Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples
- Autores
- Canales, Maria Romina; Marino Repizo, Leonardo; Reta, Mario Roberto; Cerutti, Soledad
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A multi-response optimization of a green and efficient solid phase extraction (SPE) sample treatment using non-modified multi-walled carbon nanotubes combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed for the quantification of ten heterocyclic aromatic amines (HAAs) in river and reservoir surface water samples. The proposed methodology was evaluated with the employment of experimental designs, which provided to greening the approach. Ultra-trace amounts of HAAs were retained into the SPE cartridge. Then, these analytes were removed from the carbon nanotubes with 0.8 mL of a mixture of acetonitrile/water with 0.1 % of formic acid. Under the optimal conditions, linearity was achieved for concentration levels ranging from 0.20 µg L-1 to 500 µg L-1, with regression coefficients (R2) from 0.990 to 0.998. Limits of detection varying from 0.06 µg L-1 and 0.23 µg L-1 were attained, the relative standard deviations (n=3) varied from 1.7 to 6.4, and extraction recoveries ranged from 90.6 % to 106.0 % for all the analytes. Results of the presence of HAAs found in the river samples demonstrated levels from 0.16 µg L-1 to 0.53 µg L-1; meanwhile, in the reservoir, the levels were higher, from 0.37 µg L-1 to 0.93 µg L-1. Finally, a comparative discussion was applied in order to assess the greenness of approaches for the determination of heterocyclic aromatic amines in surface water using the available metrics.
Fil: Canales, Maria Romina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Marino Repizo, Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Reta, Mario Roberto. Universidad Nacional de La Plata; Argentina
Fil: Cerutti, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina - Materia
-
Heterocyclic aromatic amines
Solid-phase extraction
Multi-walled carbon nanotubes
Green certificate - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/104581
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Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samplesCanales, Maria RominaMarino Repizo, LeonardoReta, Mario RobertoCerutti, SoledadHeterocyclic aromatic aminesSolid-phase extractionMulti-walled carbon nanotubesGreen certificatehttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A multi-response optimization of a green and efficient solid phase extraction (SPE) sample treatment using non-modified multi-walled carbon nanotubes combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed for the quantification of ten heterocyclic aromatic amines (HAAs) in river and reservoir surface water samples. The proposed methodology was evaluated with the employment of experimental designs, which provided to greening the approach. Ultra-trace amounts of HAAs were retained into the SPE cartridge. Then, these analytes were removed from the carbon nanotubes with 0.8 mL of a mixture of acetonitrile/water with 0.1 % of formic acid. Under the optimal conditions, linearity was achieved for concentration levels ranging from 0.20 µg L-1 to 500 µg L-1, with regression coefficients (R2) from 0.990 to 0.998. Limits of detection varying from 0.06 µg L-1 and 0.23 µg L-1 were attained, the relative standard deviations (n=3) varied from 1.7 to 6.4, and extraction recoveries ranged from 90.6 % to 106.0 % for all the analytes. Results of the presence of HAAs found in the river samples demonstrated levels from 0.16 µg L-1 to 0.53 µg L-1; meanwhile, in the reservoir, the levels were higher, from 0.37 µg L-1 to 0.93 µg L-1. Finally, a comparative discussion was applied in order to assess the greenness of approaches for the determination of heterocyclic aromatic amines in surface water using the available metrics.Fil: Canales, Maria Romina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Marino Repizo, Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Reta, Mario Roberto. Universidad Nacional de La Plata; ArgentinaFil: Cerutti, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaRoyal Society of Chemistry2020-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/104581Canales, Maria Romina; Marino Repizo, Leonardo; Reta, Mario Roberto; Cerutti, Soledad; Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples; Royal Society of Chemistry; Analytical Methods; 2-20201759-9660CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2020/AY/C9AY02712Binfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:47:00Zoai:ri.conicet.gov.ar:11336/104581instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:47:00.744CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples |
title |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples |
spellingShingle |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples Canales, Maria Romina Heterocyclic aromatic amines Solid-phase extraction Multi-walled carbon nanotubes Green certificate |
title_short |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples |
title_full |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples |
title_fullStr |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples |
title_full_unstemmed |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples |
title_sort |
Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples |
dc.creator.none.fl_str_mv |
Canales, Maria Romina Marino Repizo, Leonardo Reta, Mario Roberto Cerutti, Soledad |
author |
Canales, Maria Romina |
author_facet |
Canales, Maria Romina Marino Repizo, Leonardo Reta, Mario Roberto Cerutti, Soledad |
author_role |
author |
author2 |
Marino Repizo, Leonardo Reta, Mario Roberto Cerutti, Soledad |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Heterocyclic aromatic amines Solid-phase extraction Multi-walled carbon nanotubes Green certificate |
topic |
Heterocyclic aromatic amines Solid-phase extraction Multi-walled carbon nanotubes Green certificate |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
A multi-response optimization of a green and efficient solid phase extraction (SPE) sample treatment using non-modified multi-walled carbon nanotubes combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed for the quantification of ten heterocyclic aromatic amines (HAAs) in river and reservoir surface water samples. The proposed methodology was evaluated with the employment of experimental designs, which provided to greening the approach. Ultra-trace amounts of HAAs were retained into the SPE cartridge. Then, these analytes were removed from the carbon nanotubes with 0.8 mL of a mixture of acetonitrile/water with 0.1 % of formic acid. Under the optimal conditions, linearity was achieved for concentration levels ranging from 0.20 µg L-1 to 500 µg L-1, with regression coefficients (R2) from 0.990 to 0.998. Limits of detection varying from 0.06 µg L-1 and 0.23 µg L-1 were attained, the relative standard deviations (n=3) varied from 1.7 to 6.4, and extraction recoveries ranged from 90.6 % to 106.0 % for all the analytes. Results of the presence of HAAs found in the river samples demonstrated levels from 0.16 µg L-1 to 0.53 µg L-1; meanwhile, in the reservoir, the levels were higher, from 0.37 µg L-1 to 0.93 µg L-1. Finally, a comparative discussion was applied in order to assess the greenness of approaches for the determination of heterocyclic aromatic amines in surface water using the available metrics. Fil: Canales, Maria Romina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina Fil: Marino Repizo, Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina Fil: Reta, Mario Roberto. Universidad Nacional de La Plata; Argentina Fil: Cerutti, Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina |
description |
A multi-response optimization of a green and efficient solid phase extraction (SPE) sample treatment using non-modified multi-walled carbon nanotubes combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed for the quantification of ten heterocyclic aromatic amines (HAAs) in river and reservoir surface water samples. The proposed methodology was evaluated with the employment of experimental designs, which provided to greening the approach. Ultra-trace amounts of HAAs were retained into the SPE cartridge. Then, these analytes were removed from the carbon nanotubes with 0.8 mL of a mixture of acetonitrile/water with 0.1 % of formic acid. Under the optimal conditions, linearity was achieved for concentration levels ranging from 0.20 µg L-1 to 500 µg L-1, with regression coefficients (R2) from 0.990 to 0.998. Limits of detection varying from 0.06 µg L-1 and 0.23 µg L-1 were attained, the relative standard deviations (n=3) varied from 1.7 to 6.4, and extraction recoveries ranged from 90.6 % to 106.0 % for all the analytes. Results of the presence of HAAs found in the river samples demonstrated levels from 0.16 µg L-1 to 0.53 µg L-1; meanwhile, in the reservoir, the levels were higher, from 0.37 µg L-1 to 0.93 µg L-1. Finally, a comparative discussion was applied in order to assess the greenness of approaches for the determination of heterocyclic aromatic amines in surface water using the available metrics. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-02 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/104581 Canales, Maria Romina; Marino Repizo, Leonardo; Reta, Mario Roberto; Cerutti, Soledad; Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples; Royal Society of Chemistry; Analytical Methods; 2-2020 1759-9660 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/104581 |
identifier_str_mv |
Canales, Maria Romina; Marino Repizo, Leonardo; Reta, Mario Roberto; Cerutti, Soledad; Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples; Royal Society of Chemistry; Analytical Methods; 2-2020 1759-9660 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2020/AY/C9AY02712B |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Royal Society of Chemistry |
publisher.none.fl_str_mv |
Royal Society of Chemistry |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844613465565560832 |
score |
13.070432 |