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纸质出版日期:2016
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张静, 穆丽华, 赵润清, 等. 高效液相色谱法同时测定开心散提取物中3种主要成分的含量[J]. 中国实验方剂学杂志, 2016,22(4):65-68.
ZHANG Jing, MU Li-hua, ZHAO Run-qing, et al. Determination of Three Major Components in Kaixin San by HPLC[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(4): 65-68.
张静, 穆丽华, 赵润清, 等. 高效液相色谱法同时测定开心散提取物中3种主要成分的含量[J]. 中国实验方剂学杂志, 2016,22(4):65-68. DOI: 10.13422/j.cnki.syfjx.2016040065.
ZHANG Jing, MU Li-hua, ZHAO Run-qing, et al. Determination of Three Major Components in Kaixin San by HPLC[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(4): 65-68. DOI: 10.13422/j.cnki.syfjx.2016040065.
目的: 建立HPLC-ELSD同时测定开心散提取物中主要抗抑郁类成分tenuifoliside A
1-O-(E)-benzoyl-[3-O-(E)-alphatolluyl]-β-D-fructofuranosy-(2→1)-[β-D-glucop-yranosyl-(1→2)]-α-D-glucopyranoside和人参皂苷Rb1含量的方法。方法: 采用HPLC-ELSD分析方法
Agilent HC C18色谱柱(4.6 mm×250 mm
5 μm)
柱温25 ℃
流动相乙腈-0.65%乙酸铵水溶液进行梯度洗脱
流速1.0 mL ·min-1
漂移管温度115 ℃
载气流量3.2 L ·min-1
气体空气。结果: tenuifoliside A
1-O-(E)-benzoyl-[3-O-(E)-alphatolluyl]-β-D-fructofuranosy-(2→1)-[β-D-glucop-yranosyl-(1→2)]-α-D-glucopyranoside和人参皂苷Rb1分别在1.113~10.980
1.581~15.726
0.712~7.128 μg呈现良好的线性关系;精密度、稳定性和重复性均符合定量分析要求;三者的平均回收率分别为98.36%
99.58%和98.97%;百分含量分别为0.999%
1.670%和0.579%。结论: 该分析方法简便、可靠
可用于开心散提取物中 tenuifoliside A
1-O-(E)-benzoyl-[3-O-(E)-alphatolluyl]-β-D-fructofuranosy-(2→1)-[β-D-glucop-yranosyl-(1→2)]-α-D-glucopyranoside和人参皂苷Rb1的含量测定
且可以作为开心散质量控制方法之一。
Objective: To found a quantitative HPLC-ELSD method for determining tenuifoliside A
1-O-(E)-benzoyl-[3-O-(E)-alphatolluyl]-β-D-fructofuranosy-(2→1)-[β-D-glucop-yranosyl-(1→2)]-α-D-glucopyranoside and ginsenoside Rb1 from Kaixin San
which are used for anti-tumor. Method: The procedure of HPLC-ELSD was performed on the chromatographi column of Agilent HC C18 (4.6 mm×250 mm
5 μm)at 25 ℃
and the mobile phase was acetonitrile-0.65% ammonium acetate solution in gradient elution.The flow velocity was 1.0 mL · min-1.The temperature of driti tube was 115 ℃ and the gas was air
flow rate was 3.2 L · min-1. Result: Tenuifoliside A showed a good linear relationship at a range from 1.113 μg to 10.980 μg
1-O-(E)-benzoyl-[3-O-(E)-alphatolluyl]-β-D-fructofuranosy-(2→1)-[β-D-glucop-yranosyl-(1→2)]-α-D-glucopyranoside
from 1.581 μg to 15.726 μg
and ginsenoside Rb1
from 0.712 μg to 7.128 μg;Precision
stability and repeatability are comply with the requirement of quantitative analysis. The average recovery was respectively 98.36%
99.58% and 98.97%.The percentage composition was respectively 0.999%
1.670% and 0.579%. Conclusion: The method was simple and reliable
which can be used for the assaying of tenuifoliside A
1-O-(E)-benzoyl-[3-O-(E)-alphatolluyl]-β-D-fructofuranosy-(2→1)-[β-D-glucop-yranosyl-(1→2)]-α-D-glucopyranoside and ginsenoside Rb1 as well as quantity control of Kaixin San.
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