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Cyclic on-chip bacteria separation and preconcentration

Nanoparticles and biological molecules high throughput robust separation is of significant interest in many healthcare and nanoscience industrial applications. In this work, we report an on-chip automatic efficient separation and preconcentration method of dissimilar sized particles within a microfl...

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Autores principales: Ryzhkov, Vitaly V., Zverev, Alexander V., Echeistov, Vladimir V., Andronic, Mikhail, Ryzhikov, Ilya A., Budashov, Igor A., Eremenko, Arkadiy V., Kurochkin, Ilya N., Rodionov, Ilya A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713219/
https://www.ncbi.nlm.nih.gov/pubmed/33273691
http://dx.doi.org/10.1038/s41598-020-78298-y
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author Ryzhkov, Vitaly V.
Zverev, Alexander V.
Echeistov, Vladimir V.
Andronic, Mikhail
Ryzhikov, Ilya A.
Budashov, Igor A.
Eremenko, Arkadiy V.
Kurochkin, Ilya N.
Rodionov, Ilya A.
author_facet Ryzhkov, Vitaly V.
Zverev, Alexander V.
Echeistov, Vladimir V.
Andronic, Mikhail
Ryzhikov, Ilya A.
Budashov, Igor A.
Eremenko, Arkadiy V.
Kurochkin, Ilya N.
Rodionov, Ilya A.
author_sort Ryzhkov, Vitaly V.
collection PubMed
description Nanoparticles and biological molecules high throughput robust separation is of significant interest in many healthcare and nanoscience industrial applications. In this work, we report an on-chip automatic efficient separation and preconcentration method of dissimilar sized particles within a microfluidic platform using integrated membrane valves controlled microfiltration. Micro-sized E. coli bacteria are sorted from nanoparticles and preconcentrated on a microfluidic chip with six integrated pneumatic valves (sub-100 nL dead volume) using hydrophilic PVDF filter with 0.45 μm pore diameter. The proposed on-chip automatic sorting sequence includes a sample filtration, dead volume washout and retentate backflush in reverse flow. We showed that pulse backflush mode and volume control can dramatically increase microparticles sorting and preconcentration efficiency. We demonstrate that at the optimal pulse backflush regime a separation efficiency of E. coli cells up to 81.33% at a separation throughput of 120.45 μL/min can be achieved. A trimmed mode when the backflush volume is twice smaller than the initial sample results in a preconcentration efficiency of E. coli cells up to 121.96% at a throughput of 80.93 μL/min. Finally, we propose a cyclic on-chip preconcentration method which demonstrates E. coli cells preconcentration efficiency of 536% at a throughput of 1.98 μL/min and 294% preconcentration efficiency at a 10.9 μL/min throughput.
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spelling pubmed-77132192020-12-03 Cyclic on-chip bacteria separation and preconcentration Ryzhkov, Vitaly V. Zverev, Alexander V. Echeistov, Vladimir V. Andronic, Mikhail Ryzhikov, Ilya A. Budashov, Igor A. Eremenko, Arkadiy V. Kurochkin, Ilya N. Rodionov, Ilya A. Sci Rep Article Nanoparticles and biological molecules high throughput robust separation is of significant interest in many healthcare and nanoscience industrial applications. In this work, we report an on-chip automatic efficient separation and preconcentration method of dissimilar sized particles within a microfluidic platform using integrated membrane valves controlled microfiltration. Micro-sized E. coli bacteria are sorted from nanoparticles and preconcentrated on a microfluidic chip with six integrated pneumatic valves (sub-100 nL dead volume) using hydrophilic PVDF filter with 0.45 μm pore diameter. The proposed on-chip automatic sorting sequence includes a sample filtration, dead volume washout and retentate backflush in reverse flow. We showed that pulse backflush mode and volume control can dramatically increase microparticles sorting and preconcentration efficiency. We demonstrate that at the optimal pulse backflush regime a separation efficiency of E. coli cells up to 81.33% at a separation throughput of 120.45 μL/min can be achieved. A trimmed mode when the backflush volume is twice smaller than the initial sample results in a preconcentration efficiency of E. coli cells up to 121.96% at a throughput of 80.93 μL/min. Finally, we propose a cyclic on-chip preconcentration method which demonstrates E. coli cells preconcentration efficiency of 536% at a throughput of 1.98 μL/min and 294% preconcentration efficiency at a 10.9 μL/min throughput. Nature Publishing Group UK 2020-12-03 /pmc/articles/PMC7713219/ /pubmed/33273691 http://dx.doi.org/10.1038/s41598-020-78298-y Text en © The Author(s) 2020 Open AccessThis 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/.
spellingShingle Article
Ryzhkov, Vitaly V.
Zverev, Alexander V.
Echeistov, Vladimir V.
Andronic, Mikhail
Ryzhikov, Ilya A.
Budashov, Igor A.
Eremenko, Arkadiy V.
Kurochkin, Ilya N.
Rodionov, Ilya A.
Cyclic on-chip bacteria separation and preconcentration
title Cyclic on-chip bacteria separation and preconcentration
title_full Cyclic on-chip bacteria separation and preconcentration
title_fullStr Cyclic on-chip bacteria separation and preconcentration
title_full_unstemmed Cyclic on-chip bacteria separation and preconcentration
title_short Cyclic on-chip bacteria separation and preconcentration
title_sort cyclic on-chip bacteria separation and preconcentration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713219/
https://www.ncbi.nlm.nih.gov/pubmed/33273691
http://dx.doi.org/10.1038/s41598-020-78298-y
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