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Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics†
Microfluidic platforms are an attractive option for incorporating complex fluid handling into low-cost and rapid diagnostic tests. A persistent challenge for microfluidics, however, is the mismatch in the “world-to-chip” interface – it is challenging to detect analytes present at low concentrations...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734381/ https://www.ncbi.nlm.nih.gov/pubmed/28604891 http://dx.doi.org/10.1039/c7lc00440k |
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author | Rackus, Darius de Campos, Richard P. S. Chan, Calvin Karcz, Maria M. Seale, Brendon Narahari, Tanya Dixon, Christopher Chamberlainab, M. Dean Wheeler, Aaron R. |
author_facet | Rackus, Darius de Campos, Richard P. S. Chan, Calvin Karcz, Maria M. Seale, Brendon Narahari, Tanya Dixon, Christopher Chamberlainab, M. Dean Wheeler, Aaron R. |
author_sort | Rackus, Darius |
collection | PubMed |
description | Microfluidic platforms are an attractive option for incorporating complex fluid handling into low-cost and rapid diagnostic tests. A persistent challenge for microfluidics, however, is the mismatch in the “world-to-chip” interface – it is challenging to detect analytes present at low concentrations in systems that can only handle small volumes of sample. Here we describe a new technique termed pre-concentration by liquid intake by paper (P-CLIP) that addresses this mismatch, allowing digital microfluidics to interface withvolumes on the order of hundreds of microliters. In P-CLIP, a virtual microchannel is generated to pass a large volume through the device; analytes captured on magnetic particles can be isolated and then resuspended into smaller volumes for further processing and analysis. We characterize this method and demonstrate its utility with an immunoassay for Plasmodiumfalciparum lactate dehydrogenase, a malaria biomarker, and propose that the P-CLIPstrategy may be useful for a wide range of applications that are currently limited by low-abundance analytes. |
format | Online Article Text |
id | pubmed-7734381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-77343812020-12-29 Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics† Rackus, Darius de Campos, Richard P. S. Chan, Calvin Karcz, Maria M. Seale, Brendon Narahari, Tanya Dixon, Christopher Chamberlainab, M. Dean Wheeler, Aaron R. Lab Chip Paper Microfluidic platforms are an attractive option for incorporating complex fluid handling into low-cost and rapid diagnostic tests. A persistent challenge for microfluidics, however, is the mismatch in the “world-to-chip” interface – it is challenging to detect analytes present at low concentrations in systems that can only handle small volumes of sample. Here we describe a new technique termed pre-concentration by liquid intake by paper (P-CLIP) that addresses this mismatch, allowing digital microfluidics to interface withvolumes on the order of hundreds of microliters. In P-CLIP, a virtual microchannel is generated to pass a large volume through the device; analytes captured on magnetic particles can be isolated and then resuspended into smaller volumes for further processing and analysis. We characterize this method and demonstrate its utility with an immunoassay for Plasmodiumfalciparum lactate dehydrogenase, a malaria biomarker, and propose that the P-CLIPstrategy may be useful for a wide range of applications that are currently limited by low-abundance analytes. The Royal Society of Chemistry 2017-06-12 2017 /pmc/articles/PMC7734381/ /pubmed/28604891 http://dx.doi.org/10.1039/c7lc00440k Text en © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. Material from this article can be used in other publications provided that the correct acknowledgement is given with the reproduced material. |
spellingShingle | Paper Rackus, Darius de Campos, Richard P. S. Chan, Calvin Karcz, Maria M. Seale, Brendon Narahari, Tanya Dixon, Christopher Chamberlainab, M. Dean Wheeler, Aaron R. Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics† |
title | Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics† |
title_full | Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics† |
title_fullStr | Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics† |
title_full_unstemmed | Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics† |
title_short | Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics† |
title_sort | pre-concentration by liquid intake by paper (p-clip): a new technique for large volumes and digital microfluidics† |
topic | Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734381/ https://www.ncbi.nlm.nih.gov/pubmed/28604891 http://dx.doi.org/10.1039/c7lc00440k |
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