Zheng Jintao, Jiang Xiaohong, Bai Shiyao, Lai Minchao, Yu Jiacheng, Chen Mingxi, Zhou Runzhi, Jia Yue, Yan Haoyang, Liang Zheng, Wang Dian, Wu Chuyan, Liu Shan, Li Chenzhong, Yang Jinguang, Luo Yang, Jiang Cheng, Guo Keying
Department of Biotechnology and Food Engineering, Guangdong Technion-Israel Institute of Technology (GTIIT), Shantou, 515063, China.
Faculty of Biotechnology and Food Engineering, Technion-Israel Institute of Technology (IIT), Haifa, 3200003, Israel.
Adv Mater. 2025 Jun 27:e2505262. doi: 10.1002/adma.202505262.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder with no cure, making early diagnosis critical for mitigating its impact. Blood extracellular vesicles (EVs) hold promises as biomarkers for AD diagnosis, but current detection technologies lack the sensitivity and multiplexing capabilities needed for efficient diagnosis. Here, a novel label-free bioelectronic platform is presented based on an organic electrochemical transistor (OECT) integrated with a microelectrode array (MEA) for ultrasensitive detection of AD biomarkers in blood EVs, including amyloid-β (Aβ and Aβ), total tau (t-tau), and phosphorylated tau (p-tau). This platform achieves a detection limit as low as the zeptomolar (zM) level, enabling the detection of single-molecule targets. It provides a comprehensive multiplexed diagnostic model capable of delivering results within 20 min. Notably, the systematic integration of multiple AD biomarkers in blood EVs is demonstrated to significantly enhance diagnostic accuracy. This study presents a novel EVs-based multiplexed diagnostic model for AD, correctly classifying all clinical samples (n = 40), far exceeding the accuracy of a single biomarker. With its high sensitivity and rapid turnaround, this platform enables reliable AD diagnosis and holds the potential for tracking disease progression, offering a transformative tool to combat the societal burden of AD.
阿尔茨海默病(AD)是一种无法治愈的进行性神经退行性疾病,因此早期诊断对于减轻其影响至关重要。血液细胞外囊泡(EVs)有望成为AD诊断的生物标志物,但目前的检测技术缺乏高效诊断所需的灵敏度和多重检测能力。在此,我们提出了一种基于有机电化学晶体管(OECT)与微电极阵列(MEA)集成的新型无标记生物电子平台,用于超灵敏检测血液EVs中的AD生物标志物,包括淀粉样β蛋白(Aβ42和Aβ40)、总tau蛋白(t-tau)和磷酸化tau蛋白(p-tau)。该平台实现了低至zeptomolar(zM)水平的检测限,能够检测单分子靶点。它提供了一个全面的多重诊断模型,能够在20分钟内给出结果。值得注意的是,血液EVs中多种AD生物标志物的系统整合被证明可显著提高诊断准确性。本研究提出了一种基于EVs的新型AD多重诊断模型,能够正确分类所有临床样本(n = 40),远远超过单一生物标志物的准确性。凭借其高灵敏度和快速周转能力,该平台能够实现可靠的AD诊断,并具有跟踪疾病进展的潜力,为应对AD的社会负担提供了一种变革性工具。