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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Integrating chemical similarity and bioequivalence: A pilot study on quality consistency evaluation of dispensing granule and traditional decoction of Scutellariae Radix by a totality-of-the-evidence approach
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Integrating chemical similarity and bioequivalence: A pilot study on quality consistency evaluation of dispensing granule and traditional decoction of Scutellariae Radix by a totality-of-the-evidence approach

机译:集成化学相似性和生物等效性:通过证据 - 证据方法分配颗粒的质量一致性评价和传统粪便传统汤的试验研究

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摘要

There is an increasing focus on the quality consistency evaluation of dispensing granule in traditional Chinese medicines (TCMs). According to the guideline from Chinese Pharmacopoeia Commission, the substantial equivalence of dispensing granule and traditional decoction should be determined, and the chromatographic fingerprint has been recommended as a comprehensive qualitative approach to assess the quality consistency between dispensing granule and traditional decoction. However, a high-degree chemical similarity does not equal a bioequivalence. Attempting to realize the quality evaluation by integrating chemical consistency and bioequivalence, we herein proposed a totality-of-the-evidence approach based on clustering analysis and equivalence evaluation taking the dispensing granule and traditional decoction of Scutellariae Radix (SR) as a typical case. Chemical fingerprints were developed by high performance liquid chromatography coupled with photodiode array detector and quadrupole time-of-flight mass spectrometry (HPLC-PDA/QTOF-MS). Subsequently, a feature selection strategy, integrated linear and nonlinear correlation analysis, was carried out to assess the correlation between chemical profiles and biological activities. Finally, quality consistency between the dispensing granule and the traditional decoction was determined by bioactive marker-guided hierarchical clustering analysis (HCA), k-means clustering method and bioequivalence evaluation. The available evidence suggested that not all the dispensing granule of SR were sufficiently similar to the traditional decoction. This study provides an applicable methodology for quality consistency evaluation of dispensing granule and traditional decoction in TCMs. (C) 2019 Elsevier B.V. All rights reserved.
机译:在中药(TCMS)中分配颗粒的质量一致性评价越来越重要。根据中文药典委员会的指导,应确定分配颗粒和传统汤剂的大量等价,并建议使用色谱指纹作为评估分配颗粒和传统煎汤之间的质量一致性的综合定性方法。然而,高度的化学相似性不等于生物等效性。试图通过整合化学稠度和生物等效性来实现质量评价,我们在本文中提出了一种基于聚类分析和等效评价的完整验证方法,并将Cocullariae Radix(SR)的分配颗粒和传统汤剂作为典型案例。化学指纹由高性能液相色谱和耦合的光电二极管阵列检测器和四极杆飞行时间质谱法(HPLC-PDA / QTOF-MS)开发。随后,进行特征选择策略,集成线性和非线性相关分析,以评估化学分布与生物活性之间的相关性。最后,通过生物活性标记引导的分层聚类分析(HCA)测定分配颗粒与传统煎剂之间的质量一致性,K均值聚类方法和生物等效评估。可用的证据表明,并非所有SR的分配颗粒都与传统汤相似。本研究为分配颗粒和TCMS中的传统煎剂提供了适用的方法。 (c)2019 Elsevier B.v.保留所有权利。

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