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Plasma and peritoneal fluid concentrations of ceftriaxone after intravenous and intraperitoneal administration in horses

dc.contributor.authorAlonso, J. M. [UNESP]
dc.contributor.authorPeccinini, R. G. [UNESP]
dc.contributor.authorCampos, M. L. [UNESP]
dc.contributor.authorNitta, T. Y. [UNESP]
dc.contributor.authorAkutagawa, T. Y.M. [UNESP]
dc.contributor.authorCrescencio, A. P. [UNESP]
dc.contributor.authorAlves, A. L.G. [UNESP]
dc.contributor.authorRodrigues, C. A. [UNESP]
dc.contributor.authorWatanabe, M. J. [UNESP]
dc.contributor.authorHussni, C. A. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:18:09Z
dc.date.available2018-12-11T17:18:09Z
dc.date.issued2018-04-01
dc.description.abstractIntraperitoneal (IP) use of antimicrobial agents may lead to therapeutic effects with better clinical results than intravenous (IV) administration. The aim of this study was to compare plasma and peritoneal fluid concentrations of ceftriaxone after IP and IV administration in horses, and to evaluate possible adverse effects. One group of five horses received 25 mg/kg ceftriaxone diluted in 1 L saline solution by IP catheter once daily for 5 days, while a second group of five horses received 25 mg/kg ceftriaxone diluted in 250 mL saline solution by IV injection once daily for 5 days and 1 L saline solution by IP catheter once daily for 5 days. Peritoneal fluid and plasma were collected to determine ceftriaxone concentrations after the first and fifth administration. IP administration of ceftriaxone resulted in concentrations above a minimum inhibitory concentration (MIC) of 1 μg/mL for 24 h in peritoneal fluid and for 12 h in plasma, while IV administration of ceftriaxone resulted in lower peritoneal fluid concentrations, which remained above a MIC of 1 μg/mL for 12 h in peritoneal fluid and 10 h in plasma. No adverse effects were observed. Comparisons of ceftriaxone concentrations, time of occurrence of the maximum (Tmax) and minimum (Tmin) concentrations, and the mean residence time (MRT), between the two groups showed that IP administration provided greater availability of cephalosporin in peritoneal fluid. The IP use of ceftriaxone (25 mg/kg diluted in 1 L saline solution once daily) may be useful for the prophylaxis and/or treatment of peritonitis in horses.en
dc.description.affiliationDepartment of Veterinary Surgery and Anaesthesiology São Paulo State University (UNESP) School of Veterinary Medicine and Animal Science
dc.description.affiliationDepartment of Natural Active Principles and Toxicology São Paulo State University (UNESP) School of Pharmaceutical Sciences
dc.description.affiliationUnespDepartment of Veterinary Surgery and Anaesthesiology São Paulo State University (UNESP) School of Veterinary Medicine and Animal Science
dc.description.affiliationUnespDepartment of Natural Active Principles and Toxicology São Paulo State University (UNESP) School of Pharmaceutical Sciences
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCNPq: 309254/2015-9
dc.format.extent72-76
dc.identifierhttp://dx.doi.org/10.1016/j.tvjl.2018.02.006
dc.identifier.citationVeterinary Journal, v. 234, p. 72-76.
dc.identifier.doi10.1016/j.tvjl.2018.02.006
dc.identifier.file2-s2.0-85042331001.pdf
dc.identifier.issn1532-2971
dc.identifier.issn1090-0233
dc.identifier.scopus2-s2.0-85042331001
dc.identifier.urihttp://hdl.handle.net/11449/175918
dc.language.isoeng
dc.relation.ispartofVeterinary Journal
dc.relation.ispartofsjr0,979
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectCeftriaxone
dc.subjectEquine
dc.subjectIntraperitoneal
dc.subjectIntravenous
dc.subjectMinimum inhibitory concentration
dc.titlePlasma and peritoneal fluid concentrations of ceftriaxone after intravenous and intraperitoneal administration in horsesen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes7773733250141398[7]
unesp.author.lattes6020984937849801[10]
unesp.author.lattes4663463575469428[8]
unesp.author.orcid0000-0001-9092-7819[7]
unesp.author.orcid0000-0001-5421-2904[10]
unesp.author.orcid0000-0002-4837-463X[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária e Zootecnia, Botucatupt
unesp.departmentPrincípios Ativos Naturais e Toxicologia - FCFpt
unesp.departmentCirurgia e Anestesiologia Veterinária - FMVZpt

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