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  • Title/Summary/Keyword: Photoreduction fluorescence detection

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Photoreactivity of Anthraquinones for the Analysis of Ginsenosides Using Photoreduction Fluorescence Detection-HPLC

  • Park, Man-Ki;Kim, Bak-Kwang;Park, Jeong-Hill;Shin, Young-Geun;Cho, Kyung-Hee;Do, Young-Mi
    • Archives of Pharmacal Research
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    • v.19 no.6
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    • pp.562-565
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    • 1996
  • The photoreactivity of twelve anthraquinone derivatives was examined to evaluate its usefulness as a photo-reagent for the analysis of ginsenosides using photoreduction fluorescence (PRF) detection method. Among the tested compounds, 2-tert-butylandthraquinone (TBAQ), 2-chloroanthraquinone (CAQ) and anthraquinone (AQ) showed good characteristics as photoreagents. The detection limits of ginsenoside Rg1PRF-HPLC method using TBAQ, CAQ or AQ as a photo-reagent were found to be ca. 35 ng, 50 ng and 50 ng, respectively.

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Analysis of Saikosaponins by HPLC with Photoreduction Fluorescence Detection (광반응 HPLC를 이용한 시호 사포닌의 분석)

  • Shin, Young-Geun;Cho, Kyung-Hee;Kwon, Soo-Jin;Do, Young-Mi;Hwang, Gwi-Seo;Park, Jeong-Hill;Park, Man-Ki
    • YAKHAK HOEJI
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    • v.40 no.1
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    • pp.41-45
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    • 1996
  • A high performance liquid chromatography using photoreduction fluorescence detection was described for the analysis of saikosaponins. Saikosaponins were separated on an NH2 column using acetonitrile and aqueous 2-tert-butylanthraquinone(t-BAQ) as mobile phase. Column effluent was passed through a 40cm PTFE capillary tube coiled around a 10W UV lamp to reduce t-BAQ to a highly fluorescent dihydroxyanthracene derivative which was detected by a fluorescence detector. The optimal concentration of t-BAQ was found to be 6×105M and the optimal reaction time to be 2 seconds. The detection limit for saikosaponin a and d by this method was found to be about 280ng and 80ng. The dynamic linear range was over two orders and the correlation coefficient of the calibration curve of them was 0.998.

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Analysis of Ginseng Saponins by HPLC with Photoreduction Fluorescence Detection

  • Kim, Bae-Yuan;Lee, Mi-Young;Cho, Kyung-Hee;Park, Jeong-Hill;Park, Man-Ki
    • Archives of Pharmacal Research
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    • v.15 no.4
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    • pp.328-332
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    • 1992
  • A new high performance liquid chromatographic procedure is described for the analysis of ginseng saponins. Ginseng saponins were separated on Lichrosorb NH2 column and anthraquinone-2, 6-disulfonate (AQDS) solution was added to the column effluent. The effluent was passed through 1.5m-PTFE capillary coiled around 10 W-UV lamp to reduce AQDS to highly fluorescent 9. 10-dihydroxyanthracene-2, 6-disulfonate which was detected by fluorescence detector. The detection limit for the ginsenoside Rg1 by this method was found to be about 350 ng, the dynamic linear range was 102 and the correlation coefficient of the calibration curve was 0.9999.

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