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用于检测唾液中两种阿尔茨海默病生物标志物的金纳米颗粒/磁珠增强型电化学传感器

AuNP/Magnetic Bead-Enhanced Electrochemical Sensor Toward Dual Saliva Alzheimer's Biomarkers Detection.

作者信息

Zhao Pengcheng, Wang Jieyu, Mao Hongju, Zhou Lin, Wu Zhenhua, Lu Yunxing, Sun Teng, Hui Jianan, Ma Guowu

机构信息

School of Stomatology, Dalian Medical University, Dalian 116000, China.

State Key Laboratory of Transducer Technology, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, China.

出版信息

Sensors (Basel). 2025 Jun 30;25(13):4088. doi: 10.3390/s25134088.

Abstract

Alzheimer's disease (AD) early screening requires non-invasive, high-sensitivity detection of low-abundance biomarkers in complex biofluids like saliva. In this study, we present a miniaturized, silicon-based electrochemical sensor for sequential detection of two AD salivary biomarkers, lactoferrin (Lf) and amyloid β-protein 1-42 (Aβ), on a single reusable electrode. The sensor features a three-electrode system fabricated by sputter-coating a quartz substrate with gold (Au) sensing electrodes, which are further modified with gold nanoparticles (AuNPs) to form 3D dendritic structures that enhance surface area and electron transfer. To improve specificity, immunomagnetic beads (MBs) are employed to selectively capture and isolate target biomarkers from saliva samples. These MB-biomarker complexes are introduced into a polydimethylsiloxane chamber aligned with Au sensing electrodes, where a detachable magnet localizes the complexes onto the electrode surface to amplify redox signals. The AuNPs/MBs sensor achieves detection limits of 2 μg/mL for Lf and 0.1 pg/mL for Aβ, outperforming commercial ELISA kits (37.5 pg/mL for Aβ) and covering physiological salivary concentrations. After the MBs capture the biomarkers, the sensor can output the result within one minute. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements confirm enhanced electron transfer kinetics on AuNP-decorated surfaces, while linear correlations (R > 0.95) validate quantitative accuracy across biomarker ranges. The compact and integrated design eliminates reliance on bulky instrumentation and enables user-friendly operation, establishing a promising platform for portable, cost-effective AD screening and monitoring.

摘要

阿尔茨海默病(AD)的早期筛查需要对唾液等复杂生物流体中的低丰度生物标志物进行非侵入性、高灵敏度检测。在本研究中,我们展示了一种基于硅的小型化电化学传感器,用于在单个可重复使用的电极上顺序检测两种AD唾液生物标志物,即乳铁蛋白(Lf)和淀粉样β蛋白1-42(Aβ)。该传感器具有三电极系统,通过在石英基板上溅射涂覆金(Au)传感电极制成,这些电极进一步用金纳米颗粒(AuNPs)修饰,形成三维树枝状结构,以增加表面积并促进电子转移。为了提高特异性,采用免疫磁珠(MBs)从唾液样本中选择性捕获和分离目标生物标志物。这些MB-生物标志物复合物被引入与Au传感电极对齐的聚二甲基硅氧烷腔室中,其中一个可拆卸的磁体将复合物定位在电极表面,以放大氧化还原信号。AuNPs/MBs传感器对Lf的检测限为2 μg/mL,对Aβ的检测限为0.1 pg/mL,优于商业ELISA试剂盒(Aβ的检测限为37.5 pg/mL),并涵盖了生理唾液浓度范围。在MBs捕获生物标志物后,传感器可在一分钟内输出结果。循环伏安法(CV)和电化学阻抗谱(EIS)测量证实了在AuNP修饰表面上电子转移动力学的增强,而线性相关性(R>0.95)验证了跨生物标志物范围的定量准确性。紧凑的集成设计消除了对大型仪器的依赖,并实现了用户友好的操作,为便携式、经济高效的AD筛查和监测建立了一个有前景的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c2/12252058/95efa5b21278/sensors-25-04088-g001.jpg

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