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Liquid-liquid chromatography in sample pretreatment for quantitative analysis of trace component in traditional Chinese medicines by conventional liquid chromatography

机译:用常规液相色谱法进行样品预处理的样品预处理中痕量成分的液 - 液相色谱法

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A method for sample pretreatment using liquid-liquid chromatography combined with a conventional liquid chromatography was developed for quantitative determination of trace chemical component in traditional Chinese medicine. The main effective component, wilforlide A, in the traditional Chinese medicinal herb Tripterygium wilfordii as well as in its Chinese patent medicine glycosides tablets was successfully determined after sample pretreatment by liquid-liquid chromatography. A biphasic solvent system n-hexane-ethyl acetate-ethanol-water (6:4:6:4, v/v) was screened for crude sample treatment by liquidliquid chromatography. The collection time of eluted fractions containing target component could be well predicted using a continuous-stirred tank reactors model after determination of its retention time. Then, quantitative analysis of wilforlide A in Tripterygium wilfordii as well as in its tablets could be successfully determined by conventional reversed-phase high performance liquid chromatography with UV detector. Under the optimized conditions, the method showed good linearity (R-2 = 0.9999) for wilforlide A in the range of 0.01 mg mL(-1) -0.10 mg mL(-1). The limit of detection and limit of quantity were 1.35 ng mL(-1) and 4.50 ng mL(-1), respectively. The average recovery rate, intra-day and inter-day precisions of wilforlide A were 96.43%, 0.67% and 1.14%, respectively. Compared with previous studies, the present method showed advantages of complete recovery of target component in the sample pretreatment and good repeatability. (C) 2020 Elsevier B.V. All rights reserved.
机译:使用液 - 液相色谱法与常规液相色谱相结合的样品预处理方法进行定量测定中药中痕量化学成分的定量测定。通过液 - 液相色谱法预处理在样品预处理后成功测定了传统的中药草药威尔福德威尔福德威尔福德的主要有效成分威尔林A,在其中药草药糖尿布片中。将双己烷 - 乙酸乙酯 - 乙醇 - 乙醇 - 水(6:4:6:4,v / v)筛选通过液相石液色谱法处理原油样品。在测定其保留时间后,可以通过连续搅拌的罐式反应器模型进行含有靶分组分的洗脱级分的收集时间。然后,通过用UV检测器的常规反相高效液相色谱法成功地确定替代威尔福德中的钛合金A以及其片剂中的钛合金A的定量分析。在优化的条件下,该方法显示出钛的线性度(R-2 = 0.999999999),其硅树脂A在0.01mg ml(-1)-0.10mg ml(-1)的范围内。检测极限和量限制分别为1.35 ng mL(-1)和4.50ng ml(-1)。威尔林A的平均恢复率,日期和日内诊断分别为96.43%,0.67%和1.14%。与先前的研究相比,本方法显示了在样品预处理和良好的重复性中完全恢复靶分量的优点。 (c)2020 Elsevier B.v.保留所有权利。

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