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Simultaneous determination of seven bioactive lignans in Herpetospermum caudigerum by RP-HPLC method.

机译:RP-HPLC法同时测定硬皮草中的7种生物活性木脂素。

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摘要

A reversed-phase high-performance liquid chromatographic method with diode array detection was established to simultaneously determine the seven bioactive lignans in Herpetospermum caudigerum, namely ent-isolariciresinol (1), dehydrodiconiferyl alcohol (2), herpetrione (3), herpetin (4), herpetetrone (5), herpetotriol (6) amd herpetal (7). The HPLC assay was performed on a Restek Pinnacle DB C(18) column (250 x 4.6 mm, 5 microm) with gradient elution of acetonitrile and 0.1% phosphoric acid within 65 min. The detection wavelength was 240 nm. The flow-rate was 1.0 mL/min. All calibration curves showed good linearity (r(2) > 0.9998) within test ranges. The method was reproducible with intra- and inter-day variation of less than 1.98%. The method provided good accuracy with recoveries in the range 95.19-102.64% with RSDs less than 1.52%. The method was successfully applied to the quantification of seven constituents in 15 H. caudigerum samples collected from different cities. The results indicated that the developed assay could be considered as a suitable quality control method for H. caudigerum. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:建立了具有二极管阵列检测功能的反相高效液相色谱方法,以同时测定香根草中的七个生物活性木脂素,即对-异香豆素醇(1),脱氢二去甲硅烷基乙醇(2),疱疹三酮(3),疱疹素(4) ,Herpetetrone(5),herpetotriol(6)和Herpetal(7)。 HPLC测定在Restek Pinnacle DB C(18)色谱柱(250 x 4.6 mm,5微米)上进行,并在65分钟内进行乙腈和0.1%磷酸的梯度洗脱。检测波长为240nm。流速为1.0mL / min。在测试范围内,所有校准曲线均显示出良好的线性(r(2)> 0.9998)。该方法可重现,日内和日间差异小于1.98%。该方法提供了良好的准确性,回收率在95.19-102.64%之间,RSD小于1.52%。该方法已成功应用于从不同城市收集的15个沙丁草样品中7种成分的定量分析。结果表明,所开发的测定方法可以被认为是适用于C. caudigerum的质量控制方法。版权所有(c)2008 John Wiley&Sons,Ltd.

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