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Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers
Ajith Mohan Arjun
,
Sudhaunsh Deshpande,
Tom Dunlop
,
Beth Norman,
Daniela Oliviera,
Georgeta Vulpe,
Felismina Moreira,
Sanjiv Sharma
Biosensors and Bioelectronics:X
Swansea University Authors:
Tom Dunlop , Georgeta Vulpe, Sanjiv Sharma
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 (VxPDA) redox active composite and a Tau-441-specific polyaniline molecularly imprinted polymer (PANI M...
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v2 66925 2024-07-02 Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers 809395460ab1e6b53a906b136d919c41 0000-0002-5851-8713 Tom Dunlop Tom Dunlop true false d1d5815c60d63534a10a81489255c681 Georgeta Vulpe Georgeta Vulpe true false b6b7506358522f607b171ec9c94757b7 0000-0003-3828-737X Sanjiv Sharma Sanjiv Sharma true false 2024-07-02 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 (VxPDA) 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 VxPDA/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 minutes) 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. Journal Article Biosensors and Bioelectronics:X 0 0 0 0001-01-01 COLLEGE NANME COLLEGE CODE Swansea University The authors thank the MRC-AMED UK-Japan project (Multi-analyte prognostic and diagnostic screening in blood and skin for Alzheimer's disease, MR/X02153X/1) for their support. We also thank AIM providing SEM, EDS, and XPS facilities. AIM is funded in part by the EPSRC (EP/M028267/1), the European Regional Development Fund through the Welsh Government (80708) and the Welsh Government's Ser Cymru Program. 2024-07-02T15:59:04.6430298 2024-07-02T15:38:59.2727799 Faculty of Science and Engineering School of Engineering and Applied Sciences - Biomedical Engineering Ajith Mohan Arjun 0000-0001-6781-2108 1 Sudhaunsh Deshpande 2 Tom Dunlop 0000-0002-5851-8713 3 Beth Norman 4 Daniela Oliviera 5 Georgeta Vulpe 6 Felismina Moreira 7 Sanjiv Sharma 0000-0003-3828-737X 8 |
title |
Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers |
spellingShingle |
Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers Tom Dunlop Georgeta Vulpe Sanjiv Sharma |
title_short |
Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers |
title_full |
Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers |
title_fullStr |
Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers |
title_full_unstemmed |
Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers |
title_sort |
Alzheimer's diagnosis beyond cerebrospinal fluid: Probe-Free Detection of Tau Proteins using MXene based redox systems and molecularly imprinted polymers |
author_id_str_mv |
809395460ab1e6b53a906b136d919c41 d1d5815c60d63534a10a81489255c681 b6b7506358522f607b171ec9c94757b7 |
author_id_fullname_str_mv |
809395460ab1e6b53a906b136d919c41_***_Tom Dunlop d1d5815c60d63534a10a81489255c681_***_Georgeta Vulpe b6b7506358522f607b171ec9c94757b7_***_Sanjiv Sharma |
author |
Tom Dunlop Georgeta Vulpe Sanjiv Sharma |
author2 |
Ajith Mohan Arjun Sudhaunsh Deshpande Tom Dunlop Beth Norman Daniela Oliviera Georgeta Vulpe Felismina Moreira Sanjiv Sharma |
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Journal article |
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Biosensors and Bioelectronics:X |
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Swansea University |
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Faculty of Science and Engineering |
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facultyofscienceandengineering |
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Faculty of Science and Engineering |
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facultyofscienceandengineering |
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Faculty of Science and Engineering |
department_str |
School of Engineering and Applied Sciences - Biomedical Engineering{{{_:::_}}}Faculty of Science and Engineering{{{_:::_}}}School of Engineering and Applied Sciences - Biomedical Engineering |
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description |
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 (VxPDA) 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 VxPDA/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 minutes) 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. |
published_date |
0001-01-01T15:59:03Z |
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1803479776906706944 |
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11.012947 |