高效液相色谱法测定马兰中大黄素的含量  被引量:6

Determination of emodin in Kalimeris indica(L. ) Sch-Bip by HPLC

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作  者:汪跃峰[1] 刘劲松[2] 钟文武[2] 陈爱民[2] 张聪佴[2] 王刚[2] 

机构地区:[1]安徽医科大学第四附属医院 [2]安徽中医学院药学院现代中药安徽省重点实验室,安徽合肥230031

出  处:《安徽医药》2013年第3期393-394,共2页Anhui Medical and Pharmaceutical Journal

基  金:安徽省自然科学基金资助项目(No 11040606W220);康缘中医药科技创新基金资助项目(No KYCX 201003)

摘  要:目的建立测定中草药马兰中大黄素含量的高效液相色谱方法。方法甲醇回流提取药材,高效液相色谱法测定,采用的色谱柱为Kromasil-C18柱(250 mm×4.6 mm,5μm);流动相为甲醇-0.1%磷酸水溶液(80∶20);检测波长为254 nm;柱温为30℃;流速为1 mL.min-1。结果大黄素溶液在1.4~14 mg.L-1浓度范围内与其峰面积呈良好线性关系(r=0.999 3),平均加样回收率为99.61%,其RSD值为1.08%(n=6)。结论该方法准确、可靠、灵敏、简便,适合中草药马兰中大黄素含量的测定。Objective To establish an HPLC method for determination of emodin in Kalimeris indica(L.)Sch-Bip.Methods The dry medicinal herb was extracted by refluxing in methanol and determined by HPLC.A Kromasil-C18 column was used with the mobile phase composed of methanol-phosphoric acid solution(0.1%)(80∶ 20) at the flow rate of 1 mL·min-1.The detection wavelength was 254 nm and the column temperature was 30 ℃.Results Emodin showed a good linear relationship to the peak aera at a concentration range of 1.4~14 mg·L-1(r=0.999 3).The average recovery was 99.16% with RSD of 1.08%(n=6).Conclusion The method is accurate,reliable,sensitive,simple and suitable for the determination of emodin in Kalimeris indica(L.)Sch-Bip.

关 键 词:HPLC法 马兰 大黄素 

分 类 号:R286[医药卫生—中药学]

 

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