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Biomedical subjects

Shizhi Qian

Publications and source records attributed to Shizhi Qian.

10 recordsLinked to original sources

The effect of translocating cylindrical particles on the ionic current through a nanopore.

The electric field-induced translocation of cylindrical particles through nanopores with circular cross sections is studied theoretically. The coupled Nernst-Planck equations (multi-ion model, MIM) for the concentration fields of the ions in solution and the Stokes equation for the flow field are solved simultaneously. The predictions of the multi-ion model are compared with the predictions of two simplified models based on the Poisson-Boltzmann equation (PBM) and the Smoluchowski's slip velocity (SVM). The concentration field, the ionic current though the pore, and the particle's velocity are computed as functions of the particle's size, location, and electric charge; the pore's size and electric charge; the electric field intensity; and the bulk solution's concentration. In qualitative agreement with experimental data, the MIM predicts that, depending on the bulk solution's concentration, the translocating particle may either block or enhance the ionic current. When the thickness of the electric double layer is relatively large, the PBM and SVM predictions do not agree with the MIM predictions. The limitations of the PBM and SVM are delineated. The theoretical predictions are compared with and used to explain experimental data pertaining to the translocation of DNA molecules through nanopores.

Biological Transport↗

Electrophoretic motion of a spherical particle in a converging-diverging nanotube.

A charged spherical particle is concentrically positioned in a converging-diverging nanotube filled with an electrolyte solution, resulting in an electric double layer (EDL) forming around the particle's surface. In the presence of an axially applied electric field, the particle electrophoretically migrates along the axis of the nanotube due to the electrostatic and hydrodynamic forces acting on the particle. In contrast to a cylindrical nanotube with a constant cross-sectional area in which the electric field is almost uniform, the presence of a converging-diverging section in a nanotube alters the electric field, perturbs the charge distribution, and induces a pressure gradient and a recirculating flow that affect the electrostatic and hydrodynamic forces acting on both the particle and the fluid. Depending on the magnitude of the surface charge density along the nanotube's wall, the particle's electrophoretic motion may be significantly accelerated as the particle transverses the converging-diverging section. A continuum model consisting of the Nernst-Planck, Poisson, and Navier-Stokes equations for the ionic concentrations, electric potential, and flow field is implemented to compute the particle's velocity as a function of the particle's size, the nanotube's geometry, surface charges, electric field intensity, bulk electrolyte concentration, and the particle's location. When the particle is negatively charged and the wall of the nanotube is uncharged, the particle migrates in the direction opposite to that of the applied electric field and the presence of the converging-diverging section significantly accelerates the particle's motion. This, however, is not always true when the nanotube's wall is charged with the same sign as that of the particle. Once the ratio of the surface charge density of the nanotube's wall to that of the particle exceeds a certain value, the negatively charged particle will not translocate through the tube toward the anode and does not attain the maximum velocity at the throat of the converging-diverging section. One can envision such a device to be a nanofilter that allows molecules with surface charge densities much higher than that of the wall to go through the nanofilter, while preventing molecules with surface charge densities lower than that of the wall from passing through the nanofilter. The induced recirculating flow may be used to enhance mixing and to stretch, fold, and trap molecules in nanofluidic detectors and reactors.

Journal Article↗

Modulation of electroosmotic flows in electron-conducting microchannels by coupled quasi-reversible faradaic and adsorption-mediated depolarization.

A theoretical model is proposed for the description of steady electroosmotic flows within a cylindrical electron-conducting microchannel that is depolarized by faradaic and adsorption-mediated processes. The bipolar electron-transfer (e.t.) reactions are examined in the general situation where the electrolyte contains a quasi-reversible redox couple. The rate of the e.t. reactions is governed by transversal convective diffusion of the electroactive species to/from the surface and a position-dependent degree of reversibility. The nonuniform distribution of the electric field in solution, that is intimately coupled to that of the local faradaic current density, alters the double layer composition along the conducting surface via the occurrence of simultaneous electronic and ionic double layer charging processes. This in turn generates a nonlinear distribution of the zeta potential, which affects the electroosmotic flow. The highly coupled spatial profiles for the concentrations of the electroactive species, the faradaic current density, the electrokinetic potential, the electric field and the electroosmotic velocity in/along the metallic channel are solved by consistent numerical analysis of (i) the convective-diffusion equation, (ii) the generalized Butler-Volmer expression that includes mass transport and electron-transfer kinetic contributions, (iii) the continuity and Navier-Stokes equations, and (iv) the Poisson equation for finite currents. The results reported as a function of the surface properties of the channel and the kinetic characteristics of the e.t. reaction illustrate the deviations of the electroosmotic flow profiles as compared to the typical pluglike distribution predicted by Smoluchowski's equation and encountered for homogeneous and dielectric channels. Manipulation of the flow patterns by bipolar electrochemical means is a promising way to control and optimize the local detection and separation of electroactive molecules or molecules dyed with electroactive elements.

Journal Article↗

Coupling between electroosmotically driven flow and bipolar faradaic depolarization processes in electron-conducting microchannels.

A quantitative theory is proposed for the analysis of steady electroosmotically driven flows within conducting cylindrical microchannels. Beyond a threshold value of the electric field applied in the electrolyte solution and parallel to the conducting surface, electrochemical oxidation and reduction reactions take place at the two extremities of the substrate. The spatial distribution of the corresponding local faradaic currents along the bipolar electrode is intrinsically coupled to that of the electric field in solution. The nonuniform distribution of the electric field alters the double layer composition, and in particular the zeta-potential value, along the conducting surface via the occurrence of concomitant electronic and ionic double layer charging processes. The combined spatial dependencies of the lateral electric field and electrokinetic potential considerably affects the distribution of the electroosmotic velocity field in the directions parallel and perpendicular to the surface depolarized by faradaic processes. In this paper, the coupling between bipolar electrodic behavior and electroosmosis is explicitly investigated for the case of irreversible--that is, kinetically controlled--electron transfer reactions. Typical simulation results are presented and illustrate the possibility of controlling and optimizing electroosmotic flows in conducting channels by electrochemical means.

Electrochemistry↗

Thermally-actuated, phase change flow control for microfluidic systems.

An easy to implement, thermally-actuated, noninvasive method for flow control in microfluidic devices is described. This technique takes advantage of the phase change of the working liquid itself-the freezing and melting of a portion of a liquid slug-to noninvasively close and open flow passages (referred to as a phase change valve). The valve was designed for use in a miniature diagnostic system for detecting pathogens in oral fluids at the point of care. The paper describes the modeling, construction, and characteristics of the valve. The experimental results favorably agree with theoretical predictions. In addition, the paper demonstrates the use of the phase change valves for flow control, sample metering and distribution into multiple analysis paths, sealing of a polymerase chain reaction (PCR) chamber, and sample introduction into and withdrawal from a closed loop. The phase change valve is electronically addressable, does not require any moving parts, introduces only minimal dead volume, is leakage and contamination free, and is biocompatible.

Microfluidic Analytical Techniques↗

Filling carbon nanotubes with particles.

The filling of carbon nanotubes (CNTs) with fluorescent particles was studied experimentally and theoretically. The fluorescent signals emitted by the particles were visible through the walls of the nanotubes, and the particles inside the tubes were observable with an electron microscope. Taking advantage of the template-grown carbon nanotubes' transparency to fluorescent light, we measured the filling rate of the tubes with particles at room conditions. Liquids such as ethylene glycol, water, and ethylene glycol/water mixtures, laden with 50 nm diameter fluorescent particles, were brought into contact with 500 nm diameter CNTs. The liquid and the particles' transport were observed, respectively, with optical and fluorescence microscopy. The CNTs were filled controllably with particles by the complementary action of capillary forces and the evaporation of the liquid. The experimental results were compared and favorably agreed with theoretical predictions. This is the first report on fluorescence studies of particle transport in carbon nanotubes.

Capillary Action↗

Thermosiphon-based PCR reactor: experiment and modeling.

A self-actuated, flow-cycling polymerase chain reaction (PCR) reactor that takes advantage of buoyancy forces to continuously circulate reagents in a closed loop through various thermal zones has been constructed, tested, and modeled. The heating required for the PCR is advantageously used to induce fluid motion without the need for a pump. Flow velocities on the order of millimeters per second are readily attainable. In our preliminary prototype, we measured a cross-sectionally averaged velocity of 2.5 mm/s and a cycle time of 104 s. The flow velocity is nearly independent of the loop's length, making the device readily scalable. Successful amplifications of 700- and 305-bp fragments of Bacillus cereus genomic DNA have been demonstrated. Since the device does not require any moving parts, it is particularly suitable for miniature systems.

Bacillus cereus↗

Analysis of lateral flow biodetectors: competitive format.

Lateral flow (LF) biodetectors facilitate low-cost, rapid identification of various analytes. The LF cell consists of a porous membrane containing immobilized ligands at various locations. Through the action of capillary forces, a mixture of sample and reporter particles is transported to the ligand sites, where the target analytes and the reporters bind to the immobilized ligand. The concentration of the reporters is measured with a scanner. A mathematical model for two different competitive assays is constructed and used to study the performance of LF devices under various operating conditions. The model predicts the signal magnitude as a function of target analyte, reporter, and ligand concentrations, reaction rate constants, and flow rate. The predictions are compared and qualitatively agree with experimental data. The model provides insights into various experimental observations. Furthermore, the model can be used to optimize the performance of LF devices and to inexpensively and rapidly test the system under various operating conditions.

Binding Sites↗

A mathematical model of lateral flow bioreactions applied to sandwich assays.

Lateral flow (LF) biodetectors facilitate low-cost, rapid identification of various analytes at the point of care. The LF cell consists of a porous membrane containing immobilized ligands at various locations. Through the action of capillary forces, samples and reporter particles are transported to the ligand sites. The LF membrane is then scanned or probed, and the concentration of reporter particles is measured. A mathematical model for sandwich assays is constructed and used to study the performance of the LF device under various operating conditions. The model provides insights into certain experimental observations including the reduction in the level of the detected signal at high target analyte concentrations. Furthermore, the model can be used to test rapidly and inexpensively various operating conditions, assist in the device's design, and optimize the performance of the LF device.

Biosensing Techniques↗

A chaotic electroosmotic stirrer.

Two-dimensional, time-independent, and time-dependent electroosmotic flows driven by a uniform electric field in a conduit with nonuniform zeta potential distributions along its walls are investigated theoretically. The time-independent flow fields are computed with the aid of Fourier series. The series' convergence is accelerated so that highly accurate solutions are obtained with just a few terms in the series. The analytic solution is used to compute flow patterns for various distributions of the zeta potential along the conduit's boundaries. Subsequently, it is demonstrated that by time-wise periodic alternations of the zeta potentials, one can induce chaotic advection. This chaotic flow can be used to efficiently stir and mix fluids in microfluidic devices.

Journal Article↗