TY - JOUR
T1 - Hollow core photonic crystal fiber-assisted Raman spectroscopy as a tool for the detection of Alzheimers disease biomarkers
AU - Eravuchira, Pinkie J.
AU - Banchelli, Martina
AU - DAndrea, Cristiano
AU - De Angelis, Marella
AU - Matteini, Paolo
AU - Gannot, Israel
N1 - Funding Information:
Authors acknowledge the support from the European Community, the Israeli Ministry of Health, University and Research of Italy (MIUR) through the ERANET EuroNanoMed III SPEEDY Project under Grants No. 00370311000 and No. ID221. We acknowledge the previous SPIE Proceedings publications.
Publisher Copyright:
© The Authors. 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.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Significance: Alzheimers 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 Alzheimers 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 β (1-42) peptide (Aβ42), 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 Aβ42 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 Aβ42, in turn paving the way toward the development of a sensitive label-free detection tool for early diagnosis of AD.
AB - Significance: Alzheimers 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 Alzheimers 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 β (1-42) peptide (Aβ42), 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 Aβ42 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 Aβ42, in turn paving the way toward the development of a sensitive label-free detection tool for early diagnosis of AD.
KW - Alzheimers
KW - amyloid β-peptide
KW - fiber-enhanced Raman spectroscopy
KW - liquid biopsy
KW - surface-enhanced Raman spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=85087473032&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85087473032&partnerID=8YFLogxK
U2 - 10.1117/1.JBO.25.7.077001
DO - 10.1117/1.JBO.25.7.077001
M3 - Article
C2 - 32618152
AN - SCOPUS:85087473032
SN - 1083-3668
VL - 25
JO - Journal of Biomedical Optics
JF - Journal of Biomedical Optics
IS - 7
M1 - 077001
ER -