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Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging
Near-infrared (NIR) fluorescent probes are widely employed in biological detection because of their lower damage to biological samples, low background interference, and high signal-to-noise ratio. Herein, a highly water-soluble NIR probe (NIRHA) based on a hemicyanine skeleton and bearing an acrylat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076481/ https://www.ncbi.nlm.nih.gov/pubmed/35541628 http://dx.doi.org/10.1039/c9ra08555f |
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author | Qi, Shaolong Zhu, Lubao Wang, Xinyu Du, Jianshi Yang, Qingbiao Li, Yaoxian |
author_facet | Qi, Shaolong Zhu, Lubao Wang, Xinyu Du, Jianshi Yang, Qingbiao Li, Yaoxian |
author_sort | Qi, Shaolong |
collection | PubMed |
description | Near-infrared (NIR) fluorescent probes are widely employed in biological detection because of their lower damage to biological samples, low background interference, and high signal-to-noise ratio. Herein, a highly water-soluble NIR probe (NIRHA) based on a hemicyanine skeleton and bearing an acrylate moiety was synthesized. The probe showed high selectivity toward cysteine (Cys) over homocysteine (Hcy) and glutathione (GSH). The probe also had low cytotoxicity and was successfully applied in HeLa cells and mouse experiments. Results of bioimaging experiments indicated that the probe was effective for visualizing endogenous Cys in vitro and in vivo. |
format | Online Article Text |
id | pubmed-9076481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90764812022-05-09 Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging Qi, Shaolong Zhu, Lubao Wang, Xinyu Du, Jianshi Yang, Qingbiao Li, Yaoxian RSC Adv Chemistry Near-infrared (NIR) fluorescent probes are widely employed in biological detection because of their lower damage to biological samples, low background interference, and high signal-to-noise ratio. Herein, a highly water-soluble NIR probe (NIRHA) based on a hemicyanine skeleton and bearing an acrylate moiety was synthesized. The probe showed high selectivity toward cysteine (Cys) over homocysteine (Hcy) and glutathione (GSH). The probe also had low cytotoxicity and was successfully applied in HeLa cells and mouse experiments. Results of bioimaging experiments indicated that the probe was effective for visualizing endogenous Cys in vitro and in vivo. The Royal Society of Chemistry 2019-12-16 /pmc/articles/PMC9076481/ /pubmed/35541628 http://dx.doi.org/10.1039/c9ra08555f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Qi, Shaolong Zhu, Lubao Wang, Xinyu Du, Jianshi Yang, Qingbiao Li, Yaoxian Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging |
title | Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging |
title_full | Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging |
title_fullStr | Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging |
title_full_unstemmed | Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging |
title_short | Near-infrared turn-on fluorescent probe for discriminative detection of Cys and application in in vivo imaging |
title_sort | near-infrared turn-on fluorescent probe for discriminative detection of cys and application in in vivo imaging |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076481/ https://www.ncbi.nlm.nih.gov/pubmed/35541628 http://dx.doi.org/10.1039/c9ra08555f |
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