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采用 LC-MS/MS、电子显微镜和刚果红染色分析多组分中药方剂的化学和物理方法。

Chemical and Physical Methods to Analyze a Multicomponent Traditional Chinese Herbal Prescription Using LC-MS/MS, Electron Microscope, and Congo Red Staining.

机构信息

Institute of Traditional Medicine, National Yang-Ming University, Taipei 112, Taiwan.

出版信息

Evid Based Complement Alternat Med. 2013;2013:952796. doi: 10.1155/2013/952796. Epub 2013 Aug 12.

DOI:10.1155/2013/952796
PMID:23997802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3753750/
Abstract

This study develops several chemical and physical methods to evaluate the quality of a traditional Chinese formulation, Jia-Wei-Xiao-Yao-San. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) coupled with electrospray ionization was used to measure the herbal biomarkers of saikosaponin A, saikosaponin D, ferulic acid, and paeoniflorin from this herbal formula. A scanning electron microscope (SEM) and light microscopy photographs with Congo red staining were used to identify the cellulose fibers if raw herbal powder had been added to the herbal pharmaceutical product. Moreover, water solubility and crude fiber content examination were used to inspect for potential herbal additives to the herbal pharmaceutical products. The results demonstrate that the contents of the herbal ingredients of saikosaponin A, saikosaponin D, ferulic acid, and paeoniflorin were around 0.351 ± 0.017, 0.136 ± 0.010, 0.140 ± 0.005, and 2.281 ± 0.406 mg/g, respectively, for this herbal pharmaceutical product. The physical examination data demonstrate that the raw herbal powder had rough, irregular, lumpy, filamentous, and elongated shapes, as well as strong Congo red staining. In addition, water solubility and crude fiber content were not consistent in the herbal pharmaceutical products.

摘要

本研究开发了几种化学和物理方法来评估一种传统中药配方——加味逍遥散的质量。采用液相色谱-串联质谱(LC-MS/MS)结合电喷雾电离法,测定了该草药配方中柴胡皂苷 A、柴胡皂苷 D、阿魏酸和芍药苷的草药生物标志物。扫描电子显微镜(SEM)和带有刚果红染色的光学显微镜照片用于鉴定原始草药粉末是否添加到草药药物产品中。此外,水溶性和粗纤维素含量检查用于检查草药药物产品中是否存在潜在的草药添加剂。结果表明,该草药药物产品中柴胡皂苷 A、柴胡皂苷 D、阿魏酸和芍药苷的含量分别约为 0.351±0.017、0.136±0.010、0.140±0.005 和 2.281±0.406mg/g。物理检查数据表明,原始草药粉末具有粗糙、不规则、块状、丝状和细长形状,以及强烈的刚果红染色。此外,在草药药物产品中,水溶性和粗纤维素含量不一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/4f0ae1ed6c15/ECAM2013-952796.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/25a99d40a4db/ECAM2013-952796.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/5162c0a8ff44/ECAM2013-952796.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/73376f9d4dc0/ECAM2013-952796.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/4f0ae1ed6c15/ECAM2013-952796.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/25a99d40a4db/ECAM2013-952796.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/5162c0a8ff44/ECAM2013-952796.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/73376f9d4dc0/ECAM2013-952796.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e1/3753750/4f0ae1ed6c15/ECAM2013-952796.004.jpg

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