Comparative pharmacokinetics of florfenicol granule and florfenicol powder in pigs.
Liu ShuaiShuai, Gang Yang, Yongda Zhao, Qiuhua Fang, Huang XianHui
Abstract
Liu ShuaiShuai, Gang Yang, Yongda Zhao, Qiuhua Fang, Huang XianHui
Abstract
Fourteen healthy pigs were divided into two groups of 7 pigs each.The pigs in group A were orally administrated with single dose of florfenicol powder at 30 mg/kg.The pigs in group B were also orally administrated with single dose of florfenicol granule at 30 mg/kg.Comparative study on the pharmacokinetics of florfenicol powder and florfenicol granule was carried out.Plasma concentration of florfenicol was determined by HPLC.The concentration-time data of florfenicol were analyzed by non-compartmental model based on pharmacokinetic software WinNonlin 5.2.1.The main pharmacokinetic parameters of powder following oral administration were: t1/2β =(10.22±0.18) h,ke =(0.07±0.01) h-1,tmax =(1.67±0.48) h,Cmax=(24.68±1.13) μg·mL-1,AUC=(190.97±16.60) μg·mL-1·h,MRT=(8.33±0.42) h,tcp=(17.66±1.52) h.The main pharmacokinetic parameters of granule following oral administration were : t1/2β =(16.36±4.14) h,ke=(0.05±0.01) h-1,tmax=(5.71±0.47) h,Cmax=(12.23±0.78) μg·mL-1,AUC=(155.44±6.59) mg·mL-1·h,MRT=(14.96±0.35) h,tcp=(23.03±0.49) h.The results showed the granule of florfenicol after oral administration had slower elimination and longer effective time of the blood medicine density maintenance.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Fourteen healthy pigs were divided into two groups of 7 pigs each.The pigs in group A were orally administrated with single dose of florfenicol powder at 30 mg/kg.The pigs in group B were also orally administrated with single dose of florfenicol granule at 30 mg/kg.Comparative study on the pharmacokinetics of florfenicol powder and florfenicol granule was carried out.Plasma concentration of florfenicol was determined by HPLC.The concentration-time data of florfenicol were analyzed by non-compartmental model based on pharmacokinetic software WinNonlin 5.2.1.The main pharmacokinetic parameters of powder following oral administration were: t1/2β =(10.22±0.18) h,ke =(0.07±0.01) h-1,tmax =(1.67±0.48) h,Cmax=(24.68±1.13) μg·mL-1,AUC=(190.97±16.60) μg·mL-1·h,MRT=(8.33±0.42) h,tcp=(17.66±1.52) h.The main pharmacokinetic parameters of granule following oral administration were : t1/2β =(16.36±4.14) h,ke=(0.05±0.01) h-1,tmax=(5.71±0.47) h,Cmax=(12.23±0.78) μg·mL-1,AUC=(155.44±6.59) mg·mL-1·h,MRT=(14.96±0.35) h,tcp=(23.03±0.49) h.The results showed the granule of florfenicol after oral administration had slower elimination and longer effective time of the blood medicine density maintenance.
Key concepts: Florfenicol, Pharmacokinetics, Cmax, Granule (geology), Oral administration, Pharmacology, Chemistry, Medicine