dc.creatorDecundo, Julieta María
dc.creatorDieguez, Susana Nelly
dc.creatorMartínez, Guadalupe
dc.creatorRomanelli, Agustina
dc.creatorFernández Paggi, María Belén
dc.creatorPérez, Denisa Soledad
dc.creatorAmanto, Fabian A.
dc.creatorSoraci, Alejandro Luis
dc.date.accessioned2020-05-11T21:39:59Z
dc.date.accessioned2022-10-15T02:13:04Z
dc.date.available2020-05-11T21:39:59Z
dc.date.available2022-10-15T02:13:04Z
dc.date.created2020-05-11T21:39:59Z
dc.date.issued2019-07
dc.identifierDecundo, Julieta María; Dieguez, Susana Nelly; Martínez, Guadalupe; Romanelli, Agustina; Fernández Paggi, María Belén; et al.; Impact of water hardness on oxytetracycline oral bioavailability in fed and fasted piglets; Wiley Blackwell Publishing, Inc; Veterinary Medicine and Science; 5; 4; 7-2019; 517-525
dc.identifier2053-1095
dc.identifierhttp://hdl.handle.net/11336/104836
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4333925
dc.description.abstractWater hardness is a critical factor that affects oxytetracycline dissolution by chelation with cations. These interactions may lead to impaired dosing and consequently decrease absorption. Moreover, feed present in gastrointestinal tract may interact with antibiotic and alter pharmacokinetic parameters. In the present study, dissolution profiles of an oxytetracycline veterinary formulation were assessed in purified, soft and hard water. Furthermore, oxytetracycline absolute bioavailability, after oral administration of the drug dissolved in soft or hard water, was evaluated in fed and fasted piglets. A maximum dissolution of 86% and 80% was obtained in soft and hard water, respectively, while in purified water dissolution was complete. Results from in vivo study reconfirmed oxytetracycline´s very low oral bioavailability. The greatest values were attained when antibiotic was dissolved in soft water and in fasted animals. Statistically significant lower absolute bioavailability was achieved when hard water was used and/or animals were fed. Moreover, Cmax attained in all treatments was lower than MIC90 of most important swine pathogens. For these reasons, the oral use of OTC formulations, that have demonstrated low oral bioavailability, should be avoided to treat systemic diseases in pigs.
dc.languageeng
dc.publisherWiley Blackwell Publishing, Inc
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1002/vms3.185
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/epdf/10.1002/vms3.185
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBIOAVAILABILITY
dc.subjectOXYTETRACYCLINE
dc.subjectPIGLETS
dc.subjectWATER HARDNESS
dc.titleImpact of water hardness on oxytetracycline oral bioavailability in fed and fasted piglets
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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