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超越脑脊液的阿尔茨海默病诊断:使用基于MXene的氧化还原系统和分子印迹聚合物对tau蛋白进行无探针检测

Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers.

作者信息

Arjun Ajith Mohan, Deshpande Sudhaunsh, Dunlop Tom, Norman Beth, Oliviera Daniela, Vulpe Georgeta, Moreira Felismina, Sharma Sanjiv

机构信息

Dept. of Biomedical Engineering, Faculty of Science and Engineering, Swansea University, UK.

The Advanced Imaging of Materials (AIM) Facility, Faculty of Science and Engineering, Swansea University, UK.

出版信息

Biosens Bioelectron X. 2024 Oct;20:100513. doi: 10.1016/j.biosx.2024.100513.

Abstract

Phosphorylated Tau proteins are promising biomarkers for the diagnosis and prognosis of Alzheimer's disease. This study presents a novel voltametric sensor using a vanadium MXene polydopamine (VPDA) redox active composite and a Tau-441-specific polyaniline molecularly imprinted polymer (PANI MIP) for the sensitive detection of Tau-441 in interstitial fluid (ISF) and plasma. The VPDA/PANI MIP sensor demonstrates a broad detection range of 5 fg/mL to 5 ng/mL (122 aM/L to 122 pM/L) in ISF without the use of redox mediators, with a lower limit of detection (LOD) of 2.3 fg/mL (60 aM/L). Furthermore, a handheld device utilizing this technology successfully detects Tau-441 in artificial serum with high sensitivity (5 fg/mL to 150 fg/mL (122 aM/L to 366 aM/L)) and specificity within a clinically relevant range. The rapid detection time (∼32 min) and low cost (∼£20/device) of this sensor highlight its potential for minimally invasive, early AD diagnosis in clinical settings. This advancement aims to facilitate a transition away from invasive cerebrospinal fluid (CSF)-based diagnostic techniques for AD.

摘要

磷酸化 Tau 蛋白是阿尔茨海默病诊断和预后的有前景的生物标志物。本研究提出了一种新型伏安传感器,该传感器使用钒基 MXene 聚多巴胺(VPDA)氧化还原活性复合材料和 Tau-441 特异性聚苯胺分子印迹聚合物(PANI MIP),用于灵敏检测间质液(ISF)和血浆中的 Tau-441。VPDA/PANI MIP 传感器在不使用氧化还原介质的情况下,在 ISF 中的检测范围为 5 fg/mL 至 5 ng/mL(122 aM/L 至 122 pM/L),检测下限(LOD)为 2.3 fg/mL(60 aM/L)。此外,利用该技术的手持式设备成功地在临床相关范围内以高灵敏度(5 fg/mL 至 150 fg/mL(122 aM/L 至 366 aM/L))和特异性检测了人工血清中的 Tau-441。该传感器快速的检测时间(约 32 分钟)和低成本(约 20 英镑/设备)突出了其在临床环境中进行微创早期 AD 诊断的潜力。这一进展旨在推动从基于侵入性脑脊液(CSF)的 AD 诊断技术的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0531/11406148/37d5f8ee58bc/gr1.jpg

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