Rapid and sensitive determination of pyrethroids indoors using active sampling followed by ultrasound-assisted solvent extraction and gas chromatography

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Analítica, Nutrición e Bromatoloxíaes_ES
dc.contributor.authorBarro Piñeiro, Ruth
dc.contributor.authorGarcía Jares, Carmen María
dc.contributor.authorLlompart Vizoso, María del Pilar
dc.contributor.authorBollaín Rodríguez, María Herminia
dc.contributor.authorCela Torrijos, Rafael
dc.date.accessioned2024-01-30T12:32:09Z
dc.date.available2024-01-30T12:32:09Z
dc.date.issued2006-02-03
dc.description.abstractA fast and simple method to analyze pyrethroids as well as other components of frequently used domestic insecticide preparations in indoor air is presented. The proposed method, based on sampling with an adsorbent followed by ultrasound-assisted solvent extraction, was developed with the aim to simplify the traditional extraction methodologies applied up to date to determine pesticides in air. The analytes were retained on a very small amount of adsorbent, which allowed using solely 1 mL of solvent for desorption. The quantification was performed by gas chromatography with microelectron-capture detection (GC–μECD) and gas chromatography coupled to mass spectrometry (GC–MS). The influence of main factors involved in the ultrasound-assisted solvent extraction step (type of adsorbent and type of solvent, solvent volume and extraction time) was studied using an experimental design approach to account for possible factor interactions. The sampling step was studied for two adsorbents (Tenax TA and Florisil), finding that 1 m3 air could be sampled without losses of analytes. In this way, the analysis of pyrethroids in air by the proposed method could be carried out within a total time shorter than an hour, including sampling. Linearity was demonstrated in a wide concentration range. Efficiency of the total sampling–extraction process was studied at several concentration levels (2, 10, 100 and 1000 ng/m3), obtaining quantitative recoveries for all compounds, with good precision (RSD < 10%). Method detection limits were below 1 ng/m3 in air when GC–μECD was employed, and about one order of magnitude higher for GC–MS. In addition, the proposed method was applied to real samples collected in contaminated closed rooms, in which some of the target compounds were determined.es_ES
dc.description.peerreviewedSIes_ES
dc.description.sponsorshipThis research was supported by the projects BQU2003-02090 from CICYT, Spanish Commission for Research and Development (Ministerio de Ciencia y Tecnologia) and PGIDIT04PXIC23701PN and PGIDIT05RAG50302PR from Xunta de Galicia. R.B. would like to acknowledge her Doctoral grant to the Xunta de Galicia.es_ES
dc.identifier.citationBarro, R., García-Jares,C., Llompart, M., Bollain, M.H., Cela, R. (2004). Rapid and sensitive determination of pyrethroids indoors using active sampling followed by ultrasound-assisted solvent extraction and gas chromatography. "Journal of Chromatography A", vol. 1111, n. 1, 1-10es_ES
dc.identifier.doi10.1016/j.chroma.2006.01.093
dc.identifier.essn1873-3778
dc.identifier.urihttp://hdl.handle.net/10347/32104
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.chroma.2006.01.093es_ES
dc.rights© 2006 Elsevier B.V. All rights reserved. doi:10.1016/j.chroma.2006.01.093es_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectPyrethroidses_ES
dc.subjectUltrasound-assisted solvent extractiones_ES
dc.subjectAir analysises_ES
dc.subjectFactorial design optimizationes_ES
dc.subjectGas chromatographyes_ES
dc.subject.classification230103 Análisis cromatográficoes_ES
dc.titleRapid and sensitive determination of pyrethroids indoors using active sampling followed by ultrasound-assisted solvent extraction and gas chromatographyes_ES
dc.typejournal articlees_ES
dc.type.hasVersionAMes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationac5f5459-2058-41f6-b5ee-934872545db8
relation.isAuthorOfPublication6bdf401d-b737-4bd0-8be1-4da6e19d0abf
relation.isAuthorOfPublicationb3faf2dc-8b5b-458e-a409-9029aaa9fed1
relation.isAuthorOfPublication.latestForDiscoveryac5f5459-2058-41f6-b5ee-934872545db8

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