We designed and constructed a drop-on-demand (DOD) droplet dispenser using the piezo inkjet technique that is simple to construct and operate and makes use of readily available components. The droplet dispenser can be easily fitted with cost effective glass nozzles and can be readily tuned to produce consistent drop sizes. The dynamics of the droplet motion are obtained using a calibrated analog video imaging system. We observed very high accelerations for the ejected droplets that corroborate with the applied drive pulse amplitudes. The acceleration measured, near the ejection nozzle, was many times the acceleration of gravity with the largest value of 34g’s. We successfully dispensed glycol water solutions and aqueous suspensions of titanium oxide nanoparticles, with values greater than 10 in the measured pH. For the inkjet droplets deposited on smooth gold/chromium substrates (±3nm surface roughness variation), we observed the well-known coffee ring effect using optical microscopy and nanoparticle morphology using an atomic force microscope.

In this paper we present an innovative on-chip platform suitable for the simultaneous manipulation and detection of the transit of a single magnetic bead. This system is based on the controlled displacement of constrained magnetic domain walls (DWs) that are used to move and sense particles in suspension over the chip. To this scope, the high stray field from the transverse DWs created at the corners of ferromagnetic zig-zag structures is used for particles manipulation, while electrical contacts flanking a single corner are employed to simultaneously monitor the DW passage through that corner, via anisotropic magneto resistance (AMR) measurements. A single DW carrying a magnetic particle is nucleated and manipulated within the zig-zag shaped magnetic conduit, trough the action of external magnetic fields. At the same time, the variation of the voltage drop across a corner flanked by a pair of electrical leads is measured, allowing to detect the transit of the DW thanks to the change of the relative orientation of current and spins at the corner related to the peculiar micromagnetic configuration of the DW (AMR). Work is in progress in order to selectively distinguish the transit of a naked DW from that of a DW bound to a magnetic particle. This work paves the way to the development of a closed-loop microlfuidic platform for on-chip bead manipulation, where single bead can be finely moved and their motion continuously checked, via AMR electrical detection and without need of optical monitoring, in a fully integrated closed-loop system.

In this work, we demonstrate the label-free and ultrasensitive detection of troponin-T, cardiac biomarker using nanoporous membrane integrated on a microelectrode sensor platform. The nanoporous membrane allows for spatial confinement of the protein molecules. Antigen interaction with thiol immobilized antibody perturbs the electrical double layer. Charge perturbations are recorded as impedance change at low frequency using the principle of electrochemical impedance spectroscopy (EIS). The measured impedance change is used to quantitatively determine the concentration of troponin-T in tested sample. We have shown that sensitivity of sensor for troponin-T to be 1pg/mL. The accuracy and reliability of this sensor was tested by comparing the experimental troponin-T concentration values with a commercially available electrochemiluminescence assay measured with Roche Elecsys analyzer. Using this technique we were successful in detecting protein biomarkers in whole blood, human serum, and ionic buffers. This technology provides a robust analytical platform for rapid and sensitive detection of protein biomarkers, thus establishing this technology as an ideal candidate for biomarker screening in clinical settings.

Metastatic tumors can spread via release of circulating tumor cells (CTCs) into the bloodstream. Early detection of these CTCs could greatly improve cancer survival rates by enabling diagnosis, and therefore treatment, before secondary tumors arise. However, tumor cells are typically present in very low concentrations, making them difficult to detect in a fluid dominated by red blood cells (RBCs), leukocytes and serum proteins. Separation of CTCs from blood plasma, leukocytes and RBCs is predicted to improve cell capture via antibody-based methods and reduce interference in capture/detection assays. Previously, members of our team have demonstrated microfluidic, size-based separation of blood components, but have yet to integrate this sorting capability with an affinity-based detection technology. To this end, we have developed a microfluidic platform to separate CTCs from mouse blood and detect them using grating coupled surface plasmon resonance (GCSPR). We have implemented a size-based sorting array, which separates objects based upon their diameter, within a microfluidic channel. Separation of beads (2 μm, 6 μm, 10 μm) has been demonstrated, as well as separation of white blood cells and CTCs from blood. The resulting stream of large blood cells (including CTCs) is then directed onto an integrated SPR grating for affinity based capture and detection. Using GCSPR vs. conventional SPR enables detection of multiple cell types across the grating in an array-based format. We have demonstrated differential capture and detection of cells on GCSPR gratings following size-based separation of blood. Using capture antibodies specific to unique CTC surface proteins enables identification of cell types and may provide prognostic capability, beyond the diagnostic capacity of this system.