利用超高效液相色谱-四极杆飞行时间质谱法和感应效应分析法对藿香正气混合物中的异构体进行鉴定和质量控制。

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2025-03-15 Epub Date: 2024-12-18 DOI:10.1016/j.jpba.2024.116646
Yourun Chen, Chongyang Wang, Kaiwen Zhang, Meng Zhao, Qing Wang, Yanqing Zhang, Chang-Jiang-Sheng Lai
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引用次数: 0

摘要

藿香正气合剂是一种著名的中药配方,用于治疗与潮湿病原体有关的疾病。本研究采用超高效液相色谱-四极杆飞行时间质谱联用技术对藿香正气合剂中的化学成分进行了全面的定性和定量分析。共鉴定出155种化合物,其中黄酮类化合物及其苷类61种,苯乙醇类苷类36种,皂苷类23种,香豆素类14种,有机酸类9种,氨基酸类1种,核苷类和嘌呤类2种,其他化合物9种。首次建立了一种基于诱导效应和氢键的实用方法来确定PhGs异构体的洗脱顺序。测定了藿香正气合剂中9个同分异构体的相对定量和10个化合物的绝对定量,这些化合物主要来源于陈皮、甘草和厚朴。值得注意的是,在藿香正气方中首次定量到18 β -甘草次酸和9个苯乙醇苷异构体。并与藿香正气口服液的相应值进行比较。研究发现,混合物中18 β -甘草次酸含量相对较低,四种关键化合物厚朴酚、厚朴酚、甘草酸和橙皮苷的含量差异显著。本研究为进一步了解藿香正气合剂的化学成分提供了依据,为优化制剂工艺、提高疗效和建立质量标准提供了依据。
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Identification and quality control of isomers in Huo-Xiang-Zheng-Qi Mixture using ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry and inductive effects analysis.

Huo-Xiang-Zheng-Qi Mixture is a renowned traditional Chinese medicine formula used to treat ailments associated with dampness pathogens. This study employed ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry to perform a comprehensive qualitative and quantitative analysis of the chemical compounds in Huo-Xiang-Zheng-Qi Mixture. A total of 155 compounds were identified, including 61 flavonoids and their glycosides, 36 phenylethanoid glycosides, 23 saponins, 14 coumarins, 9 organic acids, 1 amino acid, 2 nucleosides and purines, and 9 additional compounds. For the first time, a practical method based on inductive effects and hydrogen bonding was developed to determine the elution order of PhGs isomers. The relative quantification of 9 isomers and the absolute quantification of 10 compounds in Huo-Xiang-Zheng-Qi Mixture were determined, primarily derived from tangerine peel, licorice and Magnolia officinalis. Notably, 18 β - glycyrrhetinic acid and 9 Phenylethanoid glycosides isomers were quantified for the first time in the Huo-Xiang-Zheng-Qi prescription. These findings were compared with corresponding values in Huo-Xiang-Zheng-Qi oral liquid. The research revealed relatively low levels of 18 β - glycyrrhetinic acid in the mixture and significant differences in the content of four key compounds: magnolol, honokiol, glycyrrhizic acid and hesperidin. This study offers valuable insights into the chemical composition of Huo-Xiang-Zheng-Qi Mixture and provides a foundation for optimizing preparation processes, improving therapeutic efficacy, and establishing quality standards.

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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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