Lucca Bruno Gabriel, Lunte Susan Marie, Tomazelli Coltro Wendell Karlos, Ferreira Valdir Souza
Instituto de Química, Universidade Federal de Mato Grosso do Sul, Campo Grande, MS, Brazil.
Electrophoresis. 2014 Dec;35(23):3363-70. doi: 10.1002/elps.201400359. Epub 2014 Oct 20.
This report describes the use of PDMS ME coupled with amperometric detection for rapid separation of ascorbic, gallic , ferulic, p-coumaric acids using reverse polarity. ME devices were fabricated in PDMS by soft lithography and detection was accomplished using an integrated carbon fiber working electrode aligned in the end-channel configuration. Separation and detection parameters were investigated and the best conditions were obtained using a run buffer consisting of 5 mM phosphate buffer (pH 6.9) and a detection voltage of 1.0 V versus Ag/AgCl reference electrode. All compounds were separated within 70 s using gated injection mode with baseline resolution and separation efficiencies between 1200 and 9000 plates. Calibration curves exhibited good linearity and the LODs achieved ranged from 1.7 to 9.7 μM. The precision for migration time and peak height provided maximum values of 4% for the intrachip studies. Lastly, the analytical method was successfully applied for the analysis of ascorbic and gallic acids in commercial beverage samples. The results achieved using ME coupled with amperometric detection were in good agreement with the values provided by the supplier. Based on the data reported here, the proposed method shows suitability to be applied for the routine analysis of beverage samples.
本报告描述了使用聚二甲基硅氧烷微流控芯片(PDMS ME)结合安培检测法,采用反相极性快速分离抗坏血酸、没食子酸、阿魏酸、对香豆酸。微流控芯片器件通过软光刻技术在聚二甲基硅氧烷中制备,检测使用集成在通道末端配置的碳纤维工作电极完成。研究了分离和检测参数,使用由5 mM磷酸盐缓冲液(pH 6.9)组成的运行缓冲液和相对于Ag/AgCl参比电极1.0 V的检测电压获得了最佳条件。所有化合物在70秒内使用门控进样模式分离,具有基线分辨率,分离效率在1200至9000塔板之间。校准曲线呈现良好的线性,检测限范围为1.7至9.7 μM。芯片内研究中迁移时间和峰高的精密度最大值为4%。最后,该分析方法成功应用于商业饮料样品中抗坏血酸和没食子酸的分析。使用微流控芯片结合安培检测获得的结果与供应商提供的值高度一致。基于此处报告的数据,所提出的方法显示适用于饮料样品的常规分析。