首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >A validated micellar electrokinetic chromatography method for the quantitation of dexamethasone, ondansetron and aprepitant, antiemetic drugs, in organogel
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A validated micellar electrokinetic chromatography method for the quantitation of dexamethasone, ondansetron and aprepitant, antiemetic drugs, in organogel

机译:一种经过验证的胶束电动色谱方法,用于定量有机凝胶中的地塞米松,恩丹西酮和阿瑞匹特,止吐药

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摘要

A micellar electrokinetic chromatography (MEKC) method was developed for the determination of three anti-vomiting drugs (aprepitant, dexamethasone and ondansetron) in pharmaceutical formulations. The method was optimized using a central composite design (CCD). Four main factors (borate buffer concentration, pH, methanol content and sodium dodecyl sulfate concentration) were optimized in order to obtain best resolutions and peak efficiencies in a minimum runtime. The separation was performed in a fused-silica capillary. After optimization, the background electrolyte consisted of a borate buffer (62.5. mM, pH 8.75) containing sodium dodecyl sulfate (77.5. mM) and methanol (3.75%). Under these conditions, a complete separation of each antiemetic drug and its respective internal standards was achieved in 38. min. The method was validated with trueness values from 94.9 to 107.2% and precision results (repeatability and intermediate precision) lower than 5.9%. MEKC-UV was the first method allowing the separation of aprepitant, dexamethasone and ondansetron and was suitable for the quantitation of these three antiemetic drugs in organogel formulations. The rapid sample preparation coupled with an automated separation technique make this method convenient for quality control of extemporaneous magistral ready-to-use formulation.
机译:开发了一种胶束电动色谱(MEKC)方法,用于测定药物制剂中的三种抗呕吐药物(阿瑞匹坦,地塞米松和恩丹西酮)。使用中央复合设计(CCD)对方法进行了优化。优化了四个主要因素(硼酸盐缓冲液浓度,pH,甲醇含量和十二烷基硫酸钠浓度),以便在最短的运行时间内获得最佳的分离度和峰效率。分离是在熔融石英毛细管中进行的。优化后,背景电解质由硼酸盐缓冲液(62.5。mM,pH 8.75)组成,其中含有十二烷基硫酸钠(77.5。mM)和甲醇(3.75%)。在这些条件下,在38分钟内即可完全分离出每种止吐药及其各自的内标。验证该方法的真实值在94.9%至107.2%之间,精度结果(重复性和中间精度)低于5.9%。 MEKC-UV是第一种允许分离阿瑞匹坦,地塞米松和昂丹司琼的方法,适用于定量有机凝胶制剂中这三种止吐药。快速的样品前处理与自动分离技术相结合,使该方法可方便地用于即席地磁即用型制剂的质量控制。

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