Abstract:
Disclosed are microfluidic devices and methods for performing analyses which, in a preferred embodiment, involve sample filtration, solid phase extraction for enrichment of target analytes and separation of target analytes via open channel electrochromatography. Small sample volumes of mixed analytes are resolvable in less than one minute using the disclosed devices and methods.
Abstract:
A method and apparatus for the manipulation of colloidal particulates and biomolecules at the interface between an insulating electrode such as silicon oxide and an electrolyte solution. Light-controlled electrokinetic assembly of particles near surfaces relies on the combination of three functional elements: the AC electric field-induced assembly of planar aggregates; the patterning of the electrolyte/silicon oxide/silicon interface to exert spatial control over the assembly process; and the real-time control of the assembly process via external illumination. The present invention provides a set of fundamental operations enabling interactive control over the creation and placement of planar arrays of several types of particles and biomolecules and the manipulation of array shape and size. The present invention enables sample preparation and handling for diagnostic assays and biochemical analysis in an array format, and the functional integration of these operations. In addition, the present invention provides a procedure for the creation of material surfaces with desired properties and for the fabrication of surface-mounted optical components. The invention is also for a system and method for programmable illumination pattern generation, including a novel method and apparatus to generate patterns of illumination and project them onto planar surfaces or onto planar interfaces such as the interface formed by an electrolyte-insulator-semiconductor (EIS), e.g., as described herein. This enables the creation of patterns or sequences of patterns using graphical design or drawing software on a personal computer and the projection of said patterns, or sequences of patterns (nulltime-varying patternsnull), onto the interface using a liquid crystal display (LCD) panel and an optical design which images the LCD panel onto the surface of interest. The use of the LCD technology provides flexibility and control over spatial layout, temporal sequences and intensities (nullgray scalesnull) of illumination patterns. The latter capability permits the creation of patterns with abruptly changing light intensities or patterns with gradually changing intensity profiles.
Abstract:
The present invention relates to a method of classifying charged molecules such as proteins for quantitative analysis. An analyte solution of the molecules is subjected to separational forces may be fluid drag and electrophoretic force in opposition. The analyte solution may be subjected to a two-phase process. The two-phase process may add both electrophoretic force based upon molecule charge, and differential mobility resistance based upon molecule mass and/or size.
Abstract:
An apparatus and method for electrochemically modifying the retention of a species on a chromatography material is disclosed. The apparatus comprises a housing having an effluent flow channel adapted to permit fluid flow therethrough. The effluent flow channel comprises chromatography material. The apparatus further comprises first and second electrodes positioned such that at least a portion of the chromatography material is disposed between the first and second electrodes, and fluid flow through the apparatus is between, and in contact with, the first and second electrodes.
Abstract:
Methods and apparatus for discriminating matter in a chamber having an inlet port and an outlet port utilizing dielectrophoresis and field flow fractionation. A carrier medium is introduced into the inlet port and is directed from the inlet port to the outlet port according to a velocity profile. A programmed voltage signal is applied to an electrode element coupled to the chamber to form a dielectrophoretic force on the matter. The dielectrophoretic force is balanced with a gravitational force to displace the matter to positions within said velocity profile in the carrier medium to discriminate the matter. A chamber having a top and bottom outlet port may be utilized to withdraw a first portion of a carrier medium from the top outlet port at a first, controllable fluid flow rate and to withdraw a second portion of the carrier medium from the bottom outlet port at a second, controllable fluid flow rate.
Abstract:
An apparatus and method for electrochemically modifying the retention of a species on a chromatography material is disclosed. The apparatus comprises a housing having an effluent flow channel adapted to permit fluid flow therethrough. The effluent flow channel comprises chromatography material. The apparatus further comprises first and second electrodes positioned such that at least a portion of the chromatography material is disposed between the first and second electrodes, and fluid flow through the apparatus is between, and in contact with, the first and second electrodes.
Abstract:
The present disclosure is directed to a novel apparatus and novel methods for the separation, characterization, and manipulation of matter. In particular, the invention combines the use of frequency-dependent dielectric and conductive properties of particulate matter and solubilized matter with the properties of the suspending and transporting medium to discriminate and separate such matter. The apparatus includes a chamber having at least one electrode element and at least one inlet and one output port into which cells are introduced and removed from the chamber. Matter carried through the chamber in a fluid stream is then displaced within the fluid by a dielectrophoretic (DEP) force caused by the energized electrode. Following displacement within the fluid, matter travels through the chamber at velocities according to the velocity profile of the chamber. After the matter has transitted through the chamber, it exits at the opposite end of the chamber at a characteristic position. Methods according to the invention involve using the apparatus for discriminating and separating matter for research, diagnosis of a condition, and therapeutic purposes. Examples of such methods may include separation of mixtures of cells, such as cancer cells from normal cells, separation of parasitized erythrocytes from normal erythrocytes, separation of nucleic acids, and others.
Abstract:
RETENTION OF SOLUTES ON THE RETARDING PHASE IS INDUCED BY APPLYING TO THE ENTIRE RETARDING PHASE AN ELECTRICAL POTENTIAL, ETHER UNIFORMLY OR WITH A GRADIENT. THE POTENTIAL MAY BE DC OR AC, IN THE LATTER CASE ADDITIONAL SEPARATION AEFFECTS ARE ATTAINABLE. THE AC PULSE SHAPE, FREQUENCY AND AMPLITUDE IS ADJUSTED WITH A PULSE GENERATOR.
Abstract:
FOR PURPOSES OF DETECTING CHANGES IN AN ELUATE IN CHROMATOGRAPHY A CELL COMPRISING A SOLID DETECTION ELECTRODE AND A REFERENCE ELECTRODE IS CONNECTED IN SERIES WITH A CHROMATOGRAPHIC SEPARATING SYSTEM, THE DETECTION ELECTRODE BEING IN DIRECT FLOWING CONTACT WITH THE ELUATE AND A LIQUID (WHICH MAY BE THE ELUATE ITSELF). A CONTROLLED POTENTIAL DIFFERENCE IS APPLIED TO THE ELECTRODES TO BRING ABOUT A CHEMICAL OXIDATION/REDUCTION REACTION OF THE SUBSTANCES BEING SEPARATED AND THE RELATIONSHIP BETWEEN AT LEAST TWO QUANTITIES INTER-RELATED BY OHM''S LAW IS OBSERVED. PROVISION IS MADE FOR A COMPENSATORY CELL AND FOR THE ELECTRO-CHEMICAL REMOVAL FROM THE ELUANT OF IMPURITIES WHICH INTERFERE WITH THE DETECTION. A PREFERRED CELL IS TUBULAR WITH THE ELECTRODES E.G. OF GRAPHITE OR GLASSY CARBON PROVIDED BY THE WALLS OF THE CELL OR EXTENDING ACROSS THE CELL.
Abstract:
A flow cell for electrophoretically-assisted capturing analytes from a flow. The flow cell includes a specimen chamber, a first membrane, a second membrane, a first electrode chamber, and a second electrode chamber. The specimen chamber may have a sample inlet and a sample outlet. A first portion of the first membrane may be coupled to a first portion of the specimen chamber. A first portion of the second membrane may be coupled to a second portion of the specimen chamber. The first electrode chamber may be configured to accept a charge. A portion of the first electrode chamber may be coupled to a second portion of the first membrane. A second electrode chamber may be configured to accept an opposite charge. A portion of the second electrode chamber may be coupled to a second portion of the second membrane.