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    Quantitative analysis of the eight major compounds in the Samsoeum using a high‑performance liquid chromatography coupled with diode array detection and electrospray ionization mass spectrometer

    Jin Bae Weon2, Hye Jin Yang2, Bohyoung Lee2, Jin Yeul Ma3, Choong Je Ma2,4 Corresponding author

    1. 1Department of Biomaterials Engineering, Division of Bioscience and Biotechnology.
    2. 2TKM Converging Research Division, Korea Institute of Oriental Medicine, 483 Exporo, Yuseong‑gu, Daejeon 305‑811, Korea.
    3. 3Research Institute of Biotechnology, Kangwon National University, Chuncheon 200‑701, Korea.

    CORRESPONDENCE

    Choong Je Ma

    TKM Converging Research Division, Korea Institute of Oriental Medicine, 483 Exporo, Yuseong‑gu, Daejeon 305‑811, Korea.

    cjma@kangwon.ac.kr

    Received: 03-06-2014; Revised: 19-06-2014.

    Volume 11, Issue 42 · pp. 320–326 · PUBLISHED 12 March 2015 · DOI: 10.4103/0973-1296.153085

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Background: Samsoeum was traditionally used for treatment of a respiratory disease. Objective: The simultaneous determination of eight major compounds, ginsenoside Rg3, caffeic acid, puerarin, costunolide, hesperidin, naringin, glycyrrhizin, and 6‑gingerol in the Samsoeum using a high‑performance liquid chromatography (HPLC) coupled with diode array detection (DAD) and an electrospray ionization mass spectrometer was developed for an accurate and reliable quality assessment. Materials and Methods: Eight compounds were qualitative identified based on their mass spectra and by comparing with standard compounds and quantitative analyzed by HPLC‑DAD. Separation of eight compounds was carried out on a LUNA C18 column (S‑5 µm, 4.6 mm i.d. ×250 mm) with gradient elution composed of acetonitrile and 0.1% trifluoroacetic acid. Results: The data showed good linearity (R2 > 0.9996). The limits of detection and the limits of quantification were <0.53 μg and 1.62 μg, respectively. Inter‑ and Intra‑day precisions (expressed as relative standard deviation values) were within 1.94% and 1.91%, respectively. The recovery of the method was in the range of 94.24–107.90%. Conclusion: The established method is effective and could be applied to quality control of Samsoeum.

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      Weon, J. B., Yang, H. J., Lee, B., Ma, J. Y., & Ma, C. J. (2015). Quantitative analysis of the eight major compounds in the Samsoeum using a high‑performance liquid chromatography coupled with diode array detection and electrospray ionization mass spectrometer. Pharmacognosy Magazine, 11(42), 320–326. https://doi.org/10.4103/0973-1296.153085