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Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA
Miniaturizing the enzyme-linked immunosorbent assay (ELISA) protocols in microfluidics is sought after by researchers for a rapid, high throughput screening, on-site diagnosis, and ease in operation for detection and quantification of biomarkers. Herein, we report the use of the centrifugation-contr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934823/ https://www.ncbi.nlm.nih.gov/pubmed/31882905 http://dx.doi.org/10.1038/s41598-019-56772-6 |
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author | Espulgar, Wilfred Tadokoro, Tatsuro Tamiya, Eiichi Saito, Masato |
author_facet | Espulgar, Wilfred Tadokoro, Tatsuro Tamiya, Eiichi Saito, Masato |
author_sort | Espulgar, Wilfred |
collection | PubMed |
description | Miniaturizing the enzyme-linked immunosorbent assay (ELISA) protocols in microfluidics is sought after by researchers for a rapid, high throughput screening, on-site diagnosis, and ease in operation for detection and quantification of biomarkers. Herein, we report the use of the centrifugation-controlled convective (C3) flow as an alternative method in fluid flow control in a ring-structured channel for enhanced on-chip ELISA. A system that consists of a rotating heater stage and a microfluidic disk chip has been developed and demonstrated to detect IgA. The ring-structured channel was partially filled with microbeads (250 µm in diameter) carrying the capture antibodies and the analyte solution was driven by thermal convection flow (50 µL/min) to promote the reaction. The remaining part of the circular channel without microbeads served as the observation area to measure the absorbance value of the labeled protein. Currently, the system is capable of conducting four reactions in parallel and can be performed within 30 min at 300 G. A detection limit of 6.16 ng/mL using 24 µL of target sample (IgA) was observed. By simply changing the capture antibodies, the system is expected to be versatile for other immunoassays. |
format | Online Article Text |
id | pubmed-6934823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69348232019-12-31 Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA Espulgar, Wilfred Tadokoro, Tatsuro Tamiya, Eiichi Saito, Masato Sci Rep Article Miniaturizing the enzyme-linked immunosorbent assay (ELISA) protocols in microfluidics is sought after by researchers for a rapid, high throughput screening, on-site diagnosis, and ease in operation for detection and quantification of biomarkers. Herein, we report the use of the centrifugation-controlled convective (C3) flow as an alternative method in fluid flow control in a ring-structured channel for enhanced on-chip ELISA. A system that consists of a rotating heater stage and a microfluidic disk chip has been developed and demonstrated to detect IgA. The ring-structured channel was partially filled with microbeads (250 µm in diameter) carrying the capture antibodies and the analyte solution was driven by thermal convection flow (50 µL/min) to promote the reaction. The remaining part of the circular channel without microbeads served as the observation area to measure the absorbance value of the labeled protein. Currently, the system is capable of conducting four reactions in parallel and can be performed within 30 min at 300 G. A detection limit of 6.16 ng/mL using 24 µL of target sample (IgA) was observed. By simply changing the capture antibodies, the system is expected to be versatile for other immunoassays. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934823/ /pubmed/31882905 http://dx.doi.org/10.1038/s41598-019-56772-6 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Espulgar, Wilfred Tadokoro, Tatsuro Tamiya, Eiichi Saito, Masato Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA |
title | Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA |
title_full | Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA |
title_fullStr | Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA |
title_full_unstemmed | Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA |
title_short | Utility of Centrifugation-Controlled Convective (C3) Flow for Rapid On-chip ELISA |
title_sort | utility of centrifugation-controlled convective (c3) flow for rapid on-chip elisa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934823/ https://www.ncbi.nlm.nih.gov/pubmed/31882905 http://dx.doi.org/10.1038/s41598-019-56772-6 |
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