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RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing
Hepatitis C virus (HCV) infections occur in approximately 3% of the world population. The development of an enhanced and extensive-scale screening is required to accomplish the World Health Organization’s (WHO) goal of eliminating HCV as a public health problem by 2030. However, standard testing met...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138684/ https://www.ncbi.nlm.nih.gov/pubmed/35624599 http://dx.doi.org/10.3390/bios12050298 |
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author | Sharma, Sandhya Thomas, Emmanuel Caputi, Massimo Asghar, Waseem |
author_facet | Sharma, Sandhya Thomas, Emmanuel Caputi, Massimo Asghar, Waseem |
author_sort | Sharma, Sandhya |
collection | PubMed |
description | Hepatitis C virus (HCV) infections occur in approximately 3% of the world population. The development of an enhanced and extensive-scale screening is required to accomplish the World Health Organization’s (WHO) goal of eliminating HCV as a public health problem by 2030. However, standard testing methods are time-consuming, expensive, and challenging to deploy in remote and underdeveloped areas. Therefore, a cost-effective, rapid, and accurate point-of-care (POC) diagnostic test is needed to properly manage the disease and reduce the economic burden caused by high case numbers. Herein, we present a fully automated reverse-transcription loop-mediated isothermal amplification (RT-LAMP)-based molecular diagnostic set-up for rapid HCV detection. The set-up consists of an automated disposable microfluidic chip, a small surface heater, and a reusable magnetic actuation platform. The microfluidic chip contains multiple chambers in which the plasma sample is processed. The system utilizes SYBR green dye to detect the amplification product with the naked eye. The efficiency of the microfluidic chip was tested with human plasma samples spiked with HCV virions, and the limit of detection observed was 500 virions/mL within 45 min. The entire virus detection process was executed inside a uniquely designed, inexpensive, disposable, and self-driven microfluidic chip with high sensitivity and specificity. |
format | Online Article Text |
id | pubmed-9138684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91386842022-05-28 RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing Sharma, Sandhya Thomas, Emmanuel Caputi, Massimo Asghar, Waseem Biosensors (Basel) Article Hepatitis C virus (HCV) infections occur in approximately 3% of the world population. The development of an enhanced and extensive-scale screening is required to accomplish the World Health Organization’s (WHO) goal of eliminating HCV as a public health problem by 2030. However, standard testing methods are time-consuming, expensive, and challenging to deploy in remote and underdeveloped areas. Therefore, a cost-effective, rapid, and accurate point-of-care (POC) diagnostic test is needed to properly manage the disease and reduce the economic burden caused by high case numbers. Herein, we present a fully automated reverse-transcription loop-mediated isothermal amplification (RT-LAMP)-based molecular diagnostic set-up for rapid HCV detection. The set-up consists of an automated disposable microfluidic chip, a small surface heater, and a reusable magnetic actuation platform. The microfluidic chip contains multiple chambers in which the plasma sample is processed. The system utilizes SYBR green dye to detect the amplification product with the naked eye. The efficiency of the microfluidic chip was tested with human plasma samples spiked with HCV virions, and the limit of detection observed was 500 virions/mL within 45 min. The entire virus detection process was executed inside a uniquely designed, inexpensive, disposable, and self-driven microfluidic chip with high sensitivity and specificity. MDPI 2022-05-05 /pmc/articles/PMC9138684/ /pubmed/35624599 http://dx.doi.org/10.3390/bios12050298 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sharma, Sandhya Thomas, Emmanuel Caputi, Massimo Asghar, Waseem RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing |
title | RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing |
title_full | RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing |
title_fullStr | RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing |
title_full_unstemmed | RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing |
title_short | RT-LAMP-Based Molecular Diagnostic Set-Up for Rapid Hepatitis C Virus Testing |
title_sort | rt-lamp-based molecular diagnostic set-up for rapid hepatitis c virus testing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138684/ https://www.ncbi.nlm.nih.gov/pubmed/35624599 http://dx.doi.org/10.3390/bios12050298 |
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