Department of Pharmaceutical Sciences, University of Florence, Via U. Schiff 6, 50019 Sesto Fiorentino, Florence, Italy.
Talanta. 2010 Nov 15;83(1):72-7. doi: 10.1016/j.talanta.2010.08.043. Epub 2010 Sep 25.
A mixture of 18 neutral UV-active compounds with different characteristics of polarity was determined by capillary electrophoresis using a pseudostationary phase constituted by a microemulsion. The test analytes were volatile fragrance compounds, included in a list of 24 chemicals classified as suspected allergens according to Directive 2003/15/CE. The considered compounds were detected at 195 nm and p-anisaldehyde was chosen as internal standard. The background electrolyte consisted of a standard microemulsion made of 90.95% 10mM borax buffer, pH 9.2, 1.05% n-heptane, 8.00% SDS/n-butanol in 1:2 ratio, to which 40 mM methyl-β-cyclodextrin was added. Temperature and voltage were set at 20 °C and 25 kV, respectively. These experimental conditions allowed separation of the compounds to be obtained in about 20 min. The method was applied to real samples made up of rinse-off scented products. The results obtained using the standard microemulsion as pseudostationary phase showed its high resolution power, capable of effectively separating a complex mixture of analytes. Microemulsion electrokinetic chromatography was confirmed to have a great potential for different analytical challenges, holding up the possibility of using this technique as a good and complementary alternative to HPLC methods for routine analysis.
采用由微乳液构成的伪固定相,通过毛细管电泳对 18 种具有不同极性特征的中性紫外活性化合物混合物进行了测定。测试分析物为挥发性香料化合物,包含在根据指令 2003/15/CE 被列为疑似过敏原的 24 种化学物质列表中。所考虑的化合物在 195nm 处被检测到,对茴香醛被选为内标。背景电解质由标准微乳液组成,该微乳液由 90.95% 10mM 硼砂缓冲液,pH9.2,1.05%正庚烷,8.00%SDS/正丁醇以 1:2 的比例组成,并添加了 40mM 甲基-β-环糊精。温度和电压分别设定为 20°C 和 25kV。这些实验条件允许在大约 20 分钟内获得化合物的分离。该方法应用于由冲洗香味产品组成的实际样品。使用标准微乳液作为伪固定相得到的结果表明其具有很高的分辨率能力,能够有效分离复杂的分析物混合物。微乳液电动色谱被证实具有应对不同分析挑战的巨大潜力,有可能将该技术用作 HPLC 方法的常规分析的良好且互补的替代方法。