Zhou Lin, Sun Zhi, Xue Wen-Hua, Liang Shu-Hong, Zuo Li-Hua, Ding Juan, Zhao Ling-Ling, Jiang Xiao-Fang, Jia Qing-Quan, Wei Hua, Liu Ke-Feng, Hu You-Hong, Zhao Jie
Department of Pharmacy, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Henan Key Laboratory of Precision Clinical Pharmacy, Zhengzhou 450052, China.
Zhongguo Zhong Yao Za Zhi. 2018 Aug;43(16):3279-3284. doi: 10.19540/j.cnki.cjcmm.20180611.006.
To establish the ultra performance liquid chromatography (UPLC) fingerprint of Dandeng Tongnao Ruanjiaonang and conduct a systemic, comprehensive quality evaluation of the drug by combining with a chemical pattern recognition method. In this study, Waters UPLC ultra-high performance liquid chromatography instrument and ACQUITY UPLCHSS T3 chromatographic colum n were employed to perform the separation with acetonitrile-0.1% formic acid aqueous solution as the mobile phase for gradient elution; and the detection wavelength was set at 256 nm to establish the UPLC fingerprint of 10 batches of Dandeng Tongnao Ruanjiaonang. Then, the further quality assessment of the drug was carried out by similarity evaluation, Cluster Analysis(CA), Principal Component Analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA). Finally, 77 peaks were recognised as common peaks in the fingerprint, and 15 peaks of them were identified using standard references. The similarity value of these 10 batches of drugs was all above 0.960, indicating a relatively stable quality. But minor differences were still discovered between the batches of the drug by CA and PCA. Finally, 6 common peaks were recognised as the quality makers using OPLS-DA method. The analysis method established in this study was scientific, accurate, reliable and simple; fingerprint combined with chemical pattern recognition technique can be used to systematically and comprehensively evaluate the drug quality of Dandeng Tongnao Ruanjiaonang; what's more, it could also provide a reference for the quality control of traditional Chinese medicine and its preparations at the same time.
建立灯盏通脑软胶囊的超高效液相色谱(UPLC)指纹图谱,并结合化学模式识别方法对该药物进行系统、全面的质量评价。本研究采用Waters UPLC超高效液相色谱仪和ACQUITY UPLCHSS T3色谱柱,以乙腈 - 0.1%甲酸水溶液为流动相进行梯度洗脱分离;检测波长设定为256 nm,建立10批灯盏通脑软胶囊的UPLC指纹图谱。然后,通过相似度评价、聚类分析(CA)、主成分分析(PCA)和正交偏最小二乘法判别分析(OPLS - DA)对该药物进行进一步的质量评价。最终,在指纹图谱中识别出77个共有峰,其中15个峰通过对照品进行了鉴定。这10批药物的相似度值均在0.960以上,表明质量相对稳定。但通过CA和PCA仍发现不同批次药物之间存在微小差异。最终,采用OPLS - DA方法识别出6个共有峰作为质量标志物。本研究建立的分析方法科学、准确、可靠且简便;指纹图谱结合化学模式识别技术可用于系统、全面地评价灯盏通脑软胶囊的药物质量;同时,也可为中药及其制剂的质量控制提供参考。