HPLC测定新疆紫草中紫草素的含量及提取方法的优化  被引量:14

Ultrasonic-assisted Extraction and Content Determination of Shikonin from Arnebiae Radix by HPLC

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作  者:崔晓秋[1] 刘云刚 

机构地区:[1]济宁医学院药学院,山东日照276826 [2]岚山生化有限公司,山东日照276800

出  处:《中国实验方剂学杂志》2014年第16期94-97,共4页Chinese Journal of Experimental Traditional Medical Formulae

基  金:济宁医学院青年基金项目(JYQ2011KM027)

摘  要:目的:采用超声方法提取新疆紫草中紫草素,并以左旋紫草素为指标,建立HPLC测定紫草素的含量.方法:利用超声波协同甲醇提取40 min;色谱条件为Shim-pack CLC-ODS-18色谱柱(4.6 mm ×250 mm,10 μm),检测波长516 nm,流动相甲醇-水(85∶15),流速1.0 mL·min-1,柱温室温.结果:左旋紫草素进样量在0.127~1.143 μg具有良好的线性关系,回归方程为y=338 763X-198 347(r =0.999 8),平均回收率99.3%,RSD 1.18%,左旋紫草素超声法提取率是回流提取法的1.29倍.结论:经方法学验证,该实验所采用的实验方法重复性好、稳定、准确、可靠,可用于中药紫草药材中紫草素的含量测定.Objective:To develop a method for ultrasonic-assisted extraction and high performance liquid chromatography (HPLC) determination of shikonin in the roots of Arnebiae Radix.Method:Shikonin was extracted by ultrasonic-assisted-methyl alcohol method.The HPLC determination condition consisted of Shim-pack CLC-ODS-18 (4.6 mm × 250 mm,10 μm) and shikonin was detected at 516 nm wavelength by using methyl alcohol-water (85∶15) as the mobile phase,column temperature at room temperature and flow rate 1.0 mL · min-1.Result:Shikonin had a good linearity relation in the range 0.127-1.143 μg (r =0.999 8),regressive equation were Y=338 763X-198 347.The average recovery was 99.3%,RSD 1.18% (n =6).In contrast with refluxing process,the extraction efficiency of ultrasonic extraction was 1.29 times.Conclusion:The methods of ultrasonic extraction and HPLC determination were proved to be accurate,reliable and repeatable.It can be used to determine natural shikonin content of Arnebiae Radix easily.

关 键 词:左旋紫草素 高效液相色谱 超声波辅助提取 紫草 

分 类 号:R284.1[医药卫生—中药学]

 

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