管内凝胶电膜结合微流控纸基装置:一种绿色、小型化的铬形态提取模式

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2022-08-01 DOI:10.1016/j.sampre.2022.100036
Hadi Tabani , Thidarat Samkumpim , Waleed Alahmad , Farzaneh Dorabadizare , Pakorn Varanusupakul
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引用次数: 9

摘要

首次制备了管内凝胶电膜微萃取(IT-G-EME)系统,然后采用微流控纸基分析装置(µPADs)作为低成本读取平台,用于三价铬(Cr(III))和六价铬(Cr(VI))作为模型阳离子和阴离子化合物的形态。在这种新的小型化提取模式中,采用透明窄孔聚合物管作为水受体相(AP, 30µL)的外壳,而琼脂糖凝胶膜作为微塞(2.5 mm)放置在管的开始。一个圆形小瓶(1.5 mL, pH 5.5)含有铬作为供体相(DP)连接在两个先前充满凝胶膜和水性AP的管之间。通过施加电势,DP中带正电的Cr(III)和带负电的Cr(VI)分别选择性地向阴极和阳极管迁移。提取后,用二苯脲(diphenylcarbazide, DPC)修饰的µPAD进行分析。在优化的提取条件下,两种分析物的检出限(LOD)均为7.0 μ g L-1, Cr(VI)和Cr(III)的提取回收率分别为72%和84%。此外,该方法还用于水样中铬种类的定量分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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In-tube gel electro-membrane combined with microfluidic paper-based device: A green and miniaturized extraction mode for the chromium speciation

For the first time, in-tube gel electro-membrane microextraction (IT-G-EME) system followed by microfluidic paper-based analytical devices (µPADs) as a low-cost reading platform was fabricated for the speciation of trivalent chromium (Cr(III)) and hexavalent chromium (Cr(VI)) as model cationic and anionic compounds. In this new miniaturized extraction mode, a transparent narrow-bore polymeric tube was used as housing of the aqueous acceptor phase (AP, 30 µL), while an agarose gel membrane was placed as a micro plug (2.5 mm) at the beginning of the tube. A circular shape vial (1.5 mL, pH 5.5) containing chromium species as donor phase (DP) was connected between two tubes which previously filled with gel membrane and aqueous AP. By applying electric potential, the positively charged Cr(III) and negatively charged Cr(VI) in the DP migrated selectively toward cathodic and anodic tubes, respectively. After extraction, each AP was analyzed by µPAD, which had already been modified with diphenylcarbazide (DPC). Under the optimized extraction conditions, a good limit of detection (LOD) equal to 7.0 µg L–1 was achieved for both analytes, while the extraction recoveries for Cr(VI) and Cr(III) were 72% and 84%. In addition, the developed approach was used for the quantification of chromium species in water samples.

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