世界中医药
文章摘要
引用本文:范晓楠1,刘梅1,胡凯莉1,苏佳灿2,奉建芳1.骨松灵颗粒质量标准研究[J].世界中医药,2015,10(10):.  
骨松灵颗粒质量标准研究
The Study of the Quality Standard of Gusongling Granules
投稿时间:2015-04-14  
DOI:10.3969/j.issn.1673-7202.2015.10.038
中文关键词:  骨松灵颗粒  淫羊藿苷  柚皮苷  毛蕊花糖苷  黄芪甲苷  薄层色谱  高效液相色谱
English Keywords:Gusongling Granules  Icariine  Naringin  Acteoside  Astragaloside  TLC  HPLC
基金项目:上海市科委中药现代化专项(编号:12401900703)
作者单位
范晓楠1,刘梅1,胡凯莉1,苏佳灿2,奉建芳1 1 上海中医药大学穆拉德中药现代化研究中心上海201203 2 第二军医大学长海医院上海200433 
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中文摘要:
      目的:建立骨松灵颗粒的质量标准。方法:采用薄层色谱法(TLC)对复方中淫羊藿、骨碎补、补骨脂、熟地黄、黄芪、当归、盐杜仲、醋龟甲进行定性鉴别;采用高效液相色谱法(HPLC)对淫羊藿中淫羊藿苷、骨碎补中柚皮苷、熟地黄中毛蕊花糖苷、黄芪中黄芪甲苷进行含量测定。结果:八味药材薄层色谱图斑点清晰,具有专属性;淫羊藿苷在0.031 5~1.712 0 ug范围内线性关系良好,r=0.999 7,平均回收率为100.23%,RSD为2.23%;柚皮苷在0.056 8~1.817 5 μg范围内线性关系良好,r=0.999 6,平均回收率为99.97%,RSD为1.22%;毛蕊花糖苷在0.060 8~1.945 6 μg范围内线性关系良好,r=0.999 8,平均回收率为99.94%,RSD为1.24%;黄芪甲苷在0.467 6~11.220 0 μg范围内线性关系良好,r=0.999 1,平均回收率为99.84%,RSD为3.35%。结论:该方法能准确可靠地进行定性、定量检测,能有效地控制骨松灵颗粒的质量。
English Summary:
      To establish the quality standard for Gusongling Granules. Methods: TLC was performed to identify the qualification of Epimedii Folium(Yinyanghuo), Drynarial Rhizoma(Gusuibu), Psoraleae Fructus(Buguzhi), Rehmanniae Radix Praeparata(Shudihuang), Astragali Radix(Huangqi), Angelicae Sinensis Radix(Danggui), Eucommiae Cortex(Yanduzhong), Testudinis Carapax Et Plastrum(Cuguijia). Besides, a HPLC method was established for the determination of icariine, naringin, acteoside, and astragaloside. Results: The spots on TLC plates were clear with specificity. Icariin showed a good linear relationship at a range between 0.0315 and 1.7120 μg, r=0.9997, the average recovery was 100.23%, and RSD was 2.23%. Naringin showed a good linear relationship at a range between 0.0568 and 1.8175 μg, r=0.9996, the average recovery was 99.97%, and RSD was 1.22%. Acteoside showed a good linear relationship at a range between 0.0608 and 1.9456 μg, r=0.9998, the average recovery was 99.94%, and RSD was 1.24%. Astragaloside showed a good linear relationship at a range between 0.4676 and 11.2200 μg, r=0.9998, the average recovery was 99.84%, and RSD was 3.35%. Conclusion: This method can be accurate and reliable in qualitative and quantitative detection, and can control the drug quality effectively.
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