-
-
2.
公开(公告)号:EP4460546A1
公开(公告)日:2024-11-13
申请号:EP23703928.4
申请日:2023-01-05
申请人: Blue Evolution, Inc.
发明人: PERRY, Beau , MCSHEERY, Tracy
-
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
发明人: ARAI, Yuuhei , NAKAJIMA, Nami
IPC分类号: C12M3/00 , C07K5/09 , C07K5/10 , C07K5/11 , C07K7/06 , C07K17/08 , C08F261/12 , C08G81/02 , C08L101/06 , C12M1/00 , C12N1/00 , C12N5/071
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.
-
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
发明人: ARAI, Yuuhei , KOBAYASHI, Daigo , ARAI, Yoshito
IPC分类号: C12M3/00 , C07K5/09 , C07K5/10 , C07K5/11 , C07K7/06 , C07K17/08 , C08F261/12 , C08G81/02 , C08L101/06 , C12M1/00 , C12N1/00 , C12N5/071
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-
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
发明人: ARAI, Yuuhei , KOBAYASHI, Daigo
IPC分类号: C12M3/00 , C07K5/09 , C07K5/10 , C07K5/11 , C07K7/06 , C07K17/08 , C08F261/12 , C08G81/02 , C08L101/06 , C12M1/00 , C12N1/00 , C12N5/071
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.
-
6.
公开(公告)号:EP4457331A1
公开(公告)日:2024-11-06
申请号:EP22838725.4
申请日:2022-12-14
-
-
公开(公告)号:EP3998073B1
公开(公告)日:2024-11-06
申请号:EP21213252.6
申请日:2016-12-02
-
9.
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.
-
公开(公告)号:EP4454672A1
公开(公告)日:2024-10-30
申请号:EP22910483.1
申请日:2022-09-15
申请人: Nitta Corporation
发明人: SHIGETA, Makoto , IKEDA, Takuji
IPC分类号: A61L101/20 , A61L2/28 , C12M1/00 , C12M1/12
摘要: This decontamination intensity sensor detects the degree of decontamination of microorganisms and/or viruses decontaminated with peracetic acid, the decontamination intensity sensor including an exposed part that is made of a metal that is corroded by the peracetic acid, and the metal is exposed.
-
-
-
-
-
-
-
-
-