银杏叶提取物的高效液相色谱定量分析新方法:单标多组分测定。

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Jianing Li, Ping Li, Hao Sun, Fan He, Qi Wu, Zhaofang Liu, Shuhong Ye, Yan Ding
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引用次数: 0

摘要

本研究建立了银杏叶(GBL)中12种主要黄酮类化合物的高效液相色谱质量控制方法,通过指纹图谱分析和多组分测定的单一标准(SSDMC)同时测定。采用SSDMC、传统外标法(ES)和中国药典法(CP)对13批GBL样品和标准提取物进行分析。该方法具有良好的线性度(r2 ~ 0.9993)、检出限(0.13 ~ 0.83 μg/mL)、定量限(0.43 ~ 2.76 μg/mL)、精密度(相对标准偏差[RSD])。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative Analysis of Ginkgo biloba Extracts Using a New HPLC Method: Single Standard for the Determination of Multiple Components.

In this study, a quality control method utilizing high-performance liquid chromatography has been developed to simultaneously determine the content of 12 major flavonoids in Ginkgo biloba leaf (GBL) through fingerprint analysis and a single standard for the determination of multiple components (SSDMC). Thirteen batches of GBL samples and standardized extracts were analyzed using the SSDMC, traditional external standard (ES) and Chinese pharmacopoeia (CP) methods. The new quality control method was credible and feasible, having been sufficiently validated for linearity (r2 > 0.9993), limits of detection (0.13-0.83 μg/mL), limits of quantification (0.43-2.76 μg/mL), precision (relative standard deviation [RSD] < 0.89%), accuracy (92-114%, RSD < 1.76%), repeatability (RSD < 1.92%) and stability (RSD < 1.96%). The flavone contents observed in the 13 batches of GBL samples and standardized extracts showed no significant difference when using SSDMC and ES methods, and their contents were slightly higher than those obtained using the CP method.

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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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