Mostrar el registro sencillo del ítem

dc.contributor.author
Langmaier, Jan  
dc.contributor.author
Garay, Fernando Sebastian  
dc.contributor.author
Kivlehan, Francine  
dc.contributor.author
Chaum, Edward  
dc.contributor.author
Lindner, Erno  
dc.date.available
2018-10-03T19:10:15Z  
dc.date.issued
2011-10  
dc.identifier.citation
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  
dc.identifier.issn
0003-2670  
dc.identifier.uri
http://hdl.handle.net/11336/61593  
dc.description.abstract
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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
2,6-Diisopropylphenol  
dc.subject
Anesthesia  
dc.subject
Cyclic Voltammetry  
dc.subject
Electrochemistry  
dc.subject
Propofol  
dc.subject
Target-Controlled Infusion Anesthesia  
dc.subject.classification
Otras Ciencias Químicas  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Electrochemical quantification of 2,6-diisopropylphenol (propofol)  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-10-01T15:23:16Z  
dc.journal.volume
704  
dc.journal.number
1-2  
dc.journal.pagination
63-67  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Langmaier, Jan. University of Memphis; Estados Unidos. Academy of Sciences of the Czech Republic; República Checa  
dc.description.fil
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  
dc.description.fil
Fil: Kivlehan, Francine. University of Memphis; Estados Unidos  
dc.description.fil
Fil: Chaum, Edward. University of Tennessee; Estados Unidos  
dc.description.fil
Fil: Lindner, Erno. University of Memphis; Estados Unidos  
dc.journal.title
Analytica Chimica Acta  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1016/j.aca.2011.08.003  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0003267011010774