Cargando…

LSPR based on-chip detection of dengue NS1 antigen in whole blood

The development of a biosensor for rapid and quantitative detection of the dengue virus continues to remain a challenge. We report a lab-on-chip device that combines membrane-based blood plasma separation and a localized surface plasmon resonance (LSPR) based biosensor for on-chip detection of dengu...

Descripción completa

Detalles Bibliográficos
Autores principales: Lathika, S., Raj, A., Sen, A. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042277/
https://www.ncbi.nlm.nih.gov/pubmed/35497567
http://dx.doi.org/10.1039/d1ra05009e
_version_ 1784694628911415296
author Lathika, S.
Raj, A.
Sen, A. K.
author_facet Lathika, S.
Raj, A.
Sen, A. K.
author_sort Lathika, S.
collection PubMed
description The development of a biosensor for rapid and quantitative detection of the dengue virus continues to remain a challenge. We report a lab-on-chip device that combines membrane-based blood plasma separation and a localized surface plasmon resonance (LSPR) based biosensor for on-chip detection of dengue NS1 antigen from a few drops of blood. The LSPR effect is realized by irradiating UV-NIR light having a spectral peak at 655 nm onto nanostructures fabricated via thermal annealing of a thin metal film. We study the effect of the resulting metal nanostructures on the LSPR performance in terms of sensitivity and limit of detection, by annealing silver films at temperatures ranging from 100 to 500 °C. The effect of annealing temperature on the nanostructure size and uniformity and the resulting optical characteristics are investigated. Further, the binding between non-targeted blood plasma proteins and NS1-antibody-functionalized nanostructures on the LSPR performance is studied by considering different blocking mechanisms. Using a nanostructure annealed at 200 °C and 2X-phosphate buffer saline with 0.05% Tween-20 as the blocking buffer, from 10 μL of whole blood, the device can detect NS1 antigen at a concentration as low as 0.047 μg mL(−1) within 30 min. Finally, we demonstrate the detection of NS1 in the blood samples of dengue-infected patients and validate our results with those obtained from the gold-standard ELISA test.
format Online
Article
Text
id pubmed-9042277
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90422772022-04-28 LSPR based on-chip detection of dengue NS1 antigen in whole blood Lathika, S. Raj, A. Sen, A. K. RSC Adv Chemistry The development of a biosensor for rapid and quantitative detection of the dengue virus continues to remain a challenge. We report a lab-on-chip device that combines membrane-based blood plasma separation and a localized surface plasmon resonance (LSPR) based biosensor for on-chip detection of dengue NS1 antigen from a few drops of blood. The LSPR effect is realized by irradiating UV-NIR light having a spectral peak at 655 nm onto nanostructures fabricated via thermal annealing of a thin metal film. We study the effect of the resulting metal nanostructures on the LSPR performance in terms of sensitivity and limit of detection, by annealing silver films at temperatures ranging from 100 to 500 °C. The effect of annealing temperature on the nanostructure size and uniformity and the resulting optical characteristics are investigated. Further, the binding between non-targeted blood plasma proteins and NS1-antibody-functionalized nanostructures on the LSPR performance is studied by considering different blocking mechanisms. Using a nanostructure annealed at 200 °C and 2X-phosphate buffer saline with 0.05% Tween-20 as the blocking buffer, from 10 μL of whole blood, the device can detect NS1 antigen at a concentration as low as 0.047 μg mL(−1) within 30 min. Finally, we demonstrate the detection of NS1 in the blood samples of dengue-infected patients and validate our results with those obtained from the gold-standard ELISA test. The Royal Society of Chemistry 2021-10-15 /pmc/articles/PMC9042277/ /pubmed/35497567 http://dx.doi.org/10.1039/d1ra05009e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Lathika, S.
Raj, A.
Sen, A. K.
LSPR based on-chip detection of dengue NS1 antigen in whole blood
title LSPR based on-chip detection of dengue NS1 antigen in whole blood
title_full LSPR based on-chip detection of dengue NS1 antigen in whole blood
title_fullStr LSPR based on-chip detection of dengue NS1 antigen in whole blood
title_full_unstemmed LSPR based on-chip detection of dengue NS1 antigen in whole blood
title_short LSPR based on-chip detection of dengue NS1 antigen in whole blood
title_sort lspr based on-chip detection of dengue ns1 antigen in whole blood
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042277/
https://www.ncbi.nlm.nih.gov/pubmed/35497567
http://dx.doi.org/10.1039/d1ra05009e
work_keys_str_mv AT lathikas lsprbasedonchipdetectionofdenguens1antigeninwholeblood
AT raja lsprbasedonchipdetectionofdenguens1antigeninwholeblood
AT senak lsprbasedonchipdetectionofdenguens1antigeninwholeblood