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Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood
Viral load measurements are an essential tool for the long-term clinical care of hum an immunodeficiency virus (HIV)-positive individuals. The gold standards in viral load instrumentation, however, are still too limited by their size, cost, and sophisticated operation for these measurements to be ub...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687746/ https://www.ncbi.nlm.nih.gov/pubmed/26705482 http://dx.doi.org/10.15302/J-ENG-2015072 |
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author | Damhorst, Gregory L. Duarte-Guevara, Carlos Chen, Weili Ghonge, Tanmay Cunningham, Brian T. Bashir, Rashid |
author_facet | Damhorst, Gregory L. Duarte-Guevara, Carlos Chen, Weili Ghonge, Tanmay Cunningham, Brian T. Bashir, Rashid |
author_sort | Damhorst, Gregory L. |
collection | PubMed |
description | Viral load measurements are an essential tool for the long-term clinical care of hum an immunodeficiency virus (HIV)-positive individuals. The gold standards in viral load instrumentation, however, are still too limited by their size, cost, and sophisticated operation for these measurements to be ubiquitous in remote settings with poor healthcare infrastructure, including parts of the world that are disproportionately affected by HIV infection. The challenge of developing a point-of-care platform capable of making viral load more accessible has been frequently approached but no solution has yet emerged that meets the practical requirements of low cost, portability, and ease-of-use. In this paper, we perform reverse-transcription loop-mediated isothermal amplification (RT-LAMP) on minimally processed HIV-spiked whole blood samples with a microfluidic and silicon microchip platform, and perform fluorescence measurements with a consumer smartphone. Our integrated assay shows amplification from as few as three viruses in a ~ 60 nL RT-LAMP droplet, corresponding to a whole blood concentration of 670 viruses per µL of whole blood. The technology contains greater power in a digital RT-LAMP approach that could be scaled up for the determination of viral load from a finger prick of blood in the clinical care of HIV-positive individuals. We demonstrate that all aspects of this viral load approach, from a drop of blood to imaging the RT-LAMP reaction, are compatible with lab-on-a-chip components and mobile instrumentation. |
format | Online Article Text |
id | pubmed-4687746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-46877462015-12-22 Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood Damhorst, Gregory L. Duarte-Guevara, Carlos Chen, Weili Ghonge, Tanmay Cunningham, Brian T. Bashir, Rashid Engineering (Beijing) Article Viral load measurements are an essential tool for the long-term clinical care of hum an immunodeficiency virus (HIV)-positive individuals. The gold standards in viral load instrumentation, however, are still too limited by their size, cost, and sophisticated operation for these measurements to be ubiquitous in remote settings with poor healthcare infrastructure, including parts of the world that are disproportionately affected by HIV infection. The challenge of developing a point-of-care platform capable of making viral load more accessible has been frequently approached but no solution has yet emerged that meets the practical requirements of low cost, portability, and ease-of-use. In this paper, we perform reverse-transcription loop-mediated isothermal amplification (RT-LAMP) on minimally processed HIV-spiked whole blood samples with a microfluidic and silicon microchip platform, and perform fluorescence measurements with a consumer smartphone. Our integrated assay shows amplification from as few as three viruses in a ~ 60 nL RT-LAMP droplet, corresponding to a whole blood concentration of 670 viruses per µL of whole blood. The technology contains greater power in a digital RT-LAMP approach that could be scaled up for the determination of viral load from a finger prick of blood in the clinical care of HIV-positive individuals. We demonstrate that all aspects of this viral load approach, from a drop of blood to imaging the RT-LAMP reaction, are compatible with lab-on-a-chip components and mobile instrumentation. 2015-10-16 2015-09 /pmc/articles/PMC4687746/ /pubmed/26705482 http://dx.doi.org/10.15302/J-ENG-2015072 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Article Damhorst, Gregory L. Duarte-Guevara, Carlos Chen, Weili Ghonge, Tanmay Cunningham, Brian T. Bashir, Rashid Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood |
title | Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated
Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood |
title_full | Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated
Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood |
title_fullStr | Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated
Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood |
title_full_unstemmed | Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated
Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood |
title_short | Smartphone-Imaged HIV-1 Reverse-Transcription Loop-Mediated
Isothermal Amplification (RT-LAMP) on a Chip from Whole Blood |
title_sort | smartphone-imaged hiv-1 reverse-transcription loop-mediated
isothermal amplification (rt-lamp) on a chip from whole blood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687746/ https://www.ncbi.nlm.nih.gov/pubmed/26705482 http://dx.doi.org/10.15302/J-ENG-2015072 |
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