| 引用本文: | 李柯,陈丹,符国成,侯茜,沈冰冰,龚小兵,李若存.复方感冒灵流浸膏的HPLC指纹图谱及化学成分鉴定[J].中国现代应用药学,2019,36(15):1887-1891. |
| LI Ke,CHEN Dan,FU Guocheng,HOU Xi,SHEN Bingbing,GONG Xiaobing,LI Ruocun.HPLC Fingerprint Analysis and Chemical Component Analysis of Fufang Ganmaoling Fluid Extract[J].Chin J Mod Appl Pharm(中国现代应用药学),2019,36(15):1887-1891. |
|
| |
|
|
| 本文已被：浏览 1895次 下载 1026次 |
码上扫一扫！ |
|
|
| 复方感冒灵流浸膏的HPLC指纹图谱及化学成分鉴定 |
|
李柯1, 陈丹2, 符国成3, 侯茜1, 沈冰冰1, 龚小兵3, 李若存1
|
|
1.湖南省中医药研究院, 长沙 410013;2.湘潭医卫职业技术学院, 湖南 湘潭 411102;3.华润三九制药有限公司, 湖南 郴州 423000
|
|
| 摘要: |
| 目的 建立复方感冒灵流浸膏HPLC指纹图谱并对其化学成分进行分析，为复方感冒灵流浸膏质量评价与药效物质基础研究提供依据。方法 采用Kromasil C18色谱柱（4.6 mm×250 mm，5 μm），以乙腈-0.1%甲酸水溶液为流动相，进行梯度洗脱，流速为1.0 mL·min-1，检测波长290 nm，柱温为30℃，测定10批复方感冒灵流浸膏。利用中药色谱相似度评价系统建立复方感冒灵流浸膏HPLC指纹图谱，并通过对照品对共有峰进行指认，应用HPLC-Q-TOF-MS/MS技术对复方感冒灵流浸膏中的化学成分进行鉴定。结果 建立了复方感冒灵流浸膏成分指纹图谱共有模式，显示12个共有峰，各峰分离度良好，各批次间共有峰相对保留时间RSD均<3.0%，样品间相似度均>0.9。鉴定出复方感冒灵流浸膏中12个化学成分，分别为奎尼酸、原儿茶酸、新绿原酸、swertiajaposide F、绿原酸、隐绿原酸、咖啡酸、二咖啡酰奎宁酸、异绿原酸B、异绿原酸A、异绿原酸C、蒙花苷。结论 该指纹图谱具有良好的精密度、重复性、稳定性，各共有峰间分离度好，可用于复方感冒灵流浸膏的质量评价；该研究为复方感冒灵流浸膏物质基础的研究提供基础。 |
| 关键词: 复方感冒灵流浸膏 高效液相色谱法 指纹图谱 化学成分 质量控制 |
| DOI：10.13748/j.cnki.issn1007-7693.2019.15.007 |
| 分类号:R917.101 |
| 基金项目:郴州市科技局科技计划项目（czgx201512）；湘发改投资（2018）236号 |
|
| HPLC Fingerprint Analysis and Chemical Component Analysis of Fufang Ganmaoling Fluid Extract |
|
LI Ke1, CHEN Dan2, FU Guocheng3, HOU Xi1, SHEN Bingbing1, GONG Xiaobing3, LI Ruocun1
|
|
1.Hunan Academy of TCM, Changsha 410013, China;2.Xiangtan Medical and Health Vocational and Technical College, Xiangtan 411102, China;3.Huarun 39 Pharmaceutical Co., Ltd., Chenzhou 423000, China
|
| Abstract: |
| OBJECTIVE To establish the HPLC fingerprint of Fufang Ganmaoling fluid extract and analyze its chemical components for its quality control and medicinal substance study. METHODS Kromasil C18 column(4.6 mm×250 mm, 5 μm) was used with acetonitrile-0.1% formic acid solution as the mobile phase for gradient elution, and the flow rate was 1.0 mL·min-1. The detection wavelength was 290 nm, the column temperature was set at 30℃. Ten batches of Fufang ganmaoling fluid extract were detected, their HPLC fingerprint was established by using Similarity Evaluation System for Chromatographic Fingerprint, and the chemical components in common peaks were identified by reference standard and HPLC-Q-TOF-MS/MS. RESULTS Fingerprints of Fufang Ganmaoling fluid extract were established and 12 common peaks were identified. The peaks were well separated, and the relative retention time of common peaks in each batch was less than 3.0% respectively; the similarity was >0.9 among different samples and 12 chemical components were identified as follows:quinic acid, protocatechuic acid, neochlorogenic acid, swertiajaposide F, chlorogenic acid, cryptochlorogenic acid, caffeic acid, dicaffeoylquinic acid, 3,4-dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid, 4,5-dicaffeoylquinic acid and buddleoside. CONCLUSION The method can be used for the quality control of Fufang Ganmaoling fluid extract with good precision, reproducibility and stability, providing basis for further studies on therapeutic efficacy of Fufang Ganmaoling fluid extract. |
| Key words: Fufang Ganmaoling fluid extract HPLC fingerprint chemical component quality control |
|
|
|
|
