ZHANG Mingyuan, MI Heming, FAN Guorong, LU Feng, QI Yunpeng. Purification of total flavones by macroporous resin and its determination of the active components from Resina Draconis[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(1): 42-44. doi: 10.3969/j.issn.1006-0111.2014.01.010
Citation:
|
ZHANG Mingyuan, MI Heming, FAN Guorong, LU Feng, QI Yunpeng. Purification of total flavones by macroporous resin and its determination of the active components from Resina Draconis[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(1): 42-44. doi: 10.3969/j.issn.1006-0111.2014.01.010
|
Purification of total flavones by macroporous resin and its determination of the active components from Resina Draconis
- 1.
Department of Pharmaceutical Analysis, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai 200433, China;Department of Pharmacy, the First Hospital of Naping, Fujian Medical University, Nanping 353000, China
- 2.
Department of Pharmaceutical Analysis, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai 200433, China
- Received Date: 2012-12-14
- Rev Recd Date:
2013-09-24
-
Abstract
Objective To purify the total flavones from Resina Draconis using D101 resin, and set up a method of simultaneously determining the contents of loureirin A and B in the extract. Methods Fractions in 70% and 95% ethanol were collected. Mixture of acetonitrile and l% acetic acid (34.5:65.5) was used as the mobile phase and ODS column was used as stationary phase to determine loureirin A and B. The detecting wave length was 280 nm. Results In the established HPLC method, the linear range of loureirin A was 11.00-275.00 g/ml, and that of loureirin B was 20.00-500.00 g/ml. Linear equation of loureirin A was Y=35 844C+44 725(r=0.999 9) and that of loureirin B was Y=28 533C-41 085, r=0.999 9.The accuracy, precision and stability of this method were satisfactory. Conclusion The proposed method was suitable for preparation of total flavones and determination of its active components from Resina Draconis.
-
References
[1]
|
(明)李时珍.本草纲目[M]. 北京:北京出版社, 2007:430. |
[2]
|
陈可冀.血瘀证与活血化瘀治疗的研究[J]. 中国中医药现代远程教育, 2005, 3 (11):10-12. |
[3]
|
曹 峥.血竭的化学成分与临床应用[J]. 中国实用医药,2009, 4(2):220. |
[4]
|
蔡 辉,胡婉英.复方血竭治疗冠心病血瘀证的实验与临床研究[J]. 南京中医学院学报, 1982, 8(4):216-220. |
[5]
|
方伟蓉, 李运曼, 邓嘉元.龙血竭总黄酮对动物心肌缺血的保护作用[J]. 中国临床药理学与治疗学, 2005, 10 (9):1020-1024. |
[6]
|
黄树莲, 陈学芬, 陈晓军, 等.广西血竭总黄酮活血化瘀作用的研究[J]. 广西医学, 1996,18(1):1-2. |
[7]
|
马建建,宋 艳,贾 敏,等.血竭总黄酮对血小板聚集、血栓形成及心肌缺血的影响[J]. 中草药, 2002, 33(11):1008-1010. |
[8]
|
乐 薇.大孔树脂精制血竭总黄酮[J]. 中南民族大学学报:自然科学版, 2008, 25(4):35-38. |
[9]
|
屠鹏飞,王钰芳,邵 杰,等.血竭中黄酮类成分提取工艺研究[J]. 中国实验方剂学杂志,2011,17(6):30-32. |
[10]
|
朱欣婷, 刘 云.大孔树脂纯化无花果叶总黄酮[J]. 中国实验方剂学杂志, 2012, 18(6):13-16. |
[11]
|
覃金玲, 宋爱华, 黄付伟, 等.大孔树脂分离纯化青皮中总黄酮的工艺研究[J]. 中国药师, 2012, 15(8):1108-1110. |
[12]
|
吴海霞.大孔树脂精制杭白菊总黄酮的上样条件研究[J]. 中国药业, 2012, 2l(14):67-69. |
[13]
|
胡迎庆,李灵芝,韩慧文.RP-HPLC测定龙血竭-龙血素A和B的含量[J]. 生命科学仪器,2003,12(6):24-25. |
[14]
|
孙胜利,宓鹤鸣,娄子洋.反相高效液相色谱法测定国产血竭中龙血素A和B的含量[J]. 第二军医大学学报,2002, 23(12):1366-1368. |
-
-
Proportional views
-