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dc.contributor.authorSantos, Gabriela Carmelinda Martins dos
dc.date.accessioned2023-12-21T18:44:24Z-
dc.date.available2023-12-21T18:44:24Z-
dc.date.issued2021-08-27
dc.identifier.citationSANTOS, Gabriela Carmelinda Martins dos. Perfil farmacocinético e eficácia contra Ctenocephalides felis felis e Rhipicephalus sanguineus do fipronil administrado pela via oral em cães. 2021. 77 f. Tese (Doutorado em Ciências Veterinárias, Biotecnologia e Inovação Tecnológica em Medicina Veterinária) - Instituto de Veterinária, Departamento de Parasitologia Animal, Universidade Federal Rural do Rio de Janeiro, Seropédica, RJ, 2021.por
dc.identifier.urihttps://rima.ufrrj.br/jspui/handle/20.500.14407/9791-
dc.description.abstractO fipronil (FIP) é um ectoparasiticida da classe dos fenilpirazóis, usado na medicina veterinária sob a forma tópica. Apoiado pelas evidências da exposição humana não controlada ao FIP e aos danos ambientais causados a partir das formulações disponíveis no mercado, o seu uso como um fármaco para administração oral tem-se tornado promissor. Nesse estudo, a eficácia do FIP contra a pulga Ctenocephalides felis felis e o carrapato Rhipicephalus sanguineus e a sua farmacocinética e a do seu principal metabólito ativo, a fipronil-sulfona (SULF), foram avaliadas após a administração oral de comprimidos em três diferentes doses (2, 4 e 6 mg/kg) em cães da raça Beagle, em um único tratamento. Nas doses de 4 mg/kg (AUC0-t= 442,39 ± 137,35 µg/mL*h) e 6 mg/kg (AUC0-t= 421,32 ± 102,84 µg/mL*h), foi possível observar percentuais de eficácia médios de 100 e 99% para a pulga e de 95 e 98% para o carrapato, respectivamente, 48h após o tratamento. Nas três doses testadas nesse estudo, o FIP apresentou perfil de rápida absorção e metabolização e lenta eliminação. Os valores de Cmax (β = 0,7653) e AUC0-t (β = 0,3209) não aumentaram proporcionalmente com o aumento da dose. As CE90 estimadas para FIP + SULF foram de 1,30 µg/mL para C. felis felis e 2,16 µg/mL para R. sanguineus. A correlação dos dados farmacocinéticos e de eficácia do FIP deste estudo demonstrou o seu potencial para ser administrado via oral na forma de comprimidos para o controle de ectoparasitas em cães, encorajando o desenvolvimento de uma nova formulação, como uma alternativa mais segura para os animais, seres humanos e o meio ambiente, alinhado ao conceito de Saúde Única.por
dc.description.sponsorshipCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superiorpor
dc.formatapplication/pdf*
dc.languageporpor
dc.publisherUniversidade Federal Rural do Rio de Janeiropor
dc.rightsAcesso Abertopor
dc.subjectFenilpirazóispor
dc.subjectOralpor
dc.subjectFarmacocinéticapor
dc.subjectDosepor
dc.subjectEficáciapor
dc.subjectEctoparasitospor
dc.subjectPhenylpyrazoleseng
dc.subjectPharmacokineticseng
dc.subjectEfficacyeng
dc.subjectEctoparasiteseng
dc.titlePerfil farmacocinético e eficácia contra Ctenocephalides felis felis e Rhipicephalus sanguineus do fipronil administrado pela via oral em cãespor
dc.title.alternativePharmacokinetic profile and efficacy against Ctenocephalides felis felis and Rhipicephalus sanguineus of fipronil administered orally in dogseng
dc.typeTesepor
dc.description.abstractOtherFipronil (FIP) is an ectoparasiticide of the phenylpyrazole class, used in veterinary medicine in topical form. Supported by evidence of uncontrolled human exposure to FIP and environmental damage caused by commercially available formulations, its use as a medicine for oral administration has become promising. In this study, the effectiveness of FIP against the flea Ctenocephalides felis felis and the tick Rhipicephalus sanguineus and its pharmacokinetics and its main active metabolite, fipronil sulfone (SULF), were evaluated after oral administration of tablets in three different doses (2, 4 and 6 mg/kg) in Beagle dogs, in a single treatment. At doses of 4 mg/kg (AUC0-t= 442.39 ± 137.35 µg/mL*h) and 6 mg/kg (AUC0-t= 421.32 ± 102.84 µg/mL*h), it was possible to observe mean efficacy percentages of 100 and 99% for the flea and 95 and 98% for the tick, respectively, 48h after treatment. In the three doses tested in this study, FIP showed a profile of rapid absorption and metabolism and slow elimination. The values of Cmax (β = 0.7653) and AUC0-t (β = 0.3209) did not increase proportionally with increasing dose. The estimated EC90 for FIP + SULF was 1.30 µg/mL for C. felis felis and 2.16 µg/mL for R. sanguineus. The correlation of the FIP pharmacokinetic and efficacy data demonstrated its potential to be administered orally in the form of tablets for the control of ectoparasites in dogs, as a safer alternative for animals, humans and environment, aligned with the One Health concept.eng
dc.contributor.advisor1Cid, Yara Peluso
dc.contributor.advisor1ID055.357.316-09por
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/0788912635109182por
dc.contributor.advisor-co1Scott, Fabio Barbour
dc.contributor.advisor-co1ID001.382.167-97por
dc.contributor.referee1Cid, Yara Peluso
dc.contributor.referee2Azevedo, Thais Ribeiro Correia
dc.contributor.referee3Cortes, Wellington da Silva
dc.contributor.referee4Klafke, Guilherme Marcondes
dc.contributor.referee5Sarcinelli, Michelle Alvares
dc.creator.ID082.988.956-65por
dc.creator.Latteshttp://lattes.cnpq.br/2717141139032580por
dc.publisher.countryBrasilpor
dc.publisher.departmentInstituto de Veterináriapor
dc.publisher.initialsUFRRJpor
dc.publisher.programPrograma de Pós-Graduação em Ciências Veterináriaspor
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