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牛蒡苷元制备方法的研究

张李赢 杨轶舜 张彤 丁越 蔡贞贞 陶建生

中药材2012,Vol.35Issue(3):467-470,4.
中药材2012,Vol.35Issue(3):467-470,4.

牛蒡苷元制备方法的研究

Research on the Preparative Method of Arctigenin

张李赢 1杨轶舜 1张彤 1丁越 1蔡贞贞 1陶建生1

作者信息

  • 1. 上海中医药大学,上海201203
  • 折叠

摘要

Abstract

Objective: To research on the preparation of Aretigenin in vitro. Methods: Took enzyme concentration,time course and substrate concentration as investigation factors,used Box-Behnken design-response surface methodology to optimize the enzyme hydrolysis path of Aretigenin. Results: The best operational path for Aretigenin was as follows; the temperature was 50 ℃ ,pH was 4. 8,enzyme concentration was 0.44 U/mL,time course was 46.81 min, substrate concentration was 0.29 mg/mL,the conversion rate was 90.94%. Conclusion: This research can be regarded as a reference in preparing Aretigenin in vitro.

关键词

牛蒡苷/牛蒡苷元/β-葡萄糖苷酶

Key words

Arctii/ Aretigenin/ β-Glucoside

分类

医药卫生

引用本文复制引用

张李赢,杨轶舜,张彤,丁越,蔡贞贞,陶建生..牛蒡苷元制备方法的研究[J].中药材,2012,35(3):467-470,4.

基金项目

教育部新世纪人才计划(NCET-10-0944) (NCET-10-0944)

国家自然科学基金(81173561) (81173561)

上海市教委曙光计划(10SG40) (10SG40)

上海市重点学科(J50302) (J50302)

中药材

OA北大核心CSCDCSTPCD

1001-4454

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