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A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore

To achieve sensitive, selective and facile detection of hydrazine in environmental and biological systems, a fluorescent probe (Che-Dcv) with a unique nonaromatic fluorophore was developed. Upon hydrazine addition in 20% DMSO–PBS buffer (pH = 7.4, 10 mM, v/v) at room temperature, the probe displayed...

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Detalles Bibliográficos
Autores principales: Liu, Jian, Li, Tao, Wang, Shun, Qi, Qingrong, Song, Hang, Li, Zicheng, Yang, Li, Huang, Wencai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049246/
https://www.ncbi.nlm.nih.gov/pubmed/35497447
http://dx.doi.org/10.1039/c9ra10882c
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author Liu, Jian
Li, Tao
Wang, Shun
Qi, Qingrong
Song, Hang
Li, Zicheng
Yang, Li
Huang, Wencai
author_facet Liu, Jian
Li, Tao
Wang, Shun
Qi, Qingrong
Song, Hang
Li, Zicheng
Yang, Li
Huang, Wencai
author_sort Liu, Jian
collection PubMed
description To achieve sensitive, selective and facile detection of hydrazine in environmental and biological systems, a fluorescent probe (Che-Dcv) with a unique nonaromatic fluorophore was developed. Upon hydrazine addition in 20% DMSO–PBS buffer (pH = 7.4, 10 mM, v/v) at room temperature, the probe displayed a strong emission at 496 nm along with a color change from brown-red to yellow. The response was attributed to the reaction of dicyanovinyl groups with hydrazine to afford hydrazone, which was supported by (1)H NMR and HRMS. The detection limit of Che-Dcv for hydrazine was estimated to be as low as 1.08 ppb and good selectivity over amines including hydroxylamine was observed. Then, the potential of probe-coated test papers to detect hydrazine in solution and vapor phase was demonstrated. Moreover, the bioimaging of hydrazine in living H1975 cells was performed successfully.
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spelling pubmed-90492462022-04-29 A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore Liu, Jian Li, Tao Wang, Shun Qi, Qingrong Song, Hang Li, Zicheng Yang, Li Huang, Wencai RSC Adv Chemistry To achieve sensitive, selective and facile detection of hydrazine in environmental and biological systems, a fluorescent probe (Che-Dcv) with a unique nonaromatic fluorophore was developed. Upon hydrazine addition in 20% DMSO–PBS buffer (pH = 7.4, 10 mM, v/v) at room temperature, the probe displayed a strong emission at 496 nm along with a color change from brown-red to yellow. The response was attributed to the reaction of dicyanovinyl groups with hydrazine to afford hydrazone, which was supported by (1)H NMR and HRMS. The detection limit of Che-Dcv for hydrazine was estimated to be as low as 1.08 ppb and good selectivity over amines including hydroxylamine was observed. Then, the potential of probe-coated test papers to detect hydrazine in solution and vapor phase was demonstrated. Moreover, the bioimaging of hydrazine in living H1975 cells was performed successfully. The Royal Society of Chemistry 2020-02-04 /pmc/articles/PMC9049246/ /pubmed/35497447 http://dx.doi.org/10.1039/c9ra10882c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Liu, Jian
Li, Tao
Wang, Shun
Qi, Qingrong
Song, Hang
Li, Zicheng
Yang, Li
Huang, Wencai
A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore
title A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore
title_full A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore
title_fullStr A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore
title_full_unstemmed A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore
title_short A sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore
title_sort sensitive and selective fluorescent probe for hydrazine with a unique nonaromatic fluorophore
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049246/
https://www.ncbi.nlm.nih.gov/pubmed/35497447
http://dx.doi.org/10.1039/c9ra10882c
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