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首页> 外文期刊>Chromatographia >Micellar Electrokinetic Chromatography as a Valuable Technique for the Quality Control of Drugs Based on the Combination of Sulfamethoxazole with Trimethoprim
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Micellar Electrokinetic Chromatography as a Valuable Technique for the Quality Control of Drugs Based on the Combination of Sulfamethoxazole with Trimethoprim

机译:胶束电动色谱法是磺胺甲恶唑与甲氧苄啶联用的一种重要的药物质量控制技术

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摘要

A micellar electrokinetic chromatographic method is presented for the determination of sulfanilic acid and sulphanilamide as degradation products of sulfamethoxazole and of 3,4,5-trimethoxybenzoic acid as degradation product of trimetoprim, by using 15 mM phosphate buffer (pH 12.6), 20 mM sodium dodecylsulfate and 5% (v/v) acetonitrile as electrolyte. The separation was carried out at 25 kV and 25 °C in a fused silica capillary (60.2 cm × 75 μm i.d.). Under these conditions, the run time was less than 10 min and the limits of quantification were 2.0–4.2 mg L−1. The reproducibility in-a-day of the assay was excellent because the relative standard deviations of the peak areas were always under 3%. The method was applied to spiked samples of a pharmaceutical commercial preparation containing the sulfamethoxazole-trimethoprim combination, and the recoveries obtained were close to 100% for both sulfanilic acid and sulfanilamide.
机译:提出了一种胶束电动色谱法,方法是使用15 mM磷酸盐缓冲液(pH 12.6),20 mM钠测定磺胺甲恶唑和3,4,5-三甲氧基苯甲酸的降解产物间苯二酚的磺胺酸和亚磺酰胺的含量十二烷基硫酸盐和5%(v / v)乙腈作为电解质。在熔融的石英毛细管(60.2cm×75μm,内径)中在25kV和25℃下进行分离。在这些条件下,运行时间少于10分钟,定量限为2.0–4.2 mg L-1 。该分析一天的重现性极佳,因为峰面积的相对标准偏差始终低于3%。该方法应用于含有磺胺甲恶唑-甲氧苄氨嘧啶组合的药物商业制剂的加标样品,对磺胺酸和磺胺酰胺的回收率均接近100%。

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