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引用本文:张春辉,王友兰,傅超.HPLC-ELSD同时测定跌打丸中三七皂苷R1、人参皂苷Rg1和人参皂苷Rb1的含量[J].中国现代应用药学,2016,33(1):91-93.
ZHANG Chunhui,WANG Youlan,FU Chao.Simultaneous Determination of Notoginsenoside R1, Ginsenoside Rg1 and Ginsenoside Rb1 in Dieda Pills by HPLC-ELSD[J].Chin J Mod Appl Pharm(中国现代应用药学),2016,33(1):91-93.
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HPLC-ELSD同时测定跌打丸中三七皂苷R1、人参皂苷Rg1和人参皂苷Rb1的含量
张春辉, 王友兰, 傅超
青岛市食品药品检验研究院,山东 青岛 266071
摘要:
目的 建立同时测定跌打丸中三七皂苷R1、人参皂苷Rg1和人参皂苷Rb1含量的HPLC-ELSD检测方法。方法 采用Phenomenex Kinetex C18色谱柱(100 mm×4.6 mm,2.6 μm),柱温30 ℃,流速0.5 mL·min-1,流动相为乙腈-水,梯度洗脱,ELSD检测器,漂移管温度110 ℃,载气(空气)体积流量3.0 L·min-1。结果 三七皂苷R1、人参皂苷Rg1、人参皂苷Rb1分别在0.158~3.16 μg(r=0.999 8),0.407~8.14 μg(r=0.999 5),0.446~8.92 μg(r=0.999 9)内呈良好的线性关系,平均加样回收率分别为97.55%(RSD=1.04%),98.09%(RSD=1.03%),97.34%(RSD=0.81%)。结论 该方法简便、快速、准确,可用于跌打丸的质量控制。
关键词:  跌打丸  三七皂苷R1  人参皂苷Rg1  人参皂苷Rb1  含量测定
DOI:
分类号:
基金项目:
Simultaneous Determination of Notoginsenoside R1, Ginsenoside Rg1 and Ginsenoside Rb1 in Dieda Pills by HPLC-ELSD
ZHANG Chunhui, WANG Youlan, FU Chao
Qingdao Institute for Food and Drug Control, Qingdao 266071, China
Abstract:
OBJECTIVE To establish a quantitative method using HPLC-ELSD to simultaneously determine three components(notoginsenoside R1, ginsenoside Rg1, ginsenoside Rb1) in Dieda pills. METHODS A Phenomenex Kinetex C18 column(100 mm×4.6 mm, 2.6 μm) was used to perform the determination, which was maintained at 30 ℃ throughout the analysis. Moble phase was composed of acetonitrile and water with flow rate at 0.5 mL·min-1 under gradient elution. The evaporation light-scattering detector was used with its drift tube temperature at 110 ℃ and the gas flow rate: 3.0 L·min-1. RESULTS Notoginsenoside R1, ginsenoside Rg1, ginsenoside Rb1 shown good linearity within 0.158-3.16 μg(r=0.999 8), 0.407-8.14 μg(r=0.999 5), 0.446-8.92 μg(r=0.999 9), and their average recoveries were 97.55%(RSD=1.04%), 98.09%(RSD= 1.03%), 97.34%(RSD=0.81%), respectively. CONCLUSION The method is simple, rapid and accurate. It show this method could be used for the quality control of Dieda Pills.
Key words:  Dieda pills  notoginsenoside R1  ginsenoside Rg1  ginsenoside Rb1  content determination
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