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高效液相色谱法测定大豆葛根软胶囊中葛根素的含量
引用本文:方加林,方恒杰.高效液相色谱法测定大豆葛根软胶囊中葛根素的含量[J].今日药学,2014(2):126-128.
作者姓名:方加林  方恒杰
作者单位:[1]揭阳市食品药品检验所,广东揭阳522000 [2]广州白云山制药总厂,广东广州510515
摘    要:目的建立HPLC法测定保健品大豆葛根软胶囊中葛根素的含量。方法采用AgilentEclipseXDB—C18柱,甲醇-0.1%醋酸水溶液(30:70)为流动相;检测波长为250nm;流速为1.0mL/min;柱温为30℃。结果葛根素在0.0282~0.282mg/mL范围内呈良好的线性关系,r:0.9992,平均回收率99.6%,RSD=1.7%(n=6)。结论本方法灵敏迅速,准确可靠,可用于保健品大豆葛根软胶囊中葛根素的含量测定。

关 键 词:葛根素  HPLC  含量测定  保健食品  油脂基质

Determination of Puerarin in High Performance Soft Capsules by Reverse-Phase Liquid Chromatography
FANG Jia-lin,FANG Heng-jie.Determination of Puerarin in High Performance Soft Capsules by Reverse-Phase Liquid Chromatography[J].Pharmacy Today,2014(2):126-128.
Authors:FANG Jia-lin  FANG Heng-jie
Institution:1. Jieyang Institule for Food and Drug Control, Jieyang, Guangdong 522000, China ; 2. Guangzhou Baiyun Shan Pharmaceutical General Factory, Guangzhou, Guangdong 510515, China)
Abstract:Objective To establish a new method for determining the content of puerarin by HPLC. Methods Agilent Eclipse XDB-CI8 column was adopted, using methanol- 0. 1% acetate acid solution (30:70), at detection wavelength of 250 nm. The flow rate was 1.0 mL/min, and column temperature was 30 ℃. Results The linear range of puerarin concentration was 0.028 2 -0. 282 mg/mL, r =0. 999 2. The average recovery of sample was 99.6%, RSD = 1.7% (n = 6 ). Conclusion This method is sensitive and accurate with good repeatability. It is suitable for the determination of puerarin.
Keywords:puerarin  HPLC  content determination  health food  oil base material
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