Pharmacokinetics of erythromycin after intravenous, intramuscular and oral administration to cats

The aim of this study was to characterise the pharmacokinetic properties of different formulations of erythromycin in cats. Erythromycin was administered as lactobionate (4 mg/kg intravenously (IV)), base (10 mg/kg, intramuscularly (IM)) and ethylsuccinate tablets or suspension (15 mg/kg orally (PO)...

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Published inThe veterinary journal (1997) Vol. 187; no. 1; pp. 129 - 132
Main Authors Albarellos, G.A., Montoya, L., Landoni, M.F.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 2011
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Summary:The aim of this study was to characterise the pharmacokinetic properties of different formulations of erythromycin in cats. Erythromycin was administered as lactobionate (4 mg/kg intravenously (IV)), base (10 mg/kg, intramuscularly (IM)) and ethylsuccinate tablets or suspension (15 mg/kg orally (PO)). After IV administration, the major pharmacokinetic parameters were (mean ± SD): area under the curve (AUC) (0–∞) 2.61 ± 1.52 μg h/mL; volume of distribution ( V z) 2.34 ± 1.76 L/kg; total body clearance ( Cl t) 2.10 ± 1.37 L/h kg; elimination half-life ( t ½ λ ) 0.75 ± 0.09 h and mean residence time (MRT) 0.88 ± 0.13 h. After IM administration, the principal pharmacokinetic parameters were (mean ± DS): peak concentration ( C max), 3.54 ± 2.16 μg/mL; time of peak ( T max), 1.22 ± 0.67 h; t ½ λ , 1.94 ± 0.21 h and MRT, 3.50 ± 0.82 h. The administration of erythromycin ethylsuccinate (tablets and suspension) did not result in measurable serum concentrations. After IM and IV administrations, erythromycin serum concentrations were above minimum inhibitory concentration (MIC) 90 = 0.5 μg/mL for 7 and 1.5 h, respectively. However, these results should be interpreted cautiously since tissue erythromycin concentrations have not been measured and can reach much higher concentrations than in blood, which may be associated with enhanced clinical efficacy.
Bibliography:http://dx.doi.org/10.1016/j.tvjl.2009.09.019
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1090-0233
1532-2971
DOI:10.1016/j.tvjl.2009.09.019