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作 者:关皎[1] 朱鹤云[1] 王佳林[1] 姜吉[1] 郝乘仪[1] 郭淑英[1] 冯波[1]
出 处:《中华中医药学刊》2017年第7期1864-1866,共3页Chinese Archives of Traditional Chinese Medicine
基 金:吉林省卫生厅科研项目(2013Z008);吉林省科技厅科研项目(200905113)
摘 要:目的:建立超快速液相色谱法同时测定黄芩中黄芩苷、汉黄芩苷、黄芩素和汉黄芩素的含量。方法:采用Shim-Pack XR-ODS柱(75 mm×3.0 mm,2.2μm);流动相为0.1%磷酸水溶液(A)-乙腈(B)梯度洗脱(0~11 min,35%~41%B;11~12 min,41%~35%B),平衡时间2 min;流速为0.4 m L·min-1;检测波长为275nm;柱温为30℃。结果:黄芩苷、汉黄芩苷、黄芩素和汉黄芩素分别在20~200μg·mL^(-1)(r=0.999 6)、4.0~40μg·mL^(-1)(r=0.999 5)、0.1~1.0μg·mL^(-1)(r=0.999 3)和0.4~4.0μg·mL^(-1)(r=0.999 6)浓度范围内与峰面积呈良好的线性关系;平均回收率(n=9)分别为99.2%,98.2%,98.7%和99.1%。结论:该方法结果准确、操作简便、具有良好的重现性和稳定性,可用于黄芩药材的质量控制。Objective: To develop an ultra -fast liquid chromatography (UFLC) method for simuhaneous detelTnina- tions of baicalin, wogonoside, baicalein and wogonin in Scutellaria Radix. Methods : Chromatographic separation was per- formed on Shim- Pack XR- ODS column(75 mm ×μ 3.0 mm, 2.2 μm). The mobile phase was 0.1% phosphoric acid ( A ) - aeetonitrile ( B ) with gradient elution ( 0 - 11 rain, 35 % - 41% B ; 11 - 12 min,41% - 35 % B ) at a flow rate of 0.4 mL · min^-1 and the equilibration time was 2 min. The detecting wavelength was set at 275 nm. The column tempera- ture was maintained at 30 ℃. Rusults : The linear ranges were 20 - 200 μg · mL^-1( r = 0. 999 6) for baicalin, 4.0 - 40 μg · mL^-1 ( r = 0. 999 5 ) for wogonoside, 0.1 - 1.0 μg· mL^-1 ( r = 0. 999 3 ) for baicalein and 0.4 - 4.0 μg· mL - ( r = 0. 999 6) for wogonin. The average recoveries ( n = 9) of four components were 99.2%, 98.2%, 98.7% and 99. 1%. Rusults: The developed method is simple, accurate with high repeatbility and stability. It is suitable for the quality control of Scutellaria Radix.
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