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Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids
A prototype dual-path microfluidic device (Rheonix CARD) capable of performing simultaneously screening (antigen or antibody) and confirmatory (nucleic acid) detection of pathogens is described. The device fully integrates sample processing, antigen or antibody detection, and nucleic acid amplificat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586469/ https://www.ncbi.nlm.nih.gov/pubmed/23509739 http://dx.doi.org/10.1155/2013/543294 |
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author | Chen, Zongyuan Abrams, William R. Geva, Eran de Dood, Claudia J. González, Jesús M. Tanke, Hans J. Niedbala, R. Sam Zhou, Peng Malamud, Daniel Corstjens, Paul L. A. M. |
author_facet | Chen, Zongyuan Abrams, William R. Geva, Eran de Dood, Claudia J. González, Jesús M. Tanke, Hans J. Niedbala, R. Sam Zhou, Peng Malamud, Daniel Corstjens, Paul L. A. M. |
author_sort | Chen, Zongyuan |
collection | PubMed |
description | A prototype dual-path microfluidic device (Rheonix CARD) capable of performing simultaneously screening (antigen or antibody) and confirmatory (nucleic acid) detection of pathogens is described. The device fully integrates sample processing, antigen or antibody detection, and nucleic acid amplification and detection, demonstrating rapid and inexpensive “sample-to-result” diagnosis with performance comparable to benchtop analysis. For the chip design, a modular approach was followed allowing the optimization of individual steps in the sample processing process. This modular design provides great versatility accommodating different disease targets independently of the production method. In the detection module, a lateral flow (LF) protocol utilizing upconverting phosphor (UCP) reporters was employed. The nucleic acid (NA) module incorporates a generic microtube containing dry reagents. Lateral flow strips and PCR primers determine the target or disease that is diagnosed. Diagnosis of HIV infection was used as a model to investigate the simultaneous detection of both human antibodies against the virus and viral RNA. The serological result is available in less than 30 min, and the confirmation by RNA amplification takes another 60 min. This approach combines a core serological portable diagnostic with a nucleic acid-based confirmatory test. |
format | Online Article Text |
id | pubmed-3586469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35864692013-03-18 Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids Chen, Zongyuan Abrams, William R. Geva, Eran de Dood, Claudia J. González, Jesús M. Tanke, Hans J. Niedbala, R. Sam Zhou, Peng Malamud, Daniel Corstjens, Paul L. A. M. Biomed Res Int Research Article A prototype dual-path microfluidic device (Rheonix CARD) capable of performing simultaneously screening (antigen or antibody) and confirmatory (nucleic acid) detection of pathogens is described. The device fully integrates sample processing, antigen or antibody detection, and nucleic acid amplification and detection, demonstrating rapid and inexpensive “sample-to-result” diagnosis with performance comparable to benchtop analysis. For the chip design, a modular approach was followed allowing the optimization of individual steps in the sample processing process. This modular design provides great versatility accommodating different disease targets independently of the production method. In the detection module, a lateral flow (LF) protocol utilizing upconverting phosphor (UCP) reporters was employed. The nucleic acid (NA) module incorporates a generic microtube containing dry reagents. Lateral flow strips and PCR primers determine the target or disease that is diagnosed. Diagnosis of HIV infection was used as a model to investigate the simultaneous detection of both human antibodies against the virus and viral RNA. The serological result is available in less than 30 min, and the confirmation by RNA amplification takes another 60 min. This approach combines a core serological portable diagnostic with a nucleic acid-based confirmatory test. Hindawi Publishing Corporation 2013 2013-02-14 /pmc/articles/PMC3586469/ /pubmed/23509739 http://dx.doi.org/10.1155/2013/543294 Text en Copyright © 2013 Zongyuan Chen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chen, Zongyuan Abrams, William R. Geva, Eran de Dood, Claudia J. González, Jesús M. Tanke, Hans J. Niedbala, R. Sam Zhou, Peng Malamud, Daniel Corstjens, Paul L. A. M. Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids |
title | Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids |
title_full | Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids |
title_fullStr | Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids |
title_full_unstemmed | Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids |
title_short | Development of a Generic Microfluidic Device for Simultaneous Detection of Antibodies and Nucleic Acids in Oral Fluids |
title_sort | development of a generic microfluidic device for simultaneous detection of antibodies and nucleic acids in oral fluids |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586469/ https://www.ncbi.nlm.nih.gov/pubmed/23509739 http://dx.doi.org/10.1155/2013/543294 |
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