Abstract: A method for preventing either the introduction of air into a liquid aspirated from a container through an aspiration line passing through a container cap, or the over-filling or non-filling of a container by a liquid dispensed through a dispensing line passing through a container cap. Such method comprises the steps of simultaneously detecting that (a) the container cap is properly positioned on and secured to a liquid container from which liquid is to be aspirated, or into which a liquid is to be dispensed, and (b) detecting that the level of liquid in the container is either above or below a predetermined level.

Abstract: An apparatus for characterizing particles suspended in a liquid sample containing electrolyte including a sample chamber to hold the liquid sample and a collection chamber to hold an electrolyte solution. A wall separates the chambers and includes an aperture to allow passage of particles between the chambers; and a pair of electrodes are disposed on opposite sides of the aperture to induce a current through the aperture. A pressure source forces the sample to pass from the sample chamber into the collection chamber; and a processor measures a signal representative of electric resistance variation between the electrodes to enable determination of the size of the particle within the liquid passing through the aperture, wherein the processor is adapted to monitor two or more parameters characterizing the flow of particles through the aperture, and to detect a potential blockage of the aperture by detecting a change in any one of the parameters.

Abstract: Transducer modules for use in a blood analysis instrument and methods for analyzing a blood sample. The transducer modules presented generally include a light source, a focus-alignment system, a flow cell, and a light scatter detection system. Electrodes within the flow cell allow for the measurement of the DC impedance and RF conductivity of cells passing through a cell-interrogation zone in the flow cell. Light scatter from the cells passing through the cell-interrogation zone is measured by the light scatter detection system. The light scatter detection system measures the light scatter parameters of upper median light scatter, lower median angle light scatter, low angle light scatter, and axial light loss.

Abstract: A microplate in which a plurality of wells that are reaction vessels, in a substantially concave shape, to analyze components of a specimen are arranged in matrix, includes a first surface that passes through an opening plane of the wells; and a second surface that is directed to an opposite side to the first surface. The microplate also includes a well-identification information indicator that is arranged on the second surface included in a boundary portion between wells next to each other, and that indicates well identification information to identify each of the wells. The boundary portion between the wells next to each other has a thickness substantially equivalent to a depth of the wells.

Abstract: A method for identifying a platelet population, preferably a population of immature, reticulated platelets, in a biological sample involves incubating the biological sample for less than 5 minutes with at least one labeled, ligand (e.g., monoclonal antibody) that binds to an epitope or antigen on platelets and with a nucleic acid dye. In one embodiment, the dye is Acridine Orange and the label on the ligand is PE-Cy7. The sample is then analyzed and one or more platelet populations is rapidly identified or quantified by passing the incubated sample through a sensing region of a flow cytometer. In one embodiment, this method occurs without a washing or physical cell separation step. The incubated sample is irradiated with a laser light source, and fluorescence of the labeled ligand and the nucleic acid dye are measured along with at least one additional parameter, e.g., light scatter, direct current, axial light loss, opacity, radio frequency, and fluorescence.

Abstract: Assay methods are disclosed involving specific binding reactions which are simplified compared to known methods. A compound capable of producing chemiluminescence is immobilized on a solid support as is a member of a specific binding pair for capturing an analyte from a sample. An activator compound that activates the chemiluminescent compound and is conjugated to a specific binding pair member is added in excess along with the sample to the solid support. Addition of a trigger solution causes a chemiluminescent reaction at the sites where the activator conjugate has been specifically bound. The assay methods are termed non-separation assays because they do not require removal or separation of excess detection label (activator conjugate) prior to the detection step. The methods are applicable to various types of assays including immunoassays, receptor-ligand assays and nucleic acid hybridization assays.

Abstract: The present invention concerns an improved apparatus for cleaning the interior of a liquid handling probe to reduce the amount time and the volume of wash fluid required to clean the probe and minimize carryover of material between different samples. In addition to the probe, the apparatus includes one or more wash fluid reservoirs, a compressed gas supply, one or more pumps, two or more valve-controlled probe lines and a controller for opening and closing the valves and actuating the pump(s) at desired time intervals. The invention further concerns a method of cleaning a liquid handling probe using the claimed apparatus and comprising sequential steps of pumping wash fluid and compressed gas through the probe.

Abstract: The present invention discloses multi-purpose metering fluid/rinse reagents for use in automated cellular analyzers that use liquid volumetric metering. The compositions contain a chelating agent, an ionizing salt, optionally a stabilizing ion, a buffer, a non-hemolytic surfactant, and optionally an antimicrobial agent. Advantageously, the compositions produce less than one part-per-million of formaldehyde over the course of one year. Methods for using the compositions are also described.

Abstract: A method of autoverifying clinical test results comprises displaying an autoverification process as a flowchart on a graphical user interface. The autoverification process is defined by a plurality of nodes and a plurality of edges connecting the nodes. The autoverification process is configured to evaluate a result and determine if the test result meets a predetermined criteria. The method further comprises receiving the test result and automatically performing the autoverification process on the test result. A system for creating and implementing the autoverification processes comprises a graphical user interface configured to display the autoverification process as a flowchart. The system includes an input configured to receive the clinical test result from a laboratory analyzer. The system also includes a processor configured to analyze the clinical test result according to the defined autoverification process.

Abstract: The present specification discloses an automated method and apparatus useful for separating and harvesting cells of interest, e.g., mononuclear cells, in a whole blood sample. The method of the invention uses the aspirating/dispensing probe of an automated sample preparation instrument to underlay a density gradient medium beneath a whole blood sample in a centrifugation tube, and the same probe is used to harvest cells of interest from a cell layer formed in the tube as a result of a centrifugation step. In harvesting cells, the probe is advanced inside the tube by a fixed, predetermined distance at which the probe tip (i.e., its aspiration port) is known to be located at, or within a predetermined distance below, the bottom of the cell layer. A predetermined volume of liquid is then aspirated through the probe tip, whereby most cells of interest (and more than 90% of those cells that can be harvested by a flawless manual method) are removed from the cell layer and collected for analysis.

Abstract: The invention relates to a mixing method for mixing at least one small quantity of liquid, in which a quantity of liquid is applied, in a reaction region and at least one surface sound wave is reacted with the quantity of liquid. The invention relates further to a mixing device for mixing at least one quantity of liquid for performing the method of the present invention, a use of the device, and a method of analysis for bond strengths on surfaces.

Abstract: Transducer modules for use in a blood analysis instrument and methods for analyzing a blood sample. The transducer modules presented generally include a light source, a focus-alignment system, a flow cell, and a light scatter detection system. Electrodes within the flow cell allow for the measurement of the DC impedance and RF conductivity of cells passing through a cell-interrogation zone in the flow cell. Light scatter from the cells passing through the cell-interrogation zone is measured by the light scatter detection system. The light scatter detection system measures the light scatter parameters of upper median light scatter, lower median angle light scatter, low angle light scatter, and axial light loss.

Abstract: A stirring determination method uses an analyzer in which a liquid contained in a vessel is stirred by an acoustic wave generated by an acoustic wave generating unit attached to the vessel, optical characteristics of a reaction solution obtained by stirring the liquid are measured, and the reaction solution is analyzed based on the optical characteristics of the reaction solution. The method includes measuring a temperature of the liquid in a position where the temperature of the liquid is different before and after the liquid is stirred; and determining whether the liquid is properly stirred based on a rate of increase in the measured temperature of the liquid.

Abstract: The analyzer (1) of the present invention comprises: a reading section (23) for storing or obtaining specimen information including a sample type of a specimen, and specimen container information; a liquid level detecting section (51) for detecting a liquid level and/or an interface of the specimen; a dispensing apparatus (5) for dispensing a specimen; a washing apparatus (6) for washing a dispensing probe (50); a calculating section (202) for calculating a contamination adhering range of an external wall surface of the dispensing probe (50), based on the sample type, specimen suction position and specimen container information stored or obtained by the reading section (23), as well as liquid level and/or interface information of the specimen detected by the liquid level detecting section (51); and a washing control section (200) for controlling a washing range based on the contamination adhering range.

Abstract: An automatic analyzer includes a wastewater suction unit that causes a suction nozzle to suction a reaction wastewater from each of plural reaction vessels transferred to a disposal position, transfers the plural suction nozzles to a cleaning position to make the suction nozzles suction a cleaning liquid, and clean the suction nozzles. The wastewater suction unit includes a pressure detector that is arranged near the suction nozzle in a pipe that guides a negative pressure for suction to each of the suction nozzles to detect pressure in each of the suction nozzles at time of suctioning of the reaction wastewater, a vessel determination unit that determines whether the reaction vessel is present or not at the disposal position, and a clog determination unit that determines whether each of the suction nozzles is clogged or not based on change in pressure in the suction nozzle and presence/absence of the reaction vessel.

Abstract: Assay methods are disclosed involving specific binding reactions which are simplified compared to known methods. A compound capable of producing chemiluminescence is immobilized on a solid support as is a member of a specific binding pair for capturing an analyte from a sample. An activator compound that activates the chemiluminescent compound and is conjugated to a specific binding pair member is added in excess along with the sample to the solid support. Addition of a trigger solution causes a chemiluminescent reaction at the sites where the activator conjugate has been specifically bound. The assay methods are termed non-separation assays because they do not require removal or separation of excess detection label (activator conjugate) prior to the detection step. The methods are applicable to various types of assays including immunoassays, receptor-ligand assays and nucleic acid hybridization assays.

Abstract: A reaction container holder capable of inhibiting the lowering of the transfer efficiency of heat transferred from a rotating member to a bottom surface of a reaction container, and an analyzer comprising the reaction container holder, are provided. In a reaction container holder comprising: a retaining member unit comprising a plurality of container retaining sections for retaining reaction containers, which house a reaction liquid containing a reagent and a specimen; and a circular rotating member for detachably fixing the unit from above and rotating, the holder keeping the container at a constant temperature by transferring heat from a heat source through the rotating member to the container, the rotating member comprises a level difference section, an upper surface of which is positioned below a bottom surface of the container retained by the unit and above a bottom part of the section, when the retaining member unit is fixed.

Abstract: A liquid agitating device includes a sound wave generator that generates a sound wave; and a transmitting portion that transmits the sound wave generated by the sound wave generator, at least a portion of the transmitting portion being in contact with a liquid, and the transmitting portion emitting the sound wave towards the liquid at the portion in contact with the liquid. The sound wave emitted toward the liquid generates a local flow within the liquid and agitates the liquid.

Abstract: Assay methods are disclosed involving specific binding reactions which are simplified compared to known methods. A compound capable of producing chemiluminescence is immobilized on a solid support as is a member of a specific binding pair for capturing an analyte from a sample. An activator compound that activates the chemiluminescent compound and is conjugated to a specific binding pair member is added in excess along with the sample to the solid support. Addition of a trigger solution causes a chemiluminescent reaction at the sites where the activator conjugate has been specifically bound. The assay methods are termed non-separation assays because they do not require removal or separation of excess detection label (activator conjugate) prior to the detection step. The methods are applicable to various types of assays including immunoassays, receptor-ligand assays and nucleic acid hybridization assays.

Abstract: A position detector is for detecting a position of liquid held in a vessel. The position detector includes a sound wave generator disposed in contact with the vessel and having a plurality of sound generating elements for generating a sound wave by electrical energy; and a measuring unit that measures electrical characteristics of each of the sound generating elements based on the electrical energy reflected from each of the sound generating elements. The position detector also includes a determining unit that determines the presence or absence of the liquid at a position of each of the sound generating elements based on difference in the electrical characteristics measured at the measuring unit.