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RPA using a multiplexed cartridge for low cost point of care diagnostics in the field
A point of care device utilising Lab-on-a-Chip technologies that is applicable for biological pathogens was designed, fabricated and tested showing sample in to answer out capabilities. The purpose of the design was to develop a cartridge with the capability to perform nucleic acid extraction and pu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884738/ https://www.ncbi.nlm.nih.gov/pubmed/29447855 http://dx.doi.org/10.1016/j.ab.2018.02.010 |
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author | Ereku, Luck Tosan Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Stead, Thomas Branavan, Manorharanehru Balachandran, Wamadeva |
author_facet | Ereku, Luck Tosan Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Stead, Thomas Branavan, Manorharanehru Balachandran, Wamadeva |
author_sort | Ereku, Luck Tosan |
collection | PubMed |
description | A point of care device utilising Lab-on-a-Chip technologies that is applicable for biological pathogens was designed, fabricated and tested showing sample in to answer out capabilities. The purpose of the design was to develop a cartridge with the capability to perform nucleic acid extraction and purification from a sample using a chitosan membrane at an acidic pH. Waste was stored within the cartridge with the use of sodium polyacrylate to solidify or gelate the sample in a single chamber. Nucleic acid elution was conducted using the RPA amplification reagents (alkaline pH). Passive valves were used to regulate the fluid flow and a multiplexer was designed to distribute the fluid into six microchambers for amplification reactions. Cartridges were produced using soft lithography of silicone from 3D printed moulds, bonded to glass substrates. The isothermal technique, RPA is employed for amplification. This paper shows the results from two separate experiments: the first using the RPA control nucleic acid, the second showing successful amplification from Chlamydia Trachomatis. Endpoint analysis conducted for the RPA analysis was gel electrophoresis that showed 143 base pair DNA was amplified successfully for positive samples whilst negative samples did not show amplification. End point analysis for Chlamydia Trachomatis samples was fluorescence detection that showed successful detection of 1 copy/μL and 10 copies/μL spiked in a MES buffer. |
format | Online Article Text |
id | pubmed-5884738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-58847382018-04-15 RPA using a multiplexed cartridge for low cost point of care diagnostics in the field Ereku, Luck Tosan Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Stead, Thomas Branavan, Manorharanehru Balachandran, Wamadeva Anal Biochem Article A point of care device utilising Lab-on-a-Chip technologies that is applicable for biological pathogens was designed, fabricated and tested showing sample in to answer out capabilities. The purpose of the design was to develop a cartridge with the capability to perform nucleic acid extraction and purification from a sample using a chitosan membrane at an acidic pH. Waste was stored within the cartridge with the use of sodium polyacrylate to solidify or gelate the sample in a single chamber. Nucleic acid elution was conducted using the RPA amplification reagents (alkaline pH). Passive valves were used to regulate the fluid flow and a multiplexer was designed to distribute the fluid into six microchambers for amplification reactions. Cartridges were produced using soft lithography of silicone from 3D printed moulds, bonded to glass substrates. The isothermal technique, RPA is employed for amplification. This paper shows the results from two separate experiments: the first using the RPA control nucleic acid, the second showing successful amplification from Chlamydia Trachomatis. Endpoint analysis conducted for the RPA analysis was gel electrophoresis that showed 143 base pair DNA was amplified successfully for positive samples whilst negative samples did not show amplification. End point analysis for Chlamydia Trachomatis samples was fluorescence detection that showed successful detection of 1 copy/μL and 10 copies/μL spiked in a MES buffer. Elsevier 2018-04-15 /pmc/articles/PMC5884738/ /pubmed/29447855 http://dx.doi.org/10.1016/j.ab.2018.02.010 Text en Crown Copyright © Published by Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ereku, Luck Tosan Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Stead, Thomas Branavan, Manorharanehru Balachandran, Wamadeva RPA using a multiplexed cartridge for low cost point of care diagnostics in the field |
title | RPA using a multiplexed cartridge for low cost point of care diagnostics in the field |
title_full | RPA using a multiplexed cartridge for low cost point of care diagnostics in the field |
title_fullStr | RPA using a multiplexed cartridge for low cost point of care diagnostics in the field |
title_full_unstemmed | RPA using a multiplexed cartridge for low cost point of care diagnostics in the field |
title_short | RPA using a multiplexed cartridge for low cost point of care diagnostics in the field |
title_sort | rpa using a multiplexed cartridge for low cost point of care diagnostics in the field |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884738/ https://www.ncbi.nlm.nih.gov/pubmed/29447855 http://dx.doi.org/10.1016/j.ab.2018.02.010 |
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