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RP-HPLC同时测定藏药波棱瓜子中7个活性木脂素成分的含量
引用本文:丛龙波,王琪,黄雅洁,袁海龙,龚千锋,杨明,肖小河.RP-HPLC同时测定藏药波棱瓜子中7个活性木脂素成分的含量[J].中国药学杂志,2008,43(12):946-949.
作者姓名:丛龙波  王琪  黄雅洁  袁海龙  龚千锋  杨明  肖小河
作者单位:1.解放军302医院解放军中药研究所 北京 100039;2.中药现代制剂教育部重点实验室江西中医学院 南昌 330004
摘    要: 目的建立一种RP-HPLC同时测定藏药波棱瓜子中7个活性木脂素成分(ent-isolariciresinol,dehydrodiconiferyl alcohol,herpet-rione,herpetin,herpetetrone,herpetotriol,herpetal)的含量。方法采用Pinnacle DB C18(4.6 mm×250 mm,5μm,RESTEK)色谱柱,以乙腈-0.1%磷酸为流动相梯度洗脱,检测波长为240 nm,流速为1.0 mL·min-1。结果Ent-isolariciresinol,dehydrodiconiferyl alcohol,herpetrione,herpetin,herpetetrone,herpetotriol和herpetal的线性范围分别为:1.29~24.80 mg·L-1(r=0.978 9),6.77~130.20 mg·L-1(r=0.100 26),10.41~200.20 mg·L-1(r=0.980 2),4.45~85.50(r=0.986 1),2.91~56.10 mg·L-1(r=0.982 8),5.80~111.60mg·L-1(r=0.100 78)和6.99~134.40 mg·L-1(r=0.986 6)。平均回收率均在95.19%~102.64%内(RSDs<1.52%)。结论本法准确可靠,灵敏度高,重现性好,结果表明,该分析方法适用于波棱瓜子药材的质量控制。

关 键 词:波棱瓜子  RP-HPLC  含量测定  质量控制
收稿时间:2007-09-27;

Simultaneous Determination of 7 Bioactive Lignans Compounds in Herpetospermum caudigerum by RPHPLC
CONG Long-bo,WANG Qi,HUANG Ya-jie,YUAN Hai-long,GONG Qian-feng,YANG Ming,XIAO Xiao-he.Simultaneous Determination of 7 Bioactive Lignans Compounds in Herpetospermum caudigerum by RPHPLC[J].Chinese Pharmaceutical Journal,2008,43(12):946-949.
Authors:CONG Long-bo  WANG Qi  HUANG Ya-jie  YUAN Hai-long  GONG Qian-feng  YANG Ming  XIAO Xiao-he
Institution:1. 302 Hospital of PLA,Institute of PLA of Chinese Medicine,Beijing 100039,China; 2. Key Lab of Modern Preparation of TCM,Ministry of Education,University of TCM,Nanchang 330004,China
Abstract:OBJECTIVE To establish a method for the determination of 7 bioactive lignan compounds in seeds of Herpetospermum caudigerum,namely ent-isolariciresinol,dehydrodiconiferyl alcohol,herpetrione,herpetin,herpetetrone,herpetotriol,herpetal.METHODS The HPLC assay was performed on a RESTEK Pinnacle DB C18 column with gradient elution.The mobile phase consisted of acetonitrile and 0.1% phosphoric acid at a flow rate of 1.0 mL·min-1.The detection wavelength was 240 nm.RESULTS The linearity was obtained over the ranges of 1.29-24.80 mg·L-1(r=0.978 9) for ent-isolariciresinol,6.77-130.20 mg·L-1(r=0.100 26) for dehydrodiconiferyl alcohol,10.41-200.20 mg·L-1(r=0.980 2) for herpetrione,45-85.50 mg·L-1(r=0.986 1) for herpetin,2.91-56.10 mg·L-1(r=0.982 8) for herpetetrone,5.80-111.60 mg·L-1(r=0.100 78) for herpetotriol and 6.99-134.40 mg·L-1(r=0.986 6) for herpetal,respectively.The recovery of the assay was in the range of 95.19%-102.64% with RSDs less than 1.52%.CONCLUSION The method is simple,sensitive and reproducible,and the results indicated that the developed assay could be considered as a suitable quality control method for Herpetospermum caudigerum.
Keywords:Herpetospermum caudigerum" target="_blank">Herpetospermum caudigerum')" href="#">Herpetospermum caudigerum  RP-HPLC  determination  quality control
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