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CHEN Hua, YU Botao, JIN Weihua, PU Zhiqiang, SONG Zonghui, FAN Kaihua. Qualitative identification and quantitative determination of Fufang Shenghua granules[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(3): 252-255. doi: 10.3969/j.issn.1006-0111.2017.03.014
Citation: CHEN Hua, YU Botao, JIN Weihua, PU Zhiqiang, SONG Zonghui, FAN Kaihua. Qualitative identification and quantitative determination of Fufang Shenghua granules[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(3): 252-255. doi: 10.3969/j.issn.1006-0111.2017.03.014

Qualitative identification and quantitative determination of Fufang Shenghua granules

doi: 10.3969/j.issn.1006-0111.2017.03.014
  • Received Date: 2016-01-26
  • Rev Recd Date: 2016-07-04
  • Objective To improve quality standard of Fufang Shenghua granules. Methods TLC was used to identify chief components in the preparation, Radix et Rhizoma Glycyrrhizae and Salvia Miltiorrhiza. HPLC was applied to identify Amarogentin and to determine the content of Salvianolic acid B. Salvianolic acid B assay was performed on Agilent HC-C18(4.6 mm×250 mm, 5 μm) column with Acetonitrile-0.1% phosphoric acid (23:77)as mobile phase. The flow rate was 1.0 ml/min. The column temperature was 30 ℃. The detection wavelength was set at 286 nm. Results The spots on TLC were fairly clear with good separation. There was no interference from the negative control samples. However, HPLC was a more accurate, reliable and objective method for qualitative identification. Salvianolic acid B showed a good linear correlation in the range of 1.56~49.92 μg/ml (r=0.999 9). The average recovery was 100.07%, RSD 1.61% (n=9). Conclusion A simple, accurate and reliable method was developed for the quality control of Fufang Shenghua granules.
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Qualitative identification and quantitative determination of Fufang Shenghua granules

doi: 10.3969/j.issn.1006-0111.2017.03.014

Abstract: Objective To improve quality standard of Fufang Shenghua granules. Methods TLC was used to identify chief components in the preparation, Radix et Rhizoma Glycyrrhizae and Salvia Miltiorrhiza. HPLC was applied to identify Amarogentin and to determine the content of Salvianolic acid B. Salvianolic acid B assay was performed on Agilent HC-C18(4.6 mm×250 mm, 5 μm) column with Acetonitrile-0.1% phosphoric acid (23:77)as mobile phase. The flow rate was 1.0 ml/min. The column temperature was 30 ℃. The detection wavelength was set at 286 nm. Results The spots on TLC were fairly clear with good separation. There was no interference from the negative control samples. However, HPLC was a more accurate, reliable and objective method for qualitative identification. Salvianolic acid B showed a good linear correlation in the range of 1.56~49.92 μg/ml (r=0.999 9). The average recovery was 100.07%, RSD 1.61% (n=9). Conclusion A simple, accurate and reliable method was developed for the quality control of Fufang Shenghua granules.

CHEN Hua, YU Botao, JIN Weihua, PU Zhiqiang, SONG Zonghui, FAN Kaihua. Qualitative identification and quantitative determination of Fufang Shenghua granules[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(3): 252-255. doi: 10.3969/j.issn.1006-0111.2017.03.014
Citation: CHEN Hua, YU Botao, JIN Weihua, PU Zhiqiang, SONG Zonghui, FAN Kaihua. Qualitative identification and quantitative determination of Fufang Shenghua granules[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(3): 252-255. doi: 10.3969/j.issn.1006-0111.2017.03.014
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