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SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers
PURPOSE: Developing a sensitive SERS-based method to quantitatively detect serum biomarkers (Aβ1-42 and P-Tau-181) for the early diagnosis of Alzheimer’s disease (AD). METHODS: In this study, a novel SERS-based sandwich immunoassay, which consists of tannin-capped silver nanoparticles and magnetic g...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943543/ https://www.ncbi.nlm.nih.gov/pubmed/33707945 http://dx.doi.org/10.2147/IJN.S293042 |
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author | Yu, Dan Yin, Qilong Wang, Jiwei Yang, Jian Chen, Zimeng Gao, Zihan Huang, Qingli Li, Shibao |
author_facet | Yu, Dan Yin, Qilong Wang, Jiwei Yang, Jian Chen, Zimeng Gao, Zihan Huang, Qingli Li, Shibao |
author_sort | Yu, Dan |
collection | PubMed |
description | PURPOSE: Developing a sensitive SERS-based method to quantitatively detect serum biomarkers (Aβ1-42 and P-Tau-181) for the early diagnosis of Alzheimer’s disease (AD). METHODS: In this study, a novel SERS-based sandwich immunoassay, which consists of tannin-capped silver nanoparticles and magnetic graphene oxide (Fe(3)O(4)@GOs), was developed. We firstly applied this method for the detection of protein standards in buffer solution, obtaining the regression equation. Then, its potential value on real serum samples of AD was further explored. RESULTS: The detection linear range of Aβ1-42 and P-Tau-181 protein standards were observed to range from 100 pg mL(−1) to 10 fg mL(−1), 100 pg mL(−1) to 1 fg mL(−1) respectively. We finally explored clinical application of the proposed method in 63 serum samples. As a result, P-tau-181 differentiated AD from non-AD dementia patients (AUC = 0.770), with a more favored ROC than Aβ1-42 (AUC = 0.383). CONCLUSION: The developed SERS-based immunoassay is successfully applied to the determination of Aβ1-42 and P-Tau-181 in human serum specimens, which provides a promising tool for the early diagnosis of AD. |
format | Online Article Text |
id | pubmed-7943543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-79435432021-03-10 SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers Yu, Dan Yin, Qilong Wang, Jiwei Yang, Jian Chen, Zimeng Gao, Zihan Huang, Qingli Li, Shibao Int J Nanomedicine Original Research PURPOSE: Developing a sensitive SERS-based method to quantitatively detect serum biomarkers (Aβ1-42 and P-Tau-181) for the early diagnosis of Alzheimer’s disease (AD). METHODS: In this study, a novel SERS-based sandwich immunoassay, which consists of tannin-capped silver nanoparticles and magnetic graphene oxide (Fe(3)O(4)@GOs), was developed. We firstly applied this method for the detection of protein standards in buffer solution, obtaining the regression equation. Then, its potential value on real serum samples of AD was further explored. RESULTS: The detection linear range of Aβ1-42 and P-Tau-181 protein standards were observed to range from 100 pg mL(−1) to 10 fg mL(−1), 100 pg mL(−1) to 1 fg mL(−1) respectively. We finally explored clinical application of the proposed method in 63 serum samples. As a result, P-tau-181 differentiated AD from non-AD dementia patients (AUC = 0.770), with a more favored ROC than Aβ1-42 (AUC = 0.383). CONCLUSION: The developed SERS-based immunoassay is successfully applied to the determination of Aβ1-42 and P-Tau-181 in human serum specimens, which provides a promising tool for the early diagnosis of AD. Dove 2021-03-05 /pmc/articles/PMC7943543/ /pubmed/33707945 http://dx.doi.org/10.2147/IJN.S293042 Text en © 2021 Yu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Yu, Dan Yin, Qilong Wang, Jiwei Yang, Jian Chen, Zimeng Gao, Zihan Huang, Qingli Li, Shibao SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers |
title | SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers |
title_full | SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers |
title_fullStr | SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers |
title_full_unstemmed | SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers |
title_short | SERS-Based Immunoassay Enhanced with Silver Probe for Selective Separation and Detection of Alzheimer’s Disease Biomarkers |
title_sort | sers-based immunoassay enhanced with silver probe for selective separation and detection of alzheimer’s disease biomarkers |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943543/ https://www.ncbi.nlm.nih.gov/pubmed/33707945 http://dx.doi.org/10.2147/IJN.S293042 |
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