2010Chinese Veterinary ScienceRequires access

Studies of pharmacokinetics of cefquinome in boar.

Zhang ChiYe, Yu JunJun, Yu DaiPeng, Yahong Liu

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Abstract

The pharmacokinetics parameters were investigated following the single intravenous injection(2mg/kg of dosage) of cefquinome in 5 healthy boars,and compared to the parameters of cefquinome in healthy swine.The concentrations of cefquinome in plasma were determined by RP-HPLC,and the concentration-time data was analyzed with WinNonlin program.It was best to fit the cefquinome concentration-time data to two-compartment open model after the single intravenous injection.The main pharmacokine-tics parameters were as follows:t1/2α=0.22h±0.05h,t1/2β=1.65h±0.46h,CL=0.29L/(h·kg)± 0.061L/(h·kg),AUC=7.2h·mg/L±1.49h·mg/L,Vss=0.59L/kg±0.66L/kg,MRT=2.16h±0.65h.The above-mentioned means were not different(P0.05) from that in the healthy swine.

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The pharmacokinetics parameters were investigated following the single intravenous injection(2mg/kg of dosage) of cefquinome in 5 healthy boars,and compared to the parameters of cefquinome in healthy swine.The concentrations of cefquinome in plasma were determined by RP-HPLC,and the concentration-time data was analyzed with WinNonlin program.It was best to fit the cefquinome concentration-time data to two-compartment open model after the single intravenous injection.The main pharmacokine-tics parameters were as follows:t1/2α=0.22h±0.05h,t1/2β=1.65h±0.46h,CL=0.29L/(h·kg)± 0.061L/(h·kg),AUC=7.2h·mg/L±1.49h·mg/L,Vss=0.59L/kg±0.66L/kg,MRT=2.16h±0.65h.The above-mentioned means were not different(P0.05) from that in the healthy swine.

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Available abstract

The pharmacokinetics parameters were investigated following the single intravenous injection(2mg/kg of dosage) of cefquinome in 5 healthy boars,and compared to the parameters of cefquinome in healthy swine.The concentrations of cefquinome in plasma were determined by RP-HPLC,and the concentration-time data was analyzed with WinNonlin program.It was best to fit the cefquinome concentration-time data to two-compartment open model after the single intravenous injection.The main pharmacokine-tics parameters were as follows:t1/2α=0.22h±0.05h,t1/2β=1.65h±0.46h,CL=0.29L/(h·kg)± 0.061L/(h·kg),AUC=7.2h·mg/L±1.49h·mg/L,Vss=0.59L/kg±0.66L/kg,MRT=2.16h±0.65h.The above-mentioned means were not different(P0.05) from that in the healthy swine.

Key concepts: Pharmacokinetics, Plasma concentration, High-performance liquid chromatography, Chromatography, Animal science, Biology, Veterinary medicine, Pharmacology

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