AC electrothermal flow (ACEF) is the fluid motion created as a result of Joule heating induced temperature gradients. ACEF is capable of performing major microfluidic operations, such as pumping, mixing, concentration, separation and assay enhancement, and is effective in biological samples with a wide range of electrical conductivity. Here, we report long-range fluid motion induced by ACEF, which creates centimeter-scale vortices. The long-range fluid motion displays a strong voltage dependence and is suppressed in microchannels with a characteristic length below similar to 300 mu m. An extended computational model of ACEF, which considers the effects of the density gradient and temperature-dependent parameters, is developed and compared experimentally by particle image velocimetry. The model captures the essence of ACEF in a wide range of channel dimensions and operating conditions. The combined experimental and computational study reveals the essential roles of buoyancy, temperature rise, and associated changes in material properties in the formation of the long-range fluid motion. Our results provide critical information for the design and modeling of ACEF based microfluidic systems toward various bioanalytical applications. (C) 2016 Elsevier Ltd. All rights reserved.

Infectious diseases resulting from bacterial pathogens are the most common causes of patient morbidity and mortality worldwide. The rapid identification of the pathogens and their antibiotic resistances is crucial for proper clinical management. However, the standard culture-based diagnostic approach requires a minimum of two days from the initial specimen collection to result reporting. As a consequence, broad-spectrum antibiotics are often prescribed under the worst-case assumption without knowledge of the pathogens or their resistances. The current clinical practice results in improper treatment of the patient and causes the rapid emergence of multi-drug resistant pathogens. A rapid diagnostics system has therefore been developed which performs hybrid electrokinetic sample preparation and volume reduction, for single-cell antimicrobial susceptibility testing (AST). The system combines multiple electrokinetic forces for sample preparation, which reduces the sample volume for over 3 orders of magnitude and minimizes the matrix effects of physiological samples for enhanced sensitivity. The device is integrated with a single-cell AST system with microfluidic confinement and electrokinetic loading to phenotypically determine the bacterial antibiotic resistance at the single-cell level. The applicability of the system has been demonstrated for performing direct AST with urine and blood samples within one hour, enabling rapid infectious disease diagnostics in non-traditional healthcare settings.

Microfluidics and its applications to Lab-on-a-Chip have attracted a lot of attention. Because of the small length scale, the flow is characterized by a low Re number. The governing equations become linear. Boundary element method (BEM) is a very good option for simulating the fluid flow with high accuracy. In this thesis, we present a 2D numerical simulation of the electrothermal flow using BEM. In electrothermal flow the volumetric force is caused by electric field and temperature gradient. The physics is mathematically modeled by (i) Laplace equation for the electrical potential, (ii) Poisson equation for the heat conduction caused by Joule heating, (iii) continuity and Stokes equation for the low Reynolds number flow. We begin by solving the electrical potential and electrical field. The heat conduction is caused by the Joule heating as the heat generation term. Superposition principle is used to solve for the temperature field. The Coulomb and dielectric forces are generated by the electrical field and temperature gradient of the system. The buoyancy force is caused by the non-uniform temperature distribution inside the system. We analyze the Stokes flow problem by superposition of fundamental solution for free-space velocity caused by body force and BEM for the corresponding homogeneous Stokes equation. It is well known that a singularity integral arises when the source point approaches the field point. To overcome this problem, we solve the free-space velocity analytically. For the BEM part, we also calculate all the integrals analytically. With this effort, our solution is more accurate. In addition, we improve the robustness of the matrix system by combining the velocity integral equation with the traction integral equation when we simulate the electrothermal pump. One of our purpose is to design a pump for the microfluidics system. Since the system is a long channel, the flow is fully developed in the area far away from the electrodes. With this assumption, the velocity profile is parabolic at the inlet and outlet of the channel. So we can get appropriate boundary conditions for the BEM part of Stokes equation. Consequently, we can simulate the electrothermal flow in an open channel. In this thesis, we will present the formulation and implementation of BEM to model electrothermal flow. Results of electrical potential, temperature field, Joule heating, electrothermal force, buoyancy force and velocity field will be presented.

Established techniques for the detection of pathogens, such as bacteria and viruses, require long timeframes for culturing. State of the art biosensors rely on the diffusion of the target analyte to the sensor surface. AC electric fields can be exploited to enhance the sampling of pathogens and concentrate them at specific locations on the sensor surface, thus overcoming these bottlenecks. AC electrokinetic effects like the dielectrophoretic force and electrothermal flows apply forces on the particle and the bulk fluid, respectively. While dielectrophoresis forces pathogens towards a target location, electrothermal flows circulates the fluid, thus replenishing the local concentration. Numerical simulations and experimental proof of principle demonstrate how AC electrokinetics can be used to collect model bioparticles on an antibody functionalized selective surface from a heterogeneous solution having physiologically relevant conductivity. The presence of parallel channels in a quadrupolar microelectrode design is identified as detrimental during the negative dielectrophoretic collection of bioparticles at the centre of the design while simultaneously providing secondary concentration points. These microelectrodes were incorporated onto the surface of a novel cantilever design for the rapid positive dielectrophoretic collection of Escherichia coli bacteria and enabled the subsequent detection of the bacteria by measuring the shift in the resonance frequency of the cantilever. Finally, a proof of principle setup for a Raman coupled, AC electrokinetically enhanced sampling and detection of viruses is shown where the presence of M13 phages are identified on a selective antibody functionalized surface using Raman spectroscopy. / Thesis (Ph.D, Chemical Engineering) -- Queen's University, 2012-01-30 19:23:48.958