The ion flux dynamics across a straight nanoslot is imaged to understand the nonequilibrium phenomenon of overlimiting current density across a nanoporous membrane. With a slow ac field, an ion-depletion front is generated intermittently from one end of the nanochannel, and a vortex instability first predicted by Rubinstein, Staude, and Kedem [ Desalination 69, 101 (1988).] is found to arrest the self-similar diffusive front growth. This electrokinetic instability evolves into a stationary interfacial vortex array that specifies the overlimiting current, independent of external stirring or convective flow.

Multi-target pathogen detection using heterogeneous medical samples require continuous filtering, sorting, and trapping of debris, bioparticles, and immunocolloids within a diagnostic chip. We present an integrated AC dielectrophoretic (DEP) microfluidic platform based on planar electrodes that form three-dimensional (3D) DEP gates. This platform can continuously perform these tasks with a throughput of $3\mu \mathrm{L}∕\min$ . Mixtures of latex particles, Escherichia coli Nissle, Lactobacillus, and Candida albicans are sorted and concentrated by these 3D DEP gates. Surface enhanced Raman scattering is used as an on-chip detection method on the concentrated bacteria. A processing rate of 500 bacteria was estimated when $100\mu \mathrm{l}$ of a heterogeneous colony of ${10}^7$ colony forming units /ml was processed in a single pass within $30\min$ .

Surface acoustic wave sensors and microfluidic platforms enable effective chemical detection and sample manipulation.

A novel approach to the analysis of exosomal RNA is presented using SAW exosome lysis and ion-exchange nanomembrane RNA sensing.

The contact line in an evaporating drop can stay pinned to form a single ring or can shrink in a discontinuous stepwise manner and generate multiple rings. We demonstrate the latter with DNA solutions and attribute it to a pinning-depinning cycle that generates new contact lines. The new contact line recedes after depinning and is repinned at an internal precipitate ring that determines the location of the next contact line. Each precursor ring is formed when DNAs are trapped by an internal microstagnation flow and precipitation dynamics hence control this unsteady drop motion.

Extracellular vesicles (EV) containing microRNAs (miRNAs) have tremendous potential as biomarkers for the early detection of disease. Here, we present a simple and rapid PCR-free integrated microfluidics platform capable of absolute quantification (<10% uncertainty) of both free-floating miRNAs and EV-miRNAs in plasma with 1 pM detection sensitivity. The assay time is only 30 minutes as opposed to 13 h and requires only ~20 μL of sample as oppose to 1 mL for conventional RT-qPCR techniques. The platform integrates a surface acoustic wave (SAW) EV lysing microfluidic chip with a concentration and sensing microfluidic chip incorporating an electrokinetic membrane sensor that is based on non-equilibrium ionic currents. Unlike conventional RT-qPCR methods, this technology does not require EV extraction, RNA purification, reverse transcription, or amplification. This platform can be easily extended for other RNA and DNA targets of interest, thus providing a viable screening tool for early disease diagnosis, prognosis, and monitoring of therapeutic response.