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Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection
Polymerase chain reaction (PCR) is a technique for nucleic acid amplification, which has been widely used in molecular biology. Owing to the limitations such as large size, high power consumption, and complicated operation, PCR is only used in hospitals or research institutions. To meet the requirem...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249063/ https://www.ncbi.nlm.nih.gov/pubmed/32380637 http://dx.doi.org/10.3390/s20092627 |
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author | Jie, Junyao Hu, Shiming Liu, Wenwen Wei, Qingquan Huang, Yizheng Yuan, Xinxin Ren, Lufeng Tan, Manqing Yu, Yude |
author_facet | Jie, Junyao Hu, Shiming Liu, Wenwen Wei, Qingquan Huang, Yizheng Yuan, Xinxin Ren, Lufeng Tan, Manqing Yu, Yude |
author_sort | Jie, Junyao |
collection | PubMed |
description | Polymerase chain reaction (PCR) is a technique for nucleic acid amplification, which has been widely used in molecular biology. Owing to the limitations such as large size, high power consumption, and complicated operation, PCR is only used in hospitals or research institutions. To meet the requirements of portable applications, we developed a fast, battery-powered, portable device for PCR amplification and end-point detection. The device consisted of a PCR thermal control system, PCR reaction chip, and fluorescence detection system. The PCR thermal control system was formed by a thermal control chip and external drive circuits. Thin-film heaters and resistance temperature detectors (RTDs) were fabricated on the thermal control chip and were regulated with external drive circuits. The average heating rate was 32 °C/s and the average cooling rate was 7.5 °C/s. The disposable reaction chips were fabricated using a silicon substrate, silicone rubber, and quartz plate. The fluorescence detection system consisted a complementary metal-oxide-semiconductor (CMOS) camera, an LED, and mirror units. The device was driven by a 24 V Li-ion battery. We amplified HPV16E6 genomic DNA using our device and achieved satisfactory results. |
format | Online Article Text |
id | pubmed-7249063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72490632020-06-10 Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection Jie, Junyao Hu, Shiming Liu, Wenwen Wei, Qingquan Huang, Yizheng Yuan, Xinxin Ren, Lufeng Tan, Manqing Yu, Yude Sensors (Basel) Article Polymerase chain reaction (PCR) is a technique for nucleic acid amplification, which has been widely used in molecular biology. Owing to the limitations such as large size, high power consumption, and complicated operation, PCR is only used in hospitals or research institutions. To meet the requirements of portable applications, we developed a fast, battery-powered, portable device for PCR amplification and end-point detection. The device consisted of a PCR thermal control system, PCR reaction chip, and fluorescence detection system. The PCR thermal control system was formed by a thermal control chip and external drive circuits. Thin-film heaters and resistance temperature detectors (RTDs) were fabricated on the thermal control chip and were regulated with external drive circuits. The average heating rate was 32 °C/s and the average cooling rate was 7.5 °C/s. The disposable reaction chips were fabricated using a silicon substrate, silicone rubber, and quartz plate. The fluorescence detection system consisted a complementary metal-oxide-semiconductor (CMOS) camera, an LED, and mirror units. The device was driven by a 24 V Li-ion battery. We amplified HPV16E6 genomic DNA using our device and achieved satisfactory results. MDPI 2020-05-05 /pmc/articles/PMC7249063/ /pubmed/32380637 http://dx.doi.org/10.3390/s20092627 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jie, Junyao Hu, Shiming Liu, Wenwen Wei, Qingquan Huang, Yizheng Yuan, Xinxin Ren, Lufeng Tan, Manqing Yu, Yude Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection |
title | Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection |
title_full | Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection |
title_fullStr | Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection |
title_full_unstemmed | Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection |
title_short | Portable and Battery-Powered PCR Device for DNA Amplification and Fluorescence Detection |
title_sort | portable and battery-powered pcr device for dna amplification and fluorescence detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249063/ https://www.ncbi.nlm.nih.gov/pubmed/32380637 http://dx.doi.org/10.3390/s20092627 |
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