Brisaert M, Gabriëls M, Plaizier-Vercammen J
Laboratory of Pharmaceutical Technology and Physical Pharmacy, Pharmaceutical Institute, Free University of Brussels, Laarbeeklaan 103, B-1090, Brussels, Belgium.
Int J Pharm. 2000 Mar 20;197(1-2):153-60. doi: 10.1016/s0378-5173(99)00462-7.
A combination of 2% erythromycin and 0.05% tretinoin in an alcohol-isopropanol lotion was prepared. Two parameters were investigated for their influence on the stability of erythromycin and/or tretinoin, namely pH and the concentration of butylhydroxytoluene (BHT) as antioxidant. To investigate these two parameters, an optimization technique was used with two factors (pH and concentration of BHT) at two levels. Accelerated stability analysis was performed at 45 degrees C in the dark to exclude isomerization of tretinoin. To analyse erythromycin and tretinoin in the combination preparation, a TLC method, previously developed in the laboratory, was used. The degradation of erythromycin seemed to be much faster than the tretinoin degradation. Optimal stability is shown in the pH range of 8.2-8.6 for erythromycin and 7.2-8.2 for tretinoin while the concentration of BHT had no significant influence.
制备了一种含2%红霉素和0.05%维甲酸的乙醇 - 异丙醇洗剂。研究了两个参数对红霉素和/或维甲酸稳定性的影响,即pH值和作为抗氧化剂的丁基羟基甲苯(BHT)浓度。为研究这两个参数,采用了一种优化技术,其中两个因素(pH值和BHT浓度)各有两个水平。在45摄氏度黑暗条件下进行加速稳定性分析以排除维甲酸的异构化。为分析复方制剂中的红霉素和维甲酸,使用了实验室先前开发的薄层色谱法。红霉素的降解似乎比维甲酸的降解快得多。红霉素在pH值8.2 - 8.6范围内以及维甲酸在pH值7.2 - 8.2范围内显示出最佳稳定性,而BHT浓度没有显著影响。