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Determination of diethanolamine in cosmetics based on micellar extraction in situ derivatization coupled with high performance liquid chromatography

机译:胶束原位衍生化-高效液相色谱法测定化妆品中的二乙醇胺

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摘要

A micellar extraction procedure in situ derivatization method was developed for extraction of diethanolamine in cosmetic samples prior to high performance liquid chromatography analysis. The diethanolamine was taken into a complex with dansyl chloride in an aqueous nonionic surfactant, Triton X-114, medium and concentrated in the surfactant-rich phase. Based on method development, the optimum parameters for the micelle-mediated extraction process were as follows: 4.0% (v/v) of Triton X-114, pH = 9, 1.5 g L-1 solution of derivative reagent, derivatization time of 15 min and derivatization temperature of 50 degrees C. In addition, the cloud point pre-concentration was optimized under the condition of 15% (m/v) sodium chloride and equilibration at 60 degrees C for 10 min. The extract obtained was analyzed by high performance liquid chromatography. The micellar extraction in situ derivatization/high performance liquid chromatography method was successfully applied for the determination of trace diethanolamine in cosmetic samples, the limit of detection (LOD) and limit of quantity (LOQ) of diethanolamine were 0.57 mu g g(-1) and 1.72 mu g g(-1), respectively. Recovery ranged from 89.9% to 96.4% with obtained relative standard deviations (RSDs) of 3.9% to 5.2%, respectively. The derivatization, extraction and enrichment were completed in the same system. The proposed method was a simple, effective and environmental friendly technique for the analysis of diethanolamine.
机译:开发了一种胶束萃取程序原位衍生方法,用于在高效液相色谱分析之前萃取化妆品样品中的二乙醇胺。将二乙醇胺与丹磺酰氯在水性非离子表面活性剂Triton X-114中混合,加入介质,并在富含表面活性剂的相中浓缩。根据方法的发展,胶束介导的提取工艺的最佳参数如下:Triton X-114的4.0%(v / v),pH = 9、1.5 g的衍生试剂L-1溶液,衍生化时间为15需要说明的是,最小沸点和衍生温度为50℃。此外,浊点预浓缩在15%(m / v)氯化钠和在60℃下平衡10分钟的条件下被优化。通过高效液相色谱法分析获得的提取物。胶束萃取原位衍生/高效液相色谱法成功地用于化妆品样品中痕量二乙醇胺的测定,二乙醇胺的检出限(LOD)和定量限(LOQ)为0.57 mu gg(-1),分别为1.72 mu gg(-1)。回收率在89.9%至96.4%之间,相对标准偏差(RSD)分别为3.9%至5.2%。衍生化,提取和富集在同一系统中完成。所提出的方法是一种简单,有效且环境友好的技术,用于二乙醇胺的分析。

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