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A digital microfluidic system with 3D microstructures for single-cell culture
Despite the precise controllability of droplet samples in digital microfluidic (DMF) systems, their capability in isolating single cells for long-time culture is still limited: typically, only a few cells can be captured on an electrode. Although fabricating small-sized hydrophilic micropatches on a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433300/ https://www.ncbi.nlm.nih.gov/pubmed/34567621 http://dx.doi.org/10.1038/s41378-019-0109-7 |
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author | Zhai, Jiao Li, Haoran Wong, Ada Hang-Heng Dong, Cheng Yi, Shuhong Jia, Yanwei Mak, Pui-In Deng, Chu-Xia Martins, Rui P. |
author_facet | Zhai, Jiao Li, Haoran Wong, Ada Hang-Heng Dong, Cheng Yi, Shuhong Jia, Yanwei Mak, Pui-In Deng, Chu-Xia Martins, Rui P. |
author_sort | Zhai, Jiao |
collection | PubMed |
description | Despite the precise controllability of droplet samples in digital microfluidic (DMF) systems, their capability in isolating single cells for long-time culture is still limited: typically, only a few cells can be captured on an electrode. Although fabricating small-sized hydrophilic micropatches on an electrode aids single-cell capture, the actuation voltage for droplet transportation has to be significantly raised, resulting in a shorter lifetime for the DMF chip and a larger risk of damaging the cells. In this work, a DMF system with 3D microstructures engineered on-chip is proposed to form semi-closed micro-wells for efficient single-cell isolation and long-time culture. Our optimum results showed that approximately 20% of the micro-wells over a 30 × 30 array were occupied by isolated single cells. In addition, low-evaporation-temperature oil and surfactant aided the system in achieving a low droplet actuation voltage of 36V, which was 4 times lower than the typical 150 V, minimizing the potential damage to the cells in the droplets and to the DMF chip. To exemplify the technological advances, drug sensitivity tests were run in our DMF system to investigate the cell response of breast cancer cells (MDA-MB-231) and breast normal cells (MCF-10A) to a widely used chemotherapeutic drug, Cisplatin (Cis). The results on-chip were consistent with those screened in conventional 96-well plates. This novel, simple and robust single-cell trapping method has great potential in biological research at the single cell level. |
format | Online Article Text |
id | pubmed-8433300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84333002021-09-24 A digital microfluidic system with 3D microstructures for single-cell culture Zhai, Jiao Li, Haoran Wong, Ada Hang-Heng Dong, Cheng Yi, Shuhong Jia, Yanwei Mak, Pui-In Deng, Chu-Xia Martins, Rui P. Microsyst Nanoeng Article Despite the precise controllability of droplet samples in digital microfluidic (DMF) systems, their capability in isolating single cells for long-time culture is still limited: typically, only a few cells can be captured on an electrode. Although fabricating small-sized hydrophilic micropatches on an electrode aids single-cell capture, the actuation voltage for droplet transportation has to be significantly raised, resulting in a shorter lifetime for the DMF chip and a larger risk of damaging the cells. In this work, a DMF system with 3D microstructures engineered on-chip is proposed to form semi-closed micro-wells for efficient single-cell isolation and long-time culture. Our optimum results showed that approximately 20% of the micro-wells over a 30 × 30 array were occupied by isolated single cells. In addition, low-evaporation-temperature oil and surfactant aided the system in achieving a low droplet actuation voltage of 36V, which was 4 times lower than the typical 150 V, minimizing the potential damage to the cells in the droplets and to the DMF chip. To exemplify the technological advances, drug sensitivity tests were run in our DMF system to investigate the cell response of breast cancer cells (MDA-MB-231) and breast normal cells (MCF-10A) to a widely used chemotherapeutic drug, Cisplatin (Cis). The results on-chip were consistent with those screened in conventional 96-well plates. This novel, simple and robust single-cell trapping method has great potential in biological research at the single cell level. Nature Publishing Group UK 2020-01-27 /pmc/articles/PMC8433300/ /pubmed/34567621 http://dx.doi.org/10.1038/s41378-019-0109-7 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhai, Jiao Li, Haoran Wong, Ada Hang-Heng Dong, Cheng Yi, Shuhong Jia, Yanwei Mak, Pui-In Deng, Chu-Xia Martins, Rui P. A digital microfluidic system with 3D microstructures for single-cell culture |
title | A digital microfluidic system with 3D microstructures for single-cell culture |
title_full | A digital microfluidic system with 3D microstructures for single-cell culture |
title_fullStr | A digital microfluidic system with 3D microstructures for single-cell culture |
title_full_unstemmed | A digital microfluidic system with 3D microstructures for single-cell culture |
title_short | A digital microfluidic system with 3D microstructures for single-cell culture |
title_sort | digital microfluidic system with 3d microstructures for single-cell culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433300/ https://www.ncbi.nlm.nih.gov/pubmed/34567621 http://dx.doi.org/10.1038/s41378-019-0109-7 |
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