A Nanomembrane-Based Nucleic Acid Sensing Platform for Portable Diagnostics

Nanowire field effect transistors (NW-FETs) can serve as ultrasensitive detectors for label-free reagents. The NW-FET sensing mechanism assumes a controlled modification in the local channel electric field created by the binding of charged molecules to the nanowire surface. Careful control of the solution Debye length is critical for unambiguous selective detection of macromolecules. Here we show the appropriate conditions under which the selective binding of macromolecules is accurately sensed with NW-FET sensors.

We have developed a highly efficient microfluidic sample preconcentration device based on the electrokinetic trapping mechanism enabled by nanofluidic filters. The device, fabricated by standard photolithography and etching techniques, generates an extended space charge region within a microchannel, which was used to both collect and trap the molecules efficiently. The electrokinetic trapping and collection can be maintained for several hours, and concentration factors as high as 10(6)-10(8) have been demonstrated. This device could be useful in various bioanalysis microsystems, due to its simplicity, performance, robustness, and integrabilty to other separation and detection systems.

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).10.1016/0011-9164(88)80013-4] 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.