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Simultaneous Sensing of Seven Pathogenic Bacteria by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles
[Image: see text] The method capable of simultaneously detecting multiple target bacterial pathogens is necessary and of great interest. In this research, we demonstrated our initial effort to simultaneously detect seven common foodborne bacteria by developing a straightforward upconversion fluoresc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648614/ https://www.ncbi.nlm.nih.gov/pubmed/31459983 http://dx.doi.org/10.1021/acsomega.9b00775 |
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author | Yin, Mingyuan Wu, Chen Li, Haijie Jia, Zhixin Deng, Qiliang Wang, Shuo Zhang, Yukui |
author_facet | Yin, Mingyuan Wu, Chen Li, Haijie Jia, Zhixin Deng, Qiliang Wang, Shuo Zhang, Yukui |
author_sort | Yin, Mingyuan |
collection | PubMed |
description | [Image: see text] The method capable of simultaneously detecting multiple target bacterial pathogens is necessary and of great interest. In this research, we demonstrated our initial effort to simultaneously detect seven common foodborne bacteria by developing a straightforward upconversion fluorescence sensing approach. The fluorescent nanosensor was constructed from a designed guanidine-functionalized upconversion fluorescent nanoparticles (UCNPs@GDN), tannic acid, and hydrogen peroxide (HP) and could quantify pathogenic bacteria in a nonspecific manner because the luminescence of the upconversion fluorescent nanoparticle was effectively strengthened in the presence of bacteria. When the developed nanosensor was applied to quantify multiple bacteria including Escherichia coli, Salmonella, Cronobacter sakazakii, Shigella flexneri, Vibrio parahaemolyticus, Staphylococcus aureus, and Listeria monocytogenes, a linear range of 10(3) to 10(8) cfu mL(–1) and a detection limit of 1.30 × 10(2) cfu mL(–1) have been obtained for the seven model mixture bacteria. In addition, the similar linear range and detection limit were also obtained for the detection of single bacteria. The present approach also exhibited acceptable recovery values ranging from 70.0 to 118.2% for bacteria in real samples (water, milk, and beef). All these results suggested that the guanidine-functionalized upconversion fluorescent nanosensor could be considered as a promising candidate for the rapid detection and surveillance of microbial pollutants in food and water. |
format | Online Article Text |
id | pubmed-6648614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66486142019-08-27 Simultaneous Sensing of Seven Pathogenic Bacteria by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles Yin, Mingyuan Wu, Chen Li, Haijie Jia, Zhixin Deng, Qiliang Wang, Shuo Zhang, Yukui ACS Omega [Image: see text] The method capable of simultaneously detecting multiple target bacterial pathogens is necessary and of great interest. In this research, we demonstrated our initial effort to simultaneously detect seven common foodborne bacteria by developing a straightforward upconversion fluorescence sensing approach. The fluorescent nanosensor was constructed from a designed guanidine-functionalized upconversion fluorescent nanoparticles (UCNPs@GDN), tannic acid, and hydrogen peroxide (HP) and could quantify pathogenic bacteria in a nonspecific manner because the luminescence of the upconversion fluorescent nanoparticle was effectively strengthened in the presence of bacteria. When the developed nanosensor was applied to quantify multiple bacteria including Escherichia coli, Salmonella, Cronobacter sakazakii, Shigella flexneri, Vibrio parahaemolyticus, Staphylococcus aureus, and Listeria monocytogenes, a linear range of 10(3) to 10(8) cfu mL(–1) and a detection limit of 1.30 × 10(2) cfu mL(–1) have been obtained for the seven model mixture bacteria. In addition, the similar linear range and detection limit were also obtained for the detection of single bacteria. The present approach also exhibited acceptable recovery values ranging from 70.0 to 118.2% for bacteria in real samples (water, milk, and beef). All these results suggested that the guanidine-functionalized upconversion fluorescent nanosensor could be considered as a promising candidate for the rapid detection and surveillance of microbial pollutants in food and water. American Chemical Society 2019-05-23 /pmc/articles/PMC6648614/ /pubmed/31459983 http://dx.doi.org/10.1021/acsomega.9b00775 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Yin, Mingyuan Wu, Chen Li, Haijie Jia, Zhixin Deng, Qiliang Wang, Shuo Zhang, Yukui Simultaneous Sensing of Seven Pathogenic Bacteria by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles |
title | Simultaneous Sensing of Seven Pathogenic Bacteria
by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles |
title_full | Simultaneous Sensing of Seven Pathogenic Bacteria
by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles |
title_fullStr | Simultaneous Sensing of Seven Pathogenic Bacteria
by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles |
title_full_unstemmed | Simultaneous Sensing of Seven Pathogenic Bacteria
by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles |
title_short | Simultaneous Sensing of Seven Pathogenic Bacteria
by Guanidine-Functionalized Upconversion Fluorescent Nanoparticles |
title_sort | simultaneous sensing of seven pathogenic bacteria
by guanidine-functionalized upconversion fluorescent nanoparticles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648614/ https://www.ncbi.nlm.nih.gov/pubmed/31459983 http://dx.doi.org/10.1021/acsomega.9b00775 |
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