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
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.