An Integrated Approach to Identify the Q‐Markers of Banxia‐Houpo Decoction Based on Nontargeted Multicomponent Profiling, Network Pharmacology, and Chemometrics

化学 化学计量学 色谱法 质谱法 厚朴酚 气相色谱-质谱法 吴茱萸碱 气相色谱法 迷迭香酸 代谢组学 黄连 八醛 汤剂 黄连 飞镖离子源 固相微萃取 传统医学 中医药 病理 有机化学 离子 己醛 抗氧化剂 电子电离 医学 替代医学 电离 生物化学
作者
Long Wang,Weigang Wu,Guoxiang Li,Haiyang Chen,Yinyin Fan,Wei Chen,Guifang Zhou,Wenlong Li
出处
期刊:Phytochemical Analysis [Wiley]
卷期号:36 (3): 832-845 被引量:3
标识
DOI:10.1002/pca.3471
摘要

INTRODUCTION: The inherent complexity of traditional Chinese medicine (TCM) poses significant challenges in directly correlating quality evaluation with clinical efficacy. Banxia-Houpo Decoction (BHD), a classical TCM formula, has demonstrated efficacy in treating globus hystericus. However, the intricate composition of BHD, which contains both volatile and non-volatile active components, complicates efforts to ensure its consistent quality and clinical effectiveness. OBJECTIVE: The aim of this study was to introduce an integrated approach that combines non-targeted multicomponent analysis, network pharmacology, and multivariate chemometrics to identify quality markers for the effective quality control of BHD. MATERIALS AND METHODS: First, a nontargeted high-definition MSE method based on ultraperformance liquid chromatography-quadrupole time-of-flight-mass spectrometry (UHPLC-QTOF-MS) was developed for the comprehensive multi-component characterization of BHD. Next, the quality markers of nonvolatile compounds in BHD were identified through network pharmacology analysis. Subsequently, volatile organic compounds (VOCs) in BHD samples were analyzed via headspace solid-phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) and headspace gas chromatography-ion mobility spectrometry (HS-GC-IMS). Finally, the orthogonal partial least squares discriminant analysis (OPLS-DA) model was applied to screen for potential markers. RESULTS: Based on in-house library-driven automated peak annotation and comparison with 25 reference compounds, 128 components were identified for the first time. Additionally, honokiol, magnolol, magnoflorine, 6-gingerol, rosmarinic acid, and adenosine were preliminarily identified as potential quality markers for BHD through network pharmacology analysis. By employing two complementary techniques, HS-SPME-GC-MS and HS-GC-IMS, a total of 145 volatile compounds was identified in the BHD samples. Four potential differential VOCs in the BHD samples were further identified based on the variable importance in projection (VIP ≥ 1.5) using HS-GC-IMS combined with chemometric analysis. CONCLUSION: In conclusion, this study not only contributes to establishing quality standards for BHD but also offers new insights into quality assessment and identification in the development of classical formulations enriched with volatile components.
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