解放军药学学报2024,Vol.37Issue(1) :1-3.DOI:10.3969/j.issn.1008-9926.2024.01.001

复方三七滴丸质量标准研究

Determination of Compound Sanqi Dripping Pills by HPLC

李思治 王剑丽 刘彬果
解放军药学学报2024,Vol.37Issue(1) :1-3.DOI:10.3969/j.issn.1008-9926.2024.01.001

复方三七滴丸质量标准研究

Determination of Compound Sanqi Dripping Pills by HPLC

李思治 1王剑丽 1刘彬果1
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作者信息

  • 1. 300142 天津,联勤保障部队第983医院
  • 折叠

摘要

目的 建立复方三七滴丸的质量标准.方法 采用薄层色谱法对制剂中的三七进行定性鉴别,高效液相色谱法测定丹参中丹参素的含量,采用ZORBAX SB-C18 色谱柱(4.6 mm×250 mm,5 μm);流动相为甲醇-水-冰醋酸(8∶91∶1);流速:1.0 ml·min-1;检测波长:280 nm.结果 薄层色谱鉴别样品斑点清晰,阴性对照无干扰;在0.5~10.0 μg的范围内,丹参素钠呈良好的线性关系(r=0.9992,n=7).加样回收率为99.8%,RSD值为0.6%.结论 建立的质量标准方法准确、重复性好、结果可靠,能有效控制复方三七滴丸的质量.

Abstract

Objective To establish a quality control method for compound Sanqi dripping pills.Methods Notoginseng in compound Sanqi dripping pills was identified via TLC.The content of salvianic acid A sodium was determined by HPLC with the ZORBAX SB-C18 column(4.6 mm×250 mm,5 μm).The mobile phrase was composed of methanl-water-1%acetic acid(8∶91∶1)at a flow rate of 1.0 ml·min-1 and detected at 280 nm.Results The spots in TLC were clear without any interference.Salvianic acid A showed a good linearity in the range of 0.5 to 10.0 μg(r=0.9992,n=7).The average recovery was 99.8%,with an RSD of 0.6%.Conclusion This method is simple and reliable,which can be used for qual-ity control of compound Sanqi pills.

关键词

高效液相色谱法/复方三七滴丸/丹参素

Key words

HPLC/compound Sanqi dripping pills/salvianic acid A

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出版年

2024
解放军药学学报
中国人民解放军总后勤部卫生部 药品仪器检验所

解放军药学学报

CSTPCD
影响因子:0.529
ISSN:1008-9926
参考文献量13
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