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Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis
The use of on-chip isotachophoresis assays for diagnostic applications is often limited by the small volumes of standard microfluidic channels. Overcoming this limitation is particularly important for detection of ‘discrete’ biological targets (such as bacteria) at low concentrations, where the volu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585209/ https://www.ncbi.nlm.nih.gov/pubmed/28874694 http://dx.doi.org/10.1038/s41598-017-10579-5 |
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author | van Kooten, Xander F. Truman-Rosentsvit, Marianna Kaigala, Govind V. Bercovici, Moran |
author_facet | van Kooten, Xander F. Truman-Rosentsvit, Marianna Kaigala, Govind V. Bercovici, Moran |
author_sort | van Kooten, Xander F. |
collection | PubMed |
description | The use of on-chip isotachophoresis assays for diagnostic applications is often limited by the small volumes of standard microfluidic channels. Overcoming this limitation is particularly important for detection of ‘discrete’ biological targets (such as bacteria) at low concentrations, where the volume of processed liquid in a standard microchannel might not contain any targets. We present a novel microfluidic chip that enables ITP focusing of target analytes from initial sample volumes of 50 μL into a concentrated zone with a volume of 500 pL, corresponding to a 100,000-fold increase in mean concentration, and a 300,000-fold increase in peak concentration. We present design considerations for limiting sample dispersion in such large-volume focusing (LVF) chips and discuss the trade-off between assay time and Joule heating, which ultimately governs the scalability of LVF designs. Finally, we demonstrate a 100-fold improvement of ITP focusing performance in the LVF chip as compared to conventional microchannels, and apply this enhancement to achieve highly sensitive detection of both molecular targets (DNA, down to 10 fM) and whole bacteria (down to 100 cfu/mL). |
format | Online Article Text |
id | pubmed-5585209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55852092017-09-06 Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis van Kooten, Xander F. Truman-Rosentsvit, Marianna Kaigala, Govind V. Bercovici, Moran Sci Rep Article The use of on-chip isotachophoresis assays for diagnostic applications is often limited by the small volumes of standard microfluidic channels. Overcoming this limitation is particularly important for detection of ‘discrete’ biological targets (such as bacteria) at low concentrations, where the volume of processed liquid in a standard microchannel might not contain any targets. We present a novel microfluidic chip that enables ITP focusing of target analytes from initial sample volumes of 50 μL into a concentrated zone with a volume of 500 pL, corresponding to a 100,000-fold increase in mean concentration, and a 300,000-fold increase in peak concentration. We present design considerations for limiting sample dispersion in such large-volume focusing (LVF) chips and discuss the trade-off between assay time and Joule heating, which ultimately governs the scalability of LVF designs. Finally, we demonstrate a 100-fold improvement of ITP focusing performance in the LVF chip as compared to conventional microchannels, and apply this enhancement to achieve highly sensitive detection of both molecular targets (DNA, down to 10 fM) and whole bacteria (down to 100 cfu/mL). Nature Publishing Group UK 2017-09-05 /pmc/articles/PMC5585209/ /pubmed/28874694 http://dx.doi.org/10.1038/s41598-017-10579-5 Text en © The Author(s) 2017 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 van Kooten, Xander F. Truman-Rosentsvit, Marianna Kaigala, Govind V. Bercovici, Moran Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis |
title | Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis |
title_full | Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis |
title_fullStr | Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis |
title_full_unstemmed | Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis |
title_short | Focusing analytes from 50 μL into 500 pL: On-chip focusing from large sample volumes using isotachophoresis |
title_sort | focusing analytes from 50 μl into 500 pl: on-chip focusing from large sample volumes using isotachophoresis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585209/ https://www.ncbi.nlm.nih.gov/pubmed/28874694 http://dx.doi.org/10.1038/s41598-017-10579-5 |
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