Cargando…
Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples
While identifying acute HIV infection is critical to providing prompt treatment to HIV-positive individuals and preventing transmission, existing laboratory-based testing methods are too complex to perform at the point of care. Specifically, molecular techniques can detect HIV RNA within 8–10 days o...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384476/ https://www.ncbi.nlm.nih.gov/pubmed/31539001 http://dx.doi.org/10.1039/c9lc00506d |
_version_ | 1783563613860003840 |
---|---|
author | Phillips, Elizabeth A. Moehling, Taylor J. Ejendal, Karin F. K. Hoilett, Orlando S. Byers, Kristin M. Basing, Laud Anthony Jankowski, Lauren A. Bennett, Jackson B. Lin, Li-Kai Stanciu, Lia A. Linnes, Jacqueline C. |
author_facet | Phillips, Elizabeth A. Moehling, Taylor J. Ejendal, Karin F. K. Hoilett, Orlando S. Byers, Kristin M. Basing, Laud Anthony Jankowski, Lauren A. Bennett, Jackson B. Lin, Li-Kai Stanciu, Lia A. Linnes, Jacqueline C. |
author_sort | Phillips, Elizabeth A. |
collection | PubMed |
description | While identifying acute HIV infection is critical to providing prompt treatment to HIV-positive individuals and preventing transmission, existing laboratory-based testing methods are too complex to perform at the point of care. Specifically, molecular techniques can detect HIV RNA within 8–10 days of transmission but require laboratory infrastructure for cold-chain reagent storage and extensive sample preparation performed by trained personnel. Here, we demonstrate our point-of-care microfluidic rapid and autonomous analysis device (microRAAD) that automatically detects HIV RNA from whole blood. Inside microRAAD, we incorporate vitrified amplification reagents, thermally-actuated valves for fluidic control, and a temperature control circuit for low-power heating. Reverse transcription loop-mediated isothermal amplification (RT-LAMP) products are visualized using a lateral flow immunoassay (LFIA), resulting in an assay limit of detection of 100 HIV-1 RNA copies when performed as a standard tube reaction. Even after three weeks of room-temperature reagent storage, microRAAD automatically isolates the virus from whole blood, amplifies HIV-1 RNA, and transports amplification products to the internal LFIA, detecting as few as 3 × 10(5) HIV-1 viral particles, or 2.3 × 10(7) virus copies per mL of whole blood, within 90 minutes. This integrated microRAAD is a low-cost and portable platform to enable automated detection of HIV and other pathogens at the point of care. |
format | Online Article Text |
id | pubmed-7384476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-73844762020-07-27 Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples Phillips, Elizabeth A. Moehling, Taylor J. Ejendal, Karin F. K. Hoilett, Orlando S. Byers, Kristin M. Basing, Laud Anthony Jankowski, Lauren A. Bennett, Jackson B. Lin, Li-Kai Stanciu, Lia A. Linnes, Jacqueline C. Lab Chip Article While identifying acute HIV infection is critical to providing prompt treatment to HIV-positive individuals and preventing transmission, existing laboratory-based testing methods are too complex to perform at the point of care. Specifically, molecular techniques can detect HIV RNA within 8–10 days of transmission but require laboratory infrastructure for cold-chain reagent storage and extensive sample preparation performed by trained personnel. Here, we demonstrate our point-of-care microfluidic rapid and autonomous analysis device (microRAAD) that automatically detects HIV RNA from whole blood. Inside microRAAD, we incorporate vitrified amplification reagents, thermally-actuated valves for fluidic control, and a temperature control circuit for low-power heating. Reverse transcription loop-mediated isothermal amplification (RT-LAMP) products are visualized using a lateral flow immunoassay (LFIA), resulting in an assay limit of detection of 100 HIV-1 RNA copies when performed as a standard tube reaction. Even after three weeks of room-temperature reagent storage, microRAAD automatically isolates the virus from whole blood, amplifies HIV-1 RNA, and transports amplification products to the internal LFIA, detecting as few as 3 × 10(5) HIV-1 viral particles, or 2.3 × 10(7) virus copies per mL of whole blood, within 90 minutes. This integrated microRAAD is a low-cost and portable platform to enable automated detection of HIV and other pathogens at the point of care. 2019-10-09 /pmc/articles/PMC7384476/ /pubmed/31539001 http://dx.doi.org/10.1039/c9lc00506d Text en This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Phillips, Elizabeth A. Moehling, Taylor J. Ejendal, Karin F. K. Hoilett, Orlando S. Byers, Kristin M. Basing, Laud Anthony Jankowski, Lauren A. Bennett, Jackson B. Lin, Li-Kai Stanciu, Lia A. Linnes, Jacqueline C. Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples |
title | Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples |
title_full | Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples |
title_fullStr | Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples |
title_full_unstemmed | Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples |
title_short | Microfluidic rapid and autonomous analytical device (microRAAD) to detect HIV from whole blood samples |
title_sort | microfluidic rapid and autonomous analytical device (microraad) to detect hiv from whole blood samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384476/ https://www.ncbi.nlm.nih.gov/pubmed/31539001 http://dx.doi.org/10.1039/c9lc00506d |
work_keys_str_mv | AT phillipselizabetha microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT moehlingtaylorj microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT ejendalkarinfk microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT hoilettorlandos microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT byerskristinm microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT basinglaudanthony microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT jankowskilaurena microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT bennettjacksonb microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT linlikai microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT stanciuliaa microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples AT linnesjacquelinec microfluidicrapidandautonomousanalyticaldevicemicroraadtodetecthivfromwholebloodsamples |