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1.
Vet Parasitol Reg Stud Reports ; 47: 100968, 2024 01.
Article in English | MEDLINE | ID: mdl-38199704

ABSTRACT

The present work evaluated the pharmacokinetics and efficacy of the association of 15cmg/kg toltrazuril +5cmg/kg fenbendazole against Eimeria spp. and gastrointestinal nematodes (GINs) in calves of different regions of Brazil (Center-West, Southeast, and South). A total of seven experiments were carried out, five of which determined formulation efficacy against Eimeria spp., considering the following aspects: therapeutic, preventive, metaphylactic, and residual efficacy. Therapeutic efficacy experiments for GINs were carried out by parasitological necropsy. The toltrazuril + fenbendazole association demonstrated ≥95% efficacy against Eimeria spp. for 21 days post-treatment (DPT). When used preventively and metaphylatically, the same association demonstrated ≥97% efficacy against E. zuernii, E. ellipsoidalis, E. cylindrica, E. bovis, E. wyomingensis and E. auburnensis. Toltrazuril + fenbendazole administered seven days before challenge was 100% effective against all these Eimeria species. Results of therapeutic, preventive, metaphylactic and residual efficacies can be related to the pharmacokinetic results, especially considering toltrazuril sulfone, which was detected in animal plasma for a longer period than the parent compound. Toltrazuril + fenbendazole achieved 100% anthelminthic efficacy against the GINs Haemonchus placei (L4), Cooperia pectinata and Oesophagostomum radiatum; 99.94% against adult H. placei; and 99.98% against C. puntacta. The association of toltrazuril + fenbendazole, associated with other measures, is an important and suitable tool for the control and treatment of Eimeria spp. and GINs in young cattle.


Subject(s)
Eimeria , Haemonchus , Animals , Cattle , Fenbendazole/therapeutic use , Triazines/therapeutic use
2.
PLoS Negl Trop Dis ; 16(3): e0010251, 2022 03.
Article in English | MEDLINE | ID: mdl-35286319

ABSTRACT

The sand flea Tunga penetrans is one of the zoonotic agents of tungiasis, a parasitic skin disease of humans and animals. The dog is one of its main reservoirs. This negatively controlled, randomized, double-masked clinical trial evaluated the therapeutic and residual efficacy of fluralaner for treatment of dogs naturally infested with T. penetrans. Sixty-two dogs from an endemically affected community in Brazil were randomly assigned to either receive oral fluralaner (Bravecto chewable tablets) at a dose of 25 to 56 mg fluralaner/kg body weight, or no treatment (31 dogs per group). Dogs were clinically examined using a severity score for acute canine tungiasis (SCADT), parasitological examinations as defined by the Fortaleza classification, and pictures of lesions on days 0 (inclusion and treatment), 7 ± 2, 14 ± 2, 21 ± 2, 28 ± 2, 60 ± 7, 90 ± 7, 120 ± 7 and 150 ± 7. The percentage of parasite-free dogs after treatment was >90% between days 14 and 90 post-treatment with 100% efficacy on study days 21, 28 and 60. Sand flea counts on fluralaner treated dogs were significantly lower (p<0.025) than control dogs on all counts from day 7 to 120. The number of live sand fleas on treated dogs was reduced by > 90% on day 7, > 95% on days 14 and 90, and 100% from day 21 to 60, and with a significant difference between groups from day 7 to 120. From day 7 to day 120, mean SCADT scores were significantly reduced in treated dogs with a mean of 0.10 compared to 1.54 on day 120 in untreated dogs. Therefore, a single oral fluralaner administration is effective for treating and achieving long lasting (> 12 weeks) prevention for tungiasis in dogs.


Subject(s)
Dog Diseases , Insecticides , Tungiasis , Animals , Brazil/epidemiology , Dog Diseases/parasitology , Dogs , Insecticides/therapeutic use , Isoxazoles , Tunga , Tungiasis/drug therapy , Tungiasis/epidemiology , Tungiasis/veterinary
3.
Parasitol Int ; 66(5): 627-634, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28527785

ABSTRACT

The present work consisted of eight studies to evaluate the ectoparasiticidal spectrum and determine the pharmacokinetic parameters of a pour-on combination of fipronil 1.25mg/kg+fluazuron 2.5mg/kg for cattle against Rhipicephalus microplus, Haematobia irritans and the larvae of Dermatobia hominis and Cochliomyia hominivorax. The analysis fipronil and fluazuron were performed by liquid chromatography using a mass detector for the detection and quantification of analytes (LC-MS/MS). Additionally, in two of these studies, the animals were artificially infested with R. microplus ticks (stall tests), and the efficacy of this formulation was compared with that of two other standalone pour-on formulations of fipronil 1.0mg/kg and fluazuron 2.5mg/kg. In the two stall studies, 28 calves were artificially infested with 5000 R. microplus (different strains), and daily collections of all of the engorged female ticks that detached from each calf were performed until 60 and 100days post-treatment (dpt). For the R. microplus field trials, 20 bovines were selected by counting the semi-engorged females, and the therapeutic and residual efficacy was evaluated by taking tick counts at 3, 7, 14, 21, 28, 35, 42, 49 and 56dpt. Forty bovines that were naturally infested with Dermatobia hominis larvae were selected, and the numbers of larvae were counted by visual and tactile inspection on 3, 7, 14, 28, 35, 42 and 49dpt. To address the efficacy on C. hominivorax larvae, two circular skin incisions (one on each side of the body) measuring approximately 4cm in diameter each were made in 12 crossbred calves, and the natural exposure of the lesions to C. hominivorax infestations was then allowed. The incisions from the 12 animals were carefully examined daily from 1 to 10dpt. Based on the PK results obtained for this pour-on combination containing fipronil 1.25mg/kg+fluazuron 2.5mg/kg, the maximum concentrations (Cmax) and the half-lives (T1/2) of these two active ingredients were detected on days 2, 5/6 and 19 (±2)/24, 4 (±3.5) days for fipronil and fluazuron, respectively. Furthermore, the combination showed higher therapeutic and residual efficacy against R. microplus (P≤0.05) when compared with commercial standalone formulations that were administered separately. A high efficacy for this new combination was also found against C. hominivorax and D. hominis larvae (efficacy≥99%). This study's results show that the combination of these two active ingredients, as opposed to their separate use, could represent a tool for extending the life cycle of these two molecules against cattle ectoparasites, especially R. microplus. Further studies would be desirable to further confirm this.


Subject(s)
Cattle Diseases/parasitology , Ectoparasitic Infestations/veterinary , Muscidae/drug effects , Phenylurea Compounds/pharmacokinetics , Pyrazoles/pharmacokinetics , Rhipicephalus/drug effects , Animals , Cattle , Cattle Diseases/drug therapy , Drug Compounding , Drug Therapy, Combination , Ectoparasitic Infestations/drug therapy , Ectoparasitic Infestations/parasitology , Female , Larva/drug effects , Phenylurea Compounds/administration & dosage , Phenylurea Compounds/therapeutic use , Pyrazoles/administration & dosage , Pyrazoles/therapeutic use , Tick Infestations/drug therapy , Tick Infestations/parasitology
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