UPLC法同时测定藿香正气滴丸中7个化学成分Simultaneous determination of seven constituents in Huoxiang Zhengqi Dripping Pill by UPLC
张永志,佟玲,李东翔,孟文婷,于治国,赵云丽
ZHANG Yong-zhi,TONG ling,LI Dong-xiang,MENG Wen-ting,YU Zhi-guo,ZHAO Yun-li
摘要(Abstract):
目的建立UPLC法同时测定藿香正气滴丸中欧前胡素、异欧前胡素、橙皮苷、和厚朴酚、厚朴酚、苍术素、甘草酸7个成分的含量。方法采用Waters Acquity UPLC BEH C18色谱柱(100 mm×2.1 mm,1.7μm),流动相:乙腈(A)-体积分数为0.2%的甲酸水溶液(B),梯度洗脱,流速:0.4 m L·min-1,柱温:30℃,检测波长:250 nm,检测欧前胡素、异欧前胡素和甘草酸,284 nm检测橙皮苷,290 nm检测和厚朴酚、厚朴酚,336 nm检测苍术素。结果欧前胡素、异欧前胡素、橙皮苷、和厚朴酚、厚朴酚、苍术素、甘草酸质量浓度分别在2.0~80.6、0.6~23.0、15.0~600.0、10.1~403.2、7.5~301.6、1.0~41.6、10.1~202.4 mg·L-1内与峰面积呈良好的线性关系(r≥0.999 5),平均回收率在98.6%~100.9%(RSD≤2.2%,n=9)。结论该方法可用于藿香正气滴丸的质量控制。
Objective To establish a UPLC method for the simultaneous determination of seven constituents,including imperatorin,isoimperatorin,hesperidin,honokiol,magnolol,atrctylodine and glycyrrhizic acid in Huoxiang Zhengqi Dripping Pill( HZDP). Methods The UPLC separation was achieved on an Waters Acquity UPLC BEH C18column( 100 mm × 2. 1 mm,1. 7 μm) with acetonitrile( A)-0. 2% formic acid solution( B) as mobile phase at the flowrate of 0. 4 m L·min- 1for gradient elution. The column temperature was30 ℃. The UV detection wavelengths were set at 250 nm for imperatorin,isoimperatorin and glycyrrhizic acid,284 nm for hesperidin,290 nm for honokiol and magnolol,336 nm for atrctylodine. Results The linear ranges of imperatorin,isoimperatorin,hesperidin,honokiol,magnolol,atrctylodine and glycyrrhizic acid were2. 0-80. 6,0. 6-23. 0,15. 0-600. 0,10. 1-403. 2,7. 5-301. 6,1. 0-41. 6 and 10. 1-202. 4 mg·L- 1,respectively.The average recoveries( n = 9) of imperatorin,isoimperatorin,hesperidin,honokiol,magnolol,atrctylodine and glycyrrhizic acid were between 98. 6% and 100. 9% with RSD less than 2. 2%. Conclusions The method is simple,accurate,and could be used for the quality control of HZDP.
关键词(KeyWords):
藿香正气滴丸;超高效液相色谱法;欧前胡素;异欧前胡素;和厚朴酚;厚朴酚;苍术素;甘草酸;含量测定
Huoxiang Zhengqi Dripping Pill;UPLC;imperatorin;isoimperatorin;honokiol;magnolol;atrc-tylodine;glycyrrhizic acid;content determination
基金项目(Foundation):
作者(Author):
张永志,佟玲,李东翔,孟文婷,于治国,赵云丽
ZHANG Yong-zhi,TONG ling,LI Dong-xiang,MENG Wen-ting,YU Zhi-guo,ZHAO Yun-li
DOI: 10.14066/j.cnki.cn21-1349/r.2015.11.004
参考文献(References):
- [1]WS3-223(Z-223)-2004(Z),国家药品标准·新药转正中药标准(第64册)[S].
- [2]阚红玉,赵卫春,孙玉侠,等.藿香正气滴丸质量标准提高研究[J].中国实验方剂学杂志,2012,18(1):72-76.
- [3]余佳文,邓开英,彭涛,等.UPLC同时测定藿香正气口服液中甘草苷、柚皮芸香苷、橙皮苷、甘草酸铵、厚朴酚、和厚朴酚的含量[J].中国中药杂志,2013,38(14):2314-2317.
- [4]刘永利,赵振霞,李冬梅,等.超高效液相色谱法同时测定藿香正气水中7种成分含量[J].中国药科大学学报,2013,44(3):249-252.
- [5]刘征辉,叶挺祥,赵洪芝,等.藿香正气水指纹图谱及模式识别对质量控制的研究[J].药物分析杂志,2012,32(11):2064-2067.
- [6]卢建秋,孙明谦,刘颖,等.高效液相色谱法同时测定藿香正气水中甘草酸、欧前胡素、异欧前胡素、厚朴酚、和厚朴酚的含量[J].药物分析杂志,2008,28(5):742-744.
- [7]罗文敏,白杨,陈会明,等.HPLC法同时测定藿香正气胶囊中8个主要成分的含量[J].药物分析杂志,2011,31(9):1776-1780.
- [8]陈佳,王钢力,姚令文,等.超高效液相色谱(UPLC)在药物分析领域中的应用[J].药物分析杂志,2008,28(11):1976-1981.
- [9]石俊敏,管佳,张庆文,等.超高效液相色谱在药物分析中的应用[J].药物分析杂志,2008,28(9):1583-1588.
- [10]阚红玉,尹俏,刘彦莉,等.GC测定藿香正气滴丸中百秋李醇的含量[J].中国现代应用药学,2013,30(7):762-764.
- [11]刘颖,刘珍清,卢建秋.毛细管气相色谱法测定藿香正气软胶囊中百秋李醇的含量[J].北京中医药大学报,2010,33(3):120-122.
- [12]郑新元,赵晨,王杰,等.GC法测定藿香正气水中百秋李醇含量[J].中国药事,2011,25(3):282-283.
- 藿香正气滴丸
- 超高效液相色谱法
- 欧前胡素
- 异欧前胡素
- 和厚朴酚
- 厚朴酚
- 苍术素
- 甘草酸
- 含量测定
Huoxiang Zhengqi Dripping Pill - UPLC
- imperatorin
- isoimperatorin
- honokiol
- magnolol
- atrc-tylodine
- glycyrrhizic acid
- content determination