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dc.contributorFacultad de Veterinariaes_ES
dc.contributor.authorMolina García, Lucía
dc.contributor.authorPérez, Jesús M.
dc.contributor.authorSarasa, Mathieu
dc.contributor.authorUreña Gutiérrez, Benjamín
dc.contributor.authorEspinosa Cerrato, José 
dc.contributor.authorAzorit, Concepción
dc.contributor.otherSanidad Animales_ES
dc.date2018
dc.date.accessioned2024-04-08T08:20:12Z
dc.date.available2024-04-08T08:20:12Z
dc.identifier.citationMolina-García, L., Pérez, J. M., Sarasa, M., Ureña-Gutiérrez, B., Espinosa, J., & Azorit, C. (2018). HPLC-QTOF method for quantifying 11-ketoetiocholanolone, a cortisol metabolite, in ruminants” feces: Optimization and validation. Ecology and Evolution, 8(18), 9218-9228. https://doi.org/10.1002/ECE3.4285es_ES
dc.identifier.issn2045-7758
dc.identifier.otherhttps://onlinelibrary.wiley.com/doi/10.1002/ece3.4285es_ES
dc.identifier.urihttps://hdl.handle.net/10612/19504
dc.descriptionThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. © 2018 The Authors. Ecology and Evolution published by John Wiley & Sons Ltdes_ES
dc.description.abstract[EN]Studies of animal ecology can benefit from a quantified understanding of eco-physiological processes and, in particular, of the physiological responses in free-ranging animals to potential stressors. The determination of fecal cortisol metabolites as a noninvasive method for monitoring stress has proved to be a powerful tool. High-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/ MS) has emerged as the most accurate method for avoiding problems related to the nonspecificity of immunoassays. In this study, we optimize and validate a reliable method using HPLC-MS/ MS for quantifying 11-ketoetiocholanolone (11-k), a representative fecal cortisol metabolite in ruminants. An appropriate extraction and purification procedure was developed taking into account the complex nature of feces. The final extract obtained was then analyzed with HPLC-MS/ MS using a quadrupole-time- of- fly (QTOF) tandem mass spectrometer with an electrospray ionization interface operating in positive mode, which allowed an unequivocal determination of the metabolite due to its accurate mass capabilities. After rigorous optimization of both sample extraction and the HPLC-QTOF parameters, making use of feces from free-ranging Iberian ibex, ideal conditions were established. Matrix-matched standards were used to calibrate the method. The limit of detection and quantification was 13-and 40-ng/ g, respectively. The validation of the method was performed with recoveries in the range of 85–110%, a figure much higher than the 60% obtained with the previous extraction methods used in our laboratory, and with relative standard deviations (RSDs) no higher than 15% for the complete analytical procedure, including extraction and analysis. The time required for the fecal 11-k analysis was greatly reduced in comparison with the previous work carried out in our laboratory. This is the first time that QTOF mass detection coupled with HPLC has been validated for 11-k quantification in feces from free-ranging ruminants such as Iberian ibex. Given the high selectivity and sensitivity attained, our method could become a useful tool for noninvasive stress quantification in ruminants.es_ES
dc.languageenges_ES
dc.publisherWiley Open Accesses_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSanidad animales_ES
dc.subjectVeterinariaes_ES
dc.subject.other11-ketoetiocholanolonees_ES
dc.subject.otherCapra pyrenaicaes_ES
dc.subject.otherFecal cortisol metaboliteses_ES
dc.subject.otherHPLC-QTOFes_ES
dc.subject.otherNoninvasive monitoringes_ES
dc.subject.otherRuminant stresses_ES
dc.subject.otherSolid phase extractiones_ES
dc.titleHPLC‐QTOF method for quantifying 11‐ketoetiocholanolone, a cortisol metabolite, in ruminants' feces: Optimization and validationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1002/ece3.4285
dc.description.peerreviewedSIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/Junta de Andalucía/Otras actuaciones de fomento de la I+D+I/RNM-118/ES/Biologia De Las Especies Cinegeticas Y Plagases_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/Junta de Andalucía/Otras actuaciones de fomento de la I+D+I/ RNM-175/ES/ Biodiversidad Y Desarrollo Sosteniblees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2045-7758
dc.journal.titleEcology and Evolutiones_ES
dc.volume.number8es_ES
dc.issue.number18es_ES
dc.page.initial9218es_ES
dc.page.final9228es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.unesco3109 Ciencias Veterinariases_ES
dc.description.projectThis study was partly funded by the Fédération Nationale des Chasseurs (France), project FNC-PSN-PR4-2013. The technical and human support provided by the CICT of Jaén University (UJA, MINECO, Junta de Andalucía, FEDER) is gratefully acknowledged. The research activities of the authors were partially supported by the PAIDI, Junta de Andalucía (RNM-118 group and RNM-175 groups), as well as by the grant P07-RNM-03087 and the European Fund for Regional Development (FEDER). This study complied with all Andalusian, Spanish and European legal requirements and guidelines regarding experimentation and animal welfare. It was approved by the Committee on Ethics of Animal Experimentation of the University of Jaén and authorized by the General Direction of Agriculture and Livestock of the Ministry of Agriculture, Fisheries and Environment of the Junta de Andalucía.es_ES


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Atribución 4.0 Internacional
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