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Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers
Significance: Alzheimer’s disease (AD) is an irreversible and progressive disorder that damages brain cells and impairs the cognitive abilities of the affected. Developing a sensitive and cost-effective method to detect Alzheimer’s biomarkers appears vital in both a diagnostic and therapeutic perspe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330420/ https://www.ncbi.nlm.nih.gov/pubmed/32618152 http://dx.doi.org/10.1117/1.JBO.25.7.077001 |
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author | Eravuchira, Pinkie J. Banchelli, Martina D’Andrea, Cristiano de Angelis, Marella Matteini, Paolo Gannot, Israel |
author_facet | Eravuchira, Pinkie J. Banchelli, Martina D’Andrea, Cristiano de Angelis, Marella Matteini, Paolo Gannot, Israel |
author_sort | Eravuchira, Pinkie J. |
collection | PubMed |
description | Significance: Alzheimer’s disease (AD) is an irreversible and progressive disorder that damages brain cells and impairs the cognitive abilities of the affected. Developing a sensitive and cost-effective method to detect Alzheimer’s biomarkers appears vital in both a diagnostic and therapeutic perspective. Aim: Our goal is to develop a sensitive and reliable tool for detection of amyloid [Formula: see text] (1-42) peptide ([Formula: see text]), a major AD biomarker, using fiber-enhanced Raman spectroscopy (FERS). Approach: A hollow core photonic crystal fiber (HCPCF) was integrated with a conventional Raman spectroscopic setup to perform FERS measurements. FERS was then coupled with surface-enhanced Raman spectroscopy (SERS) to further amplify the Raman signal thanks to a combined FERS-SERS assay. Results: A minimum 20-fold enhancement of the Raman signal of [Formula: see text] as compared to a conventional Raman spectroscopy scheme was observed using the HCPCF-based light delivery system. The signal was further boosted by decorating the fiber core with gold bipyramids generating an additional SERS effect, resulting in an overall 200 times amplification. Conclusions: The results demonstrate that the use of an HCPCF-based platform can provide sharp and intense Raman signals of [Formula: see text] , in turn paving the way toward the development of a sensitive label-free detection tool for early diagnosis of AD. |
format | Online Article Text |
id | pubmed-7330420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-73304202020-07-07 Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers Eravuchira, Pinkie J. Banchelli, Martina D’Andrea, Cristiano de Angelis, Marella Matteini, Paolo Gannot, Israel J Biomed Opt Sensing Significance: Alzheimer’s disease (AD) is an irreversible and progressive disorder that damages brain cells and impairs the cognitive abilities of the affected. Developing a sensitive and cost-effective method to detect Alzheimer’s biomarkers appears vital in both a diagnostic and therapeutic perspective. Aim: Our goal is to develop a sensitive and reliable tool for detection of amyloid [Formula: see text] (1-42) peptide ([Formula: see text]), a major AD biomarker, using fiber-enhanced Raman spectroscopy (FERS). Approach: A hollow core photonic crystal fiber (HCPCF) was integrated with a conventional Raman spectroscopic setup to perform FERS measurements. FERS was then coupled with surface-enhanced Raman spectroscopy (SERS) to further amplify the Raman signal thanks to a combined FERS-SERS assay. Results: A minimum 20-fold enhancement of the Raman signal of [Formula: see text] as compared to a conventional Raman spectroscopy scheme was observed using the HCPCF-based light delivery system. The signal was further boosted by decorating the fiber core with gold bipyramids generating an additional SERS effect, resulting in an overall 200 times amplification. Conclusions: The results demonstrate that the use of an HCPCF-based platform can provide sharp and intense Raman signals of [Formula: see text] , in turn paving the way toward the development of a sensitive label-free detection tool for early diagnosis of AD. Society of Photo-Optical Instrumentation Engineers 2020-07-02 2020-07 /pmc/articles/PMC7330420/ /pubmed/32618152 http://dx.doi.org/10.1117/1.JBO.25.7.077001 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/ Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Sensing Eravuchira, Pinkie J. Banchelli, Martina D’Andrea, Cristiano de Angelis, Marella Matteini, Paolo Gannot, Israel Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers |
title | Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers |
title_full | Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers |
title_fullStr | Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers |
title_full_unstemmed | Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers |
title_short | Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimer’s disease biomarkers |
title_sort | hollow core photonic crystal fiber-assisted raman spectroscopy as a tool for the detection of alzheimer’s disease biomarkers |
topic | Sensing |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330420/ https://www.ncbi.nlm.nih.gov/pubmed/32618152 http://dx.doi.org/10.1117/1.JBO.25.7.077001 |
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