METHOD FOR ANALYZING BLOOD COAGULATION REACTION

    公开(公告)号:EP4417978A1

    公开(公告)日:2024-08-21

    申请号:EP22880821.8

    申请日:2022-09-30

    IPC分类号: G01N35/04 G01N33/86

    CPC分类号: G01N33/86 G01N35/04

    摘要: A method for analyzing a blood coagulation reaction comprises, by a blood coagulation analysis device, measuring a coagulation reaction of a sample solution including a subject blood specimen, determining whether or not the coagulation reaction of the sample solution is completed, and when it is determined that the coagulation reaction is completed, terminating measurement of the coagulation reaction of the sample solution. The blood coagulation analysis device includes a reaction table which is rotated in one direction, and the reaction table includes a measurement port to which a cell can be attached. The coagulation reaction of the sample solution in the cell supplied to the measurement port is measured, and time series data of the measured coagulation reaction is accumulated. Whether or not the coagulation reaction is completed is determined from the accumulated time series data of the coagulation reaction, and when it is determined that the coagulation reaction is completed, measurement of the coagulation reaction of the sample solution is terminated, and the cell containing the sample solution is removed from the measurement port.

    BLOOD COAGULATION REACTION ANALYSIS METHOD
    4.
    发明公开

    公开(公告)号:EP4212880A1

    公开(公告)日:2023-07-19

    申请号:EP21866778.0

    申请日:2021-09-08

    IPC分类号: G01N33/86

    摘要: Provided is a blood coagulation reaction analysis method. The method includes measuring a blood coagulation reaction of a subject specimen and acquiring first data for calculating a blood coagulation time of the subject specimen and second data for estimating a blood coagulation abnormality factor of the subject specimen, wherein the acquiring of the second data includes: obtaining a first derivative V(i) of a coagulation reaction curve R(i); and determining a point p k where V(i) assumes X k before reaching a maximum value of V(i), Vmax, and a point q k where V(i) assumes X k after reaching Vmax.

    METHOD FOR REDUCING MEASUREMENT ERROR
    5.
    发明公开

    公开(公告)号:EP4212627A1

    公开(公告)日:2023-07-19

    申请号:EP21866847.3

    申请日:2021-09-10

    IPC分类号: C12Q1/26 C12Q1/28

    摘要: An object of the present invention is to provide a method for measuring an object to be measured in a specimen by an enzymatic method, the measurement method being able to suppress the positive influence of peroxide derived from the specimen. More specifically, an object of the present invention is to provide a measurement method and a measurement reagent that can suppress elevation in value regardless of whether or not the specimen is a catalase-free specimen. Provided is a measurement method that can accurately quantify hydrogen peroxide derived from an object to be measured, without influence derived from a specimen, by contacting the specimen with an enzyme in the presence of at least one compound selected from the group consisting of a compound represented by the following general formula (I), a benzimidazole derivative having an electron-donating substituent at position 2, and histidine, wherein R1 and R2 are the same or different and each represent hydrogen, a linear or branched alkyl group having 1 to 6 carbon atoms and optionally having a substituent, an aryl group optionally having a substituent, or an alkyloxy group having 1 to 6 carbon atoms.

    MAGNETICALLY RESPONSIVE PARTICLES, AND IMMUNOASSAY METHOD AND IMMUNOASSAY REAGENT USING SAME

    公开(公告)号:EP4130745A1

    公开(公告)日:2023-02-08

    申请号:EP21777082.5

    申请日:2021-03-24

    IPC分类号: G01N33/543 G01N33/553

    摘要: Disclosed is a sensitized magnetic responsive particle including: a magnetic responsive particle having a core particle and at least one magnetic layer disposed on the core particle, the magnetic layer containing microparticles of a magnetic metal and/or an oxide thereof; and a substance that specifically interacts with an analyte, the substance being supported on the magnetic responsive particle, wherein, assuming that a volume and a weight of the core particle are respectively v c and w c , and that a volume and a weight of the magnetic responsive particle are respectively v e and w e , the magnetic material density [(w e - w c )/(v e - v c )] satisfies the following expression 1: 2.0 ≤ w e − w c / v e − v c The magnetic responsive particle has a high magnetic collection property in spite of a small particle size. When the magnetic responsive particle is used, a reagent for an immunoassay having excellent magnetic separability and capable of realizing high sensitivity can be provided.

    HEMOGLOBIN ASSAY METHOD
    7.
    发明公开

    公开(公告)号:EP4119941A1

    公开(公告)日:2023-01-18

    申请号:EP21768942.1

    申请日:2021-03-12

    摘要: Provided is a hemoglobin assay method by which HbA0 fraction can be separated with high accuracy.
    The hemoglobin assay method includes allowing elution of a fraction containing hemoglobin A0 by ion exchange chromatography using an eluent containing a buffer at a concentration of less than 25 mM, wherein the buffer is a phosphate or a Good's buffer, and the eluent has a pH within ± 0.1 of a pKa of the buffer.

    METHOD FOR DETECTING TARGET NUCLEIC ACID USING DRIED BLOOD FILTER PAPER PIECE

    公开(公告)号:EP4108772A1

    公开(公告)日:2022-12-28

    申请号:EP21757281.7

    申请日:2021-02-19

    摘要: It is an object of the present disclosure to provide a method for reducing the influence of baseline disturbances in a method for detecting a target nucleic acid in dry blood filter paper by real-time PCR using a fluorescent dye, with a simple method. The present disclosure provides a method for detecting a target nucleic acid in dry blood filter paper by real-time PCR, the method including: (1) amplifying the target nucleic acid in the dry blood filter paper by applying thermal cycles to a sample solution containing a dry blood filter paper punch piece and a PCR reagent, wherein the PCR reagent includes a fluorescently labeled probe; (2) optically detecting the fluorescence intensity of the sample solution for each of the thermal cycles; and (3) performing quantitative analysis of the target nucleic acid using data after a predetermined number of cycles of the optically detected data.

    AUTOMATIC ANALYSIS DEVICE
    9.
    发明公开

    公开(公告)号:EP4102231A1

    公开(公告)日:2022-12-14

    申请号:EP20918005.8

    申请日:2020-12-17

    IPC分类号: G01N35/02

    摘要: An automatic analysis apparatus is provided which is capable of stirring a reagent without reducing the analysis processing capacity, with a simple configuration.
    An automatic analysis apparatus of the invention includes a reagent table 34 that is rotatable and that holds reagent vessels 74, and a plurality of magnets 36 are disposed below the reagent table 34, with orientations of magnetic poles of the magnets 36 fixed, along a movement path R of the reagent vessels 74 moving on a circumference when the reagent table 34 is rotationally driven. The plurality of magnets 36 are disposed such that the fixed orientations of the magnetic poles of the magnets vary along the movement path R, and act a magnetic force on a stirring bar 39 in each of the reagent vessels 74. When the reagent table 34 is rotated and the reagent vessels 74 pass above the magnets 36, the stirring bar 39 in each of the reagent vessels 34 is rotated and/or oscillated by the magnetic force received from the magnets 36, to stir the reagent.

    BLOOD COAGULATION TIME MEASUREMENT METHOD
    10.
    发明公开

    公开(公告)号:EP4083630A1

    公开(公告)日:2022-11-02

    申请号:EP20906355.1

    申请日:2020-12-25

    发明人: KAWABE, Toshiki

    IPC分类号: G01N33/86

    摘要: Provided is a blood coagulation time measurement method. In the method, reaction X(i) is acquired through smoothing and zero-point adjustment of a measured value P(i) for coagulation reaction of a blood specimen, and then an integration ratio Z(i) of the reaction X(i) is acquired. These values are used to calculate an index for coagulation time Tc calculation, and it is determined whether or not the index satisfies the criteria. The procedure is sequentially repeated until an index that satisfies the criteria is obtained.