Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure

In this work, the determination of 2,4-, 2,5- and 2,6-dinitrophenols and the identification of some of their metabolites in human urine and saliva is proposed. A three phase hollow fiber based liquid phase microextraction prior to ultra-high performance liquid chromatography coupled to quadrupole ti...

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Autores: Kazakova, Julia, Villar Navarro, Mercedes, Pérez Bernal, Juan Luis, Ramos Payán, María Dolores, Bello López, Miguel Ángel, Fernández Torres, Rut
Formato: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2021
País:España
Recursos:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/153302
Acesso em linha:https://hdl.handle.net/11441/153302
https://doi.org/10.1016/j.microc.2021.106193
Access Level:acceso abierto
Palavra-chave:Hollow fiber liquid phase microextraction
HF-LPME
Liquid chromatography quadrupole time-of-flight
Dinitrophenols
Human urine
Human saliva
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spelling Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposureKazakova, JuliaVillar Navarro, MercedesPérez Bernal, Juan LuisRamos Payán, María DoloresBello López, Miguel ÁngelFernández Torres, RutHollow fiber liquid phase microextractionHF-LPMELiquid chromatography quadrupole time-of-flightDinitrophenolsHuman urineHuman salivaIn this work, the determination of 2,4-, 2,5- and 2,6-dinitrophenols and the identification of some of their metabolites in human urine and saliva is proposed. A three phase hollow fiber based liquid phase microextraction prior to ultra-high performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry allowed low detection and quantitation limits of the target analytes, as well as the investigation and tentatively identification of some metabolites by accurate mass full-spectrum measurements. The chromatographic separation was accomplished on an Acquity BEH C18 column (50 mm × 2.1 mm i.d., 1.7 μm particle size) at 25 ºC using water and acetonitrile (with 0.1 % (v/v) formic acid) 20:80 v/v as mobile phase, at a flow rate of 0.5 mL/min in isocratic elution mode for 5 min. Hollow fiber liquid phase microextraction was achieved at donor phase pH 2, acceptor phase pH 13 and dihexylether as supported liquid membrane. Under the optimal conditions, detection limits for 2,4-, 2,5- and 2,6-dinitrophenol, respectively, were 0.18 μg·L-1, 0.38 μg·L-1 and 0.14 μg·L-1 in urine samples and 0.32 μg·L-1, 0.67 μg·L-1 and 0.24 μg·L-1 in saliva samples. The proposed methodology was applied on urine and saliva samples from laboratory staff likely to be or not occupationally exposed to dinitrophenols, finding quantitative levels of 2,4- and 2,6-dinitrophenol and identifying some metabolites previously reported in literature.Ministerio de Economía y Competitividad (MINECO). España CTM2015-67902-C-1-PMinisterio de Ciencia e Innovación (MICIN). España GC2018-096608-B-C22European Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER) GC2018-096608-B-C22Elsevier Inc.Química AnalíticaMinisterio de Economía y Competitividad (MINECO). EspañaMinisterio de Ciencia e Innovación (MICIN). EspañaEuropean Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER)2021info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/153302https://doi.org/10.1016/j.microc.2021.106193reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésMicrochemical journal, 166, 106193.CTM2015-67902-C-1-PGC2018-096608-B-C22https://doi.org/10.1016/j.microc.2021.106193info:eu-repo/semantics/openAccessoai:idus.us.es:11441/1533022026-06-17T12:51:07Z
dc.title.none.fl_str_mv Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
title Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
spellingShingle Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
Kazakova, Julia
Hollow fiber liquid phase microextraction
HF-LPME
Liquid chromatography quadrupole time-of-flight
Dinitrophenols
Human urine
Human saliva
title_short Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
title_full Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
title_fullStr Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
title_full_unstemmed Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
title_sort Urine and saliva biomonitoring by HF-LPME-LC/MS to assess dinitrophenols exposure
dc.creator.none.fl_str_mv Kazakova, Julia
Villar Navarro, Mercedes
Pérez Bernal, Juan Luis
Ramos Payán, María Dolores
Bello López, Miguel Ángel
Fernández Torres, Rut
author Kazakova, Julia
author_facet Kazakova, Julia
Villar Navarro, Mercedes
Pérez Bernal, Juan Luis
Ramos Payán, María Dolores
Bello López, Miguel Ángel
Fernández Torres, Rut
author_role author
author2 Villar Navarro, Mercedes
Pérez Bernal, Juan Luis
Ramos Payán, María Dolores
Bello López, Miguel Ángel
Fernández Torres, Rut
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Química Analítica
Ministerio de Economía y Competitividad (MINECO). España
Ministerio de Ciencia e Innovación (MICIN). España
European Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER)
dc.subject.none.fl_str_mv Hollow fiber liquid phase microextraction
HF-LPME
Liquid chromatography quadrupole time-of-flight
Dinitrophenols
Human urine
Human saliva
topic Hollow fiber liquid phase microextraction
HF-LPME
Liquid chromatography quadrupole time-of-flight
Dinitrophenols
Human urine
Human saliva
description In this work, the determination of 2,4-, 2,5- and 2,6-dinitrophenols and the identification of some of their metabolites in human urine and saliva is proposed. A three phase hollow fiber based liquid phase microextraction prior to ultra-high performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry allowed low detection and quantitation limits of the target analytes, as well as the investigation and tentatively identification of some metabolites by accurate mass full-spectrum measurements. The chromatographic separation was accomplished on an Acquity BEH C18 column (50 mm × 2.1 mm i.d., 1.7 μm particle size) at 25 ºC using water and acetonitrile (with 0.1 % (v/v) formic acid) 20:80 v/v as mobile phase, at a flow rate of 0.5 mL/min in isocratic elution mode for 5 min. Hollow fiber liquid phase microextraction was achieved at donor phase pH 2, acceptor phase pH 13 and dihexylether as supported liquid membrane. Under the optimal conditions, detection limits for 2,4-, 2,5- and 2,6-dinitrophenol, respectively, were 0.18 μg·L-1, 0.38 μg·L-1 and 0.14 μg·L-1 in urine samples and 0.32 μg·L-1, 0.67 μg·L-1 and 0.24 μg·L-1 in saliva samples. The proposed methodology was applied on urine and saliva samples from laboratory staff likely to be or not occupationally exposed to dinitrophenols, finding quantitative levels of 2,4- and 2,6-dinitrophenol and identifying some metabolites previously reported in literature.
publishDate 2021
dc.date.none.fl_str_mv 2021
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
format article
status_str acceptedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/11441/153302
https://doi.org/10.1016/j.microc.2021.106193
url https://hdl.handle.net/11441/153302
https://doi.org/10.1016/j.microc.2021.106193
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Microchemical journal, 166, 106193.
CTM2015-67902-C-1-P
GC2018-096608-B-C22
https://doi.org/10.1016/j.microc.2021.106193
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Inc.
publisher.none.fl_str_mv Elsevier Inc.
dc.source.none.fl_str_mv reponame:idUS. Depósito de Investigación de la Universidad de Sevilla
instname:Universidad de Sevilla (US)
instname_str Universidad de Sevilla (US)
reponame_str idUS. Depósito de Investigación de la Universidad de Sevilla
collection idUS. Depósito de Investigación de la Universidad de Sevilla
repository.name.fl_str_mv
repository.mail.fl_str_mv
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