Abstract |
The pharmacokinetic properties of norfloxacin-glycine acetate (NFLXGA) were determined in six horses following a single intravenous (i.v.) and intramuscular (i.m.) dose of 4 mgkg(-1) body weight. Following i.v. and i.m. administration, the plasma drug concentrations were best fitted by an open two-compartment model with a rapid distribution phase. After i.v. NFLXGA administration, the distribution (t(1/2alpha)) and elimination half-life (t(1/2beta)) were 0.42 (0.05) and 5.44 (1.36)h. The volume of distribution of NFLXGA at steady state (Vd(ss)) was 2.19 (0.53) Lkg(-1). After NFLXGA i.m. administration, the maximal absorption concentration (C(max)) was 0.44 (0.04) microgml(-1) at 0.86 (0.15)h (T(max)). The mean absorption (t(1/2ka)) and elimination half-life (t(1/2beta)) of NFLXGA were 0.27 (0.07) and 9.47 (2.24)h, respectively. The mean systemic bioavailability (F) following i.m. administration was 55 (12)%. The optimal dosage for each administration route was calculated from the pharmacokinetic data on the basis of the area under the inhibitory plasma concentration-time curve (AUIC) every 24h and was found to be 13.36 and 7.35 mgkg(-1) for i.m. and i.v. administration, respectively.
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Authors | S-C Park, H-I Yun |
Journal | Research in veterinary science
(Res Vet Sci)
Vol. 74
Issue 1
Pg. 79-83
(Feb 2003)
ISSN: 0034-5288 [Print] England |
PMID | 12507569
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Infective Agents
- Fluoroquinolones
- norfloxacin-glycine acetate
- Norfloxacin
- Glycine
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Topics |
- Absorption
- Animals
- Anti-Infective Agents
(administration & dosage, blood, pharmacokinetics)
- Area Under Curve
- Biological Availability
- Cross-Over Studies
- Fluoroquinolones
- Glycine
(administration & dosage, analogs & derivatives, blood, pharmacokinetics)
- Half-Life
- Horses
(metabolism)
- Injections, Intramuscular
- Injections, Intravenous
- Male
- Norfloxacin
(administration & dosage, analogs & derivatives, blood, pharmacokinetics)
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