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1.
Am J Vet Res ; 71(9): 1062-6, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20807146

RESUMO

OBJECTIVE: To determine the pharmacokinetics and tissue distribution of minocycline in horses. ANIMALS: 5 healthy Thoroughbred mares for the pharmacokinetic experiment and 6 healthy Thoroughbred mares for the tissue distribution experiment. PROCEDURES: Each mare was given 2.2 mg of minocycline hydrochloride/kg, IV. Blood samples were collected once before minocycline administration (0 hours) and 10 times within 48 hours after administration in the pharmacokinetics study, and 24 tissue samples were obtained at 0.5 and 3 hours in the distribution study. RESULTS: No adverse effects were observed in any of the mares after minocycline administration. The mean+/-SD elimination half-life was 7.70+/-1.91 hours. The total body clearance was 0.16+/-0.04 L/h/kg, and the volume of distribution at steady state was 1.53+/-0.09 L/kg. The percentage of plasma protein binding was 68.1+/-2.6%. Plasma concentration of free minocycline was 0.12 microg/mL at 12 hours. Minocycline was not detected in brain tissue, CSF or aqueous humor at 0.5 hours; however, it was found in all tissues, except in the aqueous humor, at 3 hours. CONCLUSIONS AND CLINICAL RELEVANCE: Clearance of minocycline in healthy mares was greater than that reported for humans. For effective treatment of infections with common equine pathogens, it will be necessary to administer minocycline at a dosage of 2.2 mg/kg, IV, every 12 hours. This drug could be useful for infections in many tissues, including the CNS. The pharmacokinetic and tissue distribution data should aid in the appropriate use of minocycline in horses.


Assuntos
Minociclina/farmacocinética , Animais , Antibacterianos/sangue , Antibacterianos/farmacocinética , Peso Corporal , Feminino , Meia-Vida , Cavalos , Minociclina/sangue , Distribuição Tecidual
2.
J Vet Med Sci ; 69(3): 305-7, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17409650

RESUMO

A new enzyme immunoassay (EIA) for the measurement of furosemide in horse plasma is described. The lower limit of detection of this EIA method was 7.8 ng/ml. The intra-and inter-assay coefficients of variation ranged from 2.5% to 4.9% and 7.5% to 9.8%, respectively. Cross-reactivity with other compounds was not observed. There was a high correlation (r2=0.987) between the high-performance liquid chromatography and EIA results obtained for furosemide concentrations in horse plasma. These results indicate that the newly developed EIA method is useful for the quantitative analysis of furosemide in horse plasma.


Assuntos
Furosemida/farmacocinética , Cavalos/sangue , Técnicas Imunoenzimáticas/métodos , Técnicas Imunoenzimáticas/veterinária , Animais , Cromatografia Líquida de Alta Pressão/veterinária , Relação Dose-Resposta a Droga , Furosemida/administração & dosagem , Furosemida/sangue , Sensibilidade e Especificidade
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