Disposition kinetic and bioavailability of florfenicol in buffalo calves

The Pharmacokinetics of florfenicol was studied in buffalo calves following single intravenous and intramuscular administration of 20 mg kg-1 b.wt. Florfenicol concentration in both serum and urine were determined by microbiological assay using Bacillus subtilis (ATCC 6633) as test organism. After i...

Full description

Bibliographic Details
Main Authors: A. A. M. El- Gendy, M. A. Tohamy, M. Ismail
Format: Article
Language:English
Published: Beni-Suef University 2005-12-01
Series:Journal of Veterinary Medical Research
Subjects:
Online Access:https://jvmr.journals.ekb.eg/article_77933.html
id doaj-41d605f5ac0f498daf5a893f759691cd
record_format Article
spelling doaj-41d605f5ac0f498daf5a893f759691cd2020-11-25T02:23:36ZengBeni-Suef University Journal of Veterinary Medical Research 2357-05122357-05202005-12-011526469 Disposition kinetic and bioavailability of florfenicol in buffalo calvesA. A. M. El- Gendy0 M. A. Tohamy1M. Ismail2Pharmacology Department, Faculty of Veterinary Medicine Beni-suef University, Beni-suef, EgyptPharmacology Department, Faculty of Veterinary Medicine Beni-suef University, Beni-suef, EgyptPharmacology Department, Faculty of Veterinary Medicine, Cairo University, Cairo, EgyptThe Pharmacokinetics of florfenicol was studied in buffalo calves following single intravenous and intramuscular administration of 20 mg kg-1 b.wt. Florfenicol concentration in both serum and urine were determined by microbiological assay using Bacillus subtilis (ATCC 6633) as test organism. After intravenous injection the serum florfenicol concentration time course obeys two-compartment open model with distribution (t0.5 ()) and elimination (t0.5 ()) half lives of 0.381 ± 0.004 and 2.89 + 0.263 h., respectively. Total body clearance (CLB) and steady state volume of distribution (Vdss) were 3.6 ± 0.30 ml kg-1 min-1 and 1.70 ± 0.010 l kg-1., respectively. After intramuscular administration the observed mean peak serum concentration (Cmax) was 2.32 ± 0.052 3g ml-1 achieved after maximum time (Tmax) of one hour postinjection. The systemic bioavailability after intramuscular administration was 27.43 % and the plasma protein binding was 13.5 %. https://jvmr.journals.ekb.eg/article_77933.htmldisposition; kinetic; bioavailability; florfenicol; buffalo calves
collection DOAJ
language English
format Article
sources DOAJ
author A. A. M. El- Gendy
M. A. Tohamy
M. Ismail
spellingShingle A. A. M. El- Gendy
M. A. Tohamy
M. Ismail
Disposition kinetic and bioavailability of florfenicol in buffalo calves
Journal of Veterinary Medical Research
disposition; kinetic; bioavailability; florfenicol; buffalo calves
author_facet A. A. M. El- Gendy
M. A. Tohamy
M. Ismail
author_sort A. A. M. El- Gendy
title Disposition kinetic and bioavailability of florfenicol in buffalo calves
title_short Disposition kinetic and bioavailability of florfenicol in buffalo calves
title_full Disposition kinetic and bioavailability of florfenicol in buffalo calves
title_fullStr Disposition kinetic and bioavailability of florfenicol in buffalo calves
title_full_unstemmed Disposition kinetic and bioavailability of florfenicol in buffalo calves
title_sort disposition kinetic and bioavailability of florfenicol in buffalo calves
publisher Beni-Suef University
series Journal of Veterinary Medical Research
issn 2357-0512
2357-0520
publishDate 2005-12-01
description The Pharmacokinetics of florfenicol was studied in buffalo calves following single intravenous and intramuscular administration of 20 mg kg-1 b.wt. Florfenicol concentration in both serum and urine were determined by microbiological assay using Bacillus subtilis (ATCC 6633) as test organism. After intravenous injection the serum florfenicol concentration time course obeys two-compartment open model with distribution (t0.5 ()) and elimination (t0.5 ()) half lives of 0.381 ± 0.004 and 2.89 + 0.263 h., respectively. Total body clearance (CLB) and steady state volume of distribution (Vdss) were 3.6 ± 0.30 ml kg-1 min-1 and 1.70 ± 0.010 l kg-1., respectively. After intramuscular administration the observed mean peak serum concentration (Cmax) was 2.32 ± 0.052 3g ml-1 achieved after maximum time (Tmax) of one hour postinjection. The systemic bioavailability after intramuscular administration was 27.43 % and the plasma protein binding was 13.5 %.
topic disposition; kinetic; bioavailability; florfenicol; buffalo calves
url https://jvmr.journals.ekb.eg/article_77933.html
work_keys_str_mv AT aamelgendy dispositionkineticandbioavailabilityofflorfenicolinbuffalocalves
AT matohamy dispositionkineticandbioavailabilityofflorfenicolinbuffalocalves
AT mismail dispositionkineticandbioavailabilityofflorfenicolinbuffalocalves
_version_ 1724858623276875776