Zacharis Constantinos K, Tzanavaras Paraskevas D, Notou Maria, Zotou Anastasia, Themelis Demetrius G
Department of Chemistry, Aristotle University, GR-54124 Thessaloniki, Greece.
J Pharm Biomed Anal. 2009 Feb 20;49(2):201-6. doi: 10.1016/j.jpba.2008.10.023. Epub 2008 Oct 28.
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.
已开发并验证了一种胶束电动色谱法(MEKC),用于测定药物制剂中的尼美舒利相关化合物。使用熔融石英毛细管(有效长度 = 50 cm,总长度 = 57 cm,内径 50 μm),以含有 25 mM 硼酸盐缓冲液(pH 9.5)、30 mM 十二烷基硫酸钠和 3%(v/v)乙腈的背景电解质(BGE)进行六种欧洲药典(EP)杂质(A - F)的电泳分离。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、检测限和定量限、准确度、精密度和选择性方面得到了适当验证。六种化合物的校准曲线在 5 - 12 μg/ml(0.05 - 0.12%)范围内呈线性。日内和日间实验的相对标准偏差(s(r))小于 5.0%。根据杂质不同,检测限在 0.7 至 1.6 μg/ml 之间。所提出的方法成功应用于药物制剂中尼美舒利杂质的定量分析。