Abstract: Aspects and embodiments of the instant disclosure provide a particle and/or intracellular organelle alignment agent for a particle analyzer used to analyze particles contained in a sample. An exemplary particle and/or intracellular organelle alignment agent includes an aqueous solution, a viscosity modifier, and/or a buffer.

Abstract: Aspects and embodiments of the instant disclosure provide a particle and/or intracellular organelle alignment agent for a particle analyzer used to analyze particles contained in a sample. An exemplary particle and/or intracellular organelle alignment agent includes an aqueous solution, a viscosity modifier, and/or a buffer. Embodiments also encompass systems, compositions, and methods for analyzing a sample containing particles. Particles such as blood cells can be categorized and counted by a digital image processor. A digital microscope camera can be directed, for example using certain focusing techniques, into a flowcell defining a symmetrically narrowing flowpath in which the sample stream flows in a ribbon flattened by flow and viscosity parameters between layers of sheath fluid. Blood cell images can be collected and analyzed using dynamic range extension processes and systems.

Abstract: Aspects and embodiments of the instant disclosure provide a particle and/or intracellular organelle alignment agent for a particle analyzer used to analyze particles contained in a sample. An exemplary particle and/or intracellular organelle alignment agent includes an aqueous solution, a viscosity modifier, and/or a buffer.

Abstract: The present disclosure relates to apparatus, systems, compositions, and methods for analyzing a sample containing particles. In some aspects the system comprises an analyzer which may be a visual analyzer. In one aspect, this disclosure relates to a particle imaging system comprising a flowcell through which a sample containing particles is caused to flow, and a high optical resolution imaging device which captures images for image analysis of samples. Other compositions, methods and features of this disclosure are disclosed herein.

Abstract: Particles such as blood cells can be categorized and counted by a digital image processor. A digital microscope camera can be directed into a flowcell defining a symmetrically narrowing flowpath in which the sample stream flows in a ribbon flattened by flow and viscosity parameters between layers of sheath fluid. A contrast pattern for autofocusing is provided on the flowcell, for example at an edge of a rear illumination opening. The image processor assesses focus accuracy from pixel data contrast. A positioning motor moves the microscope and/or flowcell along the optical axis for autofocusing on the contrast pattern target. The processor then displaces microscope and flowcell by a known distance between the contrast pattern and the sample stream, thus focusing on the sample stream. Blood cell images are collected from that position until autofocus is reinitiated, periodically, by input signal, or when detecting temperature changes or focus inaccuracy in the image data.

Abstract: A variable rate particle counter for adjusting the volumetric delivery rate of fluid to a flow cell based upon an initial particle count rate in order to effectively “tune” the final dilution of sample sheath flow to the particle concentration of the sample. A sheath fluid syringe pump and a test sample syringe pump are driven by motors which are adjusted by a data analyzer. The data analyzer compares a particle count rate measured by a detection assembly to a predetermined reference value and determines if the count rate is too high or to low. Accordingly, one of several pump profiles is initiated to adjust the flow rate of the sheath fluid or test sample or both. Advantageously, the low cell count precision is improved and the upper limit cell count is expanded.

Abstract: A variable rate particle counter for adjusting the volumetric delivery rate of fluid to a flow cell based upon an initial particle count rate in order to effectively “tune” the final dilution of sample sheath flow to the particle concentration of the sample. A sheath fluid syringe pump and a test sample syringe pump are driven by motors which are adjusted by a data analyzer. The data analyzer compares a particle count rate measured by a detection assembly to a predetermined reference value and determines if the count rate is too high or to low. Accordingly, one of several pump profiles is initiated to adjust the flow rate of the sheath fluid or test sample or both. Advantageously, the low cell count precision is improved and the upper limit cell count is expanded.

Abstract: A variable rate particle counter for adjusting the volumetric delivery rate of fluid to a flow cell based upon an initial particle count rate in order to effectively “tune” the final dilution of sample sheath flow to the particle concentration of the sample. A sheath fluid syringe pump and a test sample syringe pump are driven by motors which are adjusted by a data analyzer. The data analyzer compares a particle count rate measured by a detection assembly to a predetermined reference value and determines if the count rate is too high or to low. Accordingly, one of several pump profiles is initiated to adjust the flow rate of the sheath fluid or test sample or both. Advantageously, the low cell count precision is improved and the upper limit cell count is expanded.

Abstract: A reagent pump assembly for metering precise volumes of fluids, such as reagent, for an analytical instrument, such as a clinical hematology or flow cytometer instrument. The assembly includes a multilayer block having a plurality of diaphragm pumps interposed between two of the layers, controlled by application of one of vacuum or pressure, in sequence, to fill the reservoirs and expel the contents of the pump. One-way check valves are used to control the fluid flow from the reservoirs of fluids to the fluid outlet ports. The fluid outlet ports may be directly coupled to fluid inlet ports of a compatible unified flow circuit, which contains reaction chambers and a plurality of sample aliquots. Thus, the reagent pump assembly can be used to combine and mix a sample aliquots with a precise amount of reagent in a reaction chamber, preparatory for analyzing the reaction mixture.

Abstract: A unified fluid cell circuit assembly for an analytical instrument, such as a clinical hematology, immunoassy or chemistry or a flow cytometry instrument. The assembly includes a unified fluid circuit, a shear valve, a fluid pump assembly, and a plurality of solenoid valves. The unified fluid circuit is made of a plurality of acrylic plates which have formed in the various plate surfaces chamber cavities, pneumatic, hydraulic and vent line, and valve cavities. The plates, when secured together, form a plurality of reaction chambers, a plurality of control valves and various lines as a network for controlling the flow and mixing of aliquots of a sample and fluids (rinse, reagents, etc.) to perform the reactions for analyzing the sample. The fluid pump assembly is connected to the unified flow circuit and has a plurality of diaphragm pumps which pump precise volumes of fluids.

Abstract: A method and apparatus for selecting a subset of a predetermined number of test sample aliquots to mix with respective reagents using a shear valve having a maximum predetermined number of aliquot loops in an analytical instrument, including without limitation a clinical hematology or a flow cytometer instrument. Each aliquot loop can be filled with a test sample aliquot. Selected ones of the aliquot loops can be filled with a rinse solution and, using bypass passages and valves, closed off from the rinse source and a vacuum source used to empty the rinse from the non-closed off aliquot loops. The vacuum source also is used to fill the non-closed off aliquot loops with the sample to be aliquotted, so that the closed off aliquot loop remains filled with rinse. The shear valve can then be shifted to a second position, where the reagents for the non-closed off aliquot loops are pumped through those aliquot loops to mix the selected sample aliquot loops with their respective reagents.

Abstract: A valve comprises a first rigid layer having a substantially planar first surface, a second rigid layer having a substantially planar second surface facing the first surface and a substantially planar third surface opposite the second surface and a flexible layer positioned between the first and second surfaces. A valve chamber is demarcated by a concave surface in the substantially planar first surface and one surface of the flexible layer and at least one first fluid passageway in the first rigid layer opens into the valve chamber at the concave surface to alternatively apply a vacuum and pressure thereto. A fluid chamber is demarcated by another surface of the flexible layer and a concave-convex surface in the substantially planar second surface which comprises an inner circular convex portion and a concentric annular outer concave portion. At least two second fluid passageways in the second rigid layer open into the valve chamber at the convex surface.

Abstract: A method for filtering a whole blood sample using a filter element constructed and arranged to block the passage of fibrous and particulate matter which may be present in a liquid sample, such as a whole blood sample, while allowing the blood cells to pass is disclosed. In one embodiment, the filter element is part of an in-line filter assembly which assembly may include two complementary mating components. One component may take the form of a coupling provided with a male threaded portion adapted to be received into and engage the female threaded portion of the complementary mating component. This complementary mating component may be another coupling or an analysis system component, such as a valve. Each complementary mating component is adapted to receive a liquid sample carrying conduit therethrough. The coupling is also adapted to receive a filter mount which holds a filter element constructed and arranged as discussed hereinabove.

Abstract: Apparatus and method are provided for the precisely controlled and coordinated supply of sample and sheath stream fluids to a sheath stream flow cell, and comprise the use of positive displacement differential pumping means which are operable to insure consistent sample and sheath stream fluid diameters, velocity and volume flow conditions within the flow cell, thereby maximizing the accuracy and reproducibility of successive analyses.

Abstract: New and improved method and apparatus for the correction of coincident errors attendant the automated detection and counting of mixed particles having detectable characteristics of different levels in particle counting applications wherein the detection of "dominant" particles under coincident particle conditions, renders undetectable the "dominated" particles, with resulting inaccuracy in the "dominated" particle count. Such inaccuracy is corrected by modifying the "dominated" particle count in accordance with the time duration of the signals which are generated attendant the detection of the "dominated" particles.

Abstract: A multichamber cuvette for maintaining in independent and separate condition at least two reactants, one of which may be a sample, until such time that it is desired to mix them for reaction with each other for photometric analysis in the cuvette. At least one of the chambers has a pair of optical quality windows aligned with one another for analysis of the then liquid contents extending between the windows. The cuvette body is of upright construction, defining at least two such chambers laterally of one another, open at the top for filling separately or simultaneously, and interconnected adjacent their lower extremities by a passageway of inverted U shape. The passageway is of an effective height exceeding the highest filling level of each chamber by a distance at least as great as any capillary rise in the passageway beyond such level of the particular liquid in that chamber.

Abstract: A method for filtering a whole blood sample using a filter element constructed and arranged to block the passage of fibrous and particulate matter which may be present in a liquid sample, such as a whole blood sample, while allowing the blood cells to pass is disclosed. In one embodiment, the filter element is part of an in-line filter assembly which assembly may include two complementary mating components. One component may take the form of a coupling provided with a male threaded portion adapted to be received into and engage the female threaded portion of the complementary mating component. This complemnetary mating component may be another coupling or an analysis system component, such as a valve. Each complementary mating component is adapted to receive a liquid sample carrying conduit therethrough. The coupling is also adapted to receive a filter mount which holds a filter element constructed and arranged as discussed hereinabove.