Pharmacokinetic Behaviour Of Meloxicam In Loggerhead Sea Turtle (Caretta Caretta) After Im And Iv Administration

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Abstract

Data on reptile analgesia are scarce for nonsteroidal anti-inflammatory drugs (NSAIDs) and opioids and almost completely lacking in sea turtles, even though emergencies requiring correct pain management are very frequent in their rehabilitative medicine; therefore, dosage regimens extrapolated from other species involve the risk of clinical failure and damage to the animals. We describe the pharmacokinetic behavior of meloxicam in the loggerhead sea turtle (Caretta caretta). We chose meloxicam because of its selective anticyclooxygenase- 2 activity and lesser adverse side effects. No data are available on the capacity of turtles to tolerate NSAIDs, so we chose a dose of 0.1 mg/kg of meloxicam. Plasma concentrations of meloxicam were unexpectedly low both for intravenous (IV; maximum concentration [Cmax]=0.04±0.02 µg/mL) and intramuscular (IM; Cmax =0.07±0.09 µg/mL) administration. A double-peak phenomenon occurred after both IV (time for second peak concentration Tmax2 = 10.33±10.89 h) and IM (Tmax2=1.17±0.75 h). The second peak after IM injection was premature, so some difficulty and delay in absorption appears to be an appropriate explanation. Furthermore, the area under the curve, and therefore systemic bioavailability (F531.82±28.24%), after both IV (0.30±0.29) and IM (0.10±0.03) injection appeared particularly limited. Terminal elimination slope and mean residence time indicated fast elimination after IM dosing; as a consequence, plasma concentrations dropped below analytic limits in 8 h. Considering that IM is the favored route of administration of drugs in rescue centers, it is unlikely that meloxicam at 0.1 mg/kg is an appropriate choice, particularly in long-term pain management protocols

Autore Pugliese

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  • DI BELLO A.V.F.;CRESCENZO G.;CAVALIERE L.;LAI O.

Titolo volume/Rivista

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Anno di pubblicazione

2015

ISSN

0090-3558

ISBN

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Numero di citazioni Wos

6

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Settori ERC

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