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dc.contributor.authorMartínez, José-
dc.contributor.authorHernandis, Verónica-
dc.contributor.authorBadillo, Elena-
dc.contributor.authorEscudero, Elisa-
dc.contributor.authorYuste Pérez, María Teresa-
dc.contributor.authorGalecio, Juan Sebastián-
dc.contributor.authorMarín, Pedro-
dc.date.accessioned2025-02-11T11:27:34Z-
dc.date.available2025-02-11T11:27:34Z-
dc.date.issued2024-12-17-
dc.identifier.citationActa Veterinaria-Beograd 2024, 74 (4), 511-522es
dc.identifier.urihttp://hdl.handle.net/10201/150249-
dc.description© 2024 The authors This document is the published version of a published work that appeared in final form in Acta Veterinaria-Beogra. . This document is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0 To access the final edited and published work see: http://dx.doi.org/10.2478/acve-2024-0035-
dc.description.abstractDoxycycline is an antimicrobial agent used in veterinary medicine to treat a variety of bacterial infections. To date, no analytical technique utilising HPLC with fl uorescence detection has been documented for the quantifi cation of doxycycline concentrations in goat plasma or milk. Consequently, the objective of the present study was to propose a rapid HPLC assay with fl uorescence detection for the quantifi cation of doxycycline in the aforementioned samples, thereby facilitating the conduct of pharmacokinetic studies and the detection of residues in diverse goat tissues. Proteins were precipitated with methanol and trifl uoroacetic acid in a single step. Doxycycline was separated on a XBRIDGE C18 column using an isocratic method. Sample volume injected into the HPLC system was 50 µl. Fluorescence detection was conducted with an excitation wavelength of 380 nm and an emission wavelength of 520 nm. The retention times of doxycycline and danofl oxacin (internal standard) were determined to be 8.0 and 5.5 minutes, respectively. The calibration curves for plasma and milk exhibited linearity over the concentration range of 0.1 to 2 μg/mL. The limit of detection was 0.065 μg/ mL, while the limit of quantifi cation was 0.1 μg/mL in both matrices. The accuracy and precision of the method were consistently within the limits of 10.9% for plasma and 10.5% for milk. The fi ndings of this study may be employed in the quantifi cation of doxycycline in goat plasma and milk, thus facilitating the conduct of pharmacokinetic studies.es
dc.formatapplication/pdfes
dc.format.extent12es
dc.languageenges
dc.relationSin financiación externa a la Universidades
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectDoxycyclinees
dc.subjectFluorescencees
dc.subjectHPLCes
dc.subjectMilkes
dc.subjectPlasmaes
dc.titleA Fast and Accurate Method for the Quantification of Doxycycline in Goat Plasma and Milk by HPLC Using a Fluorescence Detectores
dc.typeinfo:eu-repo/semantics/articlees
dc.relation.publisherversionhttps://sciendo.com/article/10.2478/acve-2024-0035-
dc.identifier.doihttp://dx.doi.org/10.2478/acve-2024-0035-
dc.contributor.departmentDepartamento de Farmacología-
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