Abstract: A lateral flow immunoassay device includes a membrane strip for enabling capillary migration of a sample therealong with a labeled reagent disposed on the membrane. The label reagent is formulated for suspension in the sample migrating therepast. A captive reagent is immobilized on the strip on a path of sample migration and the captive reagent is formulated to bind to the labeled reagent to form a visible colored site on the strip. An element is provided for changing the strip to a color which enhances visual perception of the colored site.

Abstract: Systems and methods for high-throughput fabrication and evaluation of electrode and electrolyte material performance for solid oxide fuel cells. A system comprising a substrate, an auto-sampler operable for simultaneously controlling the flow rates of 2 or more solid oxide fuel cell components, a delivery apparatus, a mass flow controller, an x-y motion stage, and a microprocessor operable for controlling the system. A method comprising providing a library of samples, continuously and controllably supplying desired amounts of the samples to a liquid chromatography system where a multi-compositional mixture is formed, serially loading the multi-compositional mixture into a common sprayer, serially and distributively spraying the multi-compositional mixture onto a surface of a substrate, forming a discrete or continuous gradient array of the mixture reacted on the substrate, and evaluating the performance of the mixture for use in solid oxide fuel cells.

Abstract: The invention provides, inter alia, methods, devices and reagents for the preparation of native and non-denatured biomolecules using solid-phase extraction channels. The invention is particularly suited for the purification, concentration and/or analysis of protein analytes. The invention further provides, inter alia, methods, devices and reagents for the purification, concentration and/or analysis of multi-protein complexes.

Abstract: A frit for use in multi-layer microfluidic separation devices is provided. The frit comprises a polymeric membrane that may be securely bonded within the device and minimizes lateral wicking. A secure bond is ensured by treating the polymer to match its surface energy to that of the materials to which it is bound. Treatments include plasma treatment, irradiation and the application of acids.

Abstract: The invention relates to a method for solid-phase microextraction and analysis of substances in a carrier fluid, in which a collector is brought into contact with the stirred fluid containing the substances for a sufficient time and is then subjected to a solid-phase extraction directed at at least one substance adhering to the collector, and desorbed substances are transported for analysis by means of a carrier gas, in which the carrier fluid containing the substances is stirred in a receptacle of a magnetic stirrer by means of a coated magnetic stirring element as the collector, and/or the carrier fluid is made to move intimately relative to the collector by means of ultrasound, and then the stirring element is placed in a solid-phase extraction device.

Abstract: This invention provides methods of retentate chromatography for resolving analytes in a sample. The methods involve adsorbing the analytes to a substrate under a plurality of different selectivity conditions, and detecting the analytes retained on the substrate by desorption spectrometry. The methods are useful in biology and medicine, including clinical diagnostics and drug discovery.

Abstract: A system and method high throughput sample preparation and analysis using column chromatography. Each port in a plurality of ports has a port input that interfaces with a first fluid source and a port output. A fluidic circuit is coupled to each port output and to a second fluid source, the fluidic circuit for controlling fluid flow from the plurality of ports and the second fluid source. The fluidic circuit is also coupled to a plurality of chromatography columns. An interface to an analyzer receives output from at least one of the plurality of chromatography columns. The plurality of chromatography columns is moved relative to the analyzer via a translation stage, such that sample output from one of the plurality of chromatography columns can be selectively presented to the analyzer.

Abstract: A microchip-based electrospray ionization device and column with affinity adsorbents is disclosed. The invention includes a microchip array and a capillary tube or alone or attached in combination. At least a portion of the device or column has immobilized affinity adsorbents. Methods for using the device are provided as well for affinity capture of biomolecules to meet the needs for the modern life sciences such as proteomics and drug discover.

Abstract: The present invention relates to a method for presenting an analyte of a liquid sample as an MS-analyte to a mass spectrometer. More particularly, the method comprises the steps of applying a liquid sample containing the analyte to a sample inlet port of a microchannel structure of a microfluidic device, said structure also comprising an outlet port (MS-port) that is capable of being interfaced with a mass spectrometer, passing the analyte to the MS-port thereby transforming it to an MS-analyte, and presenting the MS-analyte to mass spectrometer via the MS-port.

Abstract: The structure of a capillary head section is made such that the liquid contacting surfaces of a capillary holder, a capillary, and an adhesive form a plane surface, and this shared liquid contacting surface is made a mirror surface with a surface roughness of 3.2 s or less. In the shared liquid contacting surface, the ratio of the total area of the capillaries to the internal diameter area of the capillary holder is made 60 to 73%.

Abstract: An electrolysis apparatus includes at least two coaxially spaced electrodes, at least one of which is a coil. Currents in the coil generate a magnetic field to accelerate the electrolysis process.

Abstract: Signals obtained in capillary High Performance Liquid Chromatography (HPLC) are notoriously noisy. The signal can be improved by increasing the path length of the light passing through the sample stream, but increased path length decreases resolution (resolving N closely spaced peaks in the actual separation into N peaks of almost equal separation on the chromatogram. A novel approach is to utilize a number of photocell sensors lined up along a capillary through which the solution passes. In one embodiment of this invention, the flow of the solution is stopped with the solvent spike oriented with a particular photocell sensor. Then a single, continuous scan or multiple scans of a section of the quiescent solution may be taken and integrated, summed, or statistically correlated. In another embodiment, a solvent spike is detected and tracked. A set of photocell sensors is chosen at increments of time such that the leading photocell is at the solvent spike. The set of photocells is scanned repeatedly.

Abstract: Described is a Reactor assembly for analysing the effluent stream from at least one flow—through reactor, comprising: —at least one flow-through reactor for performing at least one chemical reaction, the reactor comprising —a reaction chamber (1), comprising a reaction zone (2), the reaction chamber being connected to —at least one reactor inlet (3) for at least one reactant, 10 upstream of the reaction zone, —at least one reactor outlet (4) for the effluent stream from the reaction zone, downstream of the reaction zone, —at least one analyser (5) for subjecting the effluent stream to an analysing procedure, each reactor outlet being 15 connected to at least one analyser by an effluent conduit (6), wherein the reactor assembly further comprises —at least one dilution fluid supply means (10), for adding at least one dilution fluid to the effluent stream, downstream of the reaction zone, and a process for analysing a fluid effluent stream from a flow-through reactor com

Abstract: Liquid chromatography based on the difference of two or more kinds of separation modes, (e.g., chemical or physical properties of analytes) may improve separations when samples contain complex mixtures. In this invention, the analytes separated on the 1st analysis system (consisting of the 1st column and the 1st mobile phase) will be trapped onto individual trapping columns. Then the trapped analytes will be loaded onto the 2nd analysis system consisting of the 2nd column and the 2nd mobile phase. This invention has the trapping and loading mechanism consisting of a combination of switching valves necessary to produce the serial separations. Also this invention has the capability to affect online desalting when it is needed depending on a detector or the nature of the analyte mixture.

Abstract: The present invention is a flow distributor and integral bed support for a chromatography column. The flow distributor has an outlet extending through it and a bottom face across which is secured a bed support. The bottom face has a series of ribs extending radially outward from a center portion of the face. The bed support is secured to the flow distributor about its outer periphery and this amount of available surface area of the flow distributor and/or face that is used to secure the bed support is less than about 10%. A distribution disk is arranged over the inlet and extends across from about 1 to about 30% of the flow distributor's surface area, ending just short of the inner edge of the ribs closest to the center point of the flow distributor face. This disk is mounted on two or more legs so as to be of substantially the same height as the ribs. The disk projects the fluid flow in a 360° radial distribution without any noticeable partitioning.

Abstract: A device for storing and/or treating chemicals is described. The device includes a glass casing provided with a receiving cavity for storing chemicals therein, and further includes a transponder having a memory, the transponder being arranged in the device such that it cannot be affected by the chemicals.

Abstract: A method, system and kit for detecting the presence of an analyte includes placing a solution containing the analyte in a microcapillary tube and placing the microcapillary tube in contact with a layer of sorbent material so that the solution is withdrawn from the microcapillary tube by capillary action. A detector reagent which has been pre-deposited on the sorbent material indicates the presence of the analyte. The sorbent material, detector reagent, and the solvent for the analyte solution are selected so that the solvent is absorbed into the sorbent material and the analyte is adsorbed by the sorbent material and concentrated at the spot where the detector reagent has been pre-deposited and where the microcapillary tube contacts the sorbent material.

Abstract: A biosorbent composition, process of preparing and use thereof wherein the biosorbent composition comprises a chitosan-coated substrate. Useful substrates include support materials such as a ceramic support material. The biosorbent composition of the instant invention is useful in treating aqueous systems, including wastewater and aqueous waste streams, by removing undesired heavy metals.

Abstract: A highly sensitive and specific method for the detection and quantification of lipids is provided. Specifically, methods for the simultaneous detection and quantification of phospholipids extracted from mammalian tissues is described. The analytical methods provided disclose a modified one-dimensional thin-layer chromatography technique specifically developed to rapidly and accurantely detect and quantify phospholipids from mammalian cardiac tissues.

Abstract: A closure cap system for glass chromatography columns includes a glass cylinder with unfinished shaping or work on each end, and two sealing caps. The caps have a circumference shoulder with O-rings. The O-rings having the same diameter as the diameter of the glass cylinder unfinished ends. A base and top parts, both containing openings for receiving sealing caps and the glass cylinder. Threaded rods are received by additional openings in said top and base parts. Nuts are affixed at the end of each threaded rod. The combined action of the nuts and threaded rods apply compression forces to the caps and glass cylinder for sealing in a simple and economic manner defining the system as a disposable apparatus.

Abstract: A method and apparatus are provided for automatically separating radionuclides using a chromatographic separation process. The method includes the steps of displaying a first flow diagram on a display depicting flow of the radionuclides through a first set of separation elements of the plurality of separation processing elements, but only during a first step of the chromatographic separation process and displaying a second flow diagram on the display depicting flow of the radionuclides through a second set of separation elements of the plurality of separation processing elements, but only during a second step of the chromatographic separation process.

Abstract: The present invention is directed to an improved column for use in solid phase synthesis or purification. In a specific embodiment, the column is a disposable plastic column for use in solid phase synthesis or purification of complex chemicals, such as biomolecules and more specifically oligonucleotides. In some embodiments, the column has a top orifice with a sufficient diameter so that a fluid line or a multiple fluid line bundle may dispense fluids into the column with great efficiency. The column has an upper cavity portion configured and sized to render it compatible with dispensing pippetors, so that it can be used as a pipette tip or a pipettor can be used to aspirate the column. The column has a lower cavity portion with a shoulder for ready placement of a lower frit to contain the solid support in a central cavity portion of the column. An upper frit can be conveniently placed in the central cavity portion to seal the solid phase resin.

Abstract: An open capillary channel device for open tubular solid phase extraction of molecules capable of providing a tube enrichment factor of at least 1. The device comprises a channel having one end connected to a pump for pumping liquid and gas, and the other end can be connected to an interface for a protein chip sample applicator or a mass spectrometer, the inner surface of the channel being an extraction surface. The extraction surface can be bonded to an affinity binding agent. The affinity agent can be a chelated metal, a protein, a sugar or nucleic acid with a binding affinity for a selected analyte. The method using this device comprises binding sample molecules from a sample solution to the affinity extraction surface of the capillary channel; and desorbing a substantial portion of the sample molecules from the extraction surface with a desorbent liquid, with an extraction factor greater than 1.

Abstract: The present invention allows detection in short time while maintaining the level of the resolving power as high as when a capillary is utilized. The entire surface of an electrophoresis board 10, which is provided with a two-dimensional tubular electrophoresis pathway, is irradiated with excitation light so as to pick up fluorescence or luminescence from a sample with a two-dimensional sensor. By reading the entire electrophoresis pathway, the separated state of the sample may be confirmed during the electrophoresis. As a result, the electrophoresis may be ended when the sample is sufficiently separated and a molecular weight thereof may be determined based on the migration distance.

Abstract: Method and apparatus for suppressed ion analysis in which a sample solution of analyte (e.g., anion) in an eluent of electrolyte counterions (e.g., sodium), is chromatographically separated. Then, the counterions are suppressed in a suppression zone and removed and used to convert the analyte ions to salt form in a salt-converting zone. The suppression and salt-converting zones may be contiguous or remote, and may be performed in devices of the membrane suppresser type. Thereafter, the salts or acids or bases formed from them (e.g., in membrane suppressor devices) are detected. Also, salt conversion can be performed using two ion exchange packed bed salt convertors in which one bed is on-line while the other is regenerated, followed by a reversal of flow.

Abstract: A reversed-phase liquid chromatography using a mobile phase containing water as a main component thereof, wherein in a measurement after a flow of the mobile phase through a column is temporarily stopped and then the flow is resumed, a back pressure is applied to an outlet of the column by a back-pressure applying device which is provided between the outlet of the column and a detector.

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: Gradient performance with high pressure gradient solvent delivery system is optimized by approximation of infinite stroke volume of high pressure pumps by the addition of pulse dampening with backflow prevention to each high pressure pump. The backflow prevention adds sufficient minimum flow resistance, thereby enhancing the performance of the pulse dampening over a wider range of flow rates resulting in consistent gradient performance.

Abstract: An installation for treating samples by chromatographic separation comprises: i) means (1, 2, 4) for feeding moving phase, means (14) for supplying samples, and a multiplicity of injector means (10-i), each comprising a first inlet (11-i) for receiving a sample, a second inlet (8-i) connected to the feed means, and an outlet (13-i) for delivering the moving phase and/or the sample; ii) a stationary phase (3) defining a multiplicity of sample treatment channels (12-i), each starting at a first selected location (19-i) and terminating at a second selected location (20-i); and iii) a chamber (17) housing the stationary phase (3) and including pressurizing means for applying an external pressure to one face of the stationary phase, a multiplicity of inlets, each connected to the outlet (13-i) of an injector (10-i) to deliver the moving phase and/or the samples to the first locations (19-i), and a multiplicity of outlets (18-i) for discharging the multiplicity of samples treated in the channels (12-i) that have re

Abstract: A system for separating an aqueous stream of mixed polynucleotides into a series of length-based polynucleotide fractions and collecting one or more of the length-based polynucleotide fractions into separate containers. The system comprises a separation column containing separation media for separating an aqueous stream of mixed polynucleotides into a series of length-based polynucleotide fractions; a container including one or more single-sample containers; an ejection chamber having a separated sample inlet for receiving the length-based polynucleotide fractions, a waste outlet for discharging uncollected sample, and a capillary-sized fraction outlet positioned to discharge a selected length-based polynucleotide fraction into a single-sample container. The system also includes means for effecting discharge of a selected length-based polynucleotide fraction into the separate container.

Abstract: Systems and methods for performing multiple parallel chromatographic separations are provided. Microfluidic cartridges containing multiple separation columns allow multiple separations to be performed in a limited space by a single instrument containing high-pressure pumps and analyte detectors. The use of pressure fit interfaces allows the microfluidic cartridges to easily be removed and replaced within the instrument, either manually or robotically.

Abstract: Methods for determining total analyte concentrations and amounts, especially in combination with analyte separations are provided. Microfluidic devices are used to separate analyte mixtures and detect the individual analytes. Signal areas are summed for each individual analyte to quantitate the total analyte amount. Separate measurements of the total analyte sample are also used to determine total analyte concentration.

Abstract: What is disclosed pertains to improvement in the performance of microchannel devices by providing turns, wyes, tees, and other junctions that produce little dispersion of a sample as it traverses the turn or junction. The reduced dispersion results from contraction and expansion regions that reduce the cross-sectional area over some portion of the turn or junction. By carefully designing the geometries of these regions, sample dispersion in turns and junctions is reduced to levels comparable to the effects of ordinary diffusion. The low dispersion features are particularly suited for microfluidic devices and systems using either electromotive force, pressure, or combinations thereof as the principle of fluid transport. Such microfluidic devices and systems are useful for separation of components, sample transport, reaction, mixing, dilution or synthesis, or combinations thereof.

Abstract: A method for removing an organic solute from a solution, comprising contacting the solution with a polymer formed by copolymerizing one or more hydrophobic monomers and one or more hydrophilic monomers, whereby the solute is adsorbed onto the polymer. The solution can comprise a polar solvent such as a polar organic solvent or water or an aqueous buffer. The hydrophobic monomer can be, for example, divinylbenzene. The hydrophilic monomer can be, for example, a heterocyclic monomer, such as a vinylpyridine or N-vinylpyrrolidone.

Abstract: A device for placement of effluent comprises a substrate positioner, a deposition conduit, and a conduit positioner. The substrate positioner supports and positions a substrate on which effluent exiting from the deposition conduit is to be deposited. The conduit positioner moves an exit end of the deposition conduit relative to the substrate.

Abstract: Disclosed are apparatus for screening compound libraries using frontal chromatography in combination with mass spectrometry to identify and rank those members of the library that bind to a target receptor. The apparatus of this invention also permit a compound library to be rapidly screened to determine if any member of the library has an affinity for the target receptor as measured by a pre-selected indicator compound.

Abstract: Disclosed are methods for screening compound libraries using frontal chromatography in combination with mass spectrometry to identify and rank those members of the library that bind to a target receptor. Methods are also disclosed which permit a compound library to be rapidly screened to determine if any member of the library has an affinity for the target receptor as measured by a pre-selected indicator compound.

Abstract: A microfluidic device comprising an MS-analyte presentation unit for a EDI-MS apparatus, said unit comprising an essentially planar support plate which on one side has one, two or more ports (MS-ports) comprising an area (EDI area) for presenting the MS-analyte to a mass spectrometer. The EDI area comprises a layer I of conducting material. The characteristic feature of the device is that layer (I) has a conductive connection and/or that there is a calibrator area in the proximity of the MS-port.

Abstract: A web contactor for the purposes of continuous separation of specific proteins from a mixture of proteins comprises an endless, inert, non-porous, flexible web is coated with an activated matrix material which is, in turn, bound to a plurality of ligand molecules. The ligand molecules are chosen to correspond to a desired biological molecule or class of molecules, typically a desired protein. The web is translated over a series of rolls such that it contacts a feed solution of a mixture of biological molecules in a countercurrent manner. During contact of the web and solution, the ligand molecules which are attached to the web matrix, selectively bind to the protein or other biological molecule which are to be separated from the feed solution mixture.

Abstract: The present invention includes a method of analyzing one or more molecular components in a mixture of components. In the method, a mixture of molecular components, i.e., an analyte mixture, is separated on a capillary liquid chromatography column. The component-containing eluate from the column is deposited as a series of discrete, defined-volume microdrops, along a region of an adsorbent collection layer. During the chromatographic separation, the column eluate may also-be monitored to detect the presence of separated components in the equate. The one or more components deposited in the collection layer are then analyzed by selected analytical techniques. In related aspect, the invention includes a method of collecting one or more molecular components derived from a mixture of components, a blotter apparatus useful in the above method, and a system for analyzing one or more molecular components in a mixture of components.

Abstract: The analytical process utilized in the system of this invention comprises three (3) step distinct steps wherein an analyte of interest in a test sample is initially labeled and subsequently isolated within a porous medium of a test device. Once isolated within the medium, the label is displaced from the analyte, or from the complex with the analyte, and converted, under electrolytic condition, to a metallic species which is caused test to deposit upon a working electrode of the test device. This working electrode is part of an electrode array that is positioned coincident with the porous medium, yet maintained physically remote therefrom. This deposit is then stripped from the working electrode, under anodic stripping conditions, and the current generated within the electrode array monitored. The characteristic response curve that is produced thereby can be correlated with the identity and concentration of the analyte(s) with the test sample.

Abstract: The invention concerns a method supplying volume streams of fluids in channels or capillaries of small stream cross sections, more particularly chromatographic separating columns for the analytical fluid metrology, wherein a delivery device for delivering a volume stream of the fluid through an operating channel and a pressure measuring device for measuring the pressure in the operating channel is provided, wherein a measurement of the volume stream is possible, characterized by the following steps: a) Recording a time reference pressure course using the pressure measuring device in the operating channel, while the delivery device delivers an essentially constant, pre-determinable reference volume stream through the operating channel of a fluid with properties, more particularly flow properties, varying over time; b) Calculation of a time development of the operating pressure, which corresponds to the essentially constant and preferably small operating volume stream through the operating channel, which is d

Abstract: An ion chromatography system having a suppressor means which is provided with a main body for accommodating an ion exchanger ready for measuring; a chamber for accommodating a virgin ion exchanger, and an automatic exchanging means which discharges a used ion exchanger from the main body after an optional number of times of measurement and supplies the ion exchanger accommodated in the chamber to the main body. The ion chromatography system can measure a slight amount of ion species in a sample at a high sensitivity by conducting continuously a large number of times of measurement while the discharge of waste liquid can be minimized without causing a reduction of suppressing effect and a reduction of resolution performance of a desired ion species.

Abstract: The present invention relates to a method and apparatus for chromatographically analyzing each of a plurality of samples in detector, comprising an autosampler to contain a plurality of samples for chromatographic analysis and a plurality of chromatographic systems, each system comprising one or more pumps and one or more chromatography columns. A detector is included for detecting compounds in the samples from each of the chromatography systems along with a valve positioned between the detector and the plurality of chromatography systems, the valve permitting each sample to reach the detector in sequence. A computer control device is included which adjusts the introduction of samples from the autosampler into the plurality of chromatography systems as well as the position of the valve to sequentially separate and deliver compounds within the samples to the detector.

Abstract: One-step enzyme immunoassays in which enzyme-antibody conjugate or label and enzyme substrate are separated until separation of bound and free enzyme conjugate or label is complete. This separation is accomplished by using variable flow paths, immobilization of substrate at the test line, placement of substrate in a sac or association with a particle label, enzyme product chemical capture, delay zone dissolution and protected enzyme substrates.

Abstract: An acid or base is generated in an aqueous solution by the steps of:

Abstract: A microchip-based electrospray ionization device and column with affinity adsorbents is disclosed. The invention includes a microchip array and a capillary tube or alone or attached in combination. At least a portion of the device or column has immobilized affinity adsorbents. Methods for using the device are provided as well for affinity capture of biomolecules to meet the needs for the modern life sciences such as proteomics and drug discover.

Abstract: A method and device for increasing the loading capacity of a chromatography column through dilution of a mobile phase at the head of the column. A strong mobile phase is provided for dissolving a sample. A sample is injected into the strong mobile phase, and subsequently diluted with a weak mobile phase. The resulting sample-containing weak mobile phase is passed through a chromatography column for retention and separation of the components of the sample.

Abstract: A nucleic acid purification method and purification apparatus characterized by high washing efficiency where contamination does not occur and liquid does not remain in the nozzle tip are disclosed. The present invention provides a tip containing the solid phase capturing a nucleic acid characterized in that washing solution is fed into the tip unidirectionally from head to end.

Abstract: The present invention comprises a device and method of analyzing trace amounts of perchlorate in liquid samples comprising a concentrator column used in an ion chromatographic system that comprises an anionic capacity ranging from about 0.030 microequivalents per column to about 0.060 microequivalents per column and capable of removing substantially all perchlorate from the sample and using a multi-directional flow through said concentrator column in order to enhance perchlorate detection. The invention also comprises a packing material comprising from about 25 percent to about 80 percent of a low anionic capacity material comprising an anionic capacity of less than about 0.03 milliequivalents per milliliter mixed with from about 25 percent to about 80 percent of a high anionic capacity material comprising a anionic capacity of more than about 0.07 milliequivalents per milliliter.