RESUMO
Fipronil (FIP) is a broad-spectrum insecticide used in the industrial, residential and agricultural sectors, which presents environmental and human health risks. Studies report its presence in aquatic environments in several countries, but in Brazil reports are scarce. The aim of this work was to evaluate the presence of fipronil and fipronil sulfone in surface waters through a validated analytical method by LC-MS according to INMETRO and USEPA in eight sampling sites in two seasons (summer and autumn, 2020) in Guandu River basin, in the state of Rio de Janeiro. FIP was quantified in the concentration range of 0.132-2.44 µg/L, while FIP-S was detected in most samples. This is the first study on the occurrence of FIP and FIP-S in the Guandu River basin, presenting values high enough to justify the need for monitoring studies in a region of great importance for the city of Rio de Janeiro.
Assuntos
Rios , Espectrometria de Massas em Tandem , Brasil , Cromatografia Líquida de Alta Pressão , Monitoramento Ambiental , Humanos , Pirazóis , SulfonasRESUMO
BACKGROUND: Lynxacarus radovskyi is a fur mite of cats. Several classes of ectoparasiticides have shown success for treatment, including an isoxazoline. OBJECTIVES: To evaluate the efficacy of a single oral dose of sarolaner for the treatment of L. radovskyi mites in naturally infested cats. ANIMALS: Fourteen adult cats (six males and eight females), naturally infested with L. radovskyi. METHODS AND MATERIALS: Animals were randomized according to sex and average pretreatment mite count. The cats were assigned to two groups of seven cats each. The treated group received one 10 mg sarolaner tablet, corresponding to a dose of 2-4 mg/kg body weight, and the control group received no treatment. From each cat, three trichograms consisting of approximately 50 hairs each were collected from the dorsal neck, lateral thigh and perineum/tail region (total of nine samples per cat). The severity of infestation was scored on a scale of 0 (no parasites) to 4 (>50 mites) at baseline and days 7, 15, 30, 45 and 60 post-treatment. Efficacy was compared between the treatment and control groups using the arithmetic mean reduction of the mite score; results were analysed using the Kruskal-Wallis test followed by the Student-Newtman-Keuls test, with significance set at P < 5%. RESULTS: The efficacy of oral sarolaner was >95% at Day 30 post-treatment. Statistical differences were first observed between the means of the control and treated groups 15 days post-treatment. CONCLUSION: A single oral dose of sarolaner effectively eliminated L. radovskyi in most cats.
Assuntos
Azetidinas , Doenças do Gato , Infestações por Ácaros , Ácaros , Compostos de Espiro , Administração Oral , Animais , Azetidinas/uso terapêutico , Doenças do Gato/tratamento farmacológico , Gatos , Feminino , Masculino , Infestações por Ácaros/tratamento farmacológico , Infestações por Ácaros/veterinária , Compostos de Espiro/uso terapêutico , Resultado do TratamentoRESUMO
The horn fly, Haematobia irritans, is a bovine ectoparasite that causes large losses to cattle breeders, through lower meat and milk production and hide damage. Currently, the control of this parasite is mainly through chemicals. However, the indiscriminate use of these substances generates resistance. Pyriproxyfen belongs to an insect growth disruptors class with mechanisms of action for the control of immature forms of the insect. The aim of this study was to investigate the potential of pyriproxyfen administered orally to cattle for the control of the horn fly. In vitro bioassays were carried out by evaluating the number of adults emerged from 30 eggs per replicate, in triplicate, added in a substrate (fresh cattle feces) spiked with pyriproxyfen solutions in the concentration range of 2-130 ppb (ng.g-1). Probit analysis estimated LC50 value of 7.89 ppb and LC90 value of 70.08 ppb. The doses used in the in vivo evaluation were established based on the LC90 values and the anatomical and physiological aspects of the bovine digestive tract. Capsules containing pyriproxyfen at doses of 2.5 mg (G2.5) and 40 mg (G40) were produced and administered orally by bolus applicator for 12 days. The efficacy of pyriproxyfen against the immature forms of H. irritans was determined by incubating eggs in vitro in the feces collected on days 0, +3, +6, +10 and +13. Quantification of pyriproxyfen in feces was performed by UPLC-MS/MS, finding concentrations ranging from 13.4 to 22.6 ppb for G2.5 and between 268.5 to 509.0 ppb for G40. Pyriproxyfen administered orally is eliminated in the active form in the fecal mass and at a dose of 40 mg.day-1 (0.1 mg/kg/day) generates fecal concentrations able to produce 100 % prevention of adults emergence of H. irritans.
Assuntos
Muscidae , Espectrometria de Massas em Tandem , Animais , Bovinos , Cromatografia Líquida/veterinária , Óvulo , Piridinas , Espectrometria de Massas em Tandem/veterináriaRESUMO
The present study evaluated the rickettsial infection in a laboratory colony of cat fleas, Ctenocephalides felis felis (Bouche) in Brazil. All flea samples (30 eggs, 30 larvae, 30 cocoons, 30 males, and 30 females) tested by polymerase chain reaction (PCR) were shown to contain rickettsial DNA. PCR products, corresponding to the rickettsial gltA, htrA, ompA and ompB gene partial sequences were sequenced and showed to correspond to Rickettsia felis, indicating that the flea colony was 100% infected by R. felis. The immunofluorescence assay (IFA) showed the presence of R. felis-reactive antibodies in blood sera of 7 (87.5%) out of 8 cats that were regularly used to feed the flea colony. From 15 humans that used to work with the flea colony in the laboratory, 6 (40.0%) reacted positively to R. felis by IFA. Reactive feline and human sera showed low endpoint titers against R. felis, varying from 64 to 256. With the exception of one human serum, all R. felis-reactive sera were also reactive to Rickettsia rickettsii and/or Rickettsia parkeri antigens at similar titers to R. felis. The single human serum that was reactive solely to R. felis had an endpoint titer of 256, indicating that this person was infected by R. felis.
RESUMO
This study reports a case of parasitism by the giant kidney worm, Dioctophyme renale (Goeze, 1782), in the abdominal cavity of a domestic cat from Brazil. A female adult cat presenting prostration, dehydration, physical debility, pronounced jaundice and ascitis, was taken to the Department of Animal Parasitology of the Veterinary Institute of the Universidade Federal Rural do Rio de Janeiro, Brazil. Clinical signs suggested a case of peritonitis. The cat's clinical condition was grave and death occurred within a few days. During necropsy, a brownish-red nematode, 24.9cm long, was found in the abdominal cavity and was identified as a male adult D. renale. This study reports the first confirmed case of dioctophymatosis in the domestic cat. The parasite's aberrant location in the abdominal cavity suggests that the domestic cat is not a suitable host.
Assuntos
Doenças do Gato/parasitologia , Dioctophymatoidea/isolamento & purificação , Infecções por Enoplida/veterinária , Abdome/parasitologia , Animais , Brasil/epidemiologia , Doenças do Gato/epidemiologia , Doenças do Gato/patologia , Gatos , Dioctophymatoidea/classificação , Infecções por Enoplida/epidemiologia , Infecções por Enoplida/patologia , Evolução Fatal , Feminino , MasculinoRESUMO
The purpose of this study was to evaluate the overall efficacy, larval expulsion and larvicidal effect of spinosad on the treatment of myiasis caused by New World screwworm Cochliomyia hominivorax in naturally infested dogs. Six Beagle dogs presenting with myiasis were treated once with spinosad 560â¯mg, with dosages ranging from 43 to 577â¯mg/kg. Dogs were observed with 15â¯min post treatment, and with intervals of 15â¯min within the first hour followed by hourly evaluations up to six hours post-treatment. After this period, the remaining larvae were mechanically removed. Spontaneous expulsion of larvae was variable among dogs. All dogs received support treatment and were followed up for healing of the myiasis-associated lesion. On average, the highest larval expulsion occurred four hours after treatment. A single spinosad treatment had an overall efficacy of 79.7% (56.7-100%). The average larval expulsion rate was 73.3% (56.7-100%), reached its maximum within 6â¯h post-treatment, and the average larvicidal effect was only 23.7% (0-58.3%). No animal needed a second dosage 24â¯h post-treatment, lesions were completely healed within 8 days post-treatment. Despite not reaching the desirable 100% efficacy, spinosad treatment is an option in managing NSW myiasis, in conjunction with mechanical removal of maggots that remain in the lesion and support treatment.
Assuntos
Dípteros/efeitos dos fármacos , Cães/parasitologia , Inseticidas/uso terapêutico , Macrolídeos/uso terapêutico , Infecção por Mosca da Bicheira/veterinária , Animais , Combinação de Medicamentos , Fezes/parasitologia , Feminino , Inseticidas/administração & dosagem , Inseticidas/efeitos adversos , Larva/efeitos dos fármacos , Macrolídeos/administração & dosagem , Macrolídeos/efeitos adversos , Masculino , Infecção por Mosca da Bicheira/tratamento farmacológico , Infecção por Mosca da Bicheira/parasitologiaRESUMO
Fipronil is a phenylpyrazole class insecticide. It is widely used as an insecticide in agriculture and in the control of ectoparasites in veterinary medicine. The application of fipronil in an injectable form (subcutaneously) becomes an innovation, since there is no commercially available preparation containing fipronil herein. The present study aimed at fipronil usage, applied subcutaneously in cattle, to control Rhipicephalus microplus. The assessing criteria used in the research have been the construction of the plasma concentration curve and efficacy studies. A method using High Performance Liquid Chromatograph with ultraviolet detection was developed for determination of fipronil in bovine plasma samples, providing a fast and simple process with good reproducibility and low limit of quantification. The validation of the analytical method showed linearity, selectivity, precision, accuracy, sensitivity and stability, thus proving it as suitable for routine analysis. This method showed to be an important investigative tool in the analysis of fipronil plasma concentration in cattle. Fipronil administered via subcutaneous in bovine reached the systemic circulation (Cmax=378.06±137.44 ng/mL), was quickly absorbed (t(max)=10±0.87 h), and its elimination occurred slowly (t(1/2)=12 days), while maintaining quantifiable blood plasma levels (23.79±12.16 ng/mL) for up to 21 days after the treatment with a 1 mg/kg dosage. The in vivo efficacy tests proved that fipronil applied subcutaneously in a single dose of 1 mg/kg in cattle exhibited a mean efficacy of 82.41% against R. microplus. The potential of subcutaneous injection as an alternative treatment route in cattle encourage the development of an injectable formulation of fipronil.
Assuntos
Análise Química do Sangue/veterinária , Doenças dos Bovinos/tratamento farmacológico , Pirazóis/administração & dosagem , Pirazóis/sangue , Infestações por Carrapato/tratamento farmacológico , Acaricidas/administração & dosagem , Acaricidas/sangue , Acaricidas/farmacocinética , Animais , Bovinos , Cromatografia Líquida de Alta Pressão , Injeções Subcutâneas/veterinária , Masculino , Pirazóis/farmacocinética , Distribuição Aleatória , Rhipicephalus , Resultado do TratamentoRESUMO
Metarril SP Organic is a product based on the fungus Metarhizium anisopliae, which was developed for controlling agricultural pests. The present study evaluated the effect of Metarril SP Organic plus 10% mineral oil, for controlling Rhipicephalus microplus under field conditions. Three groups were formed: Control group, which received no treatment; Oil control group, which was bathed only with water, Tween 80 and mineral oil; and Metarril group, bathed in the oil-based formulation Metarril SP Organic. Two treatments per group were performed and to verify the effect of the treatments, all R. microplus ticks between 4.5 and 8.0mm in length on the left side of the cattle were counted on days +7, +14 and +21 after each treatment, and a sample of engorged females was collected for evaluation of biological parameters. The Metarril SP Organic oil formulation showed efficacy ranging from 8.53 to 90.53%. The average efficacy of the oil-based formulation of Metarril SP Organic was 75.09 and 46.59% compared with the groups Control and Oil control, respectively. There were no significant changes in biological parameters of engorged R. microplus females collected from animals. Although there was no significant difference in the amount of ticks between the Oil control and Metarril groups, it is believed that the association of mineral oil with Metarril SP Organic product is effective in R. microplus tick control in field. Thus, this association has potential to be used in strategic control programs of cattle tick.
Assuntos
Doenças dos Bovinos/parasitologia , Metarhizium/fisiologia , Rhipicephalus/microbiologia , Controle de Ácaros e Carrapatos/métodos , Animais , Bovinos , Doenças dos Bovinos/terapia , Óleo Mineral/farmacologia , Controle Biológico de Vetores , Rhipicephalus/efeitos dos fármacosRESUMO
With the increasing number of pets in home the human-animal relationship is increasingly close and care about control disease growing. Ivermectin (IVM) is frequently used because its proven safety. IVM is recommended for the treatment of demodectic scabies and prevention of heartworm in dogs, but informally is extremely used to control of Ctenocephalides felis felis and Rhipicephalus sanguineus. The aim of this study is evaluate the use of IVM in dogs, by the oral route at 0.6µg/kg dose, against experimental infection of these parasites using the construction of the plasma concentration curve and efficacy study. A IVM quantification method in canine plasma using HPLC-FL was developed and validated based on RE n°899/03 ANVISA. The samples collected during the efficacy test was analyzed by this validated method and prove Cmax of 350ng/mL at 4h (tmax) and AUC of 8411ng/h/mL. Spite of formulation have shown good absorption, the highest efficiency values found for Rhipcephalus sanguineus and Ctenocephalides felis felis were very low, 35% and 67% respectively, demonstrating this not be the most appropriate treatment for the control of these parasites.
Assuntos
Antiparasitários/farmacocinética , Ctenocephalides/efeitos dos fármacos , Doenças do Cão/prevenção & controle , Ivermectina/farmacocinética , Rhipicephalus sanguineus/efeitos dos fármacos , Administração Oral , Animais , Antiparasitários/administração & dosagem , Doenças do Cão/parasitologia , Cães , Infestações por Pulgas/prevenção & controle , Infestações por Pulgas/veterinária , Ivermectina/administração & dosagem , Ivermectina/sangue , Masculino , Infestações por Carrapato/prevenção & controle , Infestações por Carrapato/veterináriaRESUMO
The present study evaluated the efficacy of a single oral dose of doramectin in the control of Psoroptes ovis and Leporacarus gibbus in naturally infested rabbits. Sixteen adult rabbits were selected and distributed in two experimental groups. The treated group received 200 g/Kg of oral doramectin and the control group received the same volume of saline solution. The diagnosis of the mites was made with a stereoscopic microscope. Hairs from the dorsal part of the neck, lumbar right, lumbar left, ventral side of the tail and ventral abdomen were evaluated for L. gibbus, and ear wax evaluated for P. ovis. The evaluation of the efficiency and the clinical assessment of the lesions was made in days 0, +3, +7, +14, +21, +28, and +35 after treatment. An efficacy of 75% and 87,5% was observed for L. gibbus in days +3 and +7 after treatment, an efficacy of 100% was observed in days +14, + 21, +28 e +35. An efficacy of 100% for the control of P. ovis was observed following day +7. The clinical lesion score of the control group remained unaltered, except for one animal which conditions worsened during experimentation. In the treated group animals, regression of the lesions was observed following day +3, and on day +21 no signal of infestation by P. ovis was present. None of the animals from the treated group presented secondary collateral effects caused by the doramectin, which proved itself as an optimal alternative for mite control in naturally infested rabbits.(AU)
O objetivo do trabalho foi avaliar a eficácia da doramectina administrada por via oral no controle de Psoroptes ovis e Leporacarus gibbus em coelhos naturalmente infestados. Foram selecionados 16 coelhos adultos, distribuídos em dois grupos experimentais, compondo oito animais por grupo. O grupo tratado foi medicado com 200g/kg de doramectina por via oral, enquanto que no grupo controle foi administrado o mesmo volume de solução salina. O diagnóstico dos ácaros foi realizado com auxílio de microscópio estereoscópico. Foram coletados pelos das regiões do pescoço dorsal, lombar direita, lombar esquerda, cauda ventral e abdômen ventral para avaliação de L. gibbus e para P. ovis foi coletado cerúmen das orelhas com auxílio de zaragatoas. A avaliação da eficácia e a avaliação clínica das lesões, mensuradas em escores (grau 0 a 4), foi realizada nos dias 0, +3, +7, +14, +21, +28 e +35, após o tratamento. Foi observada eficácia de 75% e 87,5% no controle de L. gibbus nos dias +3 e +7 após o tratamento, sendo observada eficácia de 100% nos dias +14, + 21, +28 e +35. Foi observada eficácia de 100% no controle de P. ovis a partir do dia +7, permanecendo até o final do período observacional. O escore das lesões clínicas no grupo controle permaneceu de forma inalterada, exceto em um animal que piorou ao longo dos dias experimentais, enquanto nos animais do grupo tratado regrediu a partir do dia +3 e já no dia +21 após o tratamento, os animais apresentavam-se sem sinais da infestação por P. ovis. Nenhum animal do grupo tratado apresentou quaisquer efeitos colaterais secundários causados pela doramectina, que se mostrou uma ótima alternativa para o controle dos ácaros em coelhos naturalmente parasitados.(AU)
Assuntos
Animais , Coelhos , Psoroptidae , Ácaros e Carrapatos , Controle de Ácaros e Carrapatos/métodos , Antiparasitários/uso terapêutico , Infestações por Ácaros/terapia , Infestações por Ácaros/veterinária , Administração OralRESUMO
ABSTRACT: The present study evaluated the efficacy of a single oral dose of doramectin in the control of Psoroptes ovis and Leporacarus gibbus in naturally infested rabbits. Sixteen adult rabbits were selected and distributed in two experimental groups. The treated group received 200 g/Kg of oral doramectin and the control group received the same volume of saline solution. The diagnosis of the mites was made with a stereoscopic microscope. Hairs from the dorsal part of the neck, lumbar right, lumbar left, ventral side of the tail and ventral abdomen were evaluated for L. gibbus, and ear wax evaluated for P. ovis. The evaluation of the efficiency and the clinical assessment of the lesions was made in days 0, +3, +7, +14, +21, +28, and +35 after treatment. An efficacy of 75% and 87,5% was observed for L. gibbus in days +3 and +7 after treatment, an efficacy of 100% was observed in days +14, + 21, +28 e +35. An efficacy of 100% for the control of P. ovis was observed following day +7. The clinical lesion score of the control group remained unaltered, except for one animal which conditions worsened during experimentation. In the treated group animals, regression of the lesions was observed following day +3, and on day +21 no signal of infestation by P. ovis was present. None of the animals from the treated group presented secondary collateral effects caused by the doramectin, which proved itself as an optimal alternative for mite control in naturally infested rabbits.
RESUMO: O objetivo do trabalho foi avaliar a eficácia da doramectina administrada por via oral no controle de Psoroptes ovis e Leporacarus gibbus em coelhos naturalmente infestados. Foram selecionados 16 coelhos adultos, distribuídos em dois grupos experimentais, compondo oito animais por grupo. O grupo tratado foi medicado com 200g/kg de doramectina por via oral, enquanto que no grupo controle foi administrado o mesmo volume de solução salina. O diagnóstico dos ácaros foi realizado com auxílio de microscópio estereoscópico. Foram coletados pelos das regiões do pescoço dorsal, lombar direita, lombar esquerda, cauda ventral e abdômen ventral para avaliação de L. gibbus e para P. ovis foi coletado cerúmen das orelhas com auxílio de zaragatoas. A avaliação da eficácia e a avaliação clínica das lesões, mensuradas em escores (grau 0 a 4), foi realizada nos dias 0, +3, +7, +14, +21, +28 e +35, após o tratamento. Foi observada eficácia de 75% e 87,5% no controle de L. gibbus nos dias +3 e +7 após o tratamento, sendo observada eficácia de 100% nos dias +14, + 21, +28 e +35. Foi observada eficácia de 100% no controle de P. ovis a partir do dia +7, permanecendo até o final do período observacional. O escore das lesões clínicas no grupo controle permaneceu de forma inalterada, exceto em um animal que piorou ao longo dos dias experimentais, enquanto nos animais do grupo tratado regrediu a partir do dia +3 e já no dia +21 após o tratamento, os animais apresentavam-se sem sinais da infestação por P. ovis. Nenhum animal do grupo tratado apresentou quaisquer efeitos colaterais secundários causados pela doramectina, que se mostrou uma ótima alternativa para o controle dos ácaros em coelhos naturalmente parasitados.
RESUMO
The present study evaluated the efficacy of a single oral dose of doramectin in the control of Psoroptes ovis and Leporacarus gibbus in naturally infested rabbits. Sixteen adult rabbits were selected and distributed in two experimental groups. The treated group received 200 µg/Kg of oral doramectin and the control group received the same volume of saline solution. The diagnosis of the mites was made with a stereoscopic microscope. Hairs from the dorsal part of the neck, lumbar right, lumbar left, ventral side of the tail and ventral abdomen were evaluated for L. gibbus, and ear wax evaluated for P. ovis. The evaluation of the efficiency and the clinical assessment of the lesions was made in days 0, +3, +7, +14, +21, +28, and +35 after treatment. An efficacy of 75% and 87,5% was observed for L. gibbus in days +3 and +7 after treatment, an efficacy of 100% was observed in days +14, + 21, +28 e +35. An efficacy of 100% for the control of P. ovis was observed following day +7. The clinical lesion score of the control group remained unaltered, except for one animal which conditions worsened during experimentation. In the treated group animals, regression of the lesions was observed following day +3, and on day +21 no signal of infestation by P. ovis was present. None of the animals from the treated group presented secondary collateral effects caused by the doramectin, which proved itself as an optimal alternative for mite control in naturally infested rabbits.(AU)
O objetivo do trabalho foi avaliar a eficácia da doramectina administrada por via oral no controle de Psoroptes ovis e Leporacarus gibbus em coelhos naturalmente infestados. Foram selecionados 16 coelhos adultos, distribuídos em dois grupos experimentais, compondo oito animais por grupo. O grupo tratado foi medicado com 200µg/kg de doramectina por via oral, enquanto que no grupo controle foi administrado o mesmo volume de solução salina. O diagnóstico dos ácaros foi realizado com auxílio de microscópio estereoscópico. Foram coletados pelos das regiões do pescoço dorsal, lombar direita, lombar esquerda, cauda ventral e abdômen ventral para avaliação de L. gibbus e para P. ovis foi coletado cerúmen das orelhas com auxílio de zaragatoas. A avaliação da eficácia e a avaliação clínica das lesões, mensuradas em escores (grau 0 a 4), foi realizada nos dias 0, +3, +7, +14, +21, +28 e +35, após o tratamento. Foi observada eficácia de 75% e 87,5% no controle de L. gibbus nos dias +3 e +7 após o tratamento, sendo observada eficácia de 100% nos dias +14, + 21, +28 e +35. Foi observada eficácia de 100% no controle de P. ovis a partir do dia +7, permanecendo até o final do período observacional. O escore das lesões clínicas no grupo controle permaneceu de forma inalterada, exceto em um animal que piorou ao longo dos dias experimentais, enquanto nos animais do grupo tratado regrediu a partir do dia +3 e já no dia +21 após o tratamento, os animais apresentavam-se sem sinais da infestação por P. ovis. Nenhum animal do grupo tratado apresentou quaisquer efeitos colaterais secundários causados pela doramectina, que se mostrou uma ótima alternativa para o controle dos ácaros em coelhos naturalmente parasitados.(AU)
Assuntos
Animais , Coelhos , Ácaros e Carrapatos/efeitos dos fármacos , Antiparasitários/uso terapêutico , Psoroptidae , Controle de Ácaros e Carrapatos/métodos , Administração Oral , Infestações por Ácaros/terapia , Infestações por Ácaros/veterináriaRESUMO
This paper reports a case of furuncular myiasis caused by the human bot-fly Dermatobia hominis in a domestic cat from Brazil. A crossbred shorthaired female cat of approximately 3 years old, presented with three boil-like cutaneous lesions at the left cranioventral region of the neck. These were diagnosed as furuncular myiasis. The animal was sedated, and after shaving the fur, bot-fly larvae were removed from the lesion by digital compression. Afterwards, the wounds were treated with 10% iodine solution and also with wound-healing cream containing sulfanilamide, urea and beeswax. Maggots were identified as third-stage larvae of D hominis. Clinical case reports of human bot-fly myiasis in cats are relevant due to its scarce occurrence in feline veterinary practice in some countries.
Assuntos
Doenças do Gato/parasitologia , Dípteros/classificação , Furunculose/veterinária , Miíase/veterinária , Animais , Brasil , Gatos , Vetores de Doenças , Feminino , Furunculose/parasitologia , Humanos , Larva , Pescoço/parasitologia , Resultado do TratamentoRESUMO
The purpose of our study was to evaluate the larvicidal efficacy of nitenpyram for the treatment of screwworm myiasis caused by Cochliomyia hominivorax in naturally infested dogs. Seven Beagle dogs presenting with myiasis were treated with nitenpyram twice at an interval of 6 h. The animals received dosages between 1.43 and 4.42 mg/kg body weight of nitenpyram in each given treatment. The criteria used to determine the drug efficacy were larval expulsion and fall. These were quantified at 15 min intervals within the first hour followed by 2, 3, 4, 6, and 18 h post-treatment. The highest larval expulsion happened between 1 and 2 h post-treatment. The spontaneous larval expulsion percentages were 86% and 94.11% for 6 and 18 h after the first treatment, respectively. Larvae were expelled until 18 h post-treatment. After this period the remaining dead larvae were mechanically removed. Nitenpyram showed 100% efficacy on the treatment of myiasis by C. hominivorax in naturally infested dogs.
Assuntos
Dípteros/fisiologia , Doenças do Cão/parasitologia , Inseticidas/uso terapêutico , Miíase/veterinária , Piridinas/uso terapêutico , Animais , Dípteros/efeitos dos fármacos , Doenças do Cão/tratamento farmacológico , Cães , Inseticidas/administração & dosagem , Miíase/tratamento farmacológico , Miíase/parasitologia , Neonicotinoides , Piridinas/administração & dosagemRESUMO
The objective of the study was to evaluate the efficacy of pour-on formulations of fluazuron and ivermectin in different therapeutic protocols for treatment of demodicosis by means of quantifying mites with skin scraping, histological and clinical evaluation in dogs. Eighteen dogs with skin scrapings positive for Demodex canis were evaluated, divided into three groups. All the animals were treated every 14 days, completing 6 treatments for each animal (days 0, 14, 28, 42, 56 and 70). In group 1, pour-on 2.5% fluazuron was used at the dose of 20mg/kg; in the group 2 pour-on 2.5% fluazuron at a dose of 20 mg/kg in association with pour-on 0.5% ivermectin at the dose of 0.6mg/kg; and in group 3, pour-on 0.5% ivermectin alone was used, at the dose of 0.6mg/kg. The treatment was evaluated and monitored through skin scrapings and clinical follow-up of the lesions every 14 days for 84 days, and through histopathological examination at the end of each treatment protocol. The success rate was defined as the percentage of dogs in each group that had negative skin scrapings after the treatment: this was 16.67% for group 1, and 50% for groups 2 and 3. The reduction in mite counts reached effectiveness of 67.66%, 88.99% and 84.29% for groups 1, 2 and 3 respectively. The Wilcoxon test showed that there was a significant difference between the number of mites before and after treatment in groups 2 and 3. The histopathological examination revealed that only group 1 showed no significant difference in the intensity of infestation between days 0 and 84. Clinically, there was no significant difference between the evaluation before and after treatment in the three groups. pour-on 2.5% fluazuron and pour-on 0.5% ivermectin were not effective for treating canine demodicosis, either in association or as single therapy, when applied every 14 days for a period of 70 days. Quantification of mites using skin scrapings and histological evaluation proved to be ineffective, either one as sole therapeutic evaluation parameters, for canine demodicosis.(AU)
O objetivo do presente estudo foi avaliar a eficácia do fluazuron e da ivermectina pour-on em diferentes protocolos terapêuticos no tratamento da demodiciose, através da quantificação de ácaros por raspados cutâneos e exames histológicos, além da avaliação dos cães. Foram avaliados 18 cães com raspados cutâneos positivos para o ácaro Demodex canis, divididos em três grupos. Todos os animais foram tratados a cada 14 dias, totalizando seis tratamentos em cada cão (Dias 0, 14, 28, 42, 56 e 70). No grupo 1 foi utilizado fluazuron 2,5% pour-on na dosagem de 20mg/kg; no grupo 2 foi empregado fluazuron 2,5% pour-on na dosagem de 20mg/kg associado a ivermectina 0,5% pour-on, na dosagem de 0,6mg/kg e, no grupo 3, somente ivermectina 0,5% pour-on 0,6mg/kg. Raspados cutâneos e acompanhamento clínico das lesões foram realizados a cada 14 dias por 84 dias e realizado exame histopatológico ao final de cada protocolo terapêutico. A taxa de sucesso foi definida pela porcentagem de cães em cada grupo com raspados negativos ao final do tratamento, que foi 16,67% para o grupo 1 e 50% para os grupos 2 e 3. A redução na contagem no número de ácaros alcançou eficácia de até 67,66%; 88,99% e 84,29%, nos grupos 1, 2 e 3, respectivamente. O teste de Wilcoxon mostrou que houve diferença significativa entre a quantidade de ácaros antes e após o tratamento nos grupos 2 e 3. No exame histopatológico apenas o grupo 1 não apresentou diferença significativa na intensidade da infestação entre os dias 0 e 84. Clinicamente não houve diferença significativa entre as avaliações antes e após o tratamento dos três grupos. O fluazuron 2,5% pour-on e a ivermectina 0,5% pour-on associados ou como terapia única, não foram eficazes no tratamento da demodiciose canina, quando aplicados a cada 14 dias em um período de 70 dias. A quantificação de ácaros através do exame parasitológico em raspado cutâneo e em exame histopatológico demonstrou-se ineficaz como parâmetro isolado de avaliação pós-terapêutica para demodiciose canina.(AU)
Assuntos
Animais , Cães , Ivermectina/administração & dosagem , Ácaros/efeitos dos fármacos , Dermatopatias Parasitárias/veterinária , Administração CutâneaRESUMO
The objective of the study was to evaluate the efficacy of pour-on formulations of fluazuron and ivermectin in different therapeutic protocols for treatment of demodicosis by means of quantifying mites with skin scraping, histological and clinical evaluation in dogs. Eighteen dogs with skin scrapings positive for Demodex canis were evaluated, divided into three groups. All the animals were treated every 14 days, completing 6 treatments for each animal (days 0, 14, 28, 42, 56 and 70). In group 1, pour-on 2.5% fluazuron was used at the dose of 20mg/kg, in the group 2 pour-on 2.5% fluazuron at a dose of 20 mg/kg in association with pour-on 0.5% ivermectin at the dose of 0.6mg/kg, and in group 3, pour-on 0.5% ivermectin alone was used, at the dose of 0.6mg/kg. The treatment was evaluated and monitored through skin scrapings and clinical follow-up of the lesions every 14 days for 84 days, and through histopathological examination at the end of each treatment protocol. The success rate was defined as the percentage of dogs in each group that had negative skin scrapings after the treatment: this was 16.67% for group 1, and 50% for groups 2 and 3. The reduction in mite counts reached effectiveness of 67.66%, 88.99% and 84.29% for groups 1, 2 and 3 respectively. The Wilcoxon test showed that there was a significant difference between the number of mites before and after treatment in groups 2 and 3. The histopathological examination revealed that only group 1 showed no significant difference in the intensity of infestation between days 0 and 84. Clinically, there was no significant difference between the evaluation before and after treatment in the three groups. pour-on 2.5% fluazuron and pour-on 0.5% ivermectin were not effective for treating canine demodicosis, either in association or as single therapy, when applied every 14 days for a period of 70 days. Quantification of mites using skin scrapings and histological evaluation proved to be ineffective, either one as sole therapeutic evaluation parameters, for canine demodicosis.(AU)
O objetivo do presente estudo foi avaliar a eficácia do fluazuron e da ivermectina pour-on em diferentes protocolos terapêuticos no tratamento da demodiciose, através da quantificação de ácaros por raspados cutâneos e exames histológicos, além da avaliação dos cães. Foram avaliados 18 cães com raspados cutâneos positivos para o ácaro Demodex canis, divididos em três grupos. Todos os animais foram tratados a cada 14 dias, totalizando seis tratamentos em cada cão (Dias 0, 14, 28, 42, 56 e 70). No grupo 1 foi utilizado fluazuron 2,5% pour-on na dosagem de 20mg/kg, no grupo 2 foi empregado fluazuron 2,5% pour-on na dosagem de 20mg/kg associado a ivermectina 0,5% pour-on, na dosagem de 0,6mg/kg e, no grupo 3, somente ivermectina 0,5% pour-on 0,6mg/kg. Raspados cutâneos e acompanhamento clínico das lesões foram realizados a cada 14 dias por 84 dias e realizado exame histopatológico ao final de cada protocolo terapêutico. A taxa de sucesso foi definida pela porcentagem de cães em cada grupo com raspados negativos ao final do tratamento, que foi 16,67% para o grupo 1 e 50% para os grupos 2 e 3. A redução na contagem no número de ácaros alcançou eficácia de até 67,66%, 88,99% e 84,29%, nos grupos 1, 2 e 3, respectivamente. O teste de Wilcoxon mostrou que houve diferença significativa entre a quantidade de ácaros antes e após o tratamento nos grupos 2 e 3. No exame histopatológico apenas o grupo 1 não apresentou diferença significativa na intensidade da infestação entre os dias 0 e 84. Clinicamente não houve diferença significativa entre as avaliações antes e após o tratamento dos três grupos. O fluazuron 2,5% pour-on e a ivermectina 0,5% pour-on associados ou como terapia única, não foram eficazes no tratamento da demodiciose canina, quando aplicados a cada 14 dias em um período de 70 dias. A quantificação de ácaros através do exame parasitológico em raspado cutâneo e em exame histopatológico demonstrou-se ineficaz como parâmetro isolado de avaliação pós-terapêutica para demodiciose canina.(AU)
Assuntos
Animais , Cães , Cães/parasitologia , Ácaros , Ivermectina/administração & dosagem , Administração Cutânea , Dermatopatias Parasitárias/veterináriaRESUMO
O objetivo do trabalho foi avaliar a eficácia da ivermectina administrada por via oral no controle de Psoroptes ovis e Leporacarus gibbus em coelhos naturalmente infestados. Foram selecionados 20 coelhos adultos, distribuídos na mesma proporção de ambos os sexos, em dois grupos experimentais, compondo dez animais por grupo. No grupo controle foi administrado o mesmo volume do tratamento de solução salina, enquanto o grupo tratado recebeu dose única de ivermectina oral (400 µg/Kg). O diagnóstico dos ácaros foi realizado com auxílio de microscópio estereoscópico após a devida coleta de material. Para P. ovis foi realizada através de coleta do cerúmen com auxílio de zaragatoas efetuadas nas orelhas e para por L. gibbus foi realizada coleta de pelos nas regiões do pescoço dorsal, lombar direita, lombar esquerda, cauda ventral e abdômen ventral. A avaliação da eficácia e a avaliação clínica das lesões, mensuradas em escores (grau 0 a 4) foi realizada nos dias 0, +3, +7, +14, +21, +28 e + 35, após o tratamento. Foi observada a eficácia de 100% no controle de P. ovis a partir do dia +7 e para L. gibbus a partir do dia +14, mantendo-se negativos até o final do período experimental. O escore da lesão das orelhas do grupo tratado regrediu a partir do dia +14 e no dia +21 todos os animais atingiram grau 0. No grupo controle, dois animais apresentaram aumento no escore da lesão das orelhas, um coelho apresentou aumento do escore de grau 1 para 2 e outro coelho de grau 3 para 4. Não foram observadas quaisquer reações adversas nos animais tratados. A ivermectina administrada por via oral em dose única foi eficaz no controle de P. ovis e L. gibbus em coelhos naturalmente infestados...
The aim of the study was to evaluate the efficacy of oral ivermectin in the control of Psoroptes ovis and Leporacarus gibbus in naturally infested rabbits. Twenty adult rabbits were selected; they were distributed in two groups with equal proportions of both sexes, containing ten animals per group. In the control group the same volume of the treatment was administered of saline solution, meanwhile the treated group received a single dose of oral ivermectin (400µg/kg). The diagnosis of the mites was made with a stereoscopic microscope, after the proper collection of material. For P. ovis it was performed by collecting of ear wax with swabs and for L. gibbus it was performed by collecting hairs in the dorsal part of the neck, lumbar right, lumbar left, ventral side of the tail and ventral abdomen. The evaluation of the efficiency and the clinical evaluation of the lesions, measured in scores (grade 0 to 4) was made in days 0, +3, +7, +4, +21, +28, and +35, after treatment. An efficiency of 100% was observed for P. ovis following day +7, and for L. gibbus following day +14, remaining negative until the final day of the study. The score of lesions in the ears of the treated group regressed following day +14 and on day +21 all animals reached a score of 0. In the control group, two animals presented an increase in ear lesion score, one rabbit presented an increase from score 1 to 2, and the other rabbit, from score 3 to 4. No adverse reactions were observed in the treated animals. The single dose administration of oral ivermectin was successful in the control of P. ovis and L. gibbus in naturally infested rabbits...
Assuntos
Animais , Coelhos , Coelhos/parasitologia , Ivermectina/administração & dosagem , Psoroptidae , Infestações por Ácaros/tratamento farmacológicoRESUMO
O objetivo do trabalho foi avaliar a eficácia da ivermectina administrada por via oral no controle de Psoroptes ovis e Leporacarus gibbus em coelhos naturalmente infestados. Foram selecionados 20 coelhos adultos, distribuídos na mesma proporção de ambos os sexos, em dois grupos experimentais, compondo dez animais por grupo. No grupo controle foi administrado o mesmo volume do tratamento de solução salina, enquanto o grupo tratado recebeu dose única de ivermectina oral (400 µg/Kg). O diagnóstico dos ácaros foi realizado com auxílio de microscópio estereoscópico após a devida coleta de material. Para P. ovis foi realizada através de coleta do cerúmen com auxílio de zaragatoas efetuadas nas orelhas e para por L. gibbus foi realizada coleta de pelos nas regiões do pescoço dorsal, lombar direita, lombar esquerda, cauda ventral e abdômen ventral. A avaliação da eficácia e a avaliação clínica das lesões, mensuradas em escores (grau 0 a 4) foi realizada nos dias 0, +3, +7, +14, +21, +28 e + 35, após o tratamento. Foi observada a eficácia de 100% no controle de P. ovis a partir do dia +7 e para L. gibbus a partir do dia +14, mantendo-se negativos até o final do período experimental. O escore da lesão das orelhas do grupo tratado regrediu a partir do dia +14 e no dia +21 todos os animais atingiram grau 0. No grupo controle, dois animais apresentaram aumento no escore da lesão das orelhas, um coelho apresentou aumento do escore de grau 1 para 2 e outro coelho de grau 3 para 4. Não foram observadas quaisquer reações adversas nos animais tratados. A ivermectina administrada por via oral em dose única foi eficaz no controle de P. ovis e L. gibbus em coelhos naturalmente infestados.(AU)
The aim of the study was to evaluate the efficacy of oral ivermectin in the control of Psoroptes ovis and Leporacarus gibbus in naturally infested rabbits. Twenty adult rabbits were selected; they were distributed in two groups with equal proportions of both sexes, containing ten animals per group. In the control group the same volume of the treatment was administered of saline solution, meanwhile the treated group received a single dose of oral ivermectin (400µg/kg). The diagnosis of the mites was made with a stereoscopic microscope, after the proper collection of material. For P. ovis it was performed by collecting of ear wax with swabs and for L. gibbus it was performed by collecting hairs in the dorsal part of the neck, lumbar right, lumbar left, ventral side of the tail and ventral abdomen. The evaluation of the efficiency and the clinical evaluation of the lesions, measured in scores (grade 0 to 4) was made in days 0, +3, +7, +4, +21, +28, and +35, after treatment. An efficiency of 100% was observed for P. ovis following day +7, and for L. gibbus following day +14, remaining negative until the final day of the study. The score of lesions in the ears of the treated group regressed following day +14 and on day +21 all animals reached a score of 0. In the control group, two animals presented an increase in ear lesion score, one rabbit presented an increase from score 1 to 2, and the other rabbit, from score 3 to 4. No adverse reactions were observed in the treated animals. The single dose administration of oral ivermectin was successful in the control of P. ovis and L. gibbus in naturally infested rabbits.(AU)
Assuntos
Animais , Coelhos , Coelhos/parasitologia , Psoroptidae , Ivermectina/administração & dosagem , Infestações por Ácaros/tratamento farmacológicoRESUMO
Ctenocephalides felis felis is a flea species that parasitizes dogs and cats. The current study verified the in vitro virulence of the entomopathogenic fungi Metarhizium anisopliae and Beauveria bassiana to eggs and adults of C. felis felis. The fungal isolates were cultivated on rice grains in plastic bags. Conidial suspensions were then prepared by immersing the grains in Tween 80 aqueous solution (0.01%). Eggs and adults of C. felis felis were obtained from a laboratory colony. Experiments were composed of one control and four treatment groups (10(5), 10(6), 10(7), and 10(8) conidia mL(-1)). Both insect pathogens inhibited egg hatchability and caused adult mortality. Among isolates used in this study, M. anisopliae (isolate E9) was the most successful at inhibiting hatching, while B. bassiana (isolate 986) was the most powerful for causing mortality in adults. The results indicate that these entomopathogenic fungi have promising potential for use in controlling both C. felis felis egg and adult stages.
Assuntos
Beauveria/patogenicidade , Metarhizium/patogenicidade , Animais , Gatos , VirulênciaRESUMO
To evaluate the efficacy of a formulation with 0,5% of eprinomectin in cattle to control H. irritans, two trials were conducted for the control of H. irritans in the field in the state of Rio de Janeiro, using 0,5% of eprinomectin, at a dose rate of 500 mc g/kg body weight, corresponding to 10 mL/100 kg. The efficacies for days +7, +14, +21 e +28 after treatment were respectively 100%; 94,3%; 86,2% and 24,5% for the first study and 100%, 100%, 100%, and 0% for the second one.