2011Zhōnghuá yàoxué zázhìRequires access

Preparation of Oleanolic Acid Intravenous Emulsions and Its Pharmacokinetics in Rats

Yanyu Xiao

Open publisher page 1 citations

Abstract

OBJECTIVE To prepare oleanolic acid intravenous emulsions and study its pharmacokinetics in rats.METHODS Oleanolic acid intravenous emulsion was prepared by two-step emulsification using high speed stirring-ultrasonic wave.The pharmaceutical properties including appearance,content,Ke,particle size,and Zeta potential were determined.Rats were i.v.injected with oleanolic acid intravenous emulsion or oleanolic acid solution via tail veins.The concentrations in rat plasma were assayed by high-performance liquid chromatography(HPLC).The pharmacokinetic parameters were computed by 3P97 program package.RESULTS The droplets of oleanolic acid intravenous emulsion were almost spherical,The mean diameter was(176.0±3.8) nm,and Zeta potential was(-17.5±4.1) mV.The content of oleanolic acid intravenous emulsions was(87.8±1.8)%.The plasma pharmacokinetic process of the oleanolic acid intravenous emulsions obeyed a two-compartment model.t1/2β of oleanolic acid intravenous emulsions was(308.1±22.8) min,and AUC was(208.6±15.6) μg·min·mL-1,obviously higher than control preparation.CONCLUSION The intravenous emulsion has high content and even diameter.Its pharmacokinetic property has significant change with improved bioavailability.

About this research paper

What this paper is about

OBJECTIVE To prepare oleanolic acid intravenous emulsions and study its pharmacokinetics in rats.METHODS Oleanolic acid intravenous emulsion was prepared by two-step emulsification using high speed stirring-ultrasonic wave.The pharmaceutical properties including appearance,content,Ke,particle size,and Zeta potential were determined.Rats were i.v.injected with oleanolic acid intravenous emulsion or oleanolic acid solution via tail veins.The concentrations in rat plasma were assayed by high-performance liquid chromatography(HPLC).The pharmacokinetic parameters were computed by 3P97 program package.RESULTS The droplets of oleanolic acid intravenous emulsion were almost spherical,The mean diameter was(176.0±3.8) nm,and Zeta potential was(-17.5±4.1) mV.The content of oleanolic acid intravenous emulsions was(87.8±1.8)%.The plasma pharmacokinetic process of the oleanolic acid intravenous emulsions obeyed a two-compartment model.t1/2β of oleanolic acid intravenous emulsions was(308.1±22.8) min,and AUC was(208.6±15.6) μg·min·mL-1,obviously higher than control preparation.CONCLUSION The intravenous emulsion has high content and even diameter.Its pharmacokinetic property has significant change with improved bioavailability.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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

OBJECTIVE To prepare oleanolic acid intravenous emulsions and study its pharmacokinetics in rats.METHODS Oleanolic acid intravenous emulsion was prepared by two-step emulsification using high speed stirring-ultrasonic wave.The pharmaceutical properties including appearance,content,Ke,particle size,and Zeta potential were determined.Rats were i.v.injected with oleanolic acid intravenous emulsion or oleanolic acid solution via tail veins.The concentrations in rat plasma were assayed by high-performance liquid chromatography(HPLC).The pharmacokinetic parameters were computed by 3P97 program package.RESULTS The droplets of oleanolic acid intravenous emulsion were almost spherical,The mean diameter was(176.0±3.8) nm,and Zeta potential was(-17.5±4.1) mV.The content of oleanolic acid intravenous emulsions was(87.8±1.8)%.The plasma pharmacokinetic process of the oleanolic acid intravenous emulsions obeyed a two-compartment model.t1/2β of oleanolic acid intravenous emulsions was(308.1±22.8) min,and AUC was(208.6±15.6) μg·min·mL-1,obviously higher than control preparation.CONCLUSION The intravenous emulsion has high content and even diameter.Its pharmacokinetic property has significant change with improved bioavailability.

Key concepts: Oleanolic acid, Pharmacokinetics, Bioavailability, Emulsion, Chromatography, High-performance liquid chromatography, Zeta potential, Chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Preparation of Oleanolic Acid Intravenous Emulsions and Its Pharmacokinetics in Rats — Research Paper | ScholarLens