Abstract: Objective To establish a new procedure for isolating scutellarin from Erigeron multiradiatus. Methods Aproposed method was developed by combining macroporous resins with ODS column. Firstly, E. multiradiatus...Abstract: Objective To establish a new procedure for isolating scutellarin from Erigeron multiradiatus. Methods Aproposed method was developed by combining macroporous resins with ODS column. Firstly, E. multiradiatus wasextracted by ultrasound with 80% methanol. Preliminary separation was performed on macroporous resin column.The performance and adsorption characteristics of three macroporous resins, D140, D141, and D605, were comparedand the enrichment procedure was optimized. Further purification was carried out by medium pressure liquidchromatography (MPLC) with ODS column. Results It was demonstrated that D141 had better extractive effects onscutellarin. The MPLC conditions were optimized as follows: 15% ethanol aqueous as mobile phase with flow rate at2.5 mL/min. The yield and purity of the isolated scutellarin were 1.20 mg/g and 96.5%, respectively. ConclusionThe overall procedure is efficient and low-cost, which is considered suitable for the separation and purification ofscutellarin from E. multiradiatus. The results provide the scientific basis for developing and using scutellarin in clinic.展开更多
基金Fundamental Research Funds for Central Universities,Southwest University for Nationalities(09NZYZJ01)National Key Technology R&D Program in the 12th Five Year Plan of China(2012BAI27B07)
文摘Abstract: Objective To establish a new procedure for isolating scutellarin from Erigeron multiradiatus. Methods Aproposed method was developed by combining macroporous resins with ODS column. Firstly, E. multiradiatus wasextracted by ultrasound with 80% methanol. Preliminary separation was performed on macroporous resin column.The performance and adsorption characteristics of three macroporous resins, D140, D141, and D605, were comparedand the enrichment procedure was optimized. Further purification was carried out by medium pressure liquidchromatography (MPLC) with ODS column. Results It was demonstrated that D141 had better extractive effects onscutellarin. The MPLC conditions were optimized as follows: 15% ethanol aqueous as mobile phase with flow rate at2.5 mL/min. The yield and purity of the isolated scutellarin were 1.20 mg/g and 96.5%, respectively. ConclusionThe overall procedure is efficient and low-cost, which is considered suitable for the separation and purification ofscutellarin from E. multiradiatus. The results provide the scientific basis for developing and using scutellarin in clinic.