Pharmacokinetics and tissue concentrations of azithromycin in ball pythons ( Python regius )

Rob L. Coke Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506.
Present address is the San Antonio Zoo, 3903 N St Mary's St, San Antonio, TX 78212-3199.

Search for other papers by Rob L. Coke in
Current site
Google Scholar
PubMed
Close
 DVM
,
Robert P. Hunter Zoological Pharmacology Laboratory, Department of Anatomy & Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506.

Search for other papers by Robert P. Hunter in
Current site
Google Scholar
PubMed
Close
 PhD
,
Ramiro Isaza Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506.

Search for other papers by Ramiro Isaza in
Current site
Google Scholar
PubMed
Close
 DVM, MS
,
David E. Koch Department of Anatomy & Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506.

Search for other papers by David E. Koch in
Current site
Google Scholar
PubMed
Close
 MS
,
Marie A. Goatley Zoological Pharmacology Laboratory, Department of Anatomy & Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506.

Search for other papers by Marie A. Goatley in
Current site
Google Scholar
PubMed
Close
 BA
, and
James W. Carpenter Zoological Pharmacology Laboratory, Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506.

Search for other papers by James W. Carpenter in
Current site
Google Scholar
PubMed
Close
 MS, DVM

Abstract

Objective—To determine pharmacokinetics and tissue concentrations of azithromycin in ball pythons ( Python regius ) after IV or oral administration of a single dose.

Animals—2 male and 5 female ball pythons.

Procedures—Using a crossover design, each snake was given a single dose of azithromycin (10 mg/kg) IV. After a 4-week washout period, each snake was given a single dose of azithromycin (10 mg/kg) orally. Blood samples were collected prior to dose administration and 1, 3, 6, 12, 24, 48, 72, and 96 hours after azithromycin administration. Azithromycin was quantitated by use of liquid chromatography-mass spectrometry.

Results—After IV administration, azithromycin had an apparent volume of distribution of 5.69 L/kg and a plasma clearance of 0.19 L/h/kg. Harmonic means for the terminal half-life were 17 hours following IV administration and 51 hours following oral administration. Mean residence times were 37 and 94 hours following IV and oral administration, respectively. Following oral administration, azithromycin had a peak plasma concentration (Cmax) of 1.04 µg/mL, a time to Cmax of 8.4 hours, and a prolonged mean absorption time of 57 hours. Mean oral bioavailability was 77%. Tissue concentrations ranged from 4 to 140 times the corresponding plasma concentration at 24 and 72 hours after azithromycin administration.

Conclusions and Clinical Relevance—Azithromycin is well absorbed and tolerated by ball pythons. On the basis of plasma pharmacokinetics and tissue concentration data, we suggest an azithromycin dosage in ball pythons of 10 mg/kg, orally, every 2 to 7 days, depending upon the site of infection and susceptibil ity of the infective organism. (Am J Vet Res 2003;64:225–228)

Abstract

Objective—To determine pharmacokinetics and tissue concentrations of azithromycin in ball pythons ( Python regius ) after IV or oral administration of a single dose.

Animals—2 male and 5 female ball pythons.

Procedures—Using a crossover design, each snake was given a single dose of azithromycin (10 mg/kg) IV. After a 4-week washout period, each snake was given a single dose of azithromycin (10 mg/kg) orally. Blood samples were collected prior to dose administration and 1, 3, 6, 12, 24, 48, 72, and 96 hours after azithromycin administration. Azithromycin was quantitated by use of liquid chromatography-mass spectrometry.

Results—After IV administration, azithromycin had an apparent volume of distribution of 5.69 L/kg and a plasma clearance of 0.19 L/h/kg. Harmonic means for the terminal half-life were 17 hours following IV administration and 51 hours following oral administration. Mean residence times were 37 and 94 hours following IV and oral administration, respectively. Following oral administration, azithromycin had a peak plasma concentration (Cmax) of 1.04 µg/mL, a time to Cmax of 8.4 hours, and a prolonged mean absorption time of 57 hours. Mean oral bioavailability was 77%. Tissue concentrations ranged from 4 to 140 times the corresponding plasma concentration at 24 and 72 hours after azithromycin administration.

Conclusions and Clinical Relevance—Azithromycin is well absorbed and tolerated by ball pythons. On the basis of plasma pharmacokinetics and tissue concentration data, we suggest an azithromycin dosage in ball pythons of 10 mg/kg, orally, every 2 to 7 days, depending upon the site of infection and susceptibil ity of the infective organism. (Am J Vet Res 2003;64:225–228)

Advertisement