HPLC指纹图谱结合多指标含量测定的抵当芪桂汤质量评价研究OA北大核心CSTPCD
Study on Quality Evaluation of Didang Qigui Decoction by HPLC Fingerprint Combined with Multi-component Content Determination
目的 建立抵当芪桂汤HPLC指纹图谱并结合化学模式识别技术对其进行分析与评价,测定抵当芪桂汤中5种有效化学成分的含量,为其质量控制提供依据.方法 采用Agilent 5 TC-C18(2)色谱柱(250 mm×4.6 mm),以乙腈-0.1%磷酸水为流动相进行梯度洗脱,流速1.0 mL/min,柱温30℃,检测波长260 nm.采用SPSS26.0和SIMCA14.1软件对10批抵当芪桂汤进行聚类分析和主成分分析,并通过正交偏最小二乘-判别分析(OPLS-DA)筛选批间差异的标志性成分.结果 10批抵当芪桂汤的HPLC指纹图谱相似度为0.828~0.989,共标定18个共有特征峰,经对照品比对,指认芍药苷、毛蕊异黄酮苷、橙皮苷、桂皮醛、芦荟大黄素5个指标性成分,并对其进行定量分析,线性范围分别为10.000 0~320.000 0 μg/mL、2.500 0~80.000 0 μg/mL,10.000 0~320.000 0 μg/mL、10.000 0~320.000 0 μg/mL、0.078 1~5.000 0 μg/mL,平均加样回收率为100.30%~104.09%.聚类分析和主成分分析将10批抵挡芪桂汤样品分为2类,通过OPLS-DA筛选出毛蕊异黄酮苷、芍药苷、橙皮苷为质量差异的标志性成分.结论 本研究建立的抵当芪桂汤质量评价方法简便、灵敏、准确、重复性好,可为抵当芪桂汤的质量评价提供依据.
Objective To establish an HPLC fingerprint of Dingdang Qigui Decoction and analyze and evaluate it using chemical pattern recognition technology;To determine the contents of 5 effective chemical components in Dingdang Qigui Decoction;To provide a basis for its quality control.Methods The analysis was performed on Agilent 5 TC-C18(2)column(250 mm×4.6 mm).The mobile phase comprised of acetonitrile-0.1%phosphoric acid aqueous solution with the gradient elution at a flow rate of 1.0 mL/min.The detection wavelength was set at 260 nm.The column temperature was maintained at 30℃and the injection volume was 10 μL.SPSS 26.0 and SIMCA 14.1 were used to perform clustering analysis and principal component analysis on the 10 batches of Didang Qigui Decoction.The landmark components for inter batch differences were selected through orthogonal partial least squares discriminant analysis(OPLS-DA).Results The HPLC fingerprint with eighteen common peaks of Didang Qigui Decoction in 10 batches of sample was established,and the similarities of samples were between 0.828 and 0.989.Five indicative components were identified and quantitatively analyzed by comparing with the reference substances,which were paeoniflorin,mauroisoflavone glucoside,hesperidin,cinnamaldehyde and aloe rhodopsin.The linear ranges was 10.000 0-320.000 0 μg/mL,2.500 0-80.000 0 μg/mL,10.000 0-320.000 0 μg/mL,10.000 0-320.000 0 μg/mL,0.078 1-5.000 0 μg/mL,respectively,and their mean recovery ranged from 100.30%to 104.09%.Clustering analysis and principal component analysis divided 10 batches of samples from Didang Qigui Decoction into 2 categories.Through OPLS-DA screening,hairy pistil isoflavone glycosides,paeoniflorin,and hesperidin were selected as landmark components for quality differences.Conclusion The quality evaluation method for Didang Qigui Decoction established in this study is simple,sensitive,accurate,and reproducible,which can provide a basis for the quality evaluation of Didang Qigui Decoction.
郭怡佳;程都;张潇;雷莉妍;梁艳妮;王征;杨景锋
陕西中医药大学基础医学院,陕西 咸阳 712046陕西中医药大学陕西中药资源产业化省部共建协同创新中心,陕西 咸阳 712083
中医学
抵当芪桂汤高效液相色谱法指纹图谱质量评价
Didang Qigui DecoctionHPLCfingerprintquality evaluation
《中国中医药信息杂志》 2024 (003)
132-137 / 6
陕西省重点研发计划(2018ZDCXL-SF-01-02-02);陕西高校青年创新团队(2019年);陕西省教育厅重点科学研究计划项目(20JY011、20JY012)
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