马蔺子HPLC特征图谱和3个成分含量测定
投稿时间:2024-03-26     点此下载全文
引用本文:郭晓霞,徐宁,李冬华,雷虹.马蔺子HPLC特征图谱和3个成分含量测定[J].中国现代中药,2024,26(11):1886-1891
DOI:10.13313/j.issn.1673-4890.20240326002
摘要点击次数: 110
全文下载次数: 0
           
作者中文名作者英文名单位中文名单位英文名E-Mail
郭晓霞 GUO Xiao-xia 甘肃省药品检验研究院,甘肃 兰州 730070
国家药品监督管理局 中药材及饮片质量控制重点实验室,甘肃 兰州 730070
Gansu Institute for Drug Control, Lanzhou730070, China
NMPA Key Laboratory for Quality Control of Traditional Chinese Medicine, Lanzhou730070, China
 
徐宁 XU Ning 甘肃省药品检验研究院,甘肃 兰州 730070
国家药品监督管理局 中药材及饮片质量控制重点实验室,甘肃 兰州 730070
Gansu Institute for Drug Control, Lanzhou730070, China
NMPA Key Laboratory for Quality Control of Traditional Chinese Medicine, Lanzhou730070, China
 
李冬华 LI Dong-hua 甘肃省药品检验研究院,甘肃 兰州 730070
国家药品监督管理局 中药材及饮片质量控制重点实验室,甘肃 兰州 730070
Gansu Institute for Drug Control, Lanzhou730070, China
NMPA Key Laboratory for Quality Control of Traditional Chinese Medicine, Lanzhou730070, China
 
雷虹* LEI Hong 甘肃省药品检验研究院,甘肃 兰州 730070
国家药品监督管理局 中药材及饮片质量控制重点实验室,甘肃 兰州 730070
Gansu Institute for Drug Control, Lanzhou730070, China
NMPA Key Laboratory for Quality Control of Traditional Chinese Medicine, Lanzhou730070, China
 
基金项目:兰州市科技计划项目(2022-3-41);中药材及饮片质量控制重点实验室项目(2024GSMPA-KL13,2023GSMPA-KL06);甘肃省药品监督管理局项目(2022GSMPA0017)
中文摘要:目的 采用高效液相色谱法(HPLC)建立民族药马蔺子的特征图谱,测定其3个成分的含量。方法 以白藜芦醇、马蔺子甲素和马蔺子乙素为指标,采用Waters Atlantis T3色谱柱(250 mm×4.6 mm,5 μm),以乙腈-0.1%磷酸水溶液为流动相梯度洗脱,流速为1.0 mL·min–1,检测波长为254 nm,柱温为30 ℃。结果 建立马蔺子HPLC特征图谱,标定3个特征峰,55 min内马蔺子的主要色谱峰能够达到完全分离,对16批药材中3个成分进行含量测定。白藜芦醇、马蔺子甲素和马蔺子乙素质量浓度分别为0.006 08~0.121 60、0.042 66~2.133 00、0.004 82~0.241 00 mg·mL–1时与峰面积线性关系良好,平均回收率分别为90.50%、100.36%、91.81%;16批马蔺子中3个成分的质量分数分别为0.156~0.369、1.774~5.709、0.090~0.203 mg·g–1结论 建立的HPLC特征图谱专属性强,结合3个主要成分的含量测定能够为马蔺子的质量控制提供参考。
中文关键词:马蔺子  白藜芦醇  马蔺子甲素  马蔺子乙素  特征图谱  多组分含量测定  高效液相色谱法
 
HPLC Characteristic Chromatogram of Iridis Semen and Content Determination of Three Components
Abstract:Objective The high-performance liquid chromatography (HPLC) method was established to create a characteristic chromatogram for the traditional ethnic medicine Iridis Semen and to determine the content of its three components.Methods Using resveratrol, irisquinone A, and irisquinone B as indexes, a Waters Atlantis T3 chromatographic column (250 mm×4.6 mm, 5 μm) was employed. The mobile phase gradient elution consisted of acetonitrile and 0.1% phosphoric acid aqueous solution, with a flow rate of 1.0 mL·min–1. The detection wavelength was set at 254 nm, and the column temperature was maintained at 30 ℃. The results were analyzed using Chempattern Chemometric software.Results The HPLC characteristic chromatogram of Iridis Semen was established, calibrating three characteristic peaks. The main chromatographic peaks of Iridis Semen achieved complete separation within 55 min. The content of three components was determined in 16 batches of medicinal materials. The mass concentrations of resveratrol, irisquinone A, and irisquinone B exhibited good linear relationships with peak areas in the ranges of 0.006 08-0.121 60, 0.042 66-2.133 00, and 0.004 82-0.241 00 mg·mL–1, respectively, with average recoveries rates of 90.50%, 100.36%, and 91.81%. The mass fractions of the three components in 16 batches of Iridis Semen were 0.156-0.369, 1.774-5.709, and 0.090-0.203 mg·g–1, respectively.Conclusion The established HPLC characteristic chromatogram shows strong specificity. Combined with the content determination of the three main components, it can provide a reference for quality control of the Iridis Semen.
keywords:Iridis Semen  resveratrol  irisquinone A  irisquinone B  characteristic chromatogram  multi-component content determination  HPLC
查看全文   查看/发表评论  下载PDF阅读器