Dutra Elizângela Abreu, Santoro Maria Inês Rocha Miritello, Micke Gustavo Amadeu, Tavares Marina Franco Maggi, Kedor-Hackmann Erika Rosa Maria
Department of Pharmacy, Faculty of Pharmaceutical Sciences, University of São Paulo, P.O. Box 66355, 05389-970 São Paulo, SP, Brazil.
J Pharm Biomed Anal. 2006 Feb 13;40(2):242-8. doi: 10.1016/j.jpba.2005.07.009. Epub 2005 Aug 19.
In this work, a simple and reliable method for the simultaneous analysis of alpha-hydroxy acids such as tartaric, glycolic and lactic acids in cosmetic products was developed using capillary electrophoresis with indirect UV detection at 254 nm. A buffer solution containing 10 mmoll(-1) potassium phthalate (pH 4.1) and 0.5 mmoll(-1) cetyltrimethylammonium bromide as electroosmotic flow modifier allowed baseline resolution of the analytes in approximately 3 min. A few validation parameters of the proposed method include: good linearity for all compounds in the range from 10 to 100 mgl(-1) with coefficients of correlation larger than 0.9999. The average recoveries of tartaric, glycolic and lactic acids in commercial samples were 99.12, 99.41 and 99.43%, respectively. The method presented acceptable precision with average relative standard deviation of 0.54% (assay of commercial samples), 0.44% (peak area) and 0.16% (migration time).
在这项工作中,开发了一种简单可靠的方法,用于同时分析化妆品中的酒石酸、乙醇酸和乳酸等α-羟基酸,该方法采用毛细管电泳,并在254nm处进行间接紫外检测。含有10mmolL⁻¹邻苯二甲酸钾(pH 4.1)和0.5mmolL⁻¹十六烷基三甲基溴化铵作为电渗流改性剂的缓冲溶液可在约3分钟内实现分析物的基线分离。该方法的一些验证参数包括:所有化合物在10至100mgL⁻¹范围内具有良好的线性,相关系数大于0.9999。市售样品中酒石酸、乙醇酸和乳酸的平均回收率分别为99.12%、99.41%和99.43%。该方法具有可接受的精密度,平均相对标准偏差为0.54%(市售样品测定)、0.44%(峰面积)和0.16%(迁移时间)。