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基于在离子选择性毛细管传感器中用离子染料进行彻底替换的无设备微流控纸基分析器件上的 K 检测。

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

机构信息

Department of Inorganic, Analytical Chemistry , University of Geneva , Quai Ernest-Ansermet 30 , CH-1211 Geneva , Switzerland.

Department of Applied Chemistry , Keio University , 3-14-1 Hiyoshi , Kohoku-ku , 223-8522 Yokohama , Japan.

出版信息

ACS Sens. 2019 Mar 22;4(3):670-677. doi: 10.1021/acssensors.8b01521. Epub 2019 Feb 19.

Abstract

A distance-based analysis of potassium ion (K) is introduced that is performed on a microfluidic paper-based analytical device (μPAD) 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 μPAD 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 (1-6 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 Ca 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.

摘要

介绍了一种基于微流控纸基分析装置(μPAD)与离子选择性毛细管传感器相结合的钾离子(K)的距离分析方法。该概念基于两个连续步骤,即选择性地用离子染料替代分析物离子,以及在基于距离的纸读数中检测这种染料。为了实现第一步,毛细管传感器具有由癸二酸二辛酯(DOS)增塑的聚氯乙烯(PVC)膜层,该膜层在其内壁上包含钾离子载体缬氨霉素、亲脂性阳离子交换剂和离子指示剂硫代黄素 T(ThT)。在引入样品后,水样溶液中的 K 被定量提取到膜中,并被 ThT 取代。为了将离子交换信号转换为基于距离的分析,将该溶液滴加到μPAD 的入口区域,使 ThT 沿由蜡印刷定义的通道流动,从而导致 ThT 与纤维素羧酸基团静电结合。初始 K 量决定了离子交换后水溶液中 ThT 的量,因此 ThT 着色区域的距离反映了样品 K 浓度。离子交换反应在所谓的“全感应模式”下进行,在狭窄的 K 浓度范围内(1-6 mM)给出了明显的响应,而经典的光学传感器模式无法实现。毛细管传感器中不存在氢离子,有助于完全 pH 独立性,这与包含 pH 敏感指示剂的传统光学传感器不同。在单独溶液和混合溶液测试中已经证实了对 K 相对于 Na 和 Ca 的高选择性。在控温支架上成功地对浓度在 2 至 6 mM 之间的混合血清样品中的 K 进行了测量。

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