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首页> 外文期刊>Journal of the Chinese Chemical Society. >Study on Determination of Triterpenoids in Chaenomeles by High Performance Liquid Chromatography and Sample Preparation with Matrix Solid Phase Dispersion
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Study on Determination of Triterpenoids in Chaenomeles by High Performance Liquid Chromatography and Sample Preparation with Matrix Solid Phase Dispersion

机译:高效液相色谱法测定基质中的三萜类成分及基质固相分散体制备样品的研究

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摘要

A new method for the simultaneous determination of the major triterpenoids in Chaenomeles(Chinese medicinal herb)by high performance liquid chromatography(HPLC)and sample preparation with matrix solid phase dispersion(MSPD)was developed.A 0.1 g of sample was placed into an agate mortar and gently blended with 0.4 g silica gel to obtain a homogeneous mixture.This mixture was introduced into a Teflon cartridge,and the triterpenoids fraction was eluted from the cartridge with dichloromethane-acetone(85:15).The residue was dissolved with methanol after the evaporation of the solvent(dichloro-methane and acetone).The triterpenoids were separated on a ZORBAX Stable Bound(4.6 mm X 100 mm,1.8 mu m)C_(18)column by gradient elution with acetonitrile and water as the mobile phase and detected with evaporative light scattering detection.This method provides good reproducibility and sensitivity for the quantification of seven major triterpenoids,namely erythodiol,betulin,acetyl ursolic acid,ursolic acid,oleanolic acid,betulinic acid,pomolic acid,respectively.The relative standard derivations of overall intra-day variations were less than 2.0%,and the relative standard derivations of inter-day variations were less than 2.5%.The standard recoveries(three different concentrations of markers:0.1,0.5 and 2.0 mg)ranged from 97-103%.The results demonstrate that this method is simple,sensitive,selective,and suitable for the quality control of this commonly used Chinese medicinal herb.
机译:建立了同时测定木瓜中主要三萜类成分的高效液相色谱(HPLC)和基​​质固相分散体(MSPD)同时制备的新方法。将0.1 g样品置于玛瑙中用研钵将其与0.4 g硅胶轻轻混合,得到均匀的混合物。将该混合物引入Teflon柱中,用二氯甲烷-丙酮(85:15)从柱中洗脱出三萜类化合物馏分。将三萜类化合物在ZORBAX稳定结合液(4.6 mm X 100 mm,1.8μm)C_(18)色谱柱上以乙腈和水为流动相进行梯度洗脱,并进行分离。用蒸发光散射检测进行检测。该方法为定量测定七种主要的三萜类化合物,即赤藓糖醇,白蛋白,乙酰基乌索酸,乌索酸提供了良好的重现性和灵敏度。日间总变化的相对标准偏差小于2.0%,日间变化的相对标准偏差小于2.5%。标准回收率(3结果表明,该方法简便,灵敏,选择性好,适用于该常用中草药​​的质量控制。不同浓度的标记物:0.1、0.5和2.0 mg)的浓度范围为97-103%。

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