV) was used to determine the optimum conditions for the MIP-based BNP sensor, including the Py: Py3C ratio, the number of electropolymerizations, the rebinding pH, and the rebinding time. The DPV results of the new MB labeled NPs revealed directly proportional to the concentrations of rebinding BNP from 10 to 500 pg.cm-3 under optimal conditions, making them acceptable for the detection of both chronic and acute HF. This approach provides an improved detection range and may provide a novel and efficient platform for protein biomarkers.
一种分子印迹聚合物电化学传感器用于心力衰竭检测
心力衰竭(HF)患者的数量每年都在增加,这表明早期检测BNP是必要的。由于脑钠肽(BNP)有可能成为心衰诊断的心脏生物标志物,因此迫切需要寻找一种新的传感器。因此,本研究的目标是创建和开发一种基于分子印迹聚合物(MIP)而不是抗体的新型BNP检测电化学传感器。循环伏安图(CV)有效地证明了功能化多壁碳纳米管/三(联吡啶)氯化钌(f-MWCNTs/Ru)复合材料改性碳丝网印刷电极(SPCE)具有改善电极电子传递过程的优点。以吡咯(Py)和吡咯-3-羧酸(Py3C)为共聚基质制备BNP识别位点。用CV法一步电聚合了BNP和两个单体。采用差分脉冲伏安法(DPV)确定了基于mip的BNP传感器的最佳条件,包括Py: Py3C比、电聚合次数、重结合pH和重结合时间。在最佳条件下,新的MB标记NPs的DPV结果显示与再结合BNP的浓度成正比,在10 ~ 500 pg.cm-3之间,使其可用于慢性和急性HF的检测。该方法提高了检测范围,为蛋白质生物标志物的检测提供了一个新的、高效的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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