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The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells

This paper presents the instrumentation of a microfluidic analyzer enabling the characterization of single-cell biophysical properties, which includes seven key components: a microfluidic module, a pressure module, an imaging module, an impedance module, two LabVIEW platforms for instrument operatio...

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Detalles Bibliográficos
Autores principales: Wang, Ke, Zhao, Yang, Chen, Deyong, Huang, Chengjun, Fan, Beiyuan, Long, Rong, Hsieh, Chia-Hsun, Wang, Junbo, Wu, Min-Hsien, Chen, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485982/
https://www.ncbi.nlm.nih.gov/pubmed/28629175
http://dx.doi.org/10.3390/ijms18061158
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author Wang, Ke
Zhao, Yang
Chen, Deyong
Huang, Chengjun
Fan, Beiyuan
Long, Rong
Hsieh, Chia-Hsun
Wang, Junbo
Wu, Min-Hsien
Chen, Jian
author_facet Wang, Ke
Zhao, Yang
Chen, Deyong
Huang, Chengjun
Fan, Beiyuan
Long, Rong
Hsieh, Chia-Hsun
Wang, Junbo
Wu, Min-Hsien
Chen, Jian
author_sort Wang, Ke
collection PubMed
description This paper presents the instrumentation of a microfluidic analyzer enabling the characterization of single-cell biophysical properties, which includes seven key components: a microfluidic module, a pressure module, an imaging module, an impedance module, two LabVIEW platforms for instrument operation and raw data processing, respectively, and a Python code for data translation. Under the control of the LabVIEW platform for instrument operation, the pressure module flushes single cells into the microfluidic module with raw biophysical parameters sampled by the imaging and impedance modules and processed by the LabVIEW platform for raw data processing, which were further translated into intrinsic cellular biophysical parameters using the code developed in Python. Based on this system, specific membrane capacitance, cytoplasm conductivity, and instantaneous Young’s modulus of three cell types were quantified as 2.76 ± 0.57 μF/cm(2), 1.00 ± 0.14 S/m, and 3.79 ± 1.11 kPa for A549 cells (n(cell) = 202); 1.88 ± 0.31 μF/cm(2), 1.05 ± 0.16 S/m, and 3.74 ± 0.75 kPa for 95D cells (n(cell) = 257); 2.11 ± 0.38 μF/cm(2), 0.87 ± 0.11 S/m, and 5.39 ± 0.89 kPa for H460 cells (n(cell) = 246). As a semi-automatic instrument with a throughput of roughly 1 cell per second, this prototype instrument can be potentially used for the characterization of cellular biophysical properties.
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spelling pubmed-54859822017-06-29 The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells Wang, Ke Zhao, Yang Chen, Deyong Huang, Chengjun Fan, Beiyuan Long, Rong Hsieh, Chia-Hsun Wang, Junbo Wu, Min-Hsien Chen, Jian Int J Mol Sci Article This paper presents the instrumentation of a microfluidic analyzer enabling the characterization of single-cell biophysical properties, which includes seven key components: a microfluidic module, a pressure module, an imaging module, an impedance module, two LabVIEW platforms for instrument operation and raw data processing, respectively, and a Python code for data translation. Under the control of the LabVIEW platform for instrument operation, the pressure module flushes single cells into the microfluidic module with raw biophysical parameters sampled by the imaging and impedance modules and processed by the LabVIEW platform for raw data processing, which were further translated into intrinsic cellular biophysical parameters using the code developed in Python. Based on this system, specific membrane capacitance, cytoplasm conductivity, and instantaneous Young’s modulus of three cell types were quantified as 2.76 ± 0.57 μF/cm(2), 1.00 ± 0.14 S/m, and 3.79 ± 1.11 kPa for A549 cells (n(cell) = 202); 1.88 ± 0.31 μF/cm(2), 1.05 ± 0.16 S/m, and 3.74 ± 0.75 kPa for 95D cells (n(cell) = 257); 2.11 ± 0.38 μF/cm(2), 0.87 ± 0.11 S/m, and 5.39 ± 0.89 kPa for H460 cells (n(cell) = 246). As a semi-automatic instrument with a throughput of roughly 1 cell per second, this prototype instrument can be potentially used for the characterization of cellular biophysical properties. MDPI 2017-06-19 /pmc/articles/PMC5485982/ /pubmed/28629175 http://dx.doi.org/10.3390/ijms18061158 Text en © 2017 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
Wang, Ke
Zhao, Yang
Chen, Deyong
Huang, Chengjun
Fan, Beiyuan
Long, Rong
Hsieh, Chia-Hsun
Wang, Junbo
Wu, Min-Hsien
Chen, Jian
The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells
title The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells
title_full The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells
title_fullStr The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells
title_full_unstemmed The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells
title_short The Instrumentation of a Microfluidic Analyzer Enabling the Characterization of the Specific Membrane Capacitance, Cytoplasm Conductivity, and Instantaneous Young’s Modulus of Single Cells
title_sort instrumentation of a microfluidic analyzer enabling the characterization of the specific membrane capacitance, cytoplasm conductivity, and instantaneous young’s modulus of single cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485982/
https://www.ncbi.nlm.nih.gov/pubmed/28629175
http://dx.doi.org/10.3390/ijms18061158
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