Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Juiz de Fora, Cidade Universitária CEP 36036-330, Juiz de Fora, MG, Brazil.
Talanta. 2010 Jun 30;82(1):333-9. doi: 10.1016/j.talanta.2010.04.044. Epub 2010 Apr 24.
An alternative methodology for simultaneous analysis of ethambutol, isoniazid, rifampicin and pyrazinamide in pharmaceutical formulations by capillary zone electrophoresis under UV direct detection with an analysis time of 8.0 min is proposed. Background running was based on the effective mobility curve of the analytes and an optimum separation condition was achieved using a 3(3) Box-Behnken design, with Brij 35, Cu(2+) and acetic acid/sodium acetate buffer as factors. An electrolyte consisting of 50.0 mmol L(-1) of acetic acid/sodium acetate buffer, 12.5 mmol L(-1) of CuSO(4), and standard and sample solutions prepared in 2.00 mmol L(-1) of Brij 35 and 12.5 mmol L(-1) of CuSO(4) were optimized. After evaluating validation parameters, the method was successfully applied to the analysis of samples in the form of tablets and sachets.
提出了一种在毛细管区带电泳(CZE)中,采用紫外直接检测法,在 8.0 min 内同时分析药物制剂中乙胺丁醇、异烟肼、利福平及吡嗪酰胺的替代方法。背景运行基于分析物的有效迁移率曲线,采用 3(3) Box-Behnken 设计,以 Brij 35、Cu(2+)和乙酸/乙酸钠缓冲液为因素,实现了最佳分离条件。电解质由 50.0 mmol L(-1)的乙酸/乙酸钠缓冲液、12.5 mmol L(-1)的 CuSO(4)、以及在 2.00 mmol L(-1)的 Brij 35 和 12.5 mmol L(-1)的 CuSO(4)中制备的标准和样品溶液组成。在评估验证参数后,该方法成功地应用于片剂和小袋形式的样品分析。