Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/22952
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dc.contributor.authorGökbulut, Cengiz-
dc.contributor.authorAkşit, Dilek-
dc.contributor.authorMcKellar, Quintin A.-
dc.date.accessioned2021-12-02T09:01:19Z-
dc.date.available2021-12-02T09:01:19Z-
dc.date.issued2010-05-28-
dc.identifier.citationGökbulut, C. vd. (2010). "Comparative plasma disposition, bioavailability and efficacy of ivermectin following oral and pour-on administrations in horses". Veterinary Parasitology, 170(1-2), 120-126.en_US
dc.identifier.issn0304-4017-
dc.identifier.urihttps://doi.org/10.1016/j.vetpar.2010.01.041-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0304401710000750-
dc.identifier.urihttp://hdl.handle.net/11452/22952-
dc.description.abstractPour-on formulations of endectocides decrease the risk of injury for both user and animal, and are particularly convenient for animal owners who can apply the product. This study was designed to investigate the plasma disposition and efficacy of ivermectin (IVM) following pour-on, per os and intravenous administrations. Eighteen female horses weighing 510-610 kg were used in this study. The animals were allocated into three groups (per os, pour-on and intravenous groups). The equine paste, bovine pour-on and bovine injectable formulations of IVM were administered orally, topically and intravenously at the dose rates of 0.2, 0.5 and 0.2 mg/kg bodyweight, respectively. Heparinized blood samples and hair samples were collected at various times between 1 h and 40 days. The samples were analysed by high performance liquid chromatography with fluorescence detector. Faecal strongyle egg counts (EPG) were performed by a modified McMaster's technique before and at weekly intervals during 10 weeks after treatment. The results indicated that the plasma concentration and systemic availability of IVM was lower but the plasma persistence was prolonged after pour-on administration compared with per os route. IVM (paste) reduced the EPG by >95% for 10 weeks, whereas the reduction in pour-on group varied from 82 to 97%. EPG reduction in pour-on group was lower than that of per os group. Degradation on the application site, cutaneous biotransformation, binding of IVM to the haircoat and/or sebum are probably responsible for the relatively lower bioavailability of IVM in horses after pour-on administration. In conclusion, the poor plasma availability observed after pour-on administration could result in subtherapeutic plasma concentrations, which may promote the development of drug resistance in parasites.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHorseen_US
dc.subjectAnthelminticen_US
dc.subjectIvermectinen_US
dc.subjectPharmacokineticsen_US
dc.subjectEfficacyen_US
dc.subjectPour-onen_US
dc.subjectPer osen_US
dc.subjectHaircoaten_US
dc.subjectMoxidectinen_US
dc.subjectCattleen_US
dc.subjectGoatsen_US
dc.subjectDoramectinen_US
dc.subjectFormulationsen_US
dc.subjectProfilesen_US
dc.subjectDieten_US
dc.subjectPigen_US
dc.subjectParasitologyen_US
dc.subjectVeterinary sciencesen_US
dc.subjectAnimaliaen_US
dc.subjectBovinaeen_US
dc.subjectEquidaeen_US
dc.subject.meshAdministration, oralen_US
dc.subject.meshAdministration, topicalen_US
dc.subject.meshAnimalsen_US
dc.subject.meshAntiparasitic agentsen_US
dc.subject.meshArea under curveen_US
dc.subject.meshFecesen_US
dc.subject.meshFemaleen_US
dc.subject.meshHalf-lifeen_US
dc.subject.meshHorse diseasesen_US
dc.subject.meshHorsesen_US
dc.subject.meshInjections, intramuscularen_US
dc.subject.meshIvermectinen_US
dc.subject.meshParasite egg counten_US
dc.subject.meshStrongylida infectionsen_US
dc.subject.meshStrongylusen_US
dc.titleComparative plasma disposition, bioavailability and efficacy of ivermectin following oral and pour-on administrations in horsesen_US
dc.typeArticleen_US
dc.identifier.wos000278678500016tr_TR
dc.identifier.scopus2-s2.0-77952891372tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Veterinerlik Fakültesi/Klinik Öncesi Bilimler Bölümü.tr_TR
dc.contributor.orcid0000-0002-1817-5744tr_TR
dc.contributor.orcid0000-0003-2964-2245tr_TR
dc.identifier.startpage120tr_TR
dc.identifier.endpage126tr_TR
dc.identifier.volume170tr_TR
dc.identifier.issue1-2tr_TR
dc.relation.journalVeterinary Parasitologyen_US
dc.contributor.buuauthorÇırak, Veli Yılgör-
dc.contributor.buuauthorŞenlik, Bayram-
dc.contributor.buuauthorDurmaz, Murat-
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed20181429tr_TR
dc.subject.wosParasitologyen_US
dc.subject.wosVeterinary sciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ1 (Veterinary sciences)en_US
dc.wos.quartileQ2 (Parasitology)en_US
dc.contributor.scopusid6602404057tr_TR
dc.contributor.scopusid9332720500tr_TR
dc.contributor.scopusid16039333100tr_TR
dc.subject.scopusEprinomectin; Milbemycins; Abamectinen_US
dc.subject.emtreeIvermectinen_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeArea under the curveen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBiodegradationen_US
dc.subject.emtreeBlood samplingen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug bindingen_US
dc.subject.emtreeDrug bioavailabilityen_US
dc.subject.emtreeDrug blood levelen_US
dc.subject.emtreeDrug dispositionen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeDrug hair levelen_US
dc.subject.emtreeDrug retentionen_US
dc.subject.emtreeDrug transformationen_US
dc.subject.emtreeFeces analysisen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFluorescence analysisen_US
dc.subject.emtreeHigh performance liquid chromatographyen_US
dc.subject.emtreeHorseen_US
dc.subject.emtreeMaximum plasma concentrationen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreePasteen_US
dc.subject.emtreePlasma concentration-time curveen_US
dc.subject.emtreeSebumen_US
dc.subject.emtreeStrongyloideaen_US
dc.subject.emtreeTime to maximum plasma concentrationen_US
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