dc.creatorSarli, Macarena
dc.creatorMiró, Maria Victoria
dc.creatorRossner, Maria Victoria
dc.creatorNava, Santiago
dc.creatorLifschitz, Adrian Luis
dc.date.accessioned2022-09-15T12:04:05Z
dc.date.accessioned2023-03-15T14:17:37Z
dc.date.available2022-09-15T12:04:05Z
dc.date.available2023-03-15T14:17:37Z
dc.date.created2022-09-15T12:04:05Z
dc.date.issued2022-01
dc.identifierMacarena Sarli, María Victoria Miró, María Victoria Rossner, Santiago Nava, Adrián Lifschitz, Successive treatments with ivermectin (3.15%) to control the tick Rhipicephalus (Boophilus) microplus in cattle: Pharmacokinetic and efficacy assessment, Ticks and Tick-borne Diseases, Volume 13, Issue 1, 2022, 101848, ISSN 1877-959X, https://doi.org/10.1016/j.ttbdis.2021.101848
dc.identifier1877-959X
dc.identifierhttps://doi.org/10.1016/j.ttbdis.2021.101848
dc.identifierhttp://hdl.handle.net/20.500.12123/12889
dc.identifierhttps://www.sciencedirect.com/science/article/pii/S1877959X21002016
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6215827
dc.description.abstractThis study aimed to evaluate the pharmacokinetics, the potential accumulation in the body of treated animals and the efficacy of ivermectin long-acting formulation (3.15%) against the cattle tick Rhipicephalus (Boophilus) microplus in a scheme of three successive treatments. Fifteen 12-month-old heifers, naturally infested with R. microplus, were divided into two groups (G). Cattle from GI (n = 10) were subjected to three treatments with ivermectin 3.15% (IVOMEC GOLD®, Merial Argentina S.A.) at a rate of 1 mL/50 kg on days 0, 35, and 70. Cattle from GII (n = 5) were not treated. From day 1 to 202 post-treatment blood samples were taken to measure ivermectin concentrations by HPLC and female ticks (4.5–8 mm) were counted to evaluate the efficacy of the treatment. The level of tick resistance to ivermectin was evaluated before and after finishing the scheme of successive treatments by larval immersion test (LIT) bioassay from engorged females collected from GI. The area under the concentration vs. time curves (AUC0–35d) obtained post-second treatment was 1.51 ± 0.39-fold higher than those observed post-first treatment (P<0.05). The mean plasma concentrations of ivermectin 3.15% at 20 days after the first, second and third treatment were 17.0, 27.5 and 37.8 ng/mL, respectively (P<0.01). The elimination half-life of ivermectin post-third treatment was significantly longer than that was previously reported after a single dose (P<0.01). Values of therapeutic efficacy percentage reached 75.6% post-first treatment and between 95.9 and 100% after the second treatment. Ticks evaluated by LIT showed a significant increase in lethal concentrations after treatments. Although the efficacy level was high, the successive treatments with long-acting ivermectin formulation generate a significant accumulation of drug in plasma and could increase the levels of resistance to this drug in the tick population.
dc.languageeng
dc.publisherElsevier
dc.relationinfo:eu-repograntAgreement/INTA/2019-PE-E5-I109-001/2019-PE-E5-I109-001/AR./Convocatoria: Estudios para el control de enfermedades subtropicales y/o transmitidas por vectores (Tristeza Bovina, Garrapatas, Miasis, Tripanosomiasis, Lengua Azul y la
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.sourceTicks and Tick-borne Diseases 13 (1) : 101848 (January 2022)
dc.subjectRhipicephalus
dc.subjectResiduos de Medicamentos Veterinarios
dc.subjectIvermectina
dc.subjectMetastigmata
dc.subjectVeterinary Drug Residues
dc.subjectIvermectin
dc.subjectPharmacokinetics
dc.subjectFarmacocinética
dc.titleSuccessive treatments with ivermectin (3.15%) to control the tick Rhipicephalus (Boophilus) microplus in cattle: Pharmacokinetic and efficacy assessment
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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