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Systematic study on QAMS method for simultaneous determination of triterpenoid saponins in Ilex pubescens by HPLC and UPLC

机译:HPLC和UPLC同时测定毛冬青中三萜皂苷的QAMS方法的系统研究。

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摘要

The quantitative analysis of multi-components with single marker (QAMS) method was firstly established for simultaneous determination of six triterpenoid saponins (ilexgenin A (C-1), ilexsaponin A1 (C-2), ilexsaponin B1 (C-3), ilexsaponin B2 (C-4), ilexsaponin B3 (DC1), ilexoside O (DC2)) in Ilex pubescens by Ultra Performance Liquid Chromatography (UPLC) and High Performance Liquid Chromatography (HPLC). Using C1 as the internal reference, the relative correction factors (RCF) of the other five triterpenoid saponins were calculated and statistically evaluated. The durability of the method was verified with five different LC instruments and five different C-18 columns under various chromatographic conditions. The external standard method after methodology verification was chosen to check the accuracy and feasibility of the QAMS method. The results showed that the RCFs of all compounds were obtained with good reproducibility (RSD < 5.0%), whether on different chromatography instruments or under various chromatographic conditions. The relative retention value method could be adopted for accurately positioning the chromatographic peak of the six constituents, with their values of RSD ranging between 0.5% and 1.6%. Meanwhile, no significant differences were found in the quantitative results of the six saponins in nine batches of medicines calculated by the QAMS method and external standard method, whether on a HPLC system or UPLC system. The QAMS method established in our research for simultaneous determination of the six saponins is accurate and can be feasibly used to evaluate the quality of Ilex pubescens, especially when the standard substance is inconvenient to obtain.
机译:首次建立了使用单标记(QAMS)方法对多组分进行定量分析的方法,用于同时测定6种三萜皂苷(ilexgenin A(C-1),lexsaponin A1(C-2),lexsaponin B1(C-3),lexsaponin超高效液相色谱法(UPLC)和高效液相色谱法(HPLC)测定毛柔冬中的B2(C-4),冬凌草甲素B3(DC1),冬凌草甲苷O(DC2))。使用C1作为内部参考,计算并统计评估了其他五种三萜皂苷的相对校正因子(RCF)。用五种不同的LC仪器和五种不同的C-18色谱柱在各种色谱条件下验证了该方法的耐用性。选择方法论验证后的外标方法来检验QAMS方法的准确性和可行性。结果表明,无论在不同色谱仪上还是在各种色谱条件下,所有化合物的RCF均具有良好的重现性(RSD <5.0%)。可以采用相对保留值方法来精确定位这六种组分的色谱峰,其RSD值在0.5%至1.6%之间。同时,无论是在HPLC系统还是UPLC系统上,通过QAMS方法和外标方法计算的9批次药物中6种皂苷的定量结果均无显着差异。我们的研究中建立的同时测定6种皂苷的QAMS方法是准确的,可用于评估毛冬青的质量,尤其是当标准物质难以获得时。

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