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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >A simple micellar electrokinetic capillary chromatographic method for the quantitative analysis of organic expectorants.
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A simple micellar electrokinetic capillary chromatographic method for the quantitative analysis of organic expectorants.

机译:一种简单的胶束电动毛细管色谱法,用于有机祛痰剂的定量分析。

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摘要

A simple and rapid micellar electrokinetic capillary chromatographic method is described for the separation and quantification of five expectorant drugs, including ambroxol (AMB), bromhexine (BRM), carbocysteine, guaiacol and guaifenesin. The drugs were separated in a mixed solution of phosphate buffer (35 mM; pH 3.90) and acetonitrile (75:25, v/v) with sodium dodecylsulfate (120 mM) as the micellar source, and the separated drugs were directly monitored with UV detector (200 nm). Several key parameters affecting the separation and analysis of the drugs were studied and optimized. Based on the corrected peak-area ratios of the drugs to an internal standard (7-hydroxy-4-methyl-coumarin) versus the concentration of the drugs, the established method is applicable to quantify AMB and BRM each over 20-150 microM, carbocysteine over 100-1500 microM, guaiacol and guaifenesin each over 10-150 microM. The detection limits (S/N=3; 0.5 psi, 5 s injection) of the method for the analytes are in the range of 3.0-5.0microM (except that of carbocysteine at 30 microM). The precision (relative standard deviation) and accuracy (relative error) of the method for the intra-day (n=3) and inter-day (n=5) analyses of the analytes at three levels are all below 4%. The method is speedy with a run time of about 6 min for the analysis of the five analytes. Application of this method to the analysis of AMB and BRM in pharmaceutical preparations or AMB in the urine of a dosed subject proved simple and effective.
机译:描述了一种简单快速的胶束电动毛细管色谱法,用于分离和定量五种祛痰药,包括氨溴索(AMB),溴己辛(BRM),羧半胱氨酸,愈创木酚和愈创甘油醚。在磷酸盐缓冲液(35 mM; pH 3.90)和乙腈(75:25,v / v)的混合溶液中以十二烷基硫酸钠(120 mM)作为胶束源分离药物,分离出的药物直接用UV监测检测器(200 nm)。研究和优化了影响药物分离和分析的几个关键参数。根据校正后的药物与内标物(7-羟基-4-甲基香豆素)的峰面积比与药物浓度的关系,所建立的方法适用于定量20-150 microM以上的AMB和BRM,超过100-1500 microM的半胱氨酸,愈创木酚和愈创甘油醚分别超过10-150 microM。该方法对分析物的检测极限(S / N = 3; 0.5 psi,注入5 s)在3.0-5.0microM的范围内(除了30 microM的半胱氨酸外)。在三个级别对分析物进行日内(n = 3)和日间(n = 5)分析的方法的精度(相对标准偏差)和准确性(相对误差)均低于4%。该方法快速运行,运行时间约6分钟,可分析五种分析物。实践证明,该方法用于分析药物制剂中的AMB和BRM或定量研究对象尿液中的AMB是简单有效的。

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