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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...

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Autores principales: Damhorst, Gregory L., Duarte-Guevara, Carlos, Chen, Weili, Ghonge, Tanmay, Cunningham, Brian T., Bashir, Rashid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
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.
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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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