LEUKOCYTE CONCENTRATION SEPARATION DEVICE, BLOOD COLLECTION CONTAINER, AND METHOD FOR SEPARATING LEUKOCYTES

    公开(公告)号:US20230090675A1

    公开(公告)日:2023-03-23

    申请号:US17908407

    申请日:2021-03-11

    Abstract: Provided is a blood collection container with which a specimen with a high leukocyte recovery rate and a small amount of contaminating erythrocytes can be obtained. A blood collection container according to the present invention is a blood collection container by which a predetermined amount of blood is collected, the blood collection container including: a blood collection container main body; and a hemocyte separation material contained in the blood collection container main body, the hemocyte separation material having a specific gravity at 25° C. of 1.075 or more and 1.093 or less, and the blood collection container including: a configuration of including a hemagglutinating agent contained in the blood collection container main body (configuration A2); or a configuration of including an osmotic pressure regulator contained in the blood collection container main body, and when a water-soluble component contained in the blood collection container main body is dissolved with physiological saline in an amount equal to a predetermined amount of blood to be collected in the blood collection container to obtain a solution for osmotic pressure measurement, the solution for osmotic pressure measurement having an osmotic pressure of 300 mOsm/L or more and 500 mOsm/L or less (configuration B2).

    STORAGE CONTAINER FOR CELL-CONTAINING SOLUTION AND STORAGE SOLUTION

    公开(公告)号:US20230133626A1

    公开(公告)日:2023-05-04

    申请号:US17907866

    申请日:2021-03-03

    Abstract: Provided is a storage container for cell-containing solutions, which makes it possible to enhance the storage stability of cfDNA contained in a cell-containing solution even when the cell-containing solution is stored under a room temperature environment. The storage container for cell-containing solutions according to the present invention is intended to be used for storing a predetermined amount of a cell-containing solution, the storage container being provided with a container main body and a preservative solution contained in the container main body, in which the storage container has a first configuration such that the preservative solution contains a cell-membrane-permeable compound that has a molecular weight of 100 or less and cannot be frozen at 0° C. and, when a mixed solution X is prepared by collecting the predetermined amount of the cell-containing solution in the storage container for cell-containing solutions and mixing the cell-containing solution with the preservative solution, the content of the cell-membrane-permeable compound in the mixed solution X is 1 vol % to 5vol % inclusive, or the storage container has a second configuration such that the preservative solution contains a cell-membrane-impermeable compound having a molecular weight of 300 or more and, when a mixed solution X is prepared by collecting the predetermined amount of the cell-containing solution in the storage container for cell-containing solutions and mixing the cell-containing solution with the preservative solution, the content of the cell-membrane-impermeable compound in the mixed solution X is 0.5 μmol/L to 5 μmol/L inclusive.

    BLOOD COLLECTION CONTAINER
    4.
    发明申请

    公开(公告)号:US20230050815A1

    公开(公告)日:2023-02-16

    申请号:US17783156

    申请日:2020-11-30

    Abstract: Provide is a blood collection container capable of suppressing the occurrence of blood clots involving bubbles when blood containing heparin is coagulated, and capable of suppressing the production of fibrin in serum after separation when blood containing heparin is separated into serum and blood clots. A blood collection container according to the present invention includes: a blood collection container main body having an opening at one end thereof and a closed bottom at the other end thereof; a serine protease disposed in the blood collection container main body; and a heparin neutralizing agent disposed in the blood collection container main body, wherein when a region in which the serine protease is disposed is defined as a first region, and a region in which the heparin neutralizing agent is disposed is defined as a second region, the second region includes a region present on an other end side with respect to an end on the other end side of the first region.

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