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Pharmacokinetics of fentanyl, alfentanil, and sufentanil in isoflurane-anesthetized cats.

Authors :
Pypendop BH
Brosnan RJ
Majewski-Tiedeken CR
Stanley SD
Ilkiw JE
Source :
Journal of veterinary pharmacology and therapeutics [J Vet Pharmacol Ther] 2014 Feb; Vol. 37 (1), pp. 13-7. Date of Electronic Publication: 2013 Mar 21.
Publication Year :
2014

Abstract

The aim of this study was to compare the pharmacokinetics of fentanyl, alfentanil, and sufentanil in isoflurane-anesthetized cats. Six adult cats were used. Anesthesia was induced and maintained with isoflurane in oxygen. End-tidal isoflurane concentration was set at 2% and adjusted as required due to spontaneous movement. Fentanyl (10 μg/kg), alfentanil (100 μg/kg), or sufentanil (1 μg/kg) was administered intravenously as a bolus, on separate days. Blood samples were collected immediately before and for 8 h following drug administration. Plasma drug concentration was determined using liquid chromatography/mass spectrometry. Compartment models were fitted to concentration-time data. A 3-compartment model best fitted the concentration-time data for all drugs, except for 1 cat in the sufentanil group (excluded from analysis). The volume of the central compartment and the volume of distribution at steady-state (L/kg) [mean ± SEM (range)], the clearance (mL/min/kg) [harmonic mean ± pseudo-SD (range)], and the terminal half-life (min) [median (range)] were 0.25 ± 0.04 (0.09-0.34), 2.18 ± 0.16 (1.79-2.83), 18.6 ± 5.0 (15-29.8), and 151 (115-211) for fentanyl; 0.10 ± 0.01 (0.07-0.14), 0.89 ± 0.16 (0.68-1.83), 11.6 ± 2.6 (9.2-15.8), and 144 (118-501) for alfentanil; and 0.06 ± 0.01 (0.04-0.10), 0.77 ± 0.07 (0.63-0.99), 17.6 ± 4.3 (13.9-24.3), and 54 (46-76) for sufentanil. Differences in clearance and volume of distribution result in similar terminal half-lives for fentanyl and alfentanil, longer than for sufentanil.<br /> (© 2013 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2885
Volume :
37
Issue :
1
Database :
MEDLINE
Journal :
Journal of veterinary pharmacology and therapeutics
Publication Type :
Academic Journal
Accession number :
23895731
Full Text :
https://doi.org/10.1111/jvp.12047