首页> 外文期刊>Journal of food and drug analysis >Simultaneous determination of 2 aconitum alkaloids and 12 ginsenosides in Shenfu injection by ultraperformance liquid chromatography coupled with a photodiode array detector with few markers to determine multicomponents
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Simultaneous determination of 2 aconitum alkaloids and 12 ginsenosides in Shenfu injection by ultraperformance liquid chromatography coupled with a photodiode array detector with few markers to determine multicomponents

机译:超高效液相色谱-少有标记物的光电二极管阵列检测器同时测定参附注射液中2个乌头生物碱和12种人参皂苷

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摘要

Abstract A method with few markers to determine multicomponents was established and validated to evaluate the quality of Shenfu injection by ultraperformance liquid chromatography coupled with a photodiode array detector. The separations were performed on an {ACQUITY} {UPLC} {BEH} {C18} (2.1?×?50?mm2, 1.7?μm) column. Methanol and 0.1% formic acid aqueous solution were used as the mobile phase. The flow rate was 0.3?mL/min. 2 aconitum alkaloids and 12 ginsenosides could be perfectly separated within 15 minutes. Ginsenoside Rg1 and benzoylmesaconine, the easily available active components, were employed as the maker components to calculate the relative correction factors of other components in Shenfu injection, Panax ginseng and Aconitum carmichaeli. The external standard method was also established to validate the feasibility of the method with few markers to determine multicomponents. Parameter p and the principal component analysis method were employed to investigate the disparities among batches for the effective quality control of Shenfu injection. The results demonstrated that the ultraperformance liquid chromatography coupled with a photodiode array detector method with few markers to determine multicomponents could be used as a powerful tool for the quality evaluation of traditional Chinese medicines and their preparations.
机译:摘要建立了一种标记物少的多组分测定方法,并通过超高效液相色谱-光电二极管阵列检测器对申附注射液的质量进行了评价。在{ACQUITY} {UPLC} {BEH} {C18}(2.1××50×mm 2,1.7μm)柱上进行分离。甲醇和0.1%甲酸水溶液用作流动相。流速为0.3?mL / min。 15分钟内可以完美分离2种乌头生物碱和12种人参皂甙。人参皂苷Rg1和苯甲酰基美沙康宁是易于获得的活性成分,被用作制造商成分来计算参附注射液,人参和乌头中其他成分的相对校正因子。还建立了外标方法,以验证用很少的标记物测定多组分方法的可行性。采用参量p和主成分分析法研究了批号之间的差异,以有效地进行参附注射液的质量控制。结果表明,超高效液相色谱结合光电二极管阵列检测器方法,只需很少的标记物即可确定多组分,可作为中药及其制剂质量评价的有力工具。

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