2005•Journal of Jiangxi Normal UniversityRequires access

Preparation and HPLC Analysis of Ursolic Acid Separation fromHerba Hedyotidis Corymbosae

Chen Wu

Open publisher page 0 citations

Abstract

This paper explores adopting the method of ethanol extracting and agglutination separating to extract ursolic acid from Herba Hedyotidis Corymbosae and using spectrum to identify its'structure by IR, MS, NMR.A determination method of ursolic acid in Herba Hedyotidis Corymbosae by reversed-phase high performance liquid chromtograph was established. The chromatographic column, SymmetryShield RP18 (3.9 mm×150 mm,5 μm), methanol-water (88∶12, V/V) mobile phase with 1.0 mL/min flow rate, the detected wavelength (210 nm), and the column temperature(25 ℃) were adopted. The calibration curve of ursolic acid was linear under the content of 4.5~22.5 μg, the correlation coefficient was over 0.999 8. The content is 99.82% by HPLC and the gain rate is 3.65‰. The method is simple,accurate and has good repeatability and wider linear range. The method can be used to evaluate the quality of ursolic acid.

About this research paper

What this paper is about

This paper explores adopting the method of ethanol extracting and agglutination separating to extract ursolic acid from Herba Hedyotidis Corymbosae and using spectrum to identify its'structure by IR, MS, NMR.A determination method of ursolic acid in Herba Hedyotidis Corymbosae by reversed-phase high performance liquid chromtograph was established. The chromatographic column, SymmetryShield RP18 (3.9 mm×150 mm,5 μm), methanol-water (88∶12, V/V) mobile phase with 1.0 mL/min flow rate, the detected wavelength (210 nm), and the column temperature(25 ℃) were adopted. The calibration curve of ursolic acid was linear under the content of 4.5~22.5 μg, the correlation coefficient was over 0.999 8. The content is 99.82% by HPLC and the gain rate is 3.65‰. The method is simple,accurate and has good repeatability and wider linear range. The method can be used to evaluate the quality of ursolic acid.

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 paper explores adopting the method of ethanol extracting and agglutination separating to extract ursolic acid from Herba Hedyotidis Corymbosae and using spectrum to identify its'structure by IR, MS, NMR.A determination method of ursolic acid in Herba Hedyotidis Corymbosae by reversed-phase high performance liquid chromtograph was established. The chromatographic column, SymmetryShield RP18 (3.9 mm×150 mm,5 μm), methanol-water (88∶12, V/V) mobile phase with 1.0 mL/min flow rate, the detected wavelength (210 nm), and the column temperature(25 ℃) were adopted. The calibration curve of ursolic acid was linear under the content of 4.5~22.5 μg, the correlation coefficient was over 0.999 8. The content is 99.82% by HPLC and the gain rate is 3.65‰. The method is simple,accurate and has good repeatability and wider linear range. The method can be used to evaluate the quality of ursolic acid.

Key concepts: Ursolic acid, Repeatability, Chromatography, Chemistry, High-performance liquid chromatography, Calibration curve, Correlation coefficient, Content determination

Related papers

Back to paper searchBrowse research topicsOriginal source
Preparation and HPLC Analysis of Ursolic Acid Separation fromHerba Hedyotidis Corymbosae — Research Paper | ScholarLens