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Centrifugal Microfluidic Platform for Ultrasensitive Detection of Botulinum Toxin
[Image: see text] We present an innovative centrifugal microfluidic immunoassay platform (SpinDx) to address the urgent biodefense and public health need for ultrasensitive point-of-care/incident detection of botulinum toxin. The simple, sample-to-answer centrifugal microfluidic immunoassay approach...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303339/ https://www.ncbi.nlm.nih.gov/pubmed/25521812 http://dx.doi.org/10.1021/ac504054u |
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author | Koh, Chung-Yan Schaff, Ulrich Y. Piccini, Matthew E. Stanker, Larry H. Cheng, Luisa W. Ravichandran, Easwaran Singh, Bal-Ram Sommer, Greg J. Singh, Anup K. |
author_facet | Koh, Chung-Yan Schaff, Ulrich Y. Piccini, Matthew E. Stanker, Larry H. Cheng, Luisa W. Ravichandran, Easwaran Singh, Bal-Ram Sommer, Greg J. Singh, Anup K. |
author_sort | Koh, Chung-Yan |
collection | PubMed |
description | [Image: see text] We present an innovative centrifugal microfluidic immunoassay platform (SpinDx) to address the urgent biodefense and public health need for ultrasensitive point-of-care/incident detection of botulinum toxin. The simple, sample-to-answer centrifugal microfluidic immunoassay approach is based on binding of toxins to antibody-laden capture particles followed by sedimentation of the particles through a density-media in a microfluidic disk and quantification by laser-induced fluorescence. A blind, head-to-head comparison study of SpinDx versus the gold-standard mouse bioassay demonstrates 100-fold improvement in sensitivity (limit of detection = 0.09 pg/mL), while achieving total sample-to-answer time of <30 min with 2-μL required volume of the unprocessed sample. We further demonstrate quantification of botulinum toxin in both exogeneous (human blood and serum spiked with toxins) and endogeneous (serum from mice intoxicated via oral, intranasal, and intravenous routes) samples. SpinDx can analyze, without any sample preparation, multiple sample types including whole blood, serum, and food. It is readily expandable to additional analytes as the assay reagents (i.e., the capture beads and detection antibodies) are disconnected from the disk architecture and the reader, facilitating rapid development of new assays. SpinDx can also serve as a general-purpose immunoassay platform applicable to diagnosis of other conditions and diseases. |
format | Online Article Text |
id | pubmed-4303339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-43033392015-12-18 Centrifugal Microfluidic Platform for Ultrasensitive Detection of Botulinum Toxin Koh, Chung-Yan Schaff, Ulrich Y. Piccini, Matthew E. Stanker, Larry H. Cheng, Luisa W. Ravichandran, Easwaran Singh, Bal-Ram Sommer, Greg J. Singh, Anup K. Anal Chem [Image: see text] We present an innovative centrifugal microfluidic immunoassay platform (SpinDx) to address the urgent biodefense and public health need for ultrasensitive point-of-care/incident detection of botulinum toxin. The simple, sample-to-answer centrifugal microfluidic immunoassay approach is based on binding of toxins to antibody-laden capture particles followed by sedimentation of the particles through a density-media in a microfluidic disk and quantification by laser-induced fluorescence. A blind, head-to-head comparison study of SpinDx versus the gold-standard mouse bioassay demonstrates 100-fold improvement in sensitivity (limit of detection = 0.09 pg/mL), while achieving total sample-to-answer time of <30 min with 2-μL required volume of the unprocessed sample. We further demonstrate quantification of botulinum toxin in both exogeneous (human blood and serum spiked with toxins) and endogeneous (serum from mice intoxicated via oral, intranasal, and intravenous routes) samples. SpinDx can analyze, without any sample preparation, multiple sample types including whole blood, serum, and food. It is readily expandable to additional analytes as the assay reagents (i.e., the capture beads and detection antibodies) are disconnected from the disk architecture and the reader, facilitating rapid development of new assays. SpinDx can also serve as a general-purpose immunoassay platform applicable to diagnosis of other conditions and diseases. American Chemical Society 2014-12-18 2015-01-20 /pmc/articles/PMC4303339/ /pubmed/25521812 http://dx.doi.org/10.1021/ac504054u Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Koh, Chung-Yan Schaff, Ulrich Y. Piccini, Matthew E. Stanker, Larry H. Cheng, Luisa W. Ravichandran, Easwaran Singh, Bal-Ram Sommer, Greg J. Singh, Anup K. Centrifugal Microfluidic Platform for Ultrasensitive Detection of Botulinum Toxin |
title | Centrifugal Microfluidic
Platform for Ultrasensitive
Detection of Botulinum Toxin |
title_full | Centrifugal Microfluidic
Platform for Ultrasensitive
Detection of Botulinum Toxin |
title_fullStr | Centrifugal Microfluidic
Platform for Ultrasensitive
Detection of Botulinum Toxin |
title_full_unstemmed | Centrifugal Microfluidic
Platform for Ultrasensitive
Detection of Botulinum Toxin |
title_short | Centrifugal Microfluidic
Platform for Ultrasensitive
Detection of Botulinum Toxin |
title_sort | centrifugal microfluidic
platform for ultrasensitive
detection of botulinum toxin |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303339/ https://www.ncbi.nlm.nih.gov/pubmed/25521812 http://dx.doi.org/10.1021/ac504054u |
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