Jiang Ruiyuan, Sun Guoxiang
College of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Se Pu. 2012 Jan;30(1):103-6. doi: 10.3724/sp.j.1123.2011.08034.
A capillary zone electrophoresis (CZE) method was developed for the simultaneous determination of cefoperazone sodium and tazobactam sodium in the injectable powder of cefoperazone sodium and tazobactam sodium with hydrochlorothiazide as the internal standard. The operation was carried out on a quartz capillary (75 cm x 75 microm i. d. , 63 cm effective length). The electrophoretic conditions were as follows: 40 mmol/L borax solution as the back ground electrolyte (BGE), 12. 0 kV applied voltage, 220 nm as the detection wavelength; the sample solution was injected by hydraulic pressure for 10 s at the height of 10 cm. The cefoperazone and tazobactam showed good linear relationship in the ranges of 0.25-3.96 g/L and 0.062-0.99 g/L with the correlation coefficients of 0.999 5 and 0.999 6, respectively. The relative standard deviations of relative peak areas were less than 3%. The preparation was stable in 208 min. The recovery results met the methodology requirements. The method is simple, rapid, reproducible, and suitable to control the quality of cefoperazone sodium and tazobactam sodium injectable powder.
建立了一种毛细管区带电泳(CZE)法,以氢氯噻嗪为内标,同时测定注射用头孢哌酮钠舒巴坦钠中头孢哌酮钠和舒巴坦钠的含量。采用石英毛细管(75 cm×75 μm内径,有效长度63 cm)进行操作。电泳条件如下:以40 mmol/L硼砂溶液为背景电解质(BGE),施加电压12.0 kV,检测波长220 nm;样品溶液通过10 cm高度的液压进样10 s。头孢哌酮和舒巴坦在0.25~3.96 g/L和0.062~0.99 g/L范围内线性关系良好,相关系数分别为0.999 5和0.999 6。相对峰面积的相对标准偏差小于3%。制剂在208 min内稳定。回收率结果符合方法学要求。该方法简便、快速、重现性好,适用于控制注射用头孢哌酮钠舒巴坦钠的质量。