用于超灵敏蛋白质检测的高度可重复使用电化学免疫传感器

Kavya L. Singampalli, Camille Neal – Harris, Cassian Yee, Jamie S. Lin, Peter B. Lillehoj
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摘要

体液中蛋白质生物标记物的检测和定量对于疾病诊断和健康监测等许多临床应用都非常重要。目前的超灵敏蛋白质检测技术,如酶联免疫吸附测定法(ELISA)和电化学传感法,需要较长的孵育时间(1.5-3 小时),并且依赖于一次性使用的传感电极,成本高昂且产生大量废物。这项工作展示了一种可重复使用的电化学免疫传感器,该传感器采用磁性纳米粒子(MNPs)和双重标记金纳米粒子(AuNPs),用于超灵敏地测量蛋白质生物标记物。作为概念验证,该平台用于检测人体尿液中的 C-X-C motif 趋化因子配体 9 (CXCL9),这是一种与肾移植排斥反应、检查点抑制剂治疗引起的免疫性肾炎以及药物相关性急性间质性肾炎有关的生物标记物。该传感器在≈1 小时内成功检测到浓度低至 27 皮克/毫升-1 的 CXCL9。该免疫传感器还被改装到基于智能手机的手持诊断设备上,用于测量 CXCL9,其检测下限为 65 皮克/毫升-1。最后,这项工作表明,传感电极可重复使用至少 100 次测量,而分析性能的损失可以忽略不计,从而降低了与电化学传感相关的成本和浪费。
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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Highly Reusable Electrochemical Immunosensor for Ultrasensitive Protein Detection

The detection and quantification of protein biomarkers in bodily fluids is important for many clinical applications, including disease diagnosis and health monitoring. Current techniques for ultrasensitive protein detection, such as enzyme-linked immunosorbent assay (ELISA) and electrochemical sensing, involve long incubation times (1.5–3 h) and rely on single-use sensing electrodes which can be costly and generate excessive waste. This work demonstrates a reusable electrochemical immunosensor employing magnetic nanoparticles (MNPs) and dually labeled gold nanoparticles (AuNPs) for ultrasensitive measurements of protein biomarkers. As proof of concept, this platform is used to detect C-X-C motif chemokine ligand 9 (CXCL9), a biomarker associated with kidney transplant rejection, immune nephritis from checkpoint inhibitor therapy, and drug-associated acute interstitial nephritis, in human urine. The sensor successfully detects CXCL9 at concentrations as low as 27 pg mL−1 within ≈1 h. This immunosensor was also adapted onto a handheld smartphone-based diagnostic device and used for measurements of CXCL9, which exhibited a lower limit of detection of 65 pg mL−1. Lastly, this work demonstrates that the sensing electrodes can be reused for at least 100 measurements with a negligible loss in analytical performance, reducing the costs and waste associated with electrochemical sensing.

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