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An integrated microfluidic system for rapid diagnosis of dengue virus infection

This study reports an integrated microfluidic system which utilizes virus-bound magnetic bead complexes for rapid serological analysis of antibodies associated with an infection by the dengue virus. This new microfluidic system integrates one-way micropumps, a four-membrane-type micromixer, two-way...

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Autores principales: Lee, Yu-Fang, Lien, Kang-Yi, Lei, Huan-Yao, Lee, Gwo-Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125828/
https://www.ncbi.nlm.nih.gov/pubmed/19744849
http://dx.doi.org/10.1016/j.bios.2009.08.020
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author Lee, Yu-Fang
Lien, Kang-Yi
Lei, Huan-Yao
Lee, Gwo-Bin
author_facet Lee, Yu-Fang
Lien, Kang-Yi
Lei, Huan-Yao
Lee, Gwo-Bin
author_sort Lee, Yu-Fang
collection PubMed
description This study reports an integrated microfluidic system which utilizes virus-bound magnetic bead complexes for rapid serological analysis of antibodies associated with an infection by the dengue virus. This new microfluidic system integrates one-way micropumps, a four-membrane-type micromixer, two-way micropumps and an on-chip microcoil array in order to simultaneously perform the rapid detection of immunoglobulin G (IgG) and immunoglobulin M (IgM). An IgM/IgG titer in serum is used to confirm the presence of dengue virus infection. By utilizing microfluidic technologies and virus-bound magnetic beads, IgG and IgM in the serum samples are captured. This is followed by purification and isolation of these beads utilizing a magnetic field generated from the on-chip array of microcoils. Any interfering substances in the biological fluids are washed away automatically by the flow generated by the integrated pneumatic pumps. The fluorescence-labelled secondary antibodies are bound to the surface of the IgG/IgM complex attached onto the magnetic beads. Finally, the entire magnetic complex sandwich is transported automatically into a sample detection chamber. The optical signals are then measured and analyzed by a real-time optical detection module. The entire process is performed automatically on a single chip within 30 min, which is only 1/8th of the time required for a traditional method. More importantly, the detection limit has been improved to 21 pg, which is about 38 times better when compared to traditional methods. This integrated system may provide a powerful platform for the rapid diagnosis of dengue virus infection and other types of infectious diseases.
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spelling pubmed-71258282020-04-08 An integrated microfluidic system for rapid diagnosis of dengue virus infection Lee, Yu-Fang Lien, Kang-Yi Lei, Huan-Yao Lee, Gwo-Bin Biosens Bioelectron Article This study reports an integrated microfluidic system which utilizes virus-bound magnetic bead complexes for rapid serological analysis of antibodies associated with an infection by the dengue virus. This new microfluidic system integrates one-way micropumps, a four-membrane-type micromixer, two-way micropumps and an on-chip microcoil array in order to simultaneously perform the rapid detection of immunoglobulin G (IgG) and immunoglobulin M (IgM). An IgM/IgG titer in serum is used to confirm the presence of dengue virus infection. By utilizing microfluidic technologies and virus-bound magnetic beads, IgG and IgM in the serum samples are captured. This is followed by purification and isolation of these beads utilizing a magnetic field generated from the on-chip array of microcoils. Any interfering substances in the biological fluids are washed away automatically by the flow generated by the integrated pneumatic pumps. The fluorescence-labelled secondary antibodies are bound to the surface of the IgG/IgM complex attached onto the magnetic beads. Finally, the entire magnetic complex sandwich is transported automatically into a sample detection chamber. The optical signals are then measured and analyzed by a real-time optical detection module. The entire process is performed automatically on a single chip within 30 min, which is only 1/8th of the time required for a traditional method. More importantly, the detection limit has been improved to 21 pg, which is about 38 times better when compared to traditional methods. This integrated system may provide a powerful platform for the rapid diagnosis of dengue virus infection and other types of infectious diseases. Elsevier B.V. 2009-12-15 2009-08-21 /pmc/articles/PMC7125828/ /pubmed/19744849 http://dx.doi.org/10.1016/j.bios.2009.08.020 Text en Copyright © 2009 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Lee, Yu-Fang
Lien, Kang-Yi
Lei, Huan-Yao
Lee, Gwo-Bin
An integrated microfluidic system for rapid diagnosis of dengue virus infection
title An integrated microfluidic system for rapid diagnosis of dengue virus infection
title_full An integrated microfluidic system for rapid diagnosis of dengue virus infection
title_fullStr An integrated microfluidic system for rapid diagnosis of dengue virus infection
title_full_unstemmed An integrated microfluidic system for rapid diagnosis of dengue virus infection
title_short An integrated microfluidic system for rapid diagnosis of dengue virus infection
title_sort integrated microfluidic system for rapid diagnosis of dengue virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125828/
https://www.ncbi.nlm.nih.gov/pubmed/19744849
http://dx.doi.org/10.1016/j.bios.2009.08.020
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