Chemistry Department, Shiraz University, Shiraz, Iran.
Chemistry Department, Shiraz University, Shiraz, Iran.
J Chromatogr A. 2020 Jun 21;1621:461049. doi: 10.1016/j.chroma.2020.461049. Epub 2020 Mar 16.
Herein, we report three-dimensional paper chromatography (3D-PC) as a micro-chromatographic platform. The method was based on applying the origami microfluidic device for separation, coupled by colorimetric methods for simultaneous determination. The microfluidic device fabrication was a facile printing approach. Two azo food dyes, Tartrazine (E102) and Indigo carmine (E132), were selected as a model analyte, while carbonate-bicarbonate buffer was used as the mobile phase. Our micro-chromatographic device is associated with two big advantages including needing very small volume of mobile phase ( 12 µL) and ultrafast separation time (35 s). Under the optimal conditions, the method provided acceptable linear ranges of 0. 0 g L-18.0 g L (R = 0.997) for E102 and 0.070 g L-10.0 g L for E132 and the limits of detection (3σ/slope) were evaluated as 0.620 and 0.060 g L, respectively. The proposed method was successfully applied in the separation and quantification of these dyes in commercial food products such as jelly, candy, and four kinds of drink samples without any sample preparation prior to analysis. The mean recovery values for the real sample analysis were in the range of 100.14%-102.38% for E132 and E102 respectively. The inter-device relative standard deviations were in the ranges of 1.5%-11.8%. In total, our chromatographic μPAD is small (1.0 cm × 1.0 cm × 0.5 cm), portable, inexpensive, no need of specialized user, requires low volumes of sample (0.5 μL), and can perform separation using 12 μL of aqueous mobile phase in very short time.
本文报道了一种基于折纸微流控装置的三维纸色谱(3D-PC)作为微色谱平台。该方法通过应用折纸微流控装置进行分离,并结合比色法进行同时测定。微流控装置的制造采用了简单的打印方法。选择两种偶氮食用染料,Tartrazine(E102)和Indigo carmine(E132)作为模型分析物,而碳酸盐-碳酸氢盐缓冲液作为流动相。我们的微色谱装置具有两个主要优点,包括需要非常小体积的流动相(约 12 μL)和超快的分离时间(~35 s)。在最佳条件下,该方法对 E102 的线性范围为 0.0 g L-18.0 g L(R = 0.997),对 E132 的线性范围为 0.070 g L-10.0 g L,检出限(3σ/斜率)分别为 0.620 和 0.060 g L。该方法成功应用于商业食品产品(如果冻、糖果和四种饮料样品)中这些染料的分离和定量分析,无需在分析前进行样品制备。实际样品分析的平均回收率范围分别为 E132 和 E102 的 100.14%-102.38%。不同装置之间的相对标准偏差范围为 1.5%-11.8%。总的来说,我们的色谱 μPAD 体积小(1.0 cm×1.0 cm×0.5 cm),便携,价格低廉,不需要专业用户,样品用量少(0.5 μL),可在极短时间内使用 12 μL 的水相流动相进行分离。