摘要
目的 探索微波萃取 (ME)对不同形态结构中药及含不同极性成分中药的提取规律。方法 以大黄、决明子中不同极性的蒽醌类成分及金银花中绿原酸、黄芩中黄芩苷为指标成分 ,以 HPL C法测定 ,采用正交试验设计法分别考察提取率。结果 ME对大黄中不同极性蒽醌成分的提取选择性并不明显 ,而同一温度条件下 ,根茎类中药大黄中大黄素、大黄酚、大黄素甲醚的提取率明显高于种子类中药决明子中相同成分的提取率。结论 ME对不同形态结构中药的提取有选择性 。
Object To explore the regularity of microwave extraction (ME) on Chinese medicines in different morphological structure and different polar compositions. Methods Anthraquinone in Radix et Rhizoma Rhei (RRR), Semen Cassiae (SC), cholorogenic acid in Flos Lonicerae, baicalin in Radix Scutellariae were determined as index compositions by HPLC. The extraction rate was measured by orthogonal design. Results ME selectivity to different anthraquinone in RRR is not significant, while at the same temperature, the extraction rates of emodin, chrysophanol, physcion in RRR are higher than those in SC. Conclusion The ME selectivity to the different morphological structure of Chinese medicines is obvious, but to the different polar compositions is not distinct.
出处
《中草药》
CAS
CSCD
北大核心
2002年第7期604-607,共4页
Chinese Traditional and Herbal Drugs
基金
清华大学化学工程国家联合重点实验室开放课题
关键词
正交试验设计
微波萃取
HPLC法
中药提取
microwave extraction (ME)
Chinese medicines
selectivity
orthogonal design