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Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip

We have developed a novel imaging cytometry system using a poly(methyl methacrylate (PMMA)) based microfluidic chip. The system was contamination-free, because sample suspensions contacted only with a flammable PMMA chip and no other component of the system. The transparency and low-fluorescence of...

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Detalles Bibliográficos
Autores principales: Hayashi, Masahito, Hattori, Akihiro, Kim, Hyonchol, Terazono, Hideyuki, Kaneko, Tomoyuki, Yasuda, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131582/
https://www.ncbi.nlm.nih.gov/pubmed/21747698
http://dx.doi.org/10.3390/ijms12063618
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author Hayashi, Masahito
Hattori, Akihiro
Kim, Hyonchol
Terazono, Hideyuki
Kaneko, Tomoyuki
Yasuda, Kenji
author_facet Hayashi, Masahito
Hattori, Akihiro
Kim, Hyonchol
Terazono, Hideyuki
Kaneko, Tomoyuki
Yasuda, Kenji
author_sort Hayashi, Masahito
collection PubMed
description We have developed a novel imaging cytometry system using a poly(methyl methacrylate (PMMA)) based microfluidic chip. The system was contamination-free, because sample suspensions contacted only with a flammable PMMA chip and no other component of the system. The transparency and low-fluorescence of PMMA was suitable for microscopic imaging of cells flowing through microchannels on the chip. Sample particles flowing through microchannels on the chip were discriminated by an image-recognition unit with a high-speed camera in real time at the rate of 200 event/s, e.g., microparticles 2.5 μm and 3.0 μm in diameter were differentiated with an error rate of less than 2%. Desired cells were separated automatically from other cells by electrophoretic or dielectrophoretic force one by one with a separation efficiency of 90%. Cells in suspension with fluorescent dye were separated using the same kind of microfluidic chip. Sample of 5 μL with 1 × 10(6) particle/mL was processed within 40 min. Separated cells could be cultured on the microfluidic chip without contamination. The whole operation of sample handling was automated using 3D micropipetting system. These results showed that the novel imaging flow cytometry system is practically applicable for biological research and clinical diagnostics.
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spelling pubmed-31315822011-07-11 Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip Hayashi, Masahito Hattori, Akihiro Kim, Hyonchol Terazono, Hideyuki Kaneko, Tomoyuki Yasuda, Kenji Int J Mol Sci Article We have developed a novel imaging cytometry system using a poly(methyl methacrylate (PMMA)) based microfluidic chip. The system was contamination-free, because sample suspensions contacted only with a flammable PMMA chip and no other component of the system. The transparency and low-fluorescence of PMMA was suitable for microscopic imaging of cells flowing through microchannels on the chip. Sample particles flowing through microchannels on the chip were discriminated by an image-recognition unit with a high-speed camera in real time at the rate of 200 event/s, e.g., microparticles 2.5 μm and 3.0 μm in diameter were differentiated with an error rate of less than 2%. Desired cells were separated automatically from other cells by electrophoretic or dielectrophoretic force one by one with a separation efficiency of 90%. Cells in suspension with fluorescent dye were separated using the same kind of microfluidic chip. Sample of 5 μL with 1 × 10(6) particle/mL was processed within 40 min. Separated cells could be cultured on the microfluidic chip without contamination. The whole operation of sample handling was automated using 3D micropipetting system. These results showed that the novel imaging flow cytometry system is practically applicable for biological research and clinical diagnostics. Molecular Diversity Preservation International (MDPI) 2011-06-07 /pmc/articles/PMC3131582/ /pubmed/21747698 http://dx.doi.org/10.3390/ijms12063618 Text en © 2011 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Hayashi, Masahito
Hattori, Akihiro
Kim, Hyonchol
Terazono, Hideyuki
Kaneko, Tomoyuki
Yasuda, Kenji
Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip
title Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip
title_full Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip
title_fullStr Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip
title_full_unstemmed Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip
title_short Fully Automated On-Chip Imaging Flow Cytometry System with Disposable Contamination-Free Plastic Re-Cultivation Chip
title_sort fully automated on-chip imaging flow cytometry system with disposable contamination-free plastic re-cultivation chip
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131582/
https://www.ncbi.nlm.nih.gov/pubmed/21747698
http://dx.doi.org/10.3390/ijms12063618
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