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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...

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Autores principales: Yu, Dan, Yin, Qilong, Wang, Jiwei, Yang, Jian, Chen, Zimeng, Gao, Zihan, Huang, Qingli, Li, Shibao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
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.
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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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