黄连上清片中黄芩苷与欧前胡素的含量测定方法研究  被引量:1

Study on Content Determination of Baicalin and Imperatorin in Huanglianshangqing Tablets

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作  者:张小博[1] 曹恒涛[1] 王小艳[1] 

机构地区:[1]安阳市食品药品检验所,河南安阳455000

出  处:《中国执业药师》2015年第9期32-35,共4页China Licensed Pharmacist

摘  要:目的:建立黄连上清片中黄芩苷和欧前胡素的高效液相色谱含量测定方法。方法:采用高效液相色谱仪,Waters Symmetry C18柱(250 mm×4.6 mm,5μm),乙腈-水为流动相梯度洗脱,流速1.0 m L/min,检测波长:300 nm;柱温25℃,PDA检测。结果:黄芩苷在0.083~3.325μg范围内呈良好线性关系,r=0.999 9,回收率为103.54%,RSD=1.24%;欧前胡素在0.004~0.160μg范围内呈良好线性关系,r=0.999 9,回收率为102.69%,RSD=0.95%。结论 :本方法操作简便,结果准确、可靠,可用于同一波长处同时测定黄芩苷与欧前胡素的含量。Objective: To establish a method for the determination of baicalin and imperatorin in huanglianshangqing tablets by HPLC. Methods : Using high performance liquid chromatography(HPLC)and a Waters Symmetry C18column(250 mm × 4.6 mm,5 μm), the mobile phase was acetonitrile- water in gradient elution, the flow rate was 1.0 m L/min, the detection wavelength was at 300 nm, the column temperature was at 25 ℃ and detected by PDA. Results :A good linear relationship of baicalin was obtained within the range of 0.083 ~ 3.325 μg( r = 0.999 9) and the average recovery was 103.54%(RSD = 1.24%), and a good linear relationship of imperatorin was found within the range of 0.004 ~ 0.160 μg(r = 0.999 9) and the average recovery was 102.69%(RSD =0.95%). Conclusion: The method was convenient, accurate and reliable, and can be used for the simultaneous determination at the same wavelength of the contents of baicalin and imperatorin in huanglianshangqing tablets.

关 键 词:高效液相色谱 黄连上清片 黄芩苷 欧前胡素 

分 类 号:R286.0[医药卫生—中药学]

 

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