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首页> 外文期刊>Journal of Chromatographic Science >Application of experimental design in optimization of the separation condition for determination of four active components in cold medicines by flow injection-capillary electrophoresis
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Application of experimental design in optimization of the separation condition for determination of four active components in cold medicines by flow injection-capillary electrophoresis

机译:实验设计在流动注射-毛细管电泳法测定感冒药中四种有效成分的分离条件优化中的应用

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摘要

Orthogonal design (OD) was employed to optimize the separation condition of flow injection-capillary electrophoresis (FI-CE). In order to compare the optimum condition, uniform design and univariate approach were also adopted. The influences of variables such as buffer pH, buffer concentration, acetonitrile (ACN) percentage, and separation voltage were discussed. The optimum separation condition was established. The limits of detection were 1.94 × 10 ~(-2), 6.40 × 10~(-3),1.16 × 10~(-2) and 1.94 × 10~(-2) μg/mL for dextromethorphan hydrobromide (Dex), chlorphenamine hydrogen maleate (Chl), pseudoephedrine hydrochloride (Pse), and paracetamol (Par), respectively. The RSDs of peaks areas were less than 2.0%. The results showed the OD was an effective method among experimental designs for optimizing the separation conditions of CE. The optimum condition was used for separation and determination of Dex, Chl, Pse, and Par in cold medicines. The average recovery was between 96.68-101.25%.
机译:采用正交设计(OD)优化流动注射-毛细管电泳(FI-CE)的分离条件。为了比较最佳条件,还采用统一设计和单变量方法。讨论了缓冲液pH,缓冲液浓度,乙腈(ACN)百分比和分离电压等变量的影响。确定了最佳分离条件。氢溴酸右美沙芬(Dex)的检出限为1.94×10〜(-2),6.40×10〜(-3),1.16×10〜(-2)和1.94×10〜(-2)μg/ mL,分别是马来酸氯苯那敏(Chl),盐酸伪麻黄碱(Pse)和对乙酰氨基酚(Par)。峰面积的RSD小于2.0%。结果表明,OD是优化CE分离条件的实验方法之一。最佳条件用于分离和测定感冒药中的Dex,Chl,Pse和Par。平均回收率在96.68-101.25%之间。

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