REVISTA

Farmacocinética del meloxicam via oral en dosis única y repetida en conejos

Descripción: Una dosis de 1 mg/kg VO en conejos puede ser necesaria para alcanzar concentraciones clinicamente efectivas

TITULO FUENTE ORIGINAL:

Pharmacokinetics of meloxicam in rabbits after oral administration of single and multiple doses.

AUTORES:

Fredholm DV, Carpenter JW, KuKanich B, Kohles M.

REVISTA ABREV.:

Am J Vet Res.

AÑO:

2013

REFERENCIA:

Apr;74(4):636-41.

DOI:

10.2460/ajvr.74.4.636.

FECHA DE PUBLICACIÓN:

01/04/2013

RESUMEN ORIGINAL:

OBJECTIVE:
To determine the pharmacokinetics of meloxicam (1 mg/kg) in rabbits after oral administration of single and multiple doses.
ANIMALS:
6 healthy rabbits.
PROCEDURES:
A single dose of meloxicam (1 mg/kg, PO) was administered to the rabbits. After a 10-day washout period, meloxicam (1 mg/kg, PO) was administered...
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OBJECTIVE:
To determine the pharmacokinetics of meloxicam (1 mg/kg) in rabbits after oral administration of single and multiple doses.
ANIMALS:
6 healthy rabbits.
PROCEDURES:
A single dose of meloxicam (1 mg/kg, PO) was administered to the rabbits. After a 10-day washout period, meloxicam (1 mg/kg, PO) was administered to rabbits every 24 hours for 5 days. Blood samples were obtained from rabbits at predetermined intervals during both treatment periods. Plasma meloxicam concentrations were determined, and noncompartmental pharmacokinetic analysis was performed.
RESULTS:
The mean peak plasma concentration and area under the plasma concentration-versus-time curve extrapolated to infinity after administration of a single dose of meloxicam were 0.83 μg/mL and 10.37 h•μg/mL, respectively. After administration of meloxicam for 5 days, the mean peak plasma concentration was 1.33 μg/mL, and the area under the plasma concentration-versus-time curve from the time of administration of the last dose to 24 hours after that time was 18.79 h•μg/mL. For single- and multiple-dose meloxicam experiments, the mean time to maximum plasma concentration was 6.5 and 5.8 hours and the mean terminal half-life was 6.1 and 6.7 hours, respectively.
CONCLUSIONS AND CLINICAL RELEVANCE:
Plasma concentrations of meloxicam for rabbits in the present study were proportionally higher than those previously reported for rabbits receiving 0.2 mg of meloxicam/kg and were similar to those determined for animals of other species that received clinically effective doses. A dose of 1 mg/kg may be necessary to achieve clinically effective circulating concentrations of meloxicam in rabbits, although further studies are needed.

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