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YE Shengying, GUO Qi, LEI Hong, YANG Ying. Research on quality control of Huoguwan[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(2): 156-161. doi: 10.3969/j.issn.1006-0111.2018.02.012
Citation: YE Shengying, GUO Qi, LEI Hong, YANG Ying. Research on quality control of Huoguwan[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(2): 156-161. doi: 10.3969/j.issn.1006-0111.2018.02.012

Research on quality control of Huoguwan

doi: 10.3969/j.issn.1006-0111.2018.02.012
  • Received Date: 2017-06-13
  • Rev Recd Date: 2017-11-14
  • Objective To establish the quality control method for Huoguwan. Methods TLC was applied to detect the component of Danshen, Dihuang, Danggui, Chuanxiong, Sanqi, Tubiechong, and Zhicaowu in this compound preparation. HPLC was used to measure the concentration of Renshenzaogan Rg1, Rb1 and Sanqizaogan R1. Unitary C18 analytical column(4.6 mm×250 mm,5 μm)was used with acetonitrile-water as the mobile phase (Flow rate:1.0 ml/min, column temperature:30℃, wavelength:203 nm). Results Each component showed distinct spots on TLC without interference. There are good linear relationship for Sanqizhaogan R1 in the range of 39.92-399.2 μg/ml, Renshenzhaogan Rb1 in 84.28 -842.8 μg/ml and Renshenzhaogan Rg1 in 135.86-1 358.6 μg/ml. The recovery was 102.35%, 103.84% and 102.97% respectively. Conclusion The above described procedure was accurate and reproducible, which can be used as a method for the quality control of Huoguwan.
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    [3] 张宏桂, 马辰, 巫毅, 等. 复方酒剂中乌头碱含量的测定及其中毒剂量的研究[J]. 吉林大学学报(理学版),2005, 43(5):677-679.
    [4] 魏玉辉, 王晓华, 沈明谦, 等. 藤药中乌头碱含量测定HPLC方法的建立[J]. 中成药, 2008, 30(1):130-131.
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    [8] 熊梅,闫倩玲,杨文芬. 高效液相色谱梯度洗脱法测定血塞通胶囊中三七皂苷R1、人参皂苷Rg1、Rb1的含量[J].时珍国医国药, 2004, 15(3):134-135.
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Research on quality control of Huoguwan

doi: 10.3969/j.issn.1006-0111.2018.02.012

Abstract: Objective To establish the quality control method for Huoguwan. Methods TLC was applied to detect the component of Danshen, Dihuang, Danggui, Chuanxiong, Sanqi, Tubiechong, and Zhicaowu in this compound preparation. HPLC was used to measure the concentration of Renshenzaogan Rg1, Rb1 and Sanqizaogan R1. Unitary C18 analytical column(4.6 mm×250 mm,5 μm)was used with acetonitrile-water as the mobile phase (Flow rate:1.0 ml/min, column temperature:30℃, wavelength:203 nm). Results Each component showed distinct spots on TLC without interference. There are good linear relationship for Sanqizhaogan R1 in the range of 39.92-399.2 μg/ml, Renshenzhaogan Rb1 in 84.28 -842.8 μg/ml and Renshenzhaogan Rg1 in 135.86-1 358.6 μg/ml. The recovery was 102.35%, 103.84% and 102.97% respectively. Conclusion The above described procedure was accurate and reproducible, which can be used as a method for the quality control of Huoguwan.

YE Shengying, GUO Qi, LEI Hong, YANG Ying. Research on quality control of Huoguwan[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(2): 156-161. doi: 10.3969/j.issn.1006-0111.2018.02.012
Citation: YE Shengying, GUO Qi, LEI Hong, YANG Ying. Research on quality control of Huoguwan[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(2): 156-161. doi: 10.3969/j.issn.1006-0111.2018.02.012
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