A Highly Selective Colorimetric Sensor for Cysteine Detection
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1750318182577471488 |