New Quality Evaluation of Qizhi Xiangfu Pills Based on Fingerprint with Chemometric Analysis and Quantitative Analysis of Multi-Components by Single Marker.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xiaoli Xu, Lin Yang, Dezhang Zhao, Yiwu Wang, Lei Dai, Shuya Li, Dan He
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引用次数: 0

Abstract

Qizhi Xiangfu Pills (QZXFPs) is one of the most commonly used traditional Chinese medicine preparations for the treatment of dysmenorrhea, but the existing quality evaluation standards have certain shortcomings and deficiencies. An effective and scientific quality evaluation method plays a vital role in medication safety. In this study, fingerprint combined with chemometric analysis and quantitative analysis of multi-components by a single marker (QAMS) method was used to comprehensively evaluate the quality of QZXFPs. The fingerprints of 28 batches samples were established and 23 common peaks were distinguished, of which 7 peaks were identified as albiflorin, paeoniflorin, baicalin, ligustilide, cyperotundone, nootkatone and α-cyperone. The content of these seven active ingredients was determined simultaneously by the QAMS method and there was no significantly different between QAMS and the external standard method. Additionally, similarity analysis, hierarchical cluster analysis, principal component analysis and orthogonal partial least squares discrimination analysis were applied for classifying the 28 batches of samples, and to find the main components causing the quality differences between different batches. In conclusion, the established method can comprehensively evaluate the consistency of quality between different batches and provide a reference for formulation quality evaluation to ensure safe and effective application of QZXFPs.

基于指纹化学计量分析和单标记多成分定量分析的杞菊地黄丸质量评价新方法。
芪苈强心丸是治疗痛经最常用的中药制剂之一,但现有的质量评价标准存在一定的缺陷和不足。有效、科学的质量评价方法对用药安全起着至关重要的作用。本研究采用指纹图谱结合化学计量分析法和单一标记多组分定量分析法(QAMS)对芪苈强心丸的质量进行了综合评价。对28批次样品进行了指纹图谱分析,共鉴定出23个峰,其中7个峰分别为白花前胡素、芍药苷、黄芩苷、藁本内酯、香紫苏内酯、诺特卡酮和α-紫苏内酯。采用 QAMS 法同时测定了这七种有效成分的含量,结果表明 QAMS 法与外标法无显著差异。此外,还采用相似性分析、层次聚类分析、主成分分析和正交偏最小二乘判别分析等方法对 28 个批次的样品进行了分类,并找出了造成不同批次样品质量差异的主要成分。总之,所建立的方法可全面评价不同批次之间的质量一致性,为制剂质量评价提供参考,以确保安全有效地应用 QZXFP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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