College of Food and Biological Engineering, Chengdu University, Chengdu 610106, China; MIIT Public Service Platforms for Industrial Technological Base, NMPA Key Laboratory for Quality Evaluation of Traditional Chinese Medicine (Traditional Chinese Patent Medicine), Sichuan Institute for Drug Control (Sichuan Testing Center of Medical Devices), Chengdu 611731, China.
MIIT Public Service Platforms for Industrial Technological Base, NMPA Key Laboratory for Quality Evaluation of Traditional Chinese Medicine (Traditional Chinese Patent Medicine), Sichuan Institute for Drug Control (Sichuan Testing Center of Medical Devices), Chengdu 611731, China.
J Pharm Biomed Anal. 2024 Nov 15;250:116394. doi: 10.1016/j.jpba.2024.116394. Epub 2024 Aug 8.
Traditional Chinese medicine (TCM) and its preparations have become increasingly popular in recent years. Nonetheless, due to the high complexity of the compounds in Traditional Chinese Patent Medicine (TCPM), the quality differences between different dosage forms and products from various manufacturers pose numerous challenges and difficulties in quality evaluation. The Qiangli Tianma Duzhong (QLTMDZ) prescription, comprising twelve TCM, is widely used in China. Despite its prevalence, current research on QLTMDZ is limited and lacks in-depth and systematic analysis of the chemical composition of the prescription. In this study, a comprehensive strategy was proposed for characterizing the chemical profile of QLTMDZ based on UHPLC-Q-TOF-MS. A total of 122 compounds were identified in QLTMDZ under both positive and negative ion modes. Subsequently, multivariate statistical methods such as principal component analysis (PCA) and orthogonal partial least squares-discriminant analysis (OPLS-DA) were conducted in the MS-DIAL software to further elucidate quality differences among 55 batches of QLTMDZ samples from seven manufacturers. Lastly, multiple reaction monitoring (MRM) mode was utilized in conjunction with UHPLC-QQQ-MS, for the precise quantification of the identified 24 compounds within the QLTMDZ preparation and providing supplementary information in quality evaluation. The established analytical method in this study is sensitive and efficient, enabling qualitative and quantitative analysis of the chemical constituents within QLTMDZ. The application of multivariate statistical analyses effectively discriminates samples based on different dosage forms and manufacturers, thereby providing new research directions and scientific support for further studies on the quality control of the prescription.
中药及其制剂近年来越来越受欢迎。然而,由于中药复方制剂成分的高度复杂性,不同剂型和不同厂家产品之间的质量差异给质量评价带来了诸多挑战和困难。强力天麻杜仲(QLTMDZ)方由 12 种中药组成,在中国广泛应用。尽管如此,目前对 QLTMDZ 的研究有限,缺乏对该处方化学成分的深入系统分析。在本研究中,提出了一种基于 UHPLC-Q-TOF-MS 全面表征 QLTMDZ 化学特征的策略。在正、负离子模式下,共鉴定出 QLTMDZ 中的 122 种化合物。随后,在 MS-DIAL 软件中采用主成分分析(PCA)和正交偏最小二乘判别分析(OPLS-DA)等多变量统计方法,进一步阐明了来自 7 家制造商的 55 批 QLTMDZ 样品之间的质量差异。最后,采用多重反应监测(MRM)模式结合 UHPLC-QQQ-MS 对 QLTMDZ 制剂中鉴定出的 24 种化合物进行精确定量,并为质量评价提供补充信息。本研究建立的分析方法灵敏、高效,可对 QLTMDZ 中的化学成分进行定性和定量分析。多变量统计分析的应用有效地根据不同剂型和制造商对样品进行区分,为进一步研究该处方的质量控制提供了新的研究方向和科学支持。