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作 者:张凤瑞[1] 周贤[1] 刘炎[1] 翁丽丽[1] 王淑敏[1] 韩雪华[2]
机构地区:[1]长春中医药大学,吉林长春130117 [2]延边大学,吉林延吉133000
出 处:《吉林中医药》2013年第3期289-291,共3页Jilin Journal of Chinese Medicine
基 金:吉林省科技厅自然科学基金项目(编号:201105058)
摘 要:目的:建立当归补血汤中黄芪的鉴别和黄芪甲苷的含量测定方法,为当归补血汤质量标准的建立奠定基础。方法:采用薄层色谱法定性鉴别当归补血汤中的黄芪药材,并利用高效液相色谱法测定黄芪甲苷含量。色谱柱:Diamonsil ODS-C18(5μ,250 mm×4.6 mm)分析柱;流动相:乙腈-水(32∶68);流速:0.6 mL/min;柱温:35℃;载气流速:2.7 mL/min;ELSD检测器漂移管温度:100℃;进样量20μL。结果:黄芪的薄层色谱鉴别条件专属性好,高效液相色谱检测黄芪甲苷测定方法具有较好的准确性、重现性和可行性,样品在10.01~20.2μg范围内呈良好的线性关系,平均加样回收率为95.04%,RSD=0.61%。结论:所建立方法简便、准确,高效液相色谱分离效果好、线性范围宽、灵敏度高,可用于本品的质量控制。Objective: To establish the method for identifying Radix Astragali and detecting the quantity of Astragaloside IV- in Dangguibuxue Decoction and lay the foundation for the establishment of Dangguibuxue Decoction quality standard. Methods:Identify Radix Astragali qualitatively by thin layer chromatography(TLC) and detect the quantity of Astragaloside IV in Dangguibuxue Decoction by High performance liquid chromatography(HPLC). Using Diamonsil ODS-Cjs (5 tL, 250 mm x 4.6 mm) analytical column; the mobile phase was composed of a mixture of acetonitrile-water(32:68) ;the flow rate was 0.6 mL/min; the column temperature was 35 ℃ ;the flow rate of carrier gas was 2.7 mL/min; ELSD detector, drift temperature was 100 ℃ ; the sample size was 20 μL. Results: The TLC method of Radix Astragali is specific. HPLC method for de- tecting the quantity of Astragaloside IV has a good accuracy, reproducibility and feasibility. There was a good linear relationship between the absorption area value and the concentration in the range of 1.01-20.2μg for sample. The average recovery was 95.04% with the RSD of 0.61%. Conclusion:The method is simple and accurate,which has good separation efficiency, wide linear range and high sensitivity. The method can be used to control the quality of Dangguibuxue Decoction.
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