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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 >Separation and determination of nimesulide related substances for quality control purposes by micellar electrokinetic chromatography.
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Separation and determination of nimesulide related substances for quality control purposes by micellar electrokinetic chromatography.

机译:通过胶束电动色谱法分离和测定尼美舒利相关物质以进行质量控制。

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摘要

A micellar electrokinetic chromatography (MEKC) method has been developed and validated for the determination of nimesulide related compounds in pharmaceutical formulations. Electrophoretic separation of six European Pharmacopoeia (EP) impurities (A-F) was performed using a fused silica capillary (L(eff.)=50 cm, L(tot.)=57 cm, 50 microm i.d.) with a background electrolyte (BGE) containing 25 mM borate buffer (pH 9.5), 30 mM sodium dodecyl sulphate and phi=3% (v/v) acetonitrile. The influence of several factors (surfactant and buffer concentration, pH, organic modifier, applied voltage, capillary temperature and injection time) was studied. The method was suitably validated with respect to linearity, limit of detection and quantification, accuracy, precision and selectivity. The calibration curves obtained for the six compounds were linear over the range 5-12 microgml(-1) (0.05-0.12%). The relative standard deviations (s(r)) of intra- and inter-day experiments were less than 5.0%. The detection limits ranged between 0.7 and 1.6 microgml(-1) depending on the impurity. The proposed method was applied successfully to the quantification of nimesulide impurities in its pharmaceutical formulation.
机译:已经开发了胶束电动色谱(MEKC)方法,并已用于确定药物制剂中尼美舒利相关化合物的有效性。使用熔融硅胶毛细管(L(eff。)= 50 cm,L(tot。)= 57 cm,50 microm id)和背景电解质(BGE)对六种欧洲药典(EP)杂质(AF)进行电泳分离含有25 mM硼酸盐缓冲液(pH 9.5),30 mM十二烷基硫酸钠和phi = 3%(v / v)乙腈。研究了几个因素(表面活性剂和缓冲液浓度,pH,有机改性剂,施加电压,毛细管温度和进样时间)的影响。该方法在线性,检测和定量限,准确性,精密度和选择性方面经过了适当验证。六种化合物的校准曲线在5-12 microgml(-1)(0.05-0.12%)范围内是线性的。日内和日间实验的相对标准偏差(s(r))小于5.0%。根据杂质的不同,检测限范围为0.7至1.6 microgml(-1)。所提出的方法已成功应用于其药物制剂中尼美舒利杂质的定量。

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