APPARATUS AND METHOD FOR MIXING FLUIDS FOR ANALYSIS
    1.
    发明公开
    APPARATUS AND METHOD FOR MIXING FLUIDS FOR ANALYSIS 失效
    设备和方法,用于混合用于分析流体

    公开(公告)号:EP0830609A4

    公开(公告)日:1999-08-18

    申请号:EP96920585

    申请日:1996-05-31

    IPC分类号: G01N1/00 G01N1/38 G01N35/08

    摘要: In an apparatus (10) for fluid analysis, such as hematologic analysis, a plurality of reagent-mixture components are each injected by a respective pump (P1...Pn) through a valve matrix (16) and into a flow-injection unit (24). The flow-injection unit (24) defines a mixing chamber (50) including a plurality of protuberances or nubs (54) projecting inwardly toward the center of the chamber, and spaced relative to each other both axially and radially. As the reagent-mixture components are injected into the mixing chamber (50), the nubs (54) agitate the fluid flow and create turbulence, thereby dispersing the reagent-mixture components and in turn mixing the components together to create a reagent mixture. The flow rates of the reagent-mixture components are adjusted in order to select the reagent-mixture ratio as the components are combined in the flow-injection unit (24) to thereby create the selected reagent mixture. Upon passage through the flow-injection unit (24), the reagent mixture is injected into a sensing unit (20) for analyzing a particle distribution of the mixture.

    METHOD/APPARATUS FOR CELL DIFFERENTIATION MEASURING CELL SIZE, MEMBRANE INTEGRITY, INTRACELLULAR COMPLEXITY
    2.
    发明公开
    METHOD/APPARATUS FOR CELL DIFFERENTIATION MEASURING CELL SIZE, MEMBRANE INTEGRITY, INTRACELLULAR COMPLEXITY 失效
    方法/设备细胞分化用于测量ZELLENGRÖE,细胞膜的完整性和INTRAZELLULARENKOMPLEXITÄT。

    公开(公告)号:EP1005641A4

    公开(公告)日:2002-08-07

    申请号:EP98920381

    申请日:1998-05-12

    CPC分类号: G01N15/1218

    摘要: A method and apparatus are provided for differentiating cells in an automated particle analyzer (10), such as for use in hematological analysis, by measuring apparent cell size (or volume), membrane integrity and intracellular complexity ("voltaic fragility"). The cells are suspended in a selected reagent mixture. A predetermined dc voltage is applied across a sensing orifice (36) to thereby create a dc electric field within and around the orifice (36), and the reagent mixture is passed through the center of the orifice (36). The magnitude of the change in current flowing through dc electric field is measured therethrough, and based on the measured change, a signal is generated for each cell which is indicative of the apparent complexity of the cell. A visual display (54) is generated based on the signals facilitating differentiation of the cells.

    VALVE ASSEMBLY
    3.
    发明公开
    VALVE ASSEMBLY 失效
    阀单元

    公开(公告)号:EP0808434A4

    公开(公告)日:1998-12-16

    申请号:EP96906266

    申请日:1996-02-06

    IPC分类号: F16K11/02 F16K11/00

    CPC分类号: F16K11/022 Y10T137/86879

    摘要: In a valve assembly (10) exhibiting zero dead volume the port head (12, 112) is mounted on a solenoid (14) and defines an inlet port (16, 116) on one side of the valve seat (20, 120), and two outlet ports (18, 19, 118, 119) on the opposite side of the valve seat. A flexible diaphragm (22) is seated across the valve seat (20, 120) between the port head (12, 112) and the solenoid (14), and is sealed along its peripheral edge. A spring-biased valve rod (24) is coupled to the opposite side of the diaphragm (22) relative to the valve seat (20, 120), and the solenoid (14) is actuated to move the valve rod (24) and diaphragm (22) between open and closed positions. The valve assembly (10) is opened by actuating the solenoid (14) to drive the valve rod (24) and diaphragm (22) away from the valve seat (20, 120) and permit the passage of fluid across the valve seat between the inlet (16, 116) and outlet ports (18, 19, 118, 119).