In
this paper, we report a method to integrate the electrokinetic
pre-enrichment of nucleic acids within a bed of probe-modified microbeads
with their label-free electrochemical detection. In this detection
scheme, hybridization of locally enriched target nucleic acids to
the beads modulates the conduction of ions along the bead surfaces.
This is a fundamental advancement in that this mechanism is similar
to that observed in nanopore sensors, yet occurs in a bed of microbeads
with microscale interstices. In application, this approach has several
distinct advantages. First, electrokinetic enrichment requires only
a simple DC power supply, and in combination with nonoptical detection,
it makes this method amenable to point-of-care applications. Second,
the sensor is easy to fabricate and comprises a packed bed of commercially
available microbeads, which can be readily modified with a wide range
of probe types, thereby making this a versatile platform. Finally,
the sensor is highly sensitive (picomolar) despite the modest 100-fold
pre-enrichment we employ here by faradaic ion concentration polarization
(fICP). Further gains are anticipated under conditions for fICP focusing
that are known to yield higher enrichment factors (up to 100,000-fold
enrichment). Here, we demonstrate the detection of 3.7 pM single-stranded
DNA complementary to the bead-bound oligoprobe, following a 30 min
single step of enrichment and hybridization. Our results indicate
that a shift in the slope of a current–voltage curve occurs
upon hybridization and that this shift is proportional to the logarithm
of the concentration of target DNA. Finally, we investigate the proposed
mechanism of sensing by developing a numerical simulation that shows
an increase in ion flux through the bed of insulating beads, given
the changes in surface charge and zeta potential, consistent with
our experimental conditions.