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Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples

[Image: see text] Microfluidic paper-based analytical devices (μPADs) are promising biosensors that may be used in a variety of bioanalytical applications. A μPAD for automating the competitive enzyme-linked immunosorbent assay (ELISA) of small-sized target detection at the femtogram level using sub...

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Autores principales: Charernchai, Sumamal, Chikae, Miyuki, Phan, Tue Trong, Wonsawat, Wanida, Hirose, Daisuke, Takamura, Yuzuru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969870/
https://www.ncbi.nlm.nih.gov/pubmed/35302345
http://dx.doi.org/10.1021/acs.analchem.1c05401
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author Charernchai, Sumamal
Chikae, Miyuki
Phan, Tue Trong
Wonsawat, Wanida
Hirose, Daisuke
Takamura, Yuzuru
author_facet Charernchai, Sumamal
Chikae, Miyuki
Phan, Tue Trong
Wonsawat, Wanida
Hirose, Daisuke
Takamura, Yuzuru
author_sort Charernchai, Sumamal
collection PubMed
description [Image: see text] Microfluidic paper-based analytical devices (μPADs) are promising biosensors that may be used in a variety of bioanalytical applications. A μPAD for automating the competitive enzyme-linked immunosorbent assay (ELISA) of small-sized target detection at the femtogram level using submicroliter samples is reported in this study. The proposed μPAD was integrated with a sucrose valve to automate the sequential delivery of reagents, providing simple control of reagent delivery time and simple operation. The use of a sample solution dropping location at the zones on the device that had been prepared with an antibody-conjugated enzyme before immersion in a running buffer allowed minimization of sample volume to 0.6 μL, while eliminating the possible loss of a target molecule by adsorption on the membrane, thus improving detection sensitivity. Furthermore, the proposed device was successfully applied to the automation of competitive ELISA for the detection of aflatoxin B(1) (AFB(1)), a potent carcinogen that causes substantial health risks to humans worldwide, with a detection limit of 60 femtograms or 0.1 ng/mL. The method developed in this study provides high sensitivity, small sample volume, on-site and equipment-free measurements, low-cost operation, and user-friendliness. This approach could be used to analyze small-sized molecules in the fields of food safety and quality control, environmental monitoring, and clinical diagnostics.
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spelling pubmed-89698702023-03-18 Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples Charernchai, Sumamal Chikae, Miyuki Phan, Tue Trong Wonsawat, Wanida Hirose, Daisuke Takamura, Yuzuru Anal Chem [Image: see text] Microfluidic paper-based analytical devices (μPADs) are promising biosensors that may be used in a variety of bioanalytical applications. A μPAD for automating the competitive enzyme-linked immunosorbent assay (ELISA) of small-sized target detection at the femtogram level using submicroliter samples is reported in this study. The proposed μPAD was integrated with a sucrose valve to automate the sequential delivery of reagents, providing simple control of reagent delivery time and simple operation. The use of a sample solution dropping location at the zones on the device that had been prepared with an antibody-conjugated enzyme before immersion in a running buffer allowed minimization of sample volume to 0.6 μL, while eliminating the possible loss of a target molecule by adsorption on the membrane, thus improving detection sensitivity. Furthermore, the proposed device was successfully applied to the automation of competitive ELISA for the detection of aflatoxin B(1) (AFB(1)), a potent carcinogen that causes substantial health risks to humans worldwide, with a detection limit of 60 femtograms or 0.1 ng/mL. The method developed in this study provides high sensitivity, small sample volume, on-site and equipment-free measurements, low-cost operation, and user-friendliness. This approach could be used to analyze small-sized molecules in the fields of food safety and quality control, environmental monitoring, and clinical diagnostics. American Chemical Society 2022-03-18 2022-03-29 /pmc/articles/PMC8969870/ /pubmed/35302345 http://dx.doi.org/10.1021/acs.analchem.1c05401 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Charernchai, Sumamal
Chikae, Miyuki
Phan, Tue Trong
Wonsawat, Wanida
Hirose, Daisuke
Takamura, Yuzuru
Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples
title Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples
title_full Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples
title_fullStr Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples
title_full_unstemmed Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples
title_short Automated Paper-Based Femtogram Sensing Device for Competitive Enzyme-Linked Immunosorbent Assay of Aflatoxin B(1) Using Submicroliter Samples
title_sort automated paper-based femtogram sensing device for competitive enzyme-linked immunosorbent assay of aflatoxin b(1) using submicroliter samples
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969870/
https://www.ncbi.nlm.nih.gov/pubmed/35302345
http://dx.doi.org/10.1021/acs.analchem.1c05401
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