Equipment-Free Detection of K+ on Microfluidic Paper-Based Analytical Devices Based on Exhaustive Replacement with Ionic Dye in Ion-selective Capillary Sensors

被引:60
作者
Soda, Yoshiki [1 ]
Citterio, Daniel [2 ]
Bakker, Eric [1 ]
机构
[1] Univ Geneva, Dept Inorgan, Analyt Chem, Quai Ernest Ansermet 30, CH-1211 Geneva, Switzerland
[2] Keio Univ, Dept Appl Chem, Kohoku Ku, 3-14-1 Hiyoshi, Yokohama, Kanagawa 2238522, Japan
基金
瑞士国家科学基金会;
关键词
paper-based analytical devices; capillary sensor; ion-selective membrane; potassium detection; serum measurement; SOLVATOCHROMIC DYES; PATTERNED PAPER; SERUM VISCOSITY; SODIUM; POTASSIUM; BULK; ACID; PH; ELECTRODES; PLATFORM;
D O I
10.1021/acssensors.8b01521
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A distance-based analysis of potassium ion (K+) is introduced that is performed on a microfluidic paper-based analytical device (mu PAD) coupled to an ion-selective capillary sensor. The concept is based on two sequential steps, the selective replacement of analyte ion with an ionic dye, and the detection of this dye in a distance-based readout on paper. To achieve the first step, the capillary sensor holds a poly(vinyl chloride) (PVC) membrane film layer plasticized by dioctyl sebacate (DOS) that contains the potassium ionophore valinomycin, a lipophilic cation-exchanger and the ionic indicator Thioflavin T (ThT) on its inner wall. Upon introduction of the sample, K+ in the aqueous sample solution is quantitatively extracted into the film membrane and replaced with ThT. To convert the ion exchange signal into a distance-based analysis, this solution was dropped onto the inlet area of a mu PAD to flow the ThT along a channel defined by wax printing, resulting in the electrostatic binding of ThT to the cellulose carboxylic groups. The initial amount of K+ determines the amount of ThT in the aqueous solution after ion-exchange, and consequently the distance of ThT-colored area reflects the sample K+ concentration. The ion exchange reaction was operated in a so-called "exhaustive sensing mode" and gave a distinct response in a narrow range of K+ concentration (16 mM) that cannot be achieved by the classical optode sensing mode. The absence of hydrogen ions from the equilibrium competition of the capillary sensor contributed to a complete pH-independence, unlike conventional optodes that contain a pH sensitive indicator. A very high selectivity for K+ over Na+ and Ca2+ has been confirmed in separate solutions and mixed solutions tests. K+ measurements in pooled serum samples at concentrations between 2 and 6 mM are successfully demonstrated on a temperature controlled support.
引用
收藏
页码:670 / 677
页数:15
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