2009Chinese Journal of Veterinary DrugRequires access

Pharmacokinetic Study of Berberine Hydrochloride in Chickens

Qiu Yin-sheng

Open publisher page 0 citations

Abstract

This article investigated the pharmacokinetics of berberine hydrochloride in chickens.The plasma concentration of berberine was determined by HPLC.The plasma concentration-time data of berberine hydrochloride was analyzed by Drug and Statistics(DAS).Following intravenous administration(3 mg·kg-1),the drug concentration-time data was best described by a three-compartment open model,t1/2β,t1/2γ,Vc,CL and AUC were(0.41±0.24) h,(3.66±1.06) h,(25.49±21.77)L·kg-1,(43.20±16.21)L·h-1·kg-1 and(78.92±30.58)μg·L-1·h respectively.The drug concentration-time data was best described by a two-compartment open model after oral administration of 50 mg·kg-1,t1/2α,t1/2β,t1/2ka,Tmax,Cmax and AUC were(1.87±0.76) h,(4.18±3.14) h,(0.89±0.46) h,(2.64±0.63) h,(4.09±0.11)μg·L-1 and(26.18±10.73)μg·L-1·h respectively.The absolute bioavailability was 2.03% after oral administration.Berberine hydrochloride had a low rate of bioavailability by oral administration,and its elimination was fast.

About this research paper

What this paper is about

This article investigated the pharmacokinetics of berberine hydrochloride in chickens.The plasma concentration of berberine was determined by HPLC.The plasma concentration-time data of berberine hydrochloride was analyzed by Drug and Statistics(DAS).Following intravenous administration(3 mg·kg-1),the drug concentration-time data was best described by a three-compartment open model,t1/2β,t1/2γ,Vc,CL and AUC were(0.41±0.24) h,(3.66±1.06) h,(25.49±21.77)L·kg-1,(43.20±16.21)L·h-1·kg-1 and(78.92±30.58)μg·L-1·h respectively.The drug concentration-time data was best described by a two-compartment open model after oral administration of 50 mg·kg-1,t1/2α,t1/2β,t1/2ka,Tmax,Cmax and AUC were(1.87±0.76) h,(4.18±3.14) h,(0.89±0.46) h,(2.64±0.63) h,(4.09±0.11)μg·L-1 and(26.18±10.73)μg·L-1·h respectively.The absolute bioavailability was 2.03% after oral administration.Berberine hydrochloride had a low rate of bioavailability by oral administration,and its elimination was fast.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

This article investigated the pharmacokinetics of berberine hydrochloride in chickens.The plasma concentration of berberine was determined by HPLC.The plasma concentration-time data of berberine hydrochloride was analyzed by Drug and Statistics(DAS).Following intravenous administration(3 mg·kg-1),the drug concentration-time data was best described by a three-compartment open model,t1/2β,t1/2γ,Vc,CL and AUC were(0.41±0.24) h,(3.66±1.06) h,(25.49±21.77)L·kg-1,(43.20±16.21)L·h-1·kg-1 and(78.92±30.58)μg·L-1·h respectively.The drug concentration-time data was best described by a two-compartment open model after oral administration of 50 mg·kg-1,t1/2α,t1/2β,t1/2ka,Tmax,Cmax and AUC were(1.87±0.76) h,(4.18±3.14) h,(0.89±0.46) h,(2.64±0.63) h,(4.09±0.11)μg·L-1 and(26.18±10.73)μg·L-1·h respectively.The absolute bioavailability was 2.03% after oral administration.Berberine hydrochloride had a low rate of bioavailability by oral administration,and its elimination was fast.

Key concepts: Berberine, Bioavailability, Pharmacokinetics, Cmax, Berberine hydrochloride, Oral administration, Chemistry, Pharmacology

Related papers

Back to paper searchBrowse research topicsOriginal source
Pharmacokinetic Study of Berberine Hydrochloride in Chickens — Research Paper | ScholarLens