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Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections
This paper presents the design of a modular point of care test platform that integrates a proprietary sample collection device directly with a microfluidic cartridge. Cell lysis, within the cartridge, is conducted using a chemical method and nucleic acid purification is done on an activated cellulos...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Butterworth-Heinemann
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942561/ https://www.ncbi.nlm.nih.gov/pubmed/27238759 http://dx.doi.org/10.1016/j.medengphy.2016.04.022 |
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author | Branavan, Manoharanehru Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Ahern, Jeremy C. Sivanesan, Tulasi Hudson, Chris Stead, Thomas Kremer, Jessica Garg, Neha Baker, Mark Sadiq, Syed T. Balachandran, Wamadeva |
author_facet | Branavan, Manoharanehru Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Ahern, Jeremy C. Sivanesan, Tulasi Hudson, Chris Stead, Thomas Kremer, Jessica Garg, Neha Baker, Mark Sadiq, Syed T. Balachandran, Wamadeva |
author_sort | Branavan, Manoharanehru |
collection | PubMed |
description | This paper presents the design of a modular point of care test platform that integrates a proprietary sample collection device directly with a microfluidic cartridge. Cell lysis, within the cartridge, is conducted using a chemical method and nucleic acid purification is done on an activated cellulose membrane. The microfluidic device incorporates passive mixing of the lysis-binding buffers and sample using a serpentine channel. Results have shown extraction efficiencies for this new membrane of 69% and 57% compared to the commercial Qiagen extraction method of 85% and 59.4% for 0.1 ng/µL and 100 ng/µL salmon sperm DNA respectively spiked in phosphate buffered solution. Extraction experiments using the serpentine passive mixer cartridges incorporating lysis and nucleic acid purification showed extraction efficiency around 80% of the commercial Qiagen kit. Isothermal amplification was conducted using thermophillic helicase dependant amplification and recombinase polymerase amplification. A low cost benchtop real-time isothermal amplification platform has been developed capable of running six amplifications simultaneously. Results show that the platform is capable of detecting 1.32×10(6) of sample DNA through thermophillic helicase dependant amplification and 1×10(5) copy numbers Chlamydia trachomatis genomic DNA within 10 min through recombinase polymerase nucleic acid amplification tests. |
format | Online Article Text |
id | pubmed-4942561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Butterworth-Heinemann |
record_format | MEDLINE/PubMed |
spelling | pubmed-49425612016-08-01 Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections Branavan, Manoharanehru Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Ahern, Jeremy C. Sivanesan, Tulasi Hudson, Chris Stead, Thomas Kremer, Jessica Garg, Neha Baker, Mark Sadiq, Syed T. Balachandran, Wamadeva Med Eng Phys Article This paper presents the design of a modular point of care test platform that integrates a proprietary sample collection device directly with a microfluidic cartridge. Cell lysis, within the cartridge, is conducted using a chemical method and nucleic acid purification is done on an activated cellulose membrane. The microfluidic device incorporates passive mixing of the lysis-binding buffers and sample using a serpentine channel. Results have shown extraction efficiencies for this new membrane of 69% and 57% compared to the commercial Qiagen extraction method of 85% and 59.4% for 0.1 ng/µL and 100 ng/µL salmon sperm DNA respectively spiked in phosphate buffered solution. Extraction experiments using the serpentine passive mixer cartridges incorporating lysis and nucleic acid purification showed extraction efficiency around 80% of the commercial Qiagen kit. Isothermal amplification was conducted using thermophillic helicase dependant amplification and recombinase polymerase amplification. A low cost benchtop real-time isothermal amplification platform has been developed capable of running six amplifications simultaneously. Results show that the platform is capable of detecting 1.32×10(6) of sample DNA through thermophillic helicase dependant amplification and 1×10(5) copy numbers Chlamydia trachomatis genomic DNA within 10 min through recombinase polymerase nucleic acid amplification tests. Butterworth-Heinemann 2016-08 /pmc/articles/PMC4942561/ /pubmed/27238759 http://dx.doi.org/10.1016/j.medengphy.2016.04.022 Text en © 2016 The Author(s) 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 Branavan, Manoharanehru Mackay, Ruth E. Craw, Pascal Naveenathayalan, Angel Ahern, Jeremy C. Sivanesan, Tulasi Hudson, Chris Stead, Thomas Kremer, Jessica Garg, Neha Baker, Mark Sadiq, Syed T. Balachandran, Wamadeva Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections |
title | Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections
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title_full | Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections
|
title_fullStr | Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections
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title_full_unstemmed | Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections
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title_short | Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections
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title_sort | modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942561/ https://www.ncbi.nlm.nih.gov/pubmed/27238759 http://dx.doi.org/10.1016/j.medengphy.2016.04.022 |
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