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Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids

BACKGROUND: Alzheimer’s disease (AD) is a neurodegenerative chronic disorder that causes dementia and problems in thinking, cognitive impairment and behavioral changes. Amyloid-beta (Aβ) is a peptide involved in AD progression, and a high level of Aβ is highly correlated with severe AD. Identifying...

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Autores principales: Qiu, Zhengguo, Shen, Qianhe, Jiang, Chao, Yao, Li, Sun, Xiaopeng, Li, Jing, Duan, Chongzhen, Li, Rui, Li, Xiuli, Gopinath, Subash C B, Anbu, Periasamy, Lakshmipriya, Thangavel, Li, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7989959/
https://www.ncbi.nlm.nih.gov/pubmed/33776435
http://dx.doi.org/10.2147/IJN.S302396
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author Qiu, Zhengguo
Shen, Qianhe
Jiang, Chao
Yao, Li
Sun, Xiaopeng
Li, Jing
Duan, Chongzhen
Li, Rui
Li, Xiuli
Gopinath, Subash C B
Anbu, Periasamy
Lakshmipriya, Thangavel
Li, Xu
author_facet Qiu, Zhengguo
Shen, Qianhe
Jiang, Chao
Yao, Li
Sun, Xiaopeng
Li, Jing
Duan, Chongzhen
Li, Rui
Li, Xiuli
Gopinath, Subash C B
Anbu, Periasamy
Lakshmipriya, Thangavel
Li, Xu
author_sort Qiu, Zhengguo
collection PubMed
description BACKGROUND: Alzheimer’s disease (AD) is a neurodegenerative chronic disorder that causes dementia and problems in thinking, cognitive impairment and behavioral changes. Amyloid-beta (Aβ) is a peptide involved in AD progression, and a high level of Aβ is highly correlated with severe AD. Identifying and quantifying Aβ levels helps in the early treatment of AD and reduces the factors associated with AD. MATERIALS AND METHODS: This research introduced a dual probe detection system involving aptamers and antibodies to identify Aβ. Aptamers and antibodies were attached to the gold (Au) urchin and hybrid on the carbon nanohorn-modified surface. The nanohorn was immobilized on the sensor surface by using an amine linker, and then a Au urchin dual probe was immobilized. RESULTS: This dual probe-modified surface enhanced the current flow during Aβ detection compared with the surface with antibody as the probe. This dual probe interacted with higher numbers of Aβ peptides and reached the detection limit at 10 fM with R(2)=0.992. Furthermore, control experiments with nonimmune antibodies, complementary aptamer sequences and control proteins did not display the current responses, indicating the specific detection of Aβ. CONCLUSION: Aβ-spiked artificial cerebrospinal fluid showed a similar response to current changes, confirming the selective identification of Aβ.
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spelling pubmed-79899592021-03-25 Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids Qiu, Zhengguo Shen, Qianhe Jiang, Chao Yao, Li Sun, Xiaopeng Li, Jing Duan, Chongzhen Li, Rui Li, Xiuli Gopinath, Subash C B Anbu, Periasamy Lakshmipriya, Thangavel Li, Xu Int J Nanomedicine Original Research BACKGROUND: Alzheimer’s disease (AD) is a neurodegenerative chronic disorder that causes dementia and problems in thinking, cognitive impairment and behavioral changes. Amyloid-beta (Aβ) is a peptide involved in AD progression, and a high level of Aβ is highly correlated with severe AD. Identifying and quantifying Aβ levels helps in the early treatment of AD and reduces the factors associated with AD. MATERIALS AND METHODS: This research introduced a dual probe detection system involving aptamers and antibodies to identify Aβ. Aptamers and antibodies were attached to the gold (Au) urchin and hybrid on the carbon nanohorn-modified surface. The nanohorn was immobilized on the sensor surface by using an amine linker, and then a Au urchin dual probe was immobilized. RESULTS: This dual probe-modified surface enhanced the current flow during Aβ detection compared with the surface with antibody as the probe. This dual probe interacted with higher numbers of Aβ peptides and reached the detection limit at 10 fM with R(2)=0.992. Furthermore, control experiments with nonimmune antibodies, complementary aptamer sequences and control proteins did not display the current responses, indicating the specific detection of Aβ. CONCLUSION: Aβ-spiked artificial cerebrospinal fluid showed a similar response to current changes, confirming the selective identification of Aβ. Dove 2021-03-19 /pmc/articles/PMC7989959/ /pubmed/33776435 http://dx.doi.org/10.2147/IJN.S302396 Text en © 2021 Qiu 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
Qiu, Zhengguo
Shen, Qianhe
Jiang, Chao
Yao, Li
Sun, Xiaopeng
Li, Jing
Duan, Chongzhen
Li, Rui
Li, Xiuli
Gopinath, Subash C B
Anbu, Periasamy
Lakshmipriya, Thangavel
Li, Xu
Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids
title Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids
title_full Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids
title_fullStr Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids
title_full_unstemmed Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids
title_short Alzheimer’s Disease Determination by a Dual Probe on Gold Nanourchins and Nanohorn Hybrids
title_sort alzheimer’s disease determination by a dual probe on gold nanourchins and nanohorn hybrids
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7989959/
https://www.ncbi.nlm.nih.gov/pubmed/33776435
http://dx.doi.org/10.2147/IJN.S302396
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