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Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration
While droplet-based microfluidics is a powerful technique with transformative applications, most devices are passively operated and thus have limited real-time control over droplet contents. In this report, an automated droplet-based microfluidic device with pneumatic pumps and salt water electrodes...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344876/ https://www.ncbi.nlm.nih.gov/pubmed/32630555 http://dx.doi.org/10.3390/mi11060620 |
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author | Shi, Nan Easley, Christopher J. |
author_facet | Shi, Nan Easley, Christopher J. |
author_sort | Shi, Nan |
collection | PubMed |
description | While droplet-based microfluidics is a powerful technique with transformative applications, most devices are passively operated and thus have limited real-time control over droplet contents. In this report, an automated droplet-based microfluidic device with pneumatic pumps and salt water electrodes was developed to generate and coalesce up to six aqueous-in-oil droplets (2.77 nL each). Custom control software combined six droplets drawn from any of four inlet reservoirs. Using our μChopper method for lock-in fluorescence detection, we first accomplished continuous linear calibration and quantified an unknown sample. Analyte-independent signal drifts and even an abrupt decrease in excitation light intensity were corrected in real-time. The system was then validated with homogeneous insulin immunoassays that showed a nonlinear response. On-chip droplet merging with antibody-oligonucleotide (Ab-oligo) probes, insulin standards, and buffer permitted the real-time calibration and correction of large signal drifts. Full calibrations (LOD(conc) = 2 ng mL(−1) = 300 pM; LOD(amt) = 5 amol) required <1 min with merely 13.85 nL of Ab-oligo reagents, giving cost-savings 160-fold over the standard well-plate format while also automating the workflow. This proof-of-concept device—effectively a microfluidic digital-to-analog converter—is readily scalable to more droplets, and it is well-suited for the real-time automation of bioassays that call for expensive reagents. |
format | Online Article Text |
id | pubmed-7344876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73448762020-07-09 Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration Shi, Nan Easley, Christopher J. Micromachines (Basel) Article While droplet-based microfluidics is a powerful technique with transformative applications, most devices are passively operated and thus have limited real-time control over droplet contents. In this report, an automated droplet-based microfluidic device with pneumatic pumps and salt water electrodes was developed to generate and coalesce up to six aqueous-in-oil droplets (2.77 nL each). Custom control software combined six droplets drawn from any of four inlet reservoirs. Using our μChopper method for lock-in fluorescence detection, we first accomplished continuous linear calibration and quantified an unknown sample. Analyte-independent signal drifts and even an abrupt decrease in excitation light intensity were corrected in real-time. The system was then validated with homogeneous insulin immunoassays that showed a nonlinear response. On-chip droplet merging with antibody-oligonucleotide (Ab-oligo) probes, insulin standards, and buffer permitted the real-time calibration and correction of large signal drifts. Full calibrations (LOD(conc) = 2 ng mL(−1) = 300 pM; LOD(amt) = 5 amol) required <1 min with merely 13.85 nL of Ab-oligo reagents, giving cost-savings 160-fold over the standard well-plate format while also automating the workflow. This proof-of-concept device—effectively a microfluidic digital-to-analog converter—is readily scalable to more droplets, and it is well-suited for the real-time automation of bioassays that call for expensive reagents. MDPI 2020-06-25 /pmc/articles/PMC7344876/ /pubmed/32630555 http://dx.doi.org/10.3390/mi11060620 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shi, Nan Easley, Christopher J. Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration |
title | Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration |
title_full | Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration |
title_fullStr | Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration |
title_full_unstemmed | Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration |
title_short | Programmable µChopper Device with On-Chip Droplet Mergers for Continuous Assay Calibration |
title_sort | programmable µchopper device with on-chip droplet mergers for continuous assay calibration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344876/ https://www.ncbi.nlm.nih.gov/pubmed/32630555 http://dx.doi.org/10.3390/mi11060620 |
work_keys_str_mv | AT shinan programmableμchopperdevicewithonchipdropletmergersforcontinuousassaycalibration AT easleychristopherj programmableμchopperdevicewithonchipdropletmergersforcontinuousassaycalibration |