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A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells

The application of microfluidic technology to manipulate cells or biological particles is becoming one of the rapidly growing areas, and various microarray trapping devices have recently been designed for high throughput single-cell analysis and manipulation. In this paper, we design a double-slit m...

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Detalles Bibliográficos
Autores principales: Xu, Jingyi, Chen, Shulei, Wang, Dongyang, Jiang, Yue, Hao, Ming, Du, Guangyu, Ba, Dechun, Lin, Qiao, Mei, Qi, Ning, Yingchao, Su, Da, Liu, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187229/
https://www.ncbi.nlm.nih.gov/pubmed/30424091
http://dx.doi.org/10.3390/mi9040157
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author Xu, Jingyi
Chen, Shulei
Wang, Dongyang
Jiang, Yue
Hao, Ming
Du, Guangyu
Ba, Dechun
Lin, Qiao
Mei, Qi
Ning, Yingchao
Su, Da
Liu, Kun
author_facet Xu, Jingyi
Chen, Shulei
Wang, Dongyang
Jiang, Yue
Hao, Ming
Du, Guangyu
Ba, Dechun
Lin, Qiao
Mei, Qi
Ning, Yingchao
Su, Da
Liu, Kun
author_sort Xu, Jingyi
collection PubMed
description The application of microfluidic technology to manipulate cells or biological particles is becoming one of the rapidly growing areas, and various microarray trapping devices have recently been designed for high throughput single-cell analysis and manipulation. In this paper, we design a double-slit microfluidic chip for hydrodynamic cell trapping at the single-cell level, which maintains a high capture ability. The geometric effects on flow behaviour are investigated in detail for optimizing chip architecture, including the flow velocity, the fluid pressure, and the equivalent stress of cells. Based on the geometrical parameters optimized, the double-slit chip enhances the capture of HeLa cells and the drug experiment verifies the feasibility of the drug delivery.
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spelling pubmed-61872292018-11-01 A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells Xu, Jingyi Chen, Shulei Wang, Dongyang Jiang, Yue Hao, Ming Du, Guangyu Ba, Dechun Lin, Qiao Mei, Qi Ning, Yingchao Su, Da Liu, Kun Micromachines (Basel) Article The application of microfluidic technology to manipulate cells or biological particles is becoming one of the rapidly growing areas, and various microarray trapping devices have recently been designed for high throughput single-cell analysis and manipulation. In this paper, we design a double-slit microfluidic chip for hydrodynamic cell trapping at the single-cell level, which maintains a high capture ability. The geometric effects on flow behaviour are investigated in detail for optimizing chip architecture, including the flow velocity, the fluid pressure, and the equivalent stress of cells. Based on the geometrical parameters optimized, the double-slit chip enhances the capture of HeLa cells and the drug experiment verifies the feasibility of the drug delivery. MDPI 2018-03-31 /pmc/articles/PMC6187229/ /pubmed/30424091 http://dx.doi.org/10.3390/mi9040157 Text en © 2018 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
Xu, Jingyi
Chen, Shulei
Wang, Dongyang
Jiang, Yue
Hao, Ming
Du, Guangyu
Ba, Dechun
Lin, Qiao
Mei, Qi
Ning, Yingchao
Su, Da
Liu, Kun
A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells
title A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells
title_full A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells
title_fullStr A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells
title_full_unstemmed A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells
title_short A Microfluidic Chip with Double-Slit Arrays for Enhanced Capture of Single Cells
title_sort microfluidic chip with double-slit arrays for enhanced capture of single cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187229/
https://www.ncbi.nlm.nih.gov/pubmed/30424091
http://dx.doi.org/10.3390/mi9040157
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