华南理工大学学报(自然科学版) ›› 2010, Vol. 38 ›› Issue (8): 121-125.doi: 10.3969/j.issn.1000-565X.2010.08.023

• 食品科学与技术 • 上一篇    下一篇

赤芝、紫芝三萜类成分指纹图谱的优化与比较

黄生权1  魏刚2  姚松君3  刘翠玲2  宁正祥1   

  1. 1.华南理工大学 轻工与食品学院, 广东 广州 510640;2.广州中医药大学 新药开发中心, 广东 广州 510006; 3.无限极(中国)有限公司, 广东 江门 529156
  • 收稿日期:2009-12-28 修回日期:2010-03-23 出版日期:2010-08-25 发布日期:2010-08-25
  • 通信作者: 魏刚(1969-),男,研究员,主要从事中药新药研究与指纹图谱分析.E-mail:weigang021@163.com. E-mail:huangfeihong0220@sina.com
  • 作者简介:黄生权(1977-),男,博士生,主要从事中草药功能食品的研究与开发.
  • 基金资助:

    广东省自然科学基金资助项目(8151040701000020);广东省科技计划项目(2007B060401010)

Optimization and Comparison of Fingerprints of Triterpenoids from Ganoderma lucidum and Ganoderma sinense

Huang Sheng-quan Wei Gang2   Yao Song-jun3  Liu Cui-ling2  Ning Zheng-xiang1   

  1. 1. School of Light Industry and Food Sciences, South China University of Technology, Guangzhou 510640, Guangdong, China; 2. New Medicine Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong, China; 3. Infinitus (China) Co., Ltd., Jiangmen 529156, Guangdong, China
  • Received:2009-12-28 Revised:2010-03-23 Online:2010-08-25 Published:2010-08-25
  • Contact: 魏刚(1969-),男,研究员,主要从事中药新药研究与指纹图谱分析.E-mail:weigang021@163.com. E-mail:huangfeihong0220@sina.com
  • About author:黄生权(1977-),男,博士生,主要从事中草药功能食品的研究与开发.
  • Supported by:

    广东省自然科学基金资助项目(8151040701000020);广东省科技计划项目(2007B060401010)

摘要: 对高效液相色谱的色谱条件进行优化,建立灵芝三萜类成分的指纹图谱分析方法,拟定赤芝、紫芝指纹图谱的共有模式,并将其初步应用于评价赤芝与紫芝的质量差异。优化后的流动相为乙腈-2%冰醋酸(梯度洗脱),检测波长为252nm,流速为1mL/min,柱温为35℃,14批赤芝、7批紫芝共标示出29个共有峰.鉴别了3个成分(灵芝酸A、C2,G),发现灵芝酸A的峰最强;赤芝与紫芝的共有峰相对比值较接近,但紫芝的单位生药峰面积只有赤芝的5%~10%左右,说明含灵芝制剂的质量评价应采用指纹图谱与含量测定相结合的方法.采用优化后的方法获得的灵芝三萜指纹图谱表明,赤芝三萜类成分较其它文献报道多,紫芝中三萜类成分能明显检出,说明该方法准确可靠,重复性好.

关键词: 赤芝, 紫芝, 三萜类化合物, 指纹图谱, 高效液相色谱

Abstract:

By optimizing the experimental conditions of high-performance liquid chromatography ( HPLC), a method of fingerprint analysis of Glossy ganoderma was presented and a common mode of the fingerprints of Ganoderma lucidum and Ganoderma sinense was proposed, which were both initially used to estimate the quality difference. The HPLC conditions were optimized as: acetonitrile-2% acetic acid solution (gradient elution) as a mobile phase, a detection wavelength of 252 nm, a flow rate of 1 mL/min and a column temperature of 35 ℃. In the optimal conditions, 29 common peaks were separated from 14 batches of Ganoderma lucidum and 7 batches of Ganoderma sinense, and three compositions (ganoderic acids A, C2, G) were identified. The results indicate that the peak of ganoderic acid A is of the strongest intensity ; and that although the relative ratio of common peaks of Ganoderma lu- cidum is close to that of Ganoderma sinense, the peak area per unit medicine of Ganoderma sinense is only about 5% -10% of that of Ganoderma lucidum, which means that the quality evaluation of the products from Glossy ganoderma should combine both the HPLC fingerprint and the content determination. Moreover, according to the fingerprints of triterpenoids from Glossy ganoderma obtained by the optimized method, it is found that the Ganoderma lucidum contains much more triterpenoid compositions than what is reported in the literature, and that the triterpenoids in Ganoderma sinense can be easily detected. It is, thus, concluded that the proposed method is reliable, accurate and reproducible.

Key words: Ganoderma lucidum, Ganoderma sinense, triterpenoid, fingerprint, high-performance liquid chromatography