Lemus Gallego J M, Pérez Arroyo J
Department of Analytical Chemistry, Facultad de Ciencias Qui;micas, Universidad de Castilla-La Mancha, 13071, Ciudad Real, Spain.
J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Jan 25;784(1):39-47. doi: 10.1016/s1570-0232(02)00748-1.
A micellar electrokinetic capillary chromatographic method to separate prednisolone, prednisolone acetate, naphazoline, Zn-bacitracin, sulfacetamide and phenylefrine is described. The separation was carried out by using a fused-silica capillary (57 cmx75 micrometer I.D.) at 25 degrees C and 30 kV, using a 5 mM phosphate-5 mM borate buffer adjusted to pH 8.2, 50 mM sodium dodecyl sulfate (SDS) and 10% methanol-water (v/v) as background electrolyte. Under these conditions, the run time was 8 min and the limits of quantification were about 1.0 mg/l for every component. The method was applied to pharmaceutical preparations and the results provided recoveries close to 100% and the method gave good results when compared with a reference multivariate calibration spectrophotometric method.
描述了一种胶束电动毛细管色谱法,用于分离泼尼松龙、醋酸泼尼松龙、萘甲唑啉、锌杆菌肽、磺胺醋酰和去氧肾上腺素。分离在25℃和30 kV下,使用内径为75μm、长度为57 cm的熔融石英毛细管进行,以pH 8.2的5 mM磷酸盐-5 mM硼酸盐缓冲液、50 mM十二烷基硫酸钠(SDS)和10%甲醇-水(v/v)作为背景电解质。在这些条件下,运行时间为8分钟,各组分的定量限约为1.0 mg/l。该方法应用于药物制剂,结果回收率接近100%,与参考多元校准分光光度法相比,该方法给出了良好的结果。