563 research outputs found

    Dielectrophoretic manipulation of biological and non-biological analytes in a microfluidic channel

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    Micro-total-analytical systems (μTASs) for analyzing chemical/biological substances are now used across a wide variety of applications ranging from biological warfare agent detection to the healthcare industry. The first step in the operation of a μTAS consists of concentrating and separating the analytes of interest from the background matrix and positioning them into selected locations for subsequent analysis. The use of ac electric fields was demonstrated to have promising potential for a μTAS because the application of an ac field suppresses undesirable electrolytic effects in the liquid. The main purpose of this work is to study micro-scale phenomena in a flowing suspension subject to shear and high-gradient strong ac electric field. A microfluidic device equipped with dielectrophoretic gates arranged perpendicular to the flow was designed and fabricated at Sandia National Laboratories. Experiments were conducted on flowing suspensions over a broad range of flow and electric field parameters to investigate how these characteristics affect the concentration and separation of particles. It was found that dipolar interactions between suspended particles subject to a high-gradient ac field and shear lead to a new many-body phenomenon of dielectrophoresis accompanied by the field-induced phase separation in a flowing suspension. As a result, shear and electric stresses strongly compress a layer enriched with particles. The predictions of the proposed electro-hydrodynamic model for the coupled shear, dielectrophoresis, and phase separation in a flowing suspension are shown to be consistent with experimental data even though the model contains no fitting parameters. Both the model and the experiments showed that the concentration volume could be increased up to about 50%. It was demonstrated that the field-induced dielectrophoresis accompanied by the phase separation provides a new method for concentrating particles in focused regions and for separating biological and non-biological materials, a critical step in the development of miniaturizing biological assays. Specifically, experiments were performed using I um diameter polystyrene latex beads and heat-killed (Staphylococcus aureus; Molecular probes) dispersed in deionized water

    Optoelectronic tweezers for microparticle and cell manipulation

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    An optical image-driven light induced dielectrophoresis (DEP) apparatus and method are described which provide for the manipulation of particles or cells with a diameter on the order of 100 .mu.m or less. The apparatus is referred to as optoelectric tweezers (OET) and provides a number of advantages over conventional optical tweezers, in particular the ability to perform operations in parallel and over a large area without damage to living cells. The OET device generally comprises a planar liquid-filled structure having one or more portions which are photoconductive to convert incoming light to a change in the electric field pattern. The light patterns are dynamically generated to provide a number of manipulation structures that can manipulate single particles and cells or groups of particles/cells. The OET preferably includes a microscopic imaging means to provide feedback for the optical manipulation, such as detecting position and characteristics wherein the light patterns are modulated accordingly

    In Situ Preconcentration by AC Electrokinetics for Rapid and Sensitive Nanoparticle Detection

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    Reducing cost and time is a major concern in clinical diagnostics. Current molecular diagnostics are multi-step processes that usually take at least several hours or even days to complete multiple reagents delivery, incubations and several washing processes. This highly labor-intensive work and lack of automation could result in reduced reliability and low efficiency. The Laboratory-on-a-chip (LOC), taking advantage of the merger and development of microfluidics and biosensor technology, has shown promise towards a solution for performing analytical tests in a self-contained and compact unit, enabling earlier and decentralized testing. However, challenges are to integrate the fluid regulatory elements on a single platform and to detect target analytes with high sensitivity and selectivity. The goal of this research work is to develop an AC electrokinetic (ACEK) flow through concentrator for in-situ concentration of biomolecules and develop a comprehensive understanding of effects of ACEK flow on the biomolecule transport (in-situ concentration) and their impact on electronic biosensing mechanism and performance, achieving automation and miniaturization. ACEK is a new and promising technique to manipulate micro/bio-fluids and particles. It has many advantages over other techniques for its low applied voltage, portability and compatibility for integration into lab-on-a-chip devices. Numerical study on preconcentration system design in this work has provided an optimization rule for various biosensor designs using ACEK technique. And the microfluidic immunoassay lab-chip designed based on ACET effect has showed promising prospect for accelerated diagnostics. With optimized design of channel geometry, electrode patterns, and properly selected operation condition (ac frequency and voltage), the preconcentration system greatly reduced the reaction time to several minutes instead of several hours, and improved sensitivity of the assay. With the design of immunoassay lab-chip, one can quantitatively study the effect of ACET micropumping and mixing on molecular level binding. Improved sensors with single-chip form factor as a general platform could have a significant impact on a wide-range of biochemical detection and disease diagnostics including pathogen/virus detection, whole blood analysis, immune-screening, gene expression, as well as home land security

    Ultrafine Dielectrophoresis-based Technique for Virus and Biofluid Manipulation

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    abstract: Microfluidics has shown great potential in rapid isolation, sorting, and concentration of bioparticles upon its discovery. Over the past decades, significant improvements have been made in device fabrication techniques and microfluidic methodologies. As a result, considerable microfluidic-based isolation and concentration techniques have been developed, particularly for rapid pathogen detection. Among all microfluidic techniques, dielectrophoresis (DEP) is one of the most effective and efficient techniques to quickly isolate and separate polarizable particles under inhomogeneous electric field. To date, extensive studies have demonstrated that DEP devices are able to precisely manipulate cells ranging from over 10 μm (mammalian cells) down to about 1 μm (small bacteria). However, very limited DEP studies on manipulating submicron bioparticles, such as viruses, have been reported. In this dissertation, rapid capture and concentration of two different and representative types of virus particles (Sindbis virus and bacteriophage M13) with gradient insulator-based DEP (g-iDEP) has been demonstrated. Sindbis virus has a near-spherical shape with a diameter ~68 nm, while bacteriophage M13 has a filamentous shape with a length ~900 nm and a diameter ~6 nm. Under specific g-iDEP experimental conditions, the concentration of Sindbis virus can be increased two to six times within only a few seconds, using easily accessible voltages as low as 70 V. A similar phenomenon is also observed with bacteriophage M13. Meanwhile, their different DEP behavior predicts the potential of separating viruses with carefully designed microchannels and choices of experimental condition. DEP-based microfluidics also shows great potential in manipulating blood samples, specifically rapid separations of blood cells and proteins. To investigate the ability of g-iDEP device in blood sample manipulation, some proofs of principle work was accomplished including separating two cardiac disease-related proteins (myoglobin and heart-type fatty acid binding protein) and red blood cells (RBCs). Consistent separation was observed, showing retention of RBCs and passage of the two spiked protein biomarkers. The numerical concentration of RBCs was reduced (~70 percent after one minute) with the purified proteins available for detection or further processing. This study explores and extends the use of the device from differentiating similar particles to acting as a sample pretreatment step.Dissertation/ThesisDoctoral Dissertation Chemistry 201

    Optoelectronic Tweezers for Microparticle and Cell Manipulation

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    An optical image-driven light induced dielectrophoresis (DEP) apparatus and method are described which provide for the manipulation of particles or cells with a diameter on the order of 100 micromillimeters or less. The apparatus is referred to as optoelectric tweezers (OET) and provides a number of advantages over conventional optical tweezers, in particular the ability to perform operations in parallel and over a large area without damage to living cells. The OET device generally comprises a planar liquid-filled structure having one or more portions which are photoconductive to convert incoming light to a change in the electric field pattern. The light patterns are dynamically generated to provide a number of manipulation structures that can manipulate single particles and cells or group of particles/cells. The OET preferably includes a microscopic imaging means to provide feedback for the optical manipulation, such as detecting position and characteristics wherein the light patterns are modulated accordingly

    Dielectrophoretic precipitation of airborne particles.

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    Experimental and numerical modeling studies of particle separation from a gas stream using a dielectric force have shown that dielectrophoresis is an appropriate mechanism for the filtration of a particulate matter from a particle laden gas stream. Dielectrophoresis technology has the ability to produce high filtration efficiency with highly restive particles. This is the first known work producing a device that demonstrates that dielectrophoresis will separate particles from this type of fluidic system. The testing was conducted using frequencies on the order of 60 Hz, 15 kHz, and DC. The voltage ranged from 100V to 300V and the fluid velocity was varied from 1.5 m/s to 3 m/s. The dielectrophoretic separation device was designed to use interdigitated electrodes. Interdigitated electrodes are a well know device that produces dielectrophoresis in other applications [1]. The interdigitated electrodes were designed to be 20µm wide and spaced 20µm apart. The device collected particles under all frequencies, voltages, and fluid velocities; the testing shows that there is an inverse relationship between the fluid velocity and applied voltage, the lower the fluid velocity the higher the voltage; the greater the collection of particles

    Micro/Nano-Chip Electrokinetics

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    Micro/nanofluidic chips have found increasing applications in the analysis of chemical and biological samples over the past two decades. Electrokinetics has become the method of choice in these micro/nano-chips for transporting, manipulating and sensing ions, (bio)molecules, fluids and (bio)particles, etc., due to the high maneuverability, scalability, sensitivity, and integrability. The involved phenomena, which cover electroosmosis, electrophoresis, dielectrophoresis, electrohydrodynamics, electrothermal flow, diffusioosmosis, diffusiophoresis, streaming potential, current, etc., arise from either the inherent or the induced surface charge on the solid-liquid interface under DC and/or AC electric fields. To review the state-of-the-art of micro/nanochip electrokinetics, we welcome, in this Special Issue of Micromachines, all original research or review articles on the fundamentals and applications of the variety of electrokinetic phenomena in both microfluidic and nanofluidic devices

    Micromachines for Dielectrophoresis

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    An outstanding compilation that reflects the state-of-the art on Dielectrophoresis (DEP) in 2020. Contributions include: - A novel mathematical framework to analyze particle dynamics inside a circular arc microchannel using computational modeling. - A fundamental study of the passive focusing of particles in ratchet microchannels using direct-current DEP. - A novel molecular version of the Clausius-Mossotti factor that bridges the gap between theory and experiments in DEP of proteins. - The use of titanium electrodes to rapidly enrich T. brucei parasites towards a diagnostic assay. - Leveraging induced-charge electrophoresis (ICEP) to control the direction and speed of Janus particles. - An integrated device for the isolation, retrieval, and off-chip recovery of single cells. - Feasibility of using well-established CMOS processes to fabricate DEP devices. - The use of an exponential function to drive electrowetting displays to reduce flicker and improve the static display performance. - A novel waveform to drive electrophoretic displays with improved display quality and reduced flicker intensity. - Review of how combining electrode structures, single or multiple field magnitudes and/or frequencies, as well as variations in the media suspending the particles can improve the sensitivity of DEP-based particle separations. - Improvement of dielectrophoretic particle chromatography (DPC) of latex particles by exploiting differences in both their DEP mobility and their crossover frequencies
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