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采用亚 2μm 粒径填充柱的超高效合相色谱法分离酚酸类化合物的分析方法开发。

Development of an analytical method for separation of phenolic acids by ultra-performance convergence chromatography (UPC) using a column packed with a sub-2-μm particle.

机构信息

Key Laboratory of Chinese Materia Medica, Heilongjiang University of Chinese Medicine, Ministry of Education, Harbin, 150040, PR China.

Key Laboratory of Chinese Materia Medica, Heilongjiang University of Chinese Medicine, Ministry of Education, Harbin, 150040, PR China; School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, 528458, PR China.

出版信息

J Pharm Biomed Anal. 2018 May 10;153:117-125. doi: 10.1016/j.jpba.2018.02.027. Epub 2018 Feb 16.

DOI:10.1016/j.jpba.2018.02.027
PMID:29477129
Abstract

Phenolic acids are important active components of certain Traditional Chinese Medicines (TCM) and have a wide range of biological effects. Separation and purification of phenolic acids remains challenging due to difficulties with quality control using existing chromatographic methods The purpose of this study was to compare the effects of different chromatographic columns and conditions for the separation of phenolic acids. The BEH column was determined to be optimal, providing efficient separation in the shortest time (17.00 min) using gradient elution with carbon dioxide as the mobile phase, methanol/acetonitrile (70:30, v/v) with 1% TFA as the modifier, and a flow rate of 0.8 mL/min. Good peak shapes were obtained, and the peak asymmetry values were close to 1.00 for all phenolic acids. The resolution was more than 2.83 for all separated peaks. The developed method was subsequently applied to the determination of phenolic acids in Xanthii Fructus. These results are beneficial for quality control and standardization of herbal drugs using UPC, providing an efficient, rapid and environmentally friendly scientific basis for future analysis of phenolic acids.

摘要

酚酸是某些中药(TCM)的重要活性成分,具有广泛的生物效应。由于现有色谱方法的质量控制困难,酚酸的分离和纯化仍然具有挑战性。本研究旨在比较不同色谱柱和条件对酚酸分离的影响。结果表明,BEH 柱是最优的,使用二氧化碳作为流动相进行梯度洗脱,甲醇/乙腈(70:30,v/v)与 1%TFA 作为改性剂,流速为 0.8 mL/min,在最短时间(17.00 min)内提供了高效的分离。所有酚酸的峰形都很好,峰不对称值接近 1.00。所有分离峰的分辨率均大于 2.83。所建立的方法随后应用于测定葶苈子中的酚酸。这些结果有利于使用 UPC 对草药进行质量控制和标准化,为未来分析酚酸提供了高效、快速和环保的科学基础。

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