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RP-HPLC法测定不同方法加工天麻中天麻素含量 被引量:6

CONTENT DETERMINATION OF GASTRDIN IN DIFFERENTLY PROCESSED TIANMA BY RP-HPLC
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摘要 研究和评估了 3种加工新鲜天麻的方法 .方法 :新鲜天麻分别经水蒸汽法、1 2 5℃加热烘烤法和 6 0℃加热烘烤法后制成干天麻 ,用RP_HPLC法测定 .结论 :按 3种方法制备所得干天麻中的天麻素含量分别为0 .1 31 6 % ,0 .1 31 3%和 0 .0 2 70 % .实验结果分析表明 :水蒸汽法最适合中药材天麻的加工 ,有良好的外观 ;1 2 5℃加热烘烤法特别适合制药工业对天麻粉末的需要 ;6 0℃加热法是不可取的方法 .另外 。 Three processing methods of fresh Tian Ma (Rhizoma Gastrodiae) from traditional Chinese medicinal plant Gastrodia elata Blume were investigated and evaluated. Methods:To Mensurate and analyze the contents of gastrodin in Tian Ma samples processed by three methods of steaming on boiling water , roasting and heating at 125 ℃ and 60 ℃, RP-HPLC was used. Conclusion:The contents of gastrodin in processed Tian Ma were 0.1316%, 0.1313% and 0.0270%, determined by RP-HPLC, respectively. Experimental results: The processing method of steaming on boiling water was mostly suitable for merchandised Tian Ma, which owned a good appearance, roasting at 125 ℃ specially for a large scale of pharmaceutical usage of Tian Ma powder, the processing method of heating at 60 ℃ was not a good option for processing fresh Tian Ma. Additionally, instantly processing in any processing method was an important requirement of keeping the content of gastrodin in Tian Ma stabilizing.
出处 《曲阜师范大学学报(自然科学版)》 CAS 2004年第3期79-81,共3页 Journal of Qufu Normal University(Natural Science)
基金 中国科学院武汉植物园"知识创新工程"所长基金资助 ( 0 2 0 3 5 10 9)
关键词 天麻 天麻素 加工方法 RP-HPLC法 含量 Gastrodia elata blume Gastrodin processing method RP-HPLC content
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参考文献4

  • 1杨世林,兰进,徐锦堂.天麻的研究进展[J].中草药,2000,31(1):66-69. 被引量:186
  • 2李仙娟,罗晨曲.天麻不同炮制品中天麻素含量的比较分析[J].湖南中医药导报,2000,6(6):39-40. 被引量:6
  • 3Li Hongxia, Ding Mingyu, Lu Kun, et al. Identification and determination of the active compounds in Gastrodia elata Blurne by HPLC [ J ]. Journal of Liquid Chromatography & Related Technologies , 2001,24(4):579.
  • 4Zhao Yunkun, Cao Qiue, Xiang Yanqiao, et al. Identification and determination of active components in Gastrodia elata Bl. by capillary electrophoresis[ J]. Journal of Chromatography A, 1999,849(1): 277.

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