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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...

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Autores principales: Mauk, Michael G., Liu, Changchun, Song, Jinzhao, Bau, Haim H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
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.
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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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