|
|
Simultaneous determination of 7 active components in Huangqi Hugan Capsules by high performance liquid chromatography |
JI Guo-li LIU Bin▲ |
Tai′an Food and Drug Inspection and Testing Center,Shandong Province,Tai′an 271000,China |
|
|
Abstract Objective To establish a high performance liquid chromatography(HPLC)method for simultaneous determination of main components of Tetrahydropalmatine,Paeoniflorin,TanshinoneⅡA,Hesperidin,Emodin,Schisandrin A and Chrysophanol in Huangqi Hugan Capsules.Methods HPLC was used to detect the aforementioned components in Huangqi Hugan Capsules.The column was CNW Athena C18 and the mobile phase was methanol(A)and 0.1%aqueous solution of phosphoric acid(B)in gradient elution.The flow rate was 1.0 ml/min at 30℃column temperature.The detection wavelength were 210 nm for Tetrahydropalmatine,230 nm for Paeoniflorin,Hesperidin and Schisandrin A,and 265 nm for TanshinoneⅡA,Emodin,and Chrysophanol were 265 nm.The linear range,recovery,and repeatability of each component in Huangqi Hugan Capsules were examined.Results The linear ranges of Tetrahydropalmatine,Paeoniflorin,Hesperidin,Schisandrin A,Tanshinone ⅡA,Emodin and Chrysophanol were 1.26-25.20 μg/ml(r=0.9996),7.03-140.60 μg/ml(r=0.9998),3.63-72.60 μg/ml(r=0.9997),2.11-42.20 μg/ml(r=0.9994),1.98-39.60 μg/ml(r=0.9995),3.10-62.00 μg/ml(r=0.9996),and 2.28-45.60 μg/ml(r=0.9995).The average recovery of 7 components (n=6)was 99.6%,98.9%,98.7%,99.2%,98.2%,98.8%,and 98.2%,respectively.RSD was 1.7%,1.0%,1.2%,1.5%,1.2%,1.2%and 1.0%,respectively.Conclusion The method is accurate and reproducible in a high recovery,which can be used for quality control of Huangqi Hugan Capsules.
|
|
|
|
|
[1] |
谢彩娟,张志琪,张富强.RP-HPLC法同时测定延胡索药材中延胡索乙素和原阿片碱[J].陕西师范大学学报,2005,33(1):82-85.
|
[2] |
冀兰鑫,黄浩,李长志.赤芍药理作用的研究进展[J].药物评价研究,2010,33(3):233-236.
|
[3] |
张冬松,高慧媛,吴立军.橙皮苷的药理活性研究进展[J].中国现代中药,2006,8(7):25-27.
|
[4] |
王文燕,陈建光.五味子的药理作用及开发研究[J].北华大学学报,2007,8(2):128-132.
|
[5] |
张萌涛,钱亦华,唐安琪.丹参酮ⅡA药理作用的研究进展[J].医学综述,2010,16(17):2661-2664.
|
[6] |
王磊,张静泽,高文远.大黄活性成分药代动力学研究进展[J].中成药,2011,33(9):1571-1574.
|
[7] |
朱央央,余伯阳.RP-HPLC测定元胡止痛方中延胡索乙素和欧前胡素的含量[J].中成药,204,26(6):455-458.
|
[8] |
周海玲,许舜军,杨柳.HPLC法测定赤芍中芍药苷的含量[J].临床医学工程,2011,18(4):487-488.
|
[9] |
尤立华.HPLC测定复方小活络丸中芍药苷含量和乌头碱的限量[J].中国实验方剂学杂志,2013,19(9):158-160.
|
[10] |
周军,王佳,刘稚菲,等.HPLC法测定小儿磨积片中橙皮苷、甘草酸、和厚朴酚、厚朴酚及苍术素的含量[J].药物分析杂志,2010,30(9):1725-1728.
|
[11] |
宋久华,杨孝容.HPLC测定安神补心丸中五味子醇甲、五味子酯甲和五味子甲素的含量[J].中成药,2008,30(3):380-383.
|
[12] |
张亚中,金斌,黄丽丹,等.HPLC测定128批丹参舒心胶囊中丹参酮Ⅰ、隐丹参酮、丹参酮ⅡA的含量及结果分析[J].中成药,2011,33(1):65-69.
|
[13] |
陈钰蓓,马文彪,王月红.HPLC法测定心舒乐片中丹参酮ⅡA、羟基红花黄色素、苦杏仁苷[J].中成药,2012,34(3):490-494.
|
[14] |
余英,董玲,杜秋霞,等.HPLC测定妇炎灵泡腾片中大黄素、大黄酚的含量[J].中成药,2004,26(7):549-552.
|
[15] |
巫涛,顾明君.HPLC测定黄连上清胶囊中大黄素、大黄酚含量[J].中成药,2005,27(4):472-473.
|
[16] |
熊鑫,程璐,杨全伟.高效液相色谱波长切换法同时测定殃芪巴布剂中野黄芩苷、党参炔苷和延胡索乙素的含量[J].中南药学,2017,15(3):355-358.
|
[17] |
许雪峰,杜远东,任杰,等.高效液相色谱法同时测定外用伤筋药水中栀子苷和芍药苷含量[J].中国药业,2017,26(10):35-38.
|
[18] |
袁常珍,梅刚.高效液相色谱法测定参麦散结胶囊中五味子醇甲含量[J].西南医科大学学报,2017,40(2):188-191.
|
[19] |
秦龙,王娟弟,李平,等.高效液相色谱法测定肝炎康胶囊中丹参酮ⅡA和齐墩果酸含量[J].兰州大学学报(医学版),2017,43(4):69-71.
|
[20] |
张霞,程晓叶,廖曼,等.高效液相色谱法测定复方制剂中的大黄酸、大黄素、大黄酚、大黄素甲醚和二苯乙烯苷的含量[J].河北医科大学学报,2017,38(2):201-205.
|
|
|
|