首页|川木香标准汤剂UPLC指纹图谱的建立及多指标成分定量分析

川木香标准汤剂UPLC指纹图谱的建立及多指标成分定量分析

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目的:建立川木香标准汤剂的质量控制方法.方法:采用Waters CORTECS T3 超高效液相色谱柱,以乙腈-0.1%磷酸水溶液为流动相,梯度洗脱,流速为 0.35 mL·min-1,柱温为 40℃,检测波长在 0~21 min为325 nm、21~37 min为 225 nm,进样体积为 1 μL.采用超高效液相色谱法建立 14 批川木香标准汤剂的指纹图谱,确定指纹图谱共有峰,采用对照品对共有峰进行确证;通过相似度计算和化学计量学方法对不同产地川木香制备的标准汤剂进行分析,并对其中木香烃内酯、去氢木香内酯、绿原酸和 4,5-二-O-咖啡酰奎宁酸进行定量分析.结果:川木香标准汤剂指纹图谱共标记 14 个共有峰,指认了木香烃内酯、去氢木香内酯、绿原酸和 4,5-二-O-咖啡酰奎宁酸 4 个成分;相似度评价、聚类分析和主成分分析均将 14 批川木香标准汤剂分成 2 类,正交偏最小二乘法-判别分析从 14 个共有峰中筛选出 7 个差异性标志物;含量测定结果显示,来自四川阿坝的川木香制备的标准汤剂中木香烃内酯和去氢木香内酯的总质量分数最高、绿原酸和 4,5-二-O-咖啡酰奎宁酸的总质量分数最低,而其余 3 个产地川木香差异不大.结论:该方法分析时间短、准确度高、专属性好,能够为川木香标准汤剂及其相关制剂质量标准的制定提供参考.
Establishment of UPLC Fingerprint of Standard Vladimiriae Radix Decoction and Quantitative Analysis of Multiple Indicator Components
Objective:To establish a quality control method for standard Vladimiriae Radix decoction.Methods:The ultra-high performance liquid chromatography(UPLC)column Waters CORTECS T3 was used.Gradient elution was carried out using acetonitrile-0.1%phosphoric acid solution as the mobile phase.The flow rate of the mobile phase was 0.35 mL·min-1,and the column temperature was 40℃.The detection wavelength was 325 nm at 0-21 min and 225 nm at 21-37 min.The chromatographic injection volume was 1 μL.14 batches of standard Vladimiriae Radix decoction fingerprints were established by UPLC to determine the common peaks in the fingerprints.The common peaks were confirmed using reference substances.Similarity calculation and chemometrics methods were used to analyze the standard decoction prepared by Vladimiriae Radix from different regions,and four effective components,namely costunolide,dehydrocarbactone,chlorogenic acid,and 4,5-di-O-caffeoylquinic acid were quantitatively analyzed.Results:A total of 14 common peaks were identified in the fingerprints of standard Vladimiriae Radix decoction,and four components were identified:costunolide,dehydrocarbactone,chlorogenic acid,and 4,5-di-O-caffeoylquinic acid.Similarity evaluation,cluster analysis(HCA),and principal component analysis(PCA)all divided the 14 batches of standard Vladimiriae Radix decoction into two categories,and orthogonal partial least squares-discriminant analysis(OPLS-DA)screened a total of seven differential markers from the 14 common peaks.The content determination results showed that the standard decoction prepared by Vladimiriae Radix from Aba,Sichuan,had the highest total content of costunolide and dehydrocarbactone,while the total content of chlorogenic acid and 4,5-di-O-caffeoyl quinic acid was the lowest.The overall difference between Vladimiriae Radix from the other three regions was not significant.Conclusion:This method has a short analysis time,high accuracy,and good specificity,and it can provide a reference for the formulation of quality standards for standard Vladimiriae Radix decoction and its related preparations.

Vladimiriae Radixstandard decoctionUPLCfingerprintmultiple indicator component quantification

李振雨、梁月仪、卢晓莹、吕渭升、何民友、何广铭、刘晓霞、夏天睿、陈志鹏、黄爽、潘礼业

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广东一方制药有限公司/广东省中药配方颗粒企业重点实验室,广东 佛山 528244

川木香 标准汤剂 超高效液相色谱法 指纹图谱 多指标成分定量

中华人民共和国工信部产业技术基础公共服务平台项目(2022)

2022-230-221

2024

中国现代中药
中国中药协会,中国医药集团总公司,中国药材公司

中国现代中药

CSTPCD
影响因子:0.65
ISSN:1673-4890
年,卷(期):2024.26(5)
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