Jiawei Wang , Jiajia Gong , Jiakang Liu , Xudong Mao , Chunyue Huang , Chun Lei , Xiao Hu
{"title":"基于q标记的白芨质量控制综合策略研究","authors":"Jiawei Wang , Jiajia Gong , Jiakang Liu , Xudong Mao , Chunyue Huang , Chun Lei , Xiao Hu","doi":"10.1016/j.jpba.2025.117174","DOIUrl":null,"url":null,"abstract":"<div><div>Bletillae Rhizoma, the rhizome of <em>Bletilla striata</em> (Tunb.) Rchb.f. (BS), a common traditional Chinese medicine, is used to achieve haemostasis and has been widely utilized in clinics for more than 2000 years. Owing to a shortage of resources, some unofficial substitutes such as <em>Bletilla ochracea</em> (BO), <em>Bletilla formosana</em> (BF), and <em>Anthogonium gracile</em> (AG) are also available on the market. This study aims to enhance the quality control of BS and distinguish unofficial substitutes. In this study, an integrated strategy based on Q-marker was performed. Multiple techniques, including untargeted plant metabolomics, serum pharmacochemistry, and activity testing, were combined to identify the Q-marker of BS. A simultaneous quantification method based on Q-marker was established using UPLC-DAD. Through untargeted plant metabolomics, 20 components were identified as differential constituents of BS for distinguishing counterfeits. Thirty-one components were identified or tentatively characterised in the BS extract, and 24 of the 31 components were detected in the serum of treated rats based on serum pharmacochemistry analysis. Six available, differential, and absorbed components, bletilloside A, batatasin III, gymnoside III, militarine, shancigusin I, and dactylorhin A, exhibited haemostatic or anti-inflammatory activities and were selected as Q-markers of BS. The contents of the six Q-markers in BS and the counterfeits were assayed, demonstrating clear differences across BS and the counterfeit species except BF. By integrating the above results, six identified components can be considered as Q-markers of BS. These markers, which are absorbed components associated with the traditional functions and biological activities of BS, can be used for the quality control of BS.</div></div>","PeriodicalId":16685,"journal":{"name":"Journal of pharmaceutical and biomedical analysis","volume":"267 ","pages":"Article 117174"},"PeriodicalIF":3.1000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An integrated strategy for quality control of Bletillae Rhizoma based on Q-marker\",\"authors\":\"Jiawei Wang , Jiajia Gong , Jiakang Liu , Xudong Mao , Chunyue Huang , Chun Lei , Xiao Hu\",\"doi\":\"10.1016/j.jpba.2025.117174\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Bletillae Rhizoma, the rhizome of <em>Bletilla striata</em> (Tunb.) Rchb.f. (BS), a common traditional Chinese medicine, is used to achieve haemostasis and has been widely utilized in clinics for more than 2000 years. Owing to a shortage of resources, some unofficial substitutes such as <em>Bletilla ochracea</em> (BO), <em>Bletilla formosana</em> (BF), and <em>Anthogonium gracile</em> (AG) are also available on the market. This study aims to enhance the quality control of BS and distinguish unofficial substitutes. In this study, an integrated strategy based on Q-marker was performed. Multiple techniques, including untargeted plant metabolomics, serum pharmacochemistry, and activity testing, were combined to identify the Q-marker of BS. A simultaneous quantification method based on Q-marker was established using UPLC-DAD. Through untargeted plant metabolomics, 20 components were identified as differential constituents of BS for distinguishing counterfeits. Thirty-one components were identified or tentatively characterised in the BS extract, and 24 of the 31 components were detected in the serum of treated rats based on serum pharmacochemistry analysis. Six available, differential, and absorbed components, bletilloside A, batatasin III, gymnoside III, militarine, shancigusin I, and dactylorhin A, exhibited haemostatic or anti-inflammatory activities and were selected as Q-markers of BS. The contents of the six Q-markers in BS and the counterfeits were assayed, demonstrating clear differences across BS and the counterfeit species except BF. By integrating the above results, six identified components can be considered as Q-markers of BS. These markers, which are absorbed components associated with the traditional functions and biological activities of BS, can be used for the quality control of BS.</div></div>\",\"PeriodicalId\":16685,\"journal\":{\"name\":\"Journal of pharmaceutical and biomedical analysis\",\"volume\":\"267 \",\"pages\":\"Article 117174\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-09-30\",\"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/S0731708525005151\",\"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/S0731708525005151","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
An integrated strategy for quality control of Bletillae Rhizoma based on Q-marker
Bletillae Rhizoma, the rhizome of Bletilla striata (Tunb.) Rchb.f. (BS), a common traditional Chinese medicine, is used to achieve haemostasis and has been widely utilized in clinics for more than 2000 years. Owing to a shortage of resources, some unofficial substitutes such as Bletilla ochracea (BO), Bletilla formosana (BF), and Anthogonium gracile (AG) are also available on the market. This study aims to enhance the quality control of BS and distinguish unofficial substitutes. In this study, an integrated strategy based on Q-marker was performed. Multiple techniques, including untargeted plant metabolomics, serum pharmacochemistry, and activity testing, were combined to identify the Q-marker of BS. A simultaneous quantification method based on Q-marker was established using UPLC-DAD. Through untargeted plant metabolomics, 20 components were identified as differential constituents of BS for distinguishing counterfeits. Thirty-one components were identified or tentatively characterised in the BS extract, and 24 of the 31 components were detected in the serum of treated rats based on serum pharmacochemistry analysis. Six available, differential, and absorbed components, bletilloside A, batatasin III, gymnoside III, militarine, shancigusin I, and dactylorhin A, exhibited haemostatic or anti-inflammatory activities and were selected as Q-markers of BS. The contents of the six Q-markers in BS and the counterfeits were assayed, demonstrating clear differences across BS and the counterfeit species except BF. By integrating the above results, six identified components can be considered as Q-markers of BS. These markers, which are absorbed components associated with the traditional functions and biological activities of BS, can be used for the quality control of BS.
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.