Electrochemical quantification of 2,6-diisopropylphenol (propofol)

Autores
Langmaier, Jan; Garay, Fernando Sebastian; Kivlehan, Francine; Chaum, Edward; Lindner, Erno
Año de publicación
2011
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
2,6-Diisopropylphenol (propofol) is a potent anesthetic drug with fast onset of the anesthetic effect and short recovery time for the patients. Outside of the United States, propofol is widely used in performing target controlled infusion anesthesia. With the long term vision of an electrochemical sensor for in vivo monitoring and feedback controlled dosing of propofol in blood, different alternatives for the electrochemical quantification of propofol using diverse working electrodes and experimental conditions are presented in this contribution.When the electrochemical oxidation of propofol takes place on a glassy carbon working electrode, an electrochemically active film grows on the electrode surface. The reduction current of the film is proportional to the propofol concentration and the accumulation time. Based on these findings a stripping analytical method was developed for the detection of propofol in acidic solutions between 0 and 30 μM, with a detection limit of 5.5 ± 0.4 μM.By restricting the scanned potential window between 0.5. V and 1.0. V in cyclic voltammetric experiments, the formation of the electrochemically active polymer can be prevented. This allowed the development of a direct voltammetric method for assessing propofol in acidic solutions between 0 and 30 μM, with a 3.2 ± 0.1 μM (n= 3) detection limit.The stripping method has a better sensitivity but somewhat worse reproducibility because the electrode surface has to be renewed between each experiment. The direct method does not require the renewal of the electrode surface between measurements but has no adequate selectivity towards the common interfering compounds. © 2011 Elsevier B.V.
Fil: Langmaier, Jan. University of Memphis; Estados Unidos. Academy of Sciences of the Czech Republic; República Checa
Fil: Garay, Fernando Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina. University of Memphis; Estados Unidos
Fil: Kivlehan, Francine. University of Memphis; Estados Unidos
Fil: Chaum, Edward. University of Tennessee; Estados Unidos
Fil: Lindner, Erno. University of Memphis; Estados Unidos
Materia
2,6-Diisopropylphenol
Anesthesia
Cyclic Voltammetry
Electrochemistry
Propofol
Target-Controlled Infusion Anesthesia
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/61593

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spelling Electrochemical quantification of 2,6-diisopropylphenol (propofol)Langmaier, JanGaray, Fernando SebastianKivlehan, FrancineChaum, EdwardLindner, Erno2,6-DiisopropylphenolAnesthesiaCyclic VoltammetryElectrochemistryPropofolTarget-Controlled Infusion Anesthesiahttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/12,6-Diisopropylphenol (propofol) is a potent anesthetic drug with fast onset of the anesthetic effect and short recovery time for the patients. Outside of the United States, propofol is widely used in performing target controlled infusion anesthesia. With the long term vision of an electrochemical sensor for in vivo monitoring and feedback controlled dosing of propofol in blood, different alternatives for the electrochemical quantification of propofol using diverse working electrodes and experimental conditions are presented in this contribution.When the electrochemical oxidation of propofol takes place on a glassy carbon working electrode, an electrochemically active film grows on the electrode surface. The reduction current of the film is proportional to the propofol concentration and the accumulation time. Based on these findings a stripping analytical method was developed for the detection of propofol in acidic solutions between 0 and 30 μM, with a detection limit of 5.5 ± 0.4 μM.By restricting the scanned potential window between 0.5. V and 1.0. V in cyclic voltammetric experiments, the formation of the electrochemically active polymer can be prevented. This allowed the development of a direct voltammetric method for assessing propofol in acidic solutions between 0 and 30 μM, with a 3.2 ± 0.1 μM (n= 3) detection limit.The stripping method has a better sensitivity but somewhat worse reproducibility because the electrode surface has to be renewed between each experiment. The direct method does not require the renewal of the electrode surface between measurements but has no adequate selectivity towards the common interfering compounds. © 2011 Elsevier B.V.Fil: Langmaier, Jan. University of Memphis; Estados Unidos. Academy of Sciences of the Czech Republic; República ChecaFil: Garay, Fernando Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina. University of Memphis; Estados UnidosFil: Kivlehan, Francine. University of Memphis; Estados UnidosFil: Chaum, Edward. University of Tennessee; Estados UnidosFil: Lindner, Erno. University of Memphis; Estados UnidosElsevier Science2011-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/61593Langmaier, Jan; Garay, Fernando Sebastian; Kivlehan, Francine; Chaum, Edward; Lindner, Erno; Electrochemical quantification of 2,6-diisopropylphenol (propofol); Elsevier Science; Analytica Chimica Acta; 704; 1-2; 10-2011; 63-670003-2670CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.aca.2011.08.003info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0003267011010774info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:53:32Zoai:ri.conicet.gov.ar:11336/61593instacron: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:34982025-10-15 14:53:33.163CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Electrochemical quantification of 2,6-diisopropylphenol (propofol)
title Electrochemical quantification of 2,6-diisopropylphenol (propofol)
spellingShingle Electrochemical quantification of 2,6-diisopropylphenol (propofol)
Langmaier, Jan
2,6-Diisopropylphenol
Anesthesia
Cyclic Voltammetry
Electrochemistry
Propofol
Target-Controlled Infusion Anesthesia
title_short Electrochemical quantification of 2,6-diisopropylphenol (propofol)
title_full Electrochemical quantification of 2,6-diisopropylphenol (propofol)
title_fullStr Electrochemical quantification of 2,6-diisopropylphenol (propofol)
title_full_unstemmed Electrochemical quantification of 2,6-diisopropylphenol (propofol)
title_sort Electrochemical quantification of 2,6-diisopropylphenol (propofol)
dc.creator.none.fl_str_mv Langmaier, Jan
Garay, Fernando Sebastian
Kivlehan, Francine
Chaum, Edward
Lindner, Erno
author Langmaier, Jan
author_facet Langmaier, Jan
Garay, Fernando Sebastian
Kivlehan, Francine
Chaum, Edward
Lindner, Erno
author_role author
author2 Garay, Fernando Sebastian
Kivlehan, Francine
Chaum, Edward
Lindner, Erno
author2_role author
author
author
author
dc.subject.none.fl_str_mv 2,6-Diisopropylphenol
Anesthesia
Cyclic Voltammetry
Electrochemistry
Propofol
Target-Controlled Infusion Anesthesia
topic 2,6-Diisopropylphenol
Anesthesia
Cyclic Voltammetry
Electrochemistry
Propofol
Target-Controlled Infusion Anesthesia
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv 2,6-Diisopropylphenol (propofol) is a potent anesthetic drug with fast onset of the anesthetic effect and short recovery time for the patients. Outside of the United States, propofol is widely used in performing target controlled infusion anesthesia. With the long term vision of an electrochemical sensor for in vivo monitoring and feedback controlled dosing of propofol in blood, different alternatives for the electrochemical quantification of propofol using diverse working electrodes and experimental conditions are presented in this contribution.When the electrochemical oxidation of propofol takes place on a glassy carbon working electrode, an electrochemically active film grows on the electrode surface. The reduction current of the film is proportional to the propofol concentration and the accumulation time. Based on these findings a stripping analytical method was developed for the detection of propofol in acidic solutions between 0 and 30 μM, with a detection limit of 5.5 ± 0.4 μM.By restricting the scanned potential window between 0.5. V and 1.0. V in cyclic voltammetric experiments, the formation of the electrochemically active polymer can be prevented. This allowed the development of a direct voltammetric method for assessing propofol in acidic solutions between 0 and 30 μM, with a 3.2 ± 0.1 μM (n= 3) detection limit.The stripping method has a better sensitivity but somewhat worse reproducibility because the electrode surface has to be renewed between each experiment. The direct method does not require the renewal of the electrode surface between measurements but has no adequate selectivity towards the common interfering compounds. © 2011 Elsevier B.V.
Fil: Langmaier, Jan. University of Memphis; Estados Unidos. Academy of Sciences of the Czech Republic; República Checa
Fil: Garay, Fernando Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina. University of Memphis; Estados Unidos
Fil: Kivlehan, Francine. University of Memphis; Estados Unidos
Fil: Chaum, Edward. University of Tennessee; Estados Unidos
Fil: Lindner, Erno. University of Memphis; Estados Unidos
description 2,6-Diisopropylphenol (propofol) is a potent anesthetic drug with fast onset of the anesthetic effect and short recovery time for the patients. Outside of the United States, propofol is widely used in performing target controlled infusion anesthesia. With the long term vision of an electrochemical sensor for in vivo monitoring and feedback controlled dosing of propofol in blood, different alternatives for the electrochemical quantification of propofol using diverse working electrodes and experimental conditions are presented in this contribution.When the electrochemical oxidation of propofol takes place on a glassy carbon working electrode, an electrochemically active film grows on the electrode surface. The reduction current of the film is proportional to the propofol concentration and the accumulation time. Based on these findings a stripping analytical method was developed for the detection of propofol in acidic solutions between 0 and 30 μM, with a detection limit of 5.5 ± 0.4 μM.By restricting the scanned potential window between 0.5. V and 1.0. V in cyclic voltammetric experiments, the formation of the electrochemically active polymer can be prevented. This allowed the development of a direct voltammetric method for assessing propofol in acidic solutions between 0 and 30 μM, with a 3.2 ± 0.1 μM (n= 3) detection limit.The stripping method has a better sensitivity but somewhat worse reproducibility because the electrode surface has to be renewed between each experiment. The direct method does not require the renewal of the electrode surface between measurements but has no adequate selectivity towards the common interfering compounds. © 2011 Elsevier B.V.
publishDate 2011
dc.date.none.fl_str_mv 2011-10
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/11336/61593
Langmaier, Jan; Garay, Fernando Sebastian; Kivlehan, Francine; Chaum, Edward; Lindner, Erno; Electrochemical quantification of 2,6-diisopropylphenol (propofol); Elsevier Science; Analytica Chimica Acta; 704; 1-2; 10-2011; 63-67
0003-2670
CONICET Digital
CONICET
url http://hdl.handle.net/11336/61593
identifier_str_mv Langmaier, Jan; Garay, Fernando Sebastian; Kivlehan, Francine; Chaum, Edward; Lindner, Erno; Electrochemical quantification of 2,6-diisopropylphenol (propofol); Elsevier Science; Analytica Chimica Acta; 704; 1-2; 10-2011; 63-67
0003-2670
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.aca.2011.08.003
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0003267011010774
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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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
dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
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repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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