Determination of cephalexin in oral suspensions by micellar electrokinetic chromatography.

Martin Steppe, María S Aurora Prado, Marina F M Tavares, Erika R M Kedor-Hackmann, Maria Inês R M Santoro
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Abstract

A simple and efficient micellar capillary electrophoresis method for the analysis of cephalexin in oral suspensions is described. The analysis was carried out in a bare silica capillary with 75 microm i.d. and total length of 50 cm (28 cm to the detector) with a buffer solution containing 20 mM sodium tetraborate, 20 mM sodium dodecyl sulfate, and 0.1% laurylpolyoxiethylenic ether. The applied voltage was 15 kV. Detection was achieved by ultraviolet absorption at 210 nm. The calibration curve was linear within the concentration range from 40.0 to 120 microg/mL with a correlation coefficient of 0.9998. The percentage recovery was found to be 100.09 +/- 0.56. The method showed good selectivity and resolution of the drug impurities, and was found suitable to study cephalexin stability in pharmaceutical preparations.

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胶束电动色谱法测定口服混悬液中头孢氨苄的含量。
建立了一种简单有效的口服混悬液中头孢氨苄的胶束毛细管电泳分析方法。分析在75微米、总长度为50厘米(检测器长度为28厘米)的裸硅毛细管中进行,缓冲溶液含有20毫米四硼酸钠、20毫米十二烷基硫酸钠和0.1%十二烷基聚氧乙烯醚。施加电压为15kv。采用210 nm紫外吸收法进行检测。在浓度为40.0 ~ 120 μ g/mL范围内,曲线呈线性关系,相关系数为0.9998。回收率为100.09±0.56。该方法对药物杂质具有良好的选择性和分辨力,适用于头孢氨苄在药物制剂中的稳定性研究。
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