Pharmacokinetics of a single dose of enrofloxacin administered orally to captive Asian elephants (Elephas maximus)

Carlos R. Sanchez Department of Animal Health, Smithsonian National Zoological Park, 3001 Connecticut Ave NW, Washington, DC 20008-2598.

Search for other papers by Carlos R. Sanchez in
Current site
Google Scholar
PubMed
Close
 DVM
,
Suzan Z. Murray Department of Animal Health, Smithsonian National Zoological Park, 3001 Connecticut Ave NW, Washington, DC 20008-2598.

Search for other papers by Suzan Z. Murray in
Current site
Google Scholar
PubMed
Close
 DVM
,
Ramiro Isaza Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610.

Search for other papers by Ramiro Isaza in
Current site
Google Scholar
PubMed
Close
 DVM, MS
, and
Mark G. Papich Department of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606.

Search for other papers by Mark G. Papich in
Current site
Google Scholar
PubMed
Close
 DVM, MS

Abstract

Objective—To determine the pharmacokinetics of enrofloxacin after oral administration to captive elephants.

Animals—6 clinically normal adult Asian elephants (Elephas maximus).

Procedure—Each elephant received a single dose of enrofloxacin (2.5 mg/kg, PO). Three elephants received their complete diet (pellets and grain) within 2 hours after enrofloxacin administration, whereas the other 3 elephants received only hay within 6 hours after enrofloxacin administration. Serum concentrations of enrofloxacin and ciprofloxacin were measured by use of high-performance liquid chromatography.

Results—Harmonic mean half-life after oral administration was 18.4 hours for all elephants. Mean ± SD peak serum concentration of enrofloxacin was 1.31 ± 0.40 µg/mL at 5.0 ± 4.2 hours after administration. Mean area under the curve was 20.72 ± 4.25 (µg × h)/mL.

Conclusions and Clinical Relevance—Oral administration of enrofloxacin to Asian elephants has a prolonged elimination half-life, compared with the elimination half-life for adult horses. In addition, potentially therapeutic concentrations in elephants were obtained when enrofloxacin was administered orally at a dosage of 2.5 mg/kg. Analysis of these results suggests that enrofloxacin administered with feed in the manner described in this study could be a potentially useful antimicrobial for use in treatment of captive Asian elephants with infections attributable to organisms, such as Bordetella spp, Escherichia coli, Mycoplasma spp, Pasteurella spp, Haemophilus spp, Salmonella spp, and Staphylococcus spp. (Am J Vet Res 2005;66:1948–1953)

Abstract

Objective—To determine the pharmacokinetics of enrofloxacin after oral administration to captive elephants.

Animals—6 clinically normal adult Asian elephants (Elephas maximus).

Procedure—Each elephant received a single dose of enrofloxacin (2.5 mg/kg, PO). Three elephants received their complete diet (pellets and grain) within 2 hours after enrofloxacin administration, whereas the other 3 elephants received only hay within 6 hours after enrofloxacin administration. Serum concentrations of enrofloxacin and ciprofloxacin were measured by use of high-performance liquid chromatography.

Results—Harmonic mean half-life after oral administration was 18.4 hours for all elephants. Mean ± SD peak serum concentration of enrofloxacin was 1.31 ± 0.40 µg/mL at 5.0 ± 4.2 hours after administration. Mean area under the curve was 20.72 ± 4.25 (µg × h)/mL.

Conclusions and Clinical Relevance—Oral administration of enrofloxacin to Asian elephants has a prolonged elimination half-life, compared with the elimination half-life for adult horses. In addition, potentially therapeutic concentrations in elephants were obtained when enrofloxacin was administered orally at a dosage of 2.5 mg/kg. Analysis of these results suggests that enrofloxacin administered with feed in the manner described in this study could be a potentially useful antimicrobial for use in treatment of captive Asian elephants with infections attributable to organisms, such as Bordetella spp, Escherichia coli, Mycoplasma spp, Pasteurella spp, Haemophilus spp, Salmonella spp, and Staphylococcus spp. (Am J Vet Res 2005;66:1948–1953)

All Time Past Year Past 30 Days
Abstract Views 44 0 0
Full Text Views 2018 1864 629
PDF Downloads 132 61 10
Advertisement