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高效液相色谱法测定六味补血颗粒中芍药苷和阿魏酸的含量
引用本文:周琳.高效液相色谱法测定六味补血颗粒中芍药苷和阿魏酸的含量[J].中南药学,2009,7(3):187-190.
作者姓名:周琳
作者单位:湖南省永州市药品检验所,湖南,永州,425100
摘    要:目的建立HPLC法测定六味补血颗粒中芍药苷和阿魏酸的含量。方法采用UltimateXB-C18柱(250min×4.6mm,5μm);流动相为乙腈-0.1%磷酸溶液(15:85);检测波长232nm(芍药苷)、323nm(阿魏酸);流速:1.0mL·min^-1;柱温:25℃。结果芍药苷和阿魏酸的线性范围分别为0.108-0.864μg(r=0.9996,n=6)和0.0440~0.352μg(r=0.9998,n=6);芍药苷和阿魏酸的平均回收率分别为97.77%和96.78%,RSD(n=9)分别为1.33%和1.08%。结论该方法可用于六味补血颗粒中芍药苷和阿魏酸的合量测定.

关 键 词:HPLC法  芍药苷  阿魏酸

Content determination of paeoniflorin and ferulic acid in Liuwei Buxue granules by HPLC
ZHOU Lin.Content determination of paeoniflorin and ferulic acid in Liuwei Buxue granules by HPLC[J].Central South Pharmacy,2009,7(3):187-190.
Authors:ZHOU Lin
Institution:ZHOU Lin (Yongzhou Institute for Drug Control, Yongzhou Hunan , 425100)
Abstract:Objective To establish a method for the content determination of paeoniflorin and ferulic acid in Liuwei Buxue granules by HPLC. Methods Ultimate XB-C18 column (250 mm × 4.6 mm, 5μm) was used. The mobile phase was acetonitrile-0. 1% phosphoric acid solution (15 : 85), the detection wavelenghth was 230 nm for paeoni- florin and 323 nm for ferulic acid, the flow rate was 1.0 mL·min^-1, and column temperature was 25℃. Results The linear range of paeoniflorin and ferulic acid was 0. 108-0. 864μg (r=0. 999 6, n=6 ) and 0. 044 0-0. 352 μg (r=0. 999 8, n=6 ). The average recovery of paeoniflorin and ferulic acid was 97. 77% and 96.78%, RSD (n=9) was 1.33% and 1.08%. Conclusion The method may be used for the content determination of paeoniflorin and ferulic acid in Liuwei Buxue granules.
Keywords:HPLC  paeoniflorin  ferulic acid
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