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Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device
A one-step analysis method was developed for four types of amino acids using a microfluidic paper-based analytical device fabricated from chromatography filtration paper and laminate films. Aminoacyl-tRNA synthetase was used to detect each amino acid. The obtained laminated paper-based analytical de...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891284/ https://www.ncbi.nlm.nih.gov/pubmed/35236904 http://dx.doi.org/10.1038/s41598-022-07408-9 |
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author | Kugimiya, Akimitsu Wakimoto, Sho Kohda, Jiro Nakano, Yasuhisa Takano, Yu |
author_facet | Kugimiya, Akimitsu Wakimoto, Sho Kohda, Jiro Nakano, Yasuhisa Takano, Yu |
author_sort | Kugimiya, Akimitsu |
collection | PubMed |
description | A one-step analysis method was developed for four types of amino acids using a microfluidic paper-based analytical device fabricated from chromatography filtration paper and laminate films. Aminoacyl-tRNA synthetase was used to detect each amino acid. The obtained laminated paper-based analytical device (LPAD) contained four enzymatic reaction areas. Colorimetric detection was performed based on the molybdenum blue reaction. A model method for the simple, easy, and simultaneous detection of several amino acid concentrations was suggested, in contrast to the conventional methods such as HPLC or LC–MS. The method provided a selective quantification at the ranges of 3.6–100 μM for tryptophan, 10.1–100 μM for glycine, 5.9–100 μM for histidine and 5.6–100 μM for lysine with a detection limit of 1.1 μM, 3.3 μM, 1.9 μM and 1.8 μM, respectively. LPAD fabrication was considerably simple, and the subsequent detection process was easy and required a short period of time (within 15 min). |
format | Online Article Text |
id | pubmed-8891284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88912842022-03-03 Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device Kugimiya, Akimitsu Wakimoto, Sho Kohda, Jiro Nakano, Yasuhisa Takano, Yu Sci Rep Article A one-step analysis method was developed for four types of amino acids using a microfluidic paper-based analytical device fabricated from chromatography filtration paper and laminate films. Aminoacyl-tRNA synthetase was used to detect each amino acid. The obtained laminated paper-based analytical device (LPAD) contained four enzymatic reaction areas. Colorimetric detection was performed based on the molybdenum blue reaction. A model method for the simple, easy, and simultaneous detection of several amino acid concentrations was suggested, in contrast to the conventional methods such as HPLC or LC–MS. The method provided a selective quantification at the ranges of 3.6–100 μM for tryptophan, 10.1–100 μM for glycine, 5.9–100 μM for histidine and 5.6–100 μM for lysine with a detection limit of 1.1 μM, 3.3 μM, 1.9 μM and 1.8 μM, respectively. LPAD fabrication was considerably simple, and the subsequent detection process was easy and required a short period of time (within 15 min). Nature Publishing Group UK 2022-03-02 /pmc/articles/PMC8891284/ /pubmed/35236904 http://dx.doi.org/10.1038/s41598-022-07408-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kugimiya, Akimitsu Wakimoto, Sho Kohda, Jiro Nakano, Yasuhisa Takano, Yu Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device |
title | Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device |
title_full | Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device |
title_fullStr | Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device |
title_full_unstemmed | Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device |
title_short | Development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device |
title_sort | development of a one-step analysis method for several amino acids using a microfluidic paper-based analytical device |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891284/ https://www.ncbi.nlm.nih.gov/pubmed/35236904 http://dx.doi.org/10.1038/s41598-022-07408-9 |
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