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Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification
Microfluidic components and systems for rapid (<60 min), low-cost, convenient, field-deployable sequence-specific nucleic acid-based amplification tests (NAATs) are described. A microfluidic point-of-care (POC) diagnostics test to quantify HIV viral load from blood samples serves as a representat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996405/ https://www.ncbi.nlm.nih.gov/pubmed/27600235 http://dx.doi.org/10.3390/microarrays4040474 |
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author | Mauk, Michael G. Liu, Changchun Song, Jinzhao Bau, Haim H. |
author_facet | Mauk, Michael G. Liu, Changchun Song, Jinzhao Bau, Haim H. |
author_sort | Mauk, Michael G. |
collection | PubMed |
description | Microfluidic components and systems for rapid (<60 min), low-cost, convenient, field-deployable sequence-specific nucleic acid-based amplification tests (NAATs) are described. A microfluidic point-of-care (POC) diagnostics test to quantify HIV viral load from blood samples serves as a representative and instructive example to discuss the technical issues and capabilities of “lab on a chip” NAAT devices. A portable, miniaturized POC NAAT with performance comparable to conventional PCR (polymerase-chain reaction)-based tests in clinical laboratories can be realized with a disposable, palm-sized, plastic microfluidic chip in which: (1) nucleic acids (NAs) are extracted from relatively large (~mL) volume sample lysates using an embedded porous silica glass fiber or cellulose binding phase (“membrane”) to capture sample NAs in a flow-through, filtration mode; (2) NAs captured on the membrane are isothermally (~65 °C) amplified; (3) amplicon production is monitored by real-time fluorescence detection, such as with a smartphone CCD camera serving as a low-cost detector; and (4) paraffin-encapsulated, lyophilized reagents for temperature-activated release are pre-stored in the chip. Limits of Detection (LOD) better than 10(3) virons/sample can be achieved. A modified chip with conduits hosting a diffusion-mode amplification process provides a simple visual indicator to readily quantify sample NA template. In addition, a companion microfluidic device for extracting plasma from whole blood without a centrifuge, generating cell-free plasma for chip-based molecular diagnostics, is described. Extensions to a myriad of related applications including, for example, food testing, cancer screening, and insect genotyping are briefly surveyed. |
format | Online Article Text |
id | pubmed-4996405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-49964052016-09-06 Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification Mauk, Michael G. Liu, Changchun Song, Jinzhao Bau, Haim H. Microarrays (Basel) Review Microfluidic components and systems for rapid (<60 min), low-cost, convenient, field-deployable sequence-specific nucleic acid-based amplification tests (NAATs) are described. A microfluidic point-of-care (POC) diagnostics test to quantify HIV viral load from blood samples serves as a representative and instructive example to discuss the technical issues and capabilities of “lab on a chip” NAAT devices. A portable, miniaturized POC NAAT with performance comparable to conventional PCR (polymerase-chain reaction)-based tests in clinical laboratories can be realized with a disposable, palm-sized, plastic microfluidic chip in which: (1) nucleic acids (NAs) are extracted from relatively large (~mL) volume sample lysates using an embedded porous silica glass fiber or cellulose binding phase (“membrane”) to capture sample NAs in a flow-through, filtration mode; (2) NAs captured on the membrane are isothermally (~65 °C) amplified; (3) amplicon production is monitored by real-time fluorescence detection, such as with a smartphone CCD camera serving as a low-cost detector; and (4) paraffin-encapsulated, lyophilized reagents for temperature-activated release are pre-stored in the chip. Limits of Detection (LOD) better than 10(3) virons/sample can be achieved. A modified chip with conduits hosting a diffusion-mode amplification process provides a simple visual indicator to readily quantify sample NA template. In addition, a companion microfluidic device for extracting plasma from whole blood without a centrifuge, generating cell-free plasma for chip-based molecular diagnostics, is described. Extensions to a myriad of related applications including, for example, food testing, cancer screening, and insect genotyping are briefly surveyed. MDPI 2015-10-20 /pmc/articles/PMC4996405/ /pubmed/27600235 http://dx.doi.org/10.3390/microarrays4040474 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mauk, Michael G. Liu, Changchun Song, Jinzhao Bau, Haim H. Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification |
title | Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification |
title_full | Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification |
title_fullStr | Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification |
title_full_unstemmed | Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification |
title_short | Integrated Microfluidic Nucleic Acid Isolation, Isothermal Amplification, and Amplicon Quantification |
title_sort | integrated microfluidic nucleic acid isolation, isothermal amplification, and amplicon quantification |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996405/ https://www.ncbi.nlm.nih.gov/pubmed/27600235 http://dx.doi.org/10.3390/microarrays4040474 |
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