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Fingerprint and multicomponent quantitative analysis of Banxia Baizhu Tianma Decoction by HPLC |
WANG Shu-ling1 YANG Hui-min1 LI Min-hui1 XU Nan2 MEN Lian-hui1 WANG Yue1 GU Yu-xin1 BAI Xue1 TIAN Chao1#br# |
1.Medicine College of Hangzhou Normal University, Zhejiang Province, Hangzhou 310012, China;
2.Shandong Research Academy of Traditional Chinese Medicine, Shandong Province, Ji′ nan 250014, China |
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Abstract Objective To establish HPLC fingerprint of Banxia Baizhu Tianma Decoction, and simultaneously determine the contents of seven components (gastrodin, liquiritin, naringin, hesperidin, isoliquiritin, atractylodes lactone Ⅲ, glycyrrhetinic acid).To provide the basis for the quality control of Banxia Baizhu Tianma Decoction.Methods The separation was carried out on an Inert Sustain C18 column (250 mm×4.6 mm, 5 μm).The mobile phase was acetonitrile-water solution, gradient elution was used.Volume flow rate was 1.0 mL/min.Detection wavelength was 254 nm.Column temperature was 30 ℃.HPLC fingerprints of 18 batches of Banxia Baizhu Tianma Decoction samples were established,the similarity was evaluated.The common peaks were assigned and identified, and the quantity of components identified was determined.Results The similarity of fingerprints of the control and 18 batches of samples were greater than 0.983.And 25 common peaks were calibrated, including 2 from Pinellia Ternata, 1 from Gastrodia Elata, 6 from Atractylodes Macrocephala, 6 from Exocarpium Citri Rubrum, 2 from Poria Cocos and 5 from Glycyrrhiza Uralensis Fisch, of which 2 common peaks could not be clearly identified.Peak 8 was gastrodin.Peak 14 was liquiritin.Peak 15 was naringin.Peak 16 was hesperidin.Peak 19 was isoliquiritin.Peak 21 was atractylodes lactone Ⅲ.Peak 25 was glycyrrhetinic acid.Contents of the seven components respectively were: gastrodin 2.1933-5.0626 mg/g, liquiritin 0.1220-0.2867 mg/g, naringin 7.3165-15.8486 mg/g, hesperidin 0.1301-0.3928 mg/g, isoliquiritin 0.1733-0.4524 mg/g, atractylodes lactone Ⅲ0.2361-0.7849 mg/g, glycyrrhetinic acid 0.0180-0.0372 mg/g.Conclusion HPLC fingerprint and quantitative determination method of Banxia Baizhu Tianma Decoction have merits of good repeatability and stability, which provide the reference for quality control and evaluation.
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[19] |
江国荣,潘雪莲,刘少文,等.高效液相色谱法测定中药金银花中绿原酸成分的含量[J].临床合理用药,2019,12(4):122-123.
|
[20] |
徐妍,杨华蕊,肖培云,等.中药指纹图谱研究现状及展望[J].世界最新医学信息文摘,2018,18(76):91-94.
|
[1] |
王小庆,吕艳.现代分析技术在中药鉴定中的应用分析[J].世界最新医学信息文摘,2019,19(13):158.
|
[2] |
严辉,李鹏辉,郭盛,等.干姜HPLC指纹图谱建立及5种成分测定[J].中成药,2019,41(9):2246-2251.
|
[3] |
杨立伟,王海南,耿莲,等.基于标准汤剂的中药整体质量控制模式探讨[J].中国实验方剂学杂志,2018,24(8):1-6.
|
[4] |
王珏,刘史佳,朱育凤,等.基于HPLC指纹图谱的半夏及其伪品鉴别研究[J].南京中医药大学学报,2020,3(2):267-272.
|
[5] |
何利,姚晓艳,金阳,等.芍药甘草汤HPLC指纹图谱的建立和7种成分含量测定[J].中药材,2019,42(8):1837-1841.
|
[6] |
舒婷,黄湘杰.补肺活血胶囊高效液相色谱特征指纹图谱研究及多成分含量测定[J].中国药业,2019,28(23):19-23.
|
[7] |
徐男,孙蓉,崔焕月,等.化学计量学结合信息熵赋权优选半夏白术天麻汤提取工艺[J].中草药,2020,51(4):995-1002.
|
[8] |
韩旭阳,张璐,彭冰,等.UPLC-Q-TOF-MS辨析清热除湿汤药效物质基础[J].中国实验方剂学杂志,2019,25(6):150-155.
|
[9] |
尹宁宁,周黎明,刘军田,等.HPLC法同时测定21种中药饮片中4种黄曲霉毒素的含量[J].山东中医药杂志,2019,38(11):1067-1071.
|
[10] |
许艺凡,周冰,张聪,等.HPLC法同时测定芩黄颗粒中黄芩苷和甘草酸的含量[J].中国兽药杂志,2020,54(2):29-33.
|
[11] |
张家祺,陈颖,胡诚,等.HPLC法检测茵陈五苓散中3种有效成分的含量[J].上海中医药大学学报,2020,34(2):86-89.
|
[12] |
胡婷,高智强,尹彦超,等.UPLC法测定乌拉尔甘草与光果甘草中7个黄酮类成分的含量[J].药物分析杂志,2019,39(5):763-771.
|
[13] |
杨冰月,敬勇,赖月月,等.HPLC法同时测定半夏中5个代表性成分的含量[J].药物分析杂志,2019,39(11):1992-1997.
|
[14] |
李超,董自波,蒋金来,等.HPLC法测定蒲公英中菊苣酸、咖啡酸与绿原酸[J].中草药,2015,46(23):3577-3580.
|
[15] |
洪博,刘军,张杰,等.甘遂半夏汤的UPLC-DAD指纹图谱研究[J].中国药房,2018,29(17):2373-2376.
|
[16] |
徐男,王亮,时海燕,等.基于整合药理学平台探究半夏白术天麻汤治疗高血压的分子机制[J].中国实验方剂学杂志,2019,25(2):109-117.
|
[17] |
李强,杜思邈,张忠亮,等.中药指纹图谱技术进展及未来发展方向展望[J].中草药,2013,44(22):3095-3104.
|
[18] |
薛刚强,曹宝帅,高淑丽,等.LC-MS/MS 法同时测定回春育子颗粒中9种成分的含量[J].中国药房,2018,29(9):1213-1217.
|
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