4.6 Article

Development of a Reverse-Phase High-Performance Liquid Chromatography and Liquid Chromatography Tandem Mass Spectrometry Methods for Quality Control of Daegunjoong-Tang

期刊

APPLIED SCIENCES-BASEL
卷 11, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/app11083437

关键词

high-performance liquid chromatography; liquid chromatography tandem mass spectrometry; quality control; Daegunjoong-tang

资金

  1. Korea Institute of Oriental Medicine [KSN2021310]
  2. National Research Council of Science & Technology (NST), Republic of Korea [KSN2021310] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

In this study, a protocol for quality control of Daegunjoong-tang (DGJT) based on reverse-phase HPLC and LC-MS/MS analysis was developed to separate, verify, and quantify four marker analytes. The developed methods successfully detected the marker analytes in the samples, which will be useful for evaluating the quality of DGJT.
Daegunjoong-tang (DGJT) is an oriental medicine consisting of four medicinal herbs (Zingiber officinale Rosc., Panax ginseng C.A.Mey., Oryza sativa L., and Zanthoxylum schinifolium Sieb. et Zucc.) that is used to treat intestinal- and cancer-related diseases. In this study, a protocol for quality control of DGJT based on reverse-phase high-performance liquid chromatography (HPLC) and liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis were developed. In HPLC analysis, the marker analytes (hyperoside, quercitrin, ginsenoside Rg1, and 6-gingerol) were separated, verified, and quantified using a mobile phase of 0.1% (v/v) aqueous formic acid-0.1% (v/v) formic acid in acetonitrile system, and a C18 reverse-phase column (4.6 mm x 250 mm, particle size; 5 m) maintained at 40 degrees C. In LC-MS/MS analysis, all analytes were separated using a Waters Acquity UPLC BEH C-18 column (2.1 mm x 100 mm, particle size; 1.7 mu m). Using the developed HPLC and LC-MS/MS methods, the four marker analytes were found in the samples at 0.95-13.86 mg/g (HPLC) and 0.27-2.42 mg/g (LC-MS/MS). The assay will be useful for evaluating the quality of DGJT.

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