Multiple solid-phase microextraction in a non equilibrium situation. Application in quantitative analysis of chlorophenols and chloroanisoles related to cork taint in wine

Multiple HS-solid-phase microextraction (MHS-SPME) is a modification of SPME developed for quantitative analysis that avoids possible matrix effects based on an exhaustive analyte extraction from the sample. In this paper, the theory of this process associated with a non-equilibrium situation has be...

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Detalles Bibliográficos
Autores: Martínez-Uruñuela, A., González-Sáiz, J.M. [0000-0002-4463-8343], Pizarro, C. [0000-0001-6450-8741]
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2005
País:España
Institución:Universidad de La Rioja (UR)
Repositorio:RIUR. Repositorio Institucional de la Universidad de La Rioja
OAI Identifier:oai:portal.dialnet.es:doc/5bbc6991b750603269e81d98
Acceso en línea:https://investigacion.unirioja.es/documentos/5bbc6991b750603269e81d98
Access Level:acceso abierto
Palabra clave:Chloroanisoles
Chlorophenols
Cork taint
GC/MS/MS
Multiple solid-phase microextraction
Wine
Descripción
Sumario:Multiple HS-solid-phase microextraction (MHS-SPME) is a modification of SPME developed for quantitative analysis that avoids possible matrix effects based on an exhaustive analyte extraction from the sample. In this paper, the theory of this process associated with a non-equilibrium situation has been presented. The application of an optimised HS-SPME-based method in the analysis of chloroanisoles and chlorophenols, previously acetylated, associated with the occurrence of cork taint in different red, white and rosé wine samples, has revealed the existence of matrix effects. This fact determines the choice of standard addition as the adequate technique for the quantification of these compounds in real samples. MHS-SPME is proposed as a good alternative technique with respect to HS-SPME because it avoids matrix effects, simplifies the quantification of these compounds in real samples and reduces analysis time, providing sensitivity below chloroanisole sensory threshold with acceptable precision. © 2005 Elsevier B.V. All rights reserved.