CELL CULTURE SCAFFOLD MATERIAL
    3.
    发明公开

    公开(公告)号:EP4458948A1

    公开(公告)日:2024-11-06

    申请号:EP22916003.1

    申请日:2022-12-26

    摘要: Provided is a scaffold material for cell culture with which the culture stability of cells can be maintained over an extended period of time. A scaffold material for cell culture according to the present invention contains a peptide-conjugated (meth)acrylic copolymer having a (meth)acrylic copolymer moiety and a peptide moiety bonded to the (meth)acrylic copolymer moiety, the following relaxation time (CS 2 ) being 5 milliseconds or less. Relaxation time (CS 2 ): a relaxation time of a CS component, which is a component having the lowest molecular mobility among three components, when the scaffold material for cell culture after being brought into contact with heavy water at 25°C for 18 hours is measured by a CPMG method using pulsed NMR, and the obtained free induction decay curve of spin-spin relaxation of 1 H is separated into three components.

    SCAFFOLD MATERIAL FOR CELL CULTURE
    4.
    发明公开

    公开(公告)号:EP4458946A1

    公开(公告)日:2024-11-06

    申请号:EP22916001.5

    申请日:2022-12-26

    摘要: Provided is a scaffold material for cell culture with which the culture stability of cells can be maintained over an extended period of time. A scaffold material for cell culture according to the present invention contains a peptide-conjugated (meth)acrylic copolymer having a (meth)acrylic copolymer moiety and a peptide moiety bonded to the (meth)acrylic copolymer moiety, when the peptide-conjugated (meth)acrylic copolymer is subjected to high performance liquid chromatography measurement under the following condition 1, a peak top of a main peak having the largest area among signals being not detected within a retention time of 4 minutes:
    the condition 1 being:
    a column of C18 (Inner diameter 3.0 mm × length 150 mm, filler particle size 3.5 µm),
    a column temperature of 40°C,
    a flow rate of 0.3 mL/min,
    a detector of an evaporative light scattering detector,
    a mobile phase A (liquid A) of a 0.1 wt% aqueous formic acid solution,
    a mobile phase B (liquid B) of isopropyl alcohol,
    a retention time of 0 minutes, in which the liquid A/the liquid B (volume ratio) is 70%/30%,
    a retention time of 0 minutes to 15 minutes, in which the liquid A/the liquid B (volume ratio) is changed from 70%/30% to 0%/100%, and
    a retention time of 15 minutes to 30 minutes, in which the liquid A/the liquid B (volume ratio) = 0%/100% is maintained

    SCAFFOLD MATERIAL FOR CELL CULTURE
    5.
    发明公开

    公开(公告)号:EP4458945A1

    公开(公告)日:2024-11-06

    申请号:EP22916000.7

    申请日:2022-12-26

    摘要: Provided is a scaffold material for cell culture with which the culture stability of cells can be maintained over an extended period of time. A scaffold material for cell culture according to the present invention contains a peptide-conjugated (meth)acrylic copolymer having a (meth)acrylic copolymer moiety and a peptide moiety bonded to the (meth)acrylic copolymer moiety, the (meth)acrylic copolymer moiety having a structural unit derived from a (meth)acrylate compound (A) represented by the following Formula (A1) or the following Formula (A2), and a content ratio of the structural unit derived from the (meth)acrylate compound (A) being 25 mol% or more and 98 mol% or less in 100 mol% of the total structural units of the (meth)acrylic copolymer moiety. In the Formula (A1), R represents a hydrocarbon group having 2 or more and 18 or less carbon atoms. In the Formula (A2), R represents a hydrocarbon group having 2 or more and 18 or less carbon atoms.

    SYSTEMS AND METHODS FOR TISSUE PROCESSING AND PREPARATION OF CELL SUSPENSION THEREFROM

    公开(公告)号:EP4455258A2

    公开(公告)日:2024-10-30

    申请号:EP24199321.1

    申请日:2014-03-14

    IPC分类号: C12M1/00

    摘要: The present invention provides for methods and at least partially automated devices suitable for producing a transplantable cellular suspension of living tissue suitable for promoting tissue regeneration in an epithelium-related procedure, as well as compositions produced therefrom. Tissue regeneration in humans is extremely limited and constitutes a major challenge to the repair of damaged organ function. Wound treatment is a typical area where tissue regeneration is required. Wounds (lacerations or openings) in mammalian tissue can result in tissue disruption and coagulation of the microvasculature at the wound face.