Gomez María R, Sombra Lorena, Olsina Roberto A, Martínez Luis D, Silva María F
Cátedra de Control de Calidad de Medicamentos, Facultad de Química, Bioquímica y Farmacia, Chacabuco y Pedernera, Universidad Nacional de San Luis, 5700 San Luis, Argentina.
Farmaco. 2005 Jan;60(1):85-90. doi: 10.1016/j.farmac.2004.11.002. Epub 2004 Dec 22.
The present work describes a simple, accurate and rapid method for the separation and simultaneous determination of codeine, diphenhydramine, ephedrine and noscapine present in cough-cold syrup formulations by capillary zone electrophoresis. Factors affecting the separation were the buffer pH and concentration, applied voltage, and presence of additives. Separations were carried out in less than 10 min with a 20 mM sodium tetraborate buffer, pH 8.50. The carrier electrolyte gave baseline separation with good resolution, great reproducibility and accuracy. Calibration plots were linear over at least three orders of magnitude of analyte concentrations, the lower limits of detection being within the range 0.42-1.33 microg ml(-1). Detection was performed by UV absorbance at wavelengths of 205 and 250 nm. Quantification of the components in actual syrup formulations was calculated against the responses of freshly prepared external standard solutions. The method was validated and met all analysis requirements of quality assurance and quality control. The procedure was fast and reliable and commercial pharmaceuticals could be analyzed without prior sample clean-up procedure.
本研究描述了一种通过毛细管区带电泳分离并同时测定止咳感冒糖浆制剂中可待因、苯海拉明、麻黄碱和那可丁的简单、准确且快速的方法。影响分离的因素有缓冲液的pH值和浓度、施加电压以及添加剂的存在。使用20 mM pH 8.50的硼酸钠缓冲液,分离在不到10分钟内完成。载体电解质实现了基线分离,具有良好的分辨率、重现性和准确性。校准曲线在至少三个分析物浓度数量级范围内呈线性,检测下限在0.42 - 1.33 μg ml⁻¹范围内。通过在205和250 nm波长处的紫外吸光度进行检测。实际糖浆制剂中各成分的定量是根据新制备的外标溶液的响应进行计算的。该方法经过验证,符合质量保证和质量控制的所有分析要求。该方法快速可靠,无需预先进行样品净化程序即可分析市售药品。