{"title":"通过对30种东亚传统中药制剂的对比分析,揭示了1H NMR谱法在中药质量控制中的适用性","authors":"Eunah Jeong, Huong T. Pham, Kyo Bin Kang","doi":"10.1016/j.jpba.2025.117089","DOIUrl":null,"url":null,"abstract":"<div><div>Multi-herbal formulations in East Asian traditional medicine have long played an important role in disease treatment and modern drug discovery. Despite extensive efforts toward standardization, quality control remains challenging due to their chemical complexity and richness in polar metabolites, which complicate chromatography-based methods. Nuclear Magnetic Resonance (NMR) spectroscopy offers an alternative solution; however, previous studies have mainly focused on single formulations, with limited systematic analysis across multiple formulations. This study explores the applicability of <sup>1</sup>H NMR spectroscopy for quality control in East Asian traditional medicine products by analyzing 86 batch samples from 30 formulations, manufactured in a GMP-certified facility. Pearson correlation efficients between binned spectra were calculated to evaluate both batch-to-batch and formulation-to-formulation similarities. Batch-to-batch correlations were consistently high (r > 0.99), indicating excellent reproducibility. In contrast, formulation-to-formulation correlations ranged from 0.72 to 1.00, largely influenced by saccharide abundance. Additionally, three major specialized metabolites—paeoniflorin, naringin, and baicalin—were identified based on their characteristic proton signals, and their presence correlated with the herbal composition of each formulation. These findings highlight the potential of <sup>1</sup>H NMR analysis as an effective solution for the quality control of traditional medicines, addressing the challenges posed by their chemical complexity while ensuring consistency and providing detailed insights into metabolite variations among formulations.</div></div>","PeriodicalId":16685,"journal":{"name":"Journal of pharmaceutical and biomedical analysis","volume":"266 ","pages":"Article 117089"},"PeriodicalIF":3.1000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative analysis of 30 East Asian traditional medicine formulations revealed the applicability of 1H NMR spectroscopy in quality control\",\"authors\":\"Eunah Jeong, Huong T. Pham, Kyo Bin Kang\",\"doi\":\"10.1016/j.jpba.2025.117089\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Multi-herbal formulations in East Asian traditional medicine have long played an important role in disease treatment and modern drug discovery. Despite extensive efforts toward standardization, quality control remains challenging due to their chemical complexity and richness in polar metabolites, which complicate chromatography-based methods. Nuclear Magnetic Resonance (NMR) spectroscopy offers an alternative solution; however, previous studies have mainly focused on single formulations, with limited systematic analysis across multiple formulations. This study explores the applicability of <sup>1</sup>H NMR spectroscopy for quality control in East Asian traditional medicine products by analyzing 86 batch samples from 30 formulations, manufactured in a GMP-certified facility. Pearson correlation efficients between binned spectra were calculated to evaluate both batch-to-batch and formulation-to-formulation similarities. Batch-to-batch correlations were consistently high (r > 0.99), indicating excellent reproducibility. In contrast, formulation-to-formulation correlations ranged from 0.72 to 1.00, largely influenced by saccharide abundance. Additionally, three major specialized metabolites—paeoniflorin, naringin, and baicalin—were identified based on their characteristic proton signals, and their presence correlated with the herbal composition of each formulation. These findings highlight the potential of <sup>1</sup>H NMR analysis as an effective solution for the quality control of traditional medicines, addressing the challenges posed by their chemical complexity while ensuring consistency and providing detailed insights into metabolite variations among formulations.</div></div>\",\"PeriodicalId\":16685,\"journal\":{\"name\":\"Journal of pharmaceutical and biomedical analysis\",\"volume\":\"266 \",\"pages\":\"Article 117089\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pharmaceutical and biomedical analysis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0731708525004303\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmaceutical and biomedical analysis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0731708525004303","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Comparative analysis of 30 East Asian traditional medicine formulations revealed the applicability of 1H NMR spectroscopy in quality control
Multi-herbal formulations in East Asian traditional medicine have long played an important role in disease treatment and modern drug discovery. Despite extensive efforts toward standardization, quality control remains challenging due to their chemical complexity and richness in polar metabolites, which complicate chromatography-based methods. Nuclear Magnetic Resonance (NMR) spectroscopy offers an alternative solution; however, previous studies have mainly focused on single formulations, with limited systematic analysis across multiple formulations. This study explores the applicability of 1H NMR spectroscopy for quality control in East Asian traditional medicine products by analyzing 86 batch samples from 30 formulations, manufactured in a GMP-certified facility. Pearson correlation efficients between binned spectra were calculated to evaluate both batch-to-batch and formulation-to-formulation similarities. Batch-to-batch correlations were consistently high (r > 0.99), indicating excellent reproducibility. In contrast, formulation-to-formulation correlations ranged from 0.72 to 1.00, largely influenced by saccharide abundance. Additionally, three major specialized metabolites—paeoniflorin, naringin, and baicalin—were identified based on their characteristic proton signals, and their presence correlated with the herbal composition of each formulation. These findings highlight the potential of 1H NMR analysis as an effective solution for the quality control of traditional medicines, addressing the challenges posed by their chemical complexity while ensuring consistency and providing detailed insights into metabolite variations among formulations.
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.