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Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip

This research demonstrates the development of a transmission-mode localized surface plasmon resonance (LSPR) sensor chip using a cuvette cell system for the sensitive detection of a biomolecule marker such as C-reactive protein (CRP). In order to develop a highly sensitive LSPR sensor chip, plasmoni...

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Autores principales: Oh, Seo Yeong, Heo, Nam Su, Bajpai, Vivek K., Jang, Sung-Chan, Ok, Gyeongsik, Cho, Youngjin, Huh, Yun Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839135/
https://www.ncbi.nlm.nih.gov/pubmed/31737618
http://dx.doi.org/10.3389/fbioe.2019.00299
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author Oh, Seo Yeong
Heo, Nam Su
Bajpai, Vivek K.
Jang, Sung-Chan
Ok, Gyeongsik
Cho, Youngjin
Huh, Yun Suk
author_facet Oh, Seo Yeong
Heo, Nam Su
Bajpai, Vivek K.
Jang, Sung-Chan
Ok, Gyeongsik
Cho, Youngjin
Huh, Yun Suk
author_sort Oh, Seo Yeong
collection PubMed
description This research demonstrates the development of a transmission-mode localized surface plasmon resonance (LSPR) sensor chip using a cuvette cell system for the sensitive detection of a biomolecule marker such as C-reactive protein (CRP). In order to develop a highly sensitive LSPR sensor chip, plasmonically active gold nanoparticles (AuNPs) were decorated onto various transparent substrates in the form of a uniform, high-density single layer using a self-assembly process. The transparent substrate surface was modified with amine functional groups via (3-Aminopropyl)triethoxysilane (APTES) treatment, and the ligand concentration and temperature (0.5% APTES at 60°C) were then optimized to control the binding energy with AuNPs. The optimized plasmonically active strip was subsequently prepared by dipping the amine-functionalized substrate into AuNPs for 8 h. The optimized plasmonic strip functionalized with anti-CRP was transformed into a portable LSPR sensor chip by placing it inside a cuvette cell system, and its detection performance was evaluated using CRP as a model sample. The detection limit for CRP using our LSPR sensor chip was 0.01 μg/mL, and the detection dynamic range was 0.01–10 μg/mL with a %CV of <10%, thus confirming its selectivity and good reproducibility. These findings illustrate that the highly sensitive portable LSPR biosensor developed in this study is expected to be widely used in a diverse range of fields such as diagnosis, medical care, environmental monitoring, and food quality control.
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spelling pubmed-68391352019-11-15 Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip Oh, Seo Yeong Heo, Nam Su Bajpai, Vivek K. Jang, Sung-Chan Ok, Gyeongsik Cho, Youngjin Huh, Yun Suk Front Bioeng Biotechnol Bioengineering and Biotechnology This research demonstrates the development of a transmission-mode localized surface plasmon resonance (LSPR) sensor chip using a cuvette cell system for the sensitive detection of a biomolecule marker such as C-reactive protein (CRP). In order to develop a highly sensitive LSPR sensor chip, plasmonically active gold nanoparticles (AuNPs) were decorated onto various transparent substrates in the form of a uniform, high-density single layer using a self-assembly process. The transparent substrate surface was modified with amine functional groups via (3-Aminopropyl)triethoxysilane (APTES) treatment, and the ligand concentration and temperature (0.5% APTES at 60°C) were then optimized to control the binding energy with AuNPs. The optimized plasmonically active strip was subsequently prepared by dipping the amine-functionalized substrate into AuNPs for 8 h. The optimized plasmonic strip functionalized with anti-CRP was transformed into a portable LSPR sensor chip by placing it inside a cuvette cell system, and its detection performance was evaluated using CRP as a model sample. The detection limit for CRP using our LSPR sensor chip was 0.01 μg/mL, and the detection dynamic range was 0.01–10 μg/mL with a %CV of <10%, thus confirming its selectivity and good reproducibility. These findings illustrate that the highly sensitive portable LSPR biosensor developed in this study is expected to be widely used in a diverse range of fields such as diagnosis, medical care, environmental monitoring, and food quality control. Frontiers Media S.A. 2019-11-01 /pmc/articles/PMC6839135/ /pubmed/31737618 http://dx.doi.org/10.3389/fbioe.2019.00299 Text en Copyright © 2019 Oh, Heo, Bajpai, Jang, Ok, Cho and Huh. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Oh, Seo Yeong
Heo, Nam Su
Bajpai, Vivek K.
Jang, Sung-Chan
Ok, Gyeongsik
Cho, Youngjin
Huh, Yun Suk
Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip
title Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip
title_full Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip
title_fullStr Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip
title_full_unstemmed Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip
title_short Development of a Cuvette-Based LSPR Sensor Chip Using a Plasmonically Active Transparent Strip
title_sort development of a cuvette-based lspr sensor chip using a plasmonically active transparent strip
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839135/
https://www.ncbi.nlm.nih.gov/pubmed/31737618
http://dx.doi.org/10.3389/fbioe.2019.00299
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