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Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring
BACKGROUND: Azo dyes are the most widely used synthetic colorants in the textile, food, pharmaceutical, cosmetic, and other industries, accounting for nearly 70% of all dyestuffs consumed. Recently, much research attention has been paid to efficient monitoring of these hazardous chemicals and their...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pasteur Institute of Iran
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7748117/ https://www.ncbi.nlm.nih.gov/pubmed/33129235 http://dx.doi.org/10.29252/ibj.25.1.8 |
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author | Hajipour, Fahimeh Asad, Sedigheh Amoozegar, Mohammad Ali Javidparvar, Ali Asghar Tang, Jialun Zhong, Haizheng Khajeh, Khosro |
author_facet | Hajipour, Fahimeh Asad, Sedigheh Amoozegar, Mohammad Ali Javidparvar, Ali Asghar Tang, Jialun Zhong, Haizheng Khajeh, Khosro |
author_sort | Hajipour, Fahimeh |
collection | PubMed |
description | BACKGROUND: Azo dyes are the most widely used synthetic colorants in the textile, food, pharmaceutical, cosmetic, and other industries, accounting for nearly 70% of all dyestuffs consumed. Recently, much research attention has been paid to efficient monitoring of these hazardous chemicals and their related metabolites because of their potentially harmful effect on environmental issues. In contrast to the complex and expensive instrumental procedures, the detection system based on the QDs with the superior optochemical properties provides a new era in the pollution sensing and prevention. METHODS: We have developed a QD-enzyme hybrid system to probe MR in aqueous solutions using a fluorescence quenching procedure. RESULTS: The azoreductase enzyme catalyzed the reduction of azo group in MR, which can efficiently decrease the FRET between the QDs and MR molecules. The correlation between the QDs photoluminescence recovery and MR enzymatic decolorization at the neutral phosphate buffer permitted the creation of a fluorescence quenching-based sensor. The synthesized biosensor can be used for the accurate detection of MR in a linear calibration over MR concentrations of 5-84 μM, with the LOD of 0.5 μM in response time of three minutes. CONCLUSION: Our findings revealed that this fluorometric sensor has the potential to be successfully applied for monitoring a wide linear range of MR concentration with the relative standard deviation of 4% rather than the other method. |
format | Online Article Text |
id | pubmed-7748117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Pasteur Institute of Iran |
record_format | MEDLINE/PubMed |
spelling | pubmed-77481172021-01-06 Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring Hajipour, Fahimeh Asad, Sedigheh Amoozegar, Mohammad Ali Javidparvar, Ali Asghar Tang, Jialun Zhong, Haizheng Khajeh, Khosro Iran Biomed J Full Length BACKGROUND: Azo dyes are the most widely used synthetic colorants in the textile, food, pharmaceutical, cosmetic, and other industries, accounting for nearly 70% of all dyestuffs consumed. Recently, much research attention has been paid to efficient monitoring of these hazardous chemicals and their related metabolites because of their potentially harmful effect on environmental issues. In contrast to the complex and expensive instrumental procedures, the detection system based on the QDs with the superior optochemical properties provides a new era in the pollution sensing and prevention. METHODS: We have developed a QD-enzyme hybrid system to probe MR in aqueous solutions using a fluorescence quenching procedure. RESULTS: The azoreductase enzyme catalyzed the reduction of azo group in MR, which can efficiently decrease the FRET between the QDs and MR molecules. The correlation between the QDs photoluminescence recovery and MR enzymatic decolorization at the neutral phosphate buffer permitted the creation of a fluorescence quenching-based sensor. The synthesized biosensor can be used for the accurate detection of MR in a linear calibration over MR concentrations of 5-84 μM, with the LOD of 0.5 μM in response time of three minutes. CONCLUSION: Our findings revealed that this fluorometric sensor has the potential to be successfully applied for monitoring a wide linear range of MR concentration with the relative standard deviation of 4% rather than the other method. Pasteur Institute of Iran 2021-01 2020-09-12 /pmc/articles/PMC7748117/ /pubmed/33129235 http://dx.doi.org/10.29252/ibj.25.1.8 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Length Hajipour, Fahimeh Asad, Sedigheh Amoozegar, Mohammad Ali Javidparvar, Ali Asghar Tang, Jialun Zhong, Haizheng Khajeh, Khosro Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring |
title | Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring |
title_full | Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring |
title_fullStr | Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring |
title_full_unstemmed | Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring |
title_short | Developing a Fluorescent Hybrid Nanobiosensor Based on Quantum Dots and Azoreductase Enzyme for Methyl Red Monitoring |
title_sort | developing a fluorescent hybrid nanobiosensor based on quantum dots and azoreductase enzyme for methyl red monitoring |
topic | Full Length |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7748117/ https://www.ncbi.nlm.nih.gov/pubmed/33129235 http://dx.doi.org/10.29252/ibj.25.1.8 |
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