首页|藏药七味血病丸质量标准的研究

藏药七味血病丸质量标准的研究

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目的 建立藏药七味血病丸的质量标准。方法 用薄层色谱法(thin-layer chromatography,TLC)对成方中的木香和余甘子进行定性鉴别;用高效液相色谱法(high performance liquid chromatography,HPLC)测定成方中没食子酸、土木香内酯和异土木香内酯的含量。色谱柱为C18柱,流动相为乙腈-1 mL·L-1磷酸溶液,梯度洗脱;流速为1。0 mL·min-1;检测波长为225 nm;进样量为 5 µL。结果 TLC斑点清晰且阴性样品无干扰;没食子酸、土木香内酯、异土木香内酯的质量浓度分别在 0。892~4。461、0。975~4。874、0。956~4。780 mg·mL-1范围内与其峰面积呈良好的线性关系。结论 该方法专属性强、灵敏度高、操作简便,可用于藏成药七味血病丸的定性及定量分析,为本品质量标准的研究和提高提供了参考数据与实验基础。
Study on the quality standard of Tibetan medicine Qiwei Xuebing Pills
Objective To establish the quality standard of Tibetan medicine,Qiwei Xuebing Pills.Methods Radix Aucklandiae in the prescription was identified by thin-layer chromatography(TLC).The contents of gallic acid,coumarin,and iso-coumarin in the pills were determined by high performance liquid chromatography(HPLC).The chromatographic column was packed with C18.The mobile phase was acetonitrile 1 mL·L-1 phosphoric acid solution,in gradient elution mode.The flow rate was 1 mL·min-1,The detection wavelength was 225 nm and the injection volume was 5 µL.Results TLC spots were clear and negative samples showed no interference.There were good linear relationship between the mass concentrations of gallic acid,coumarin,and isoquercetin with their peak areas in the ranges of 0.892-4.461,0.975-4.874,and 0.956-4.780 mg·mL-1,respectively.Conclusion The method exhibited satisfactory specificity and sensitivity,also being user-friendly.The method is suitable for both qualitative and quantitative analysis of Tibetan medicine,Qiwei Xuebing Pills.This provides reference data and experimental basis for the research and improvement of the quality standards of this product.

Tibetan medicineQiwei Xuebing PillsHPLC

扎西措、桑乾才让、慕晓旭、多杰才让、万玛太、鲁雪、马应风、王丽娟

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青海省藏医院,西宁 810007

藏药 七味血病丸 高效液相色谱法

第七批全国老中医药专家学术经验继承工作项目

[2022]76号

2024

西北药学杂志
西安交通大学,陕西省药学会

西北药学杂志

CSTPCD
影响因子:0.912
ISSN:1004-2407
年,卷(期):2024.39(4)