A Highly Selective Colorimetric Sensor for Cysteine Detection

Detalhes bibliográficos
Autor(a) principal: Peng,Mengjiao
Data de Publicação: 2020
Outros Autores: Wang,Hui, Gibson,Gregory L., Shang,Hua, Yang,Jianmin, Chen,Yan, Lu,Yin
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000200305
Resumo: Introducing a hybrid xanthene as a fluorophore, an ‘ensemble’-based fluorescent sensor (E)-2-(6-(diethylamino)-2-((2-hydroxyphenylimino)methyl)-3-oxo-3H-xanthen-9-yl)benzoic acid (a) was designed and synthesised for detection of cysteine. Cysteine can release CuII ion from the non-fluorescent a-CuII complex. Then hydrolytic cleavage of Schiff base a produces a pink fluorescent compound 2-(6-(diethylamino)-2-formyl-3-oxo-3H-xanthen-9-yl)benzoic acid (2). We call this process a fluorescence off-on change. An obvious color change from purple a to pink 2 can be easily observed by the naked-eye. The calibration curve showed that the fluorescence intensity at 560 nm linearly increased over the cysteine concentration range of 0.379-100 µmol L-1 with a limit of detection of 0.379 µmol L-1. Sensor a-CuII displayed excellent selectivity for cysteine, even homocysteine and glutathione did not show influence. The sensor was also used for detecting cysteine in human breast adenocarcinoma cells, which illustrates the practical value. Overall, the sensor appears to be useful for rapid, convenient and selective cysteine detection in living tissues.
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spelling A Highly Selective Colorimetric Sensor for Cysteine Detectionfluorescent sensorcysteine detectioncolorimetrichigh selectivityIntroducing a hybrid xanthene as a fluorophore, an ‘ensemble’-based fluorescent sensor (E)-2-(6-(diethylamino)-2-((2-hydroxyphenylimino)methyl)-3-oxo-3H-xanthen-9-yl)benzoic acid (a) was designed and synthesised for detection of cysteine. Cysteine can release CuII ion from the non-fluorescent a-CuII complex. Then hydrolytic cleavage of Schiff base a produces a pink fluorescent compound 2-(6-(diethylamino)-2-formyl-3-oxo-3H-xanthen-9-yl)benzoic acid (2). We call this process a fluorescence off-on change. An obvious color change from purple a to pink 2 can be easily observed by the naked-eye. The calibration curve showed that the fluorescence intensity at 560 nm linearly increased over the cysteine concentration range of 0.379-100 µmol L-1 with a limit of detection of 0.379 µmol L-1. Sensor a-CuII displayed excellent selectivity for cysteine, even homocysteine and glutathione did not show influence. The sensor was also used for detecting cysteine in human breast adenocarcinoma cells, which illustrates the practical value. Overall, the sensor appears to be useful for rapid, convenient and selective cysteine detection in living tissues.Sociedade Brasileira de Química2020-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000200305Journal of the Brazilian Chemical Society v.31 n.2 2020reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20190177info:eu-repo/semantics/openAccessPeng,MengjiaoWang,HuiGibson,Gregory L.Shang,HuaYang,JianminChen,YanLu,Yineng2020-01-17T00:00:00Zoai:scielo:S0103-50532020000200305Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2020-01-17T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv A Highly Selective Colorimetric Sensor for Cysteine Detection
title A Highly Selective Colorimetric Sensor for Cysteine Detection
spellingShingle A Highly Selective Colorimetric Sensor for Cysteine Detection
Peng,Mengjiao
fluorescent sensor
cysteine detection
colorimetric
high selectivity
title_short A Highly Selective Colorimetric Sensor for Cysteine Detection
title_full A Highly Selective Colorimetric Sensor for Cysteine Detection
title_fullStr A Highly Selective Colorimetric Sensor for Cysteine Detection
title_full_unstemmed A Highly Selective Colorimetric Sensor for Cysteine Detection
title_sort A Highly Selective Colorimetric Sensor for Cysteine Detection
author Peng,Mengjiao
author_facet Peng,Mengjiao
Wang,Hui
Gibson,Gregory L.
Shang,Hua
Yang,Jianmin
Chen,Yan
Lu,Yin
author_role author
author2 Wang,Hui
Gibson,Gregory L.
Shang,Hua
Yang,Jianmin
Chen,Yan
Lu,Yin
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Peng,Mengjiao
Wang,Hui
Gibson,Gregory L.
Shang,Hua
Yang,Jianmin
Chen,Yan
Lu,Yin
dc.subject.por.fl_str_mv fluorescent sensor
cysteine detection
colorimetric
high selectivity
topic fluorescent sensor
cysteine detection
colorimetric
high selectivity
description Introducing a hybrid xanthene as a fluorophore, an ‘ensemble’-based fluorescent sensor (E)-2-(6-(diethylamino)-2-((2-hydroxyphenylimino)methyl)-3-oxo-3H-xanthen-9-yl)benzoic acid (a) was designed and synthesised for detection of cysteine. Cysteine can release CuII ion from the non-fluorescent a-CuII complex. Then hydrolytic cleavage of Schiff base a produces a pink fluorescent compound 2-(6-(diethylamino)-2-formyl-3-oxo-3H-xanthen-9-yl)benzoic acid (2). We call this process a fluorescence off-on change. An obvious color change from purple a to pink 2 can be easily observed by the naked-eye. The calibration curve showed that the fluorescence intensity at 560 nm linearly increased over the cysteine concentration range of 0.379-100 µmol L-1 with a limit of detection of 0.379 µmol L-1. Sensor a-CuII displayed excellent selectivity for cysteine, even homocysteine and glutathione did not show influence. The sensor was also used for detecting cysteine in human breast adenocarcinoma cells, which illustrates the practical value. Overall, the sensor appears to be useful for rapid, convenient and selective cysteine detection in living tissues.
publishDate 2020
dc.date.none.fl_str_mv 2020-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000200305
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000200305
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20190177
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.31 n.2 2020
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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