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Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays

For highly sensitive point-of-care (POC) diagnostics, we explored the limit of thermal contrast amplification (TCA) reading of gold nanoparticles (GNPs/mm(2)) at test regions in immunoassays. More specifically, we built and compared fast (minute scale) and ultrafast (seconds scale) TCA setups using...

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Autores principales: Liu, Yilin, Zhan, Li, Kangas, Joseph, Wang, Yiru, Bischof, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321340/
https://www.ncbi.nlm.nih.gov/pubmed/35882876
http://dx.doi.org/10.1038/s41598-022-14841-3
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author Liu, Yilin
Zhan, Li
Kangas, Joseph
Wang, Yiru
Bischof, John
author_facet Liu, Yilin
Zhan, Li
Kangas, Joseph
Wang, Yiru
Bischof, John
author_sort Liu, Yilin
collection PubMed
description For highly sensitive point-of-care (POC) diagnostics, we explored the limit of thermal contrast amplification (TCA) reading of gold nanoparticles (GNPs/mm(2)) at test regions in immunoassays. More specifically, we built and compared fast (minute scale) and ultrafast (seconds scale) TCA setups using continuous-wave (CW) and ms pulsed lasers, respectively. TCA improved the limit of detection (LoD) for silica-core gold nanoshells (GNSs) preloaded in nitrocellulose (NC) membrane as model lateral flow immunoassays (LFAs) by 10- to 20-fold over visual reading. While the ultrafast TCA led to higher thermal signals, this came with a twofold loss in LoD vs. fast TCA primarily due to noise within the infrared sensor and a necessity to limit power to avoid burning. To allow higher laser power, and therefore amplification fold, we also explored transparent glass coverslip substrate as a model microfluidic immunoassay (MIA). We found the ultrafast TCA reading of GNS-coated coverslips achieved a maximal signal amplification (57-fold) over visual reading of model LFAs. Therefore, ultrafast TCA-MIA is promising for ultrasensitive and ultrafast diagnostics. Further advantages of using TCA in MIA vs. LFA could include lower sample volume, multiplexed tests, higher throughput, and fast reading. In summary, TCA technology is able to enhance the sensitivity and speed of reading GNPs (GNPs/mm(2)) within both LFAs and MIAs.
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spelling pubmed-93213402022-07-27 Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays Liu, Yilin Zhan, Li Kangas, Joseph Wang, Yiru Bischof, John Sci Rep Article For highly sensitive point-of-care (POC) diagnostics, we explored the limit of thermal contrast amplification (TCA) reading of gold nanoparticles (GNPs/mm(2)) at test regions in immunoassays. More specifically, we built and compared fast (minute scale) and ultrafast (seconds scale) TCA setups using continuous-wave (CW) and ms pulsed lasers, respectively. TCA improved the limit of detection (LoD) for silica-core gold nanoshells (GNSs) preloaded in nitrocellulose (NC) membrane as model lateral flow immunoassays (LFAs) by 10- to 20-fold over visual reading. While the ultrafast TCA led to higher thermal signals, this came with a twofold loss in LoD vs. fast TCA primarily due to noise within the infrared sensor and a necessity to limit power to avoid burning. To allow higher laser power, and therefore amplification fold, we also explored transparent glass coverslip substrate as a model microfluidic immunoassay (MIA). We found the ultrafast TCA reading of GNS-coated coverslips achieved a maximal signal amplification (57-fold) over visual reading of model LFAs. Therefore, ultrafast TCA-MIA is promising for ultrasensitive and ultrafast diagnostics. Further advantages of using TCA in MIA vs. LFA could include lower sample volume, multiplexed tests, higher throughput, and fast reading. In summary, TCA technology is able to enhance the sensitivity and speed of reading GNPs (GNPs/mm(2)) within both LFAs and MIAs. Nature Publishing Group UK 2022-07-26 /pmc/articles/PMC9321340/ /pubmed/35882876 http://dx.doi.org/10.1038/s41598-022-14841-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liu, Yilin
Zhan, Li
Kangas, Joseph
Wang, Yiru
Bischof, John
Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays
title Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays
title_full Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays
title_fullStr Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays
title_full_unstemmed Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays
title_short Fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays
title_sort fast and ultrafast thermal contrast amplification of gold nanoparticle-based immunoassays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321340/
https://www.ncbi.nlm.nih.gov/pubmed/35882876
http://dx.doi.org/10.1038/s41598-022-14841-3
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