Iranian journal of pharmacology & therapeutics · 2005 · 10 citations · 8 references
PharmacyPharmacokineticsPharmacologyBioavailabilityDrug ClearancePharmacokinetic ModelingArea Under The CurveDrug DispositionDrug Half-lifeHalf-life EstimationPharmacokinetics Of AntimicrobialsArea Under The Plasma Concentration-time CurveDrug Elimination Half-lifeFirst-order Elimination KineticsHigh-performance Liquid ChromatographyIntramuscular Medication AdministrationPharmacokinetic Parameter AnalysisPharmacokinetic ParametersPlasma Concentration - Time Profile
The pharmacokinetic studies of enrofloxacin were investigated in yak (Bos grunniens L.) after administration of enrofloxacin by intramuscular route at 5 mg⋅kg -1 body weight. Blood samples were collected from the jugular vein at predetermined time intervals after drug administration. Plasma was separated and analysed for enrofloxacin by reverse-phase high performance liquid chromatography. Various pharmacokinetic parameters were calculated using a non-compartmental model. The elimination half-life (t½), area under plasma concentration-time curve (AUC), area under the moment curve (AUMC), mean residence time (MRT), apparent volume of distribution (Vd), total body clearance (ClB) and apparent first-order elimination rate constant (K) of enrofloxacin were 2.79±0.60 h, 5.35±1.29 μg⋅h⋅mL -1 , 21.50±8.60 μg⋅h 2 ⋅mL -1 , 4.02±0.87 h, 3.76±0.83 L⋅kg -1 , 935.09 ± 236.45 mL⋅h -1 ⋅kg -1 and 0.25±0.07 h -1 , respectively after the administration of enrofloxacin. Because of faster elimination time, excellent tissue penetration, shorter halflife, low MRT after intramuscular administration of enrofloxacin at a dose rate of 5 mg⋅kg -1 , it is recommended for use in yaks at therapeutic dose.
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The Pharmacological Basis of Therapeutics
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Pharmacokinetic properties of enrofloxacin in rabbits
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