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公开(公告)号:US20190017046A1
公开(公告)日:2019-01-17
申请号:US16144475
申请日:2018-09-27
Applicant: FUJIFILM Corporation
Inventor: Hayato MIYOSHI , Toshihide YOSHITANI , Tadanori YAMADA
IPC: C12N15/11 , A61K47/42 , A61K47/64 , C08J3/24 , C07K14/435
Abstract: Objects of the present invention are to provide a preparation, which satisfies both a sufficient drug carrying amount and a preferred decomposition rate, and a method for manufacturing the preparation and to provide a member for a preparation used in the preparation of the present invention described above and a method for manufacturing the member. According to the present invention, there are provided a preparation containing a crosslinked substance of an anionic polypeptide and a cationic, polypeptide and a cationic drug; a method for manufacturing the preparation including a freezing step, a drying step, a crosslinking step, and a drug adding step; a member for a preparation formed of a crosslinked substance of an anionic polypeptide and a cationic polypeptide; and a method for manufacturing the member for a preparation.
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公开(公告)号:US20210227802A1
公开(公告)日:2021-07-29
申请号:US17225127
申请日:2021-04-08
Applicant: FUJIFILM CORPORATION
Inventor: Yutaka MAENO , Kazutaka CHIBANA , Hidehiro MOCHIZUKI , Tadanori YAMADA
IPC: A01K61/54
Abstract: There are provided a pearl culture material containing at least one selected from the group consisting of a pearl nucleus and a mantle, and the at least one selected from the group consisting of a pearl nucleus and a mantle contains a protein having 10 EU/g or less of an endotoxin amount, a nucleus insertion method, and a pearl culture material composition.
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公开(公告)号:US20220228112A1
公开(公告)日:2022-07-21
申请号:US17707215
申请日:2022-03-29
Applicant: FUJIFILM Corporation
Inventor: Yusuke MORI , Tadanori YAMADA
IPC: C12N5/071
Abstract: An object of the present invention is to provide a medium with which hepatocytes can be cultured while a metabolic function thereof is maintained, a method of producing a hepatocyte using the above medium, and the hepatocyte that is obtained by the above method. According to the present invention, there is provided a medium for culturing a hepatocyte, containing one or more of a ROCK inhibitor, nicotinamide, and an analogous substance of the nicotinamide, in which a content of a serum component is less than 5% by volume, a content of an EGF receptor activating factor is less than 1 ng/mL, and a content of an ALK inhibitor is less than 0.1 μmol/L.
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公开(公告)号:US20200296940A1
公开(公告)日:2020-09-24
申请号:US16862590
申请日:2020-04-30
Applicant: FUJIFILM CORPORATION
Inventor: Akihito AMAO , Kazutaka CHIBANA , Hidehiro MOCHIZUKI , Tadanori YAMADA
IPC: A01K61/57 , C09D189/00 , C07K14/78 , A01K61/56
Abstract: Provided are a pearl culture material in which at least one selected from the group consisting of a pearl nucleus and a mantle piece is coated with a protein containing a repeating sequence of GXY triplets which may be separated by one or more amino acids, and one or more RGD motifs, and having a polydispersity of less than 20; and a coating composition including the protein.
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公开(公告)号:US20200071651A1
公开(公告)日:2020-03-05
申请号:US16674613
申请日:2019-11-05
Applicant: FUJIFILM Corporation
Inventor: Toshiki TAKEI , Tadanori YAMADA , Ryuta TAKEGAMI , Kuniyuki KAMINAGA
Abstract: An object of the present invention is to provide a separation substrate having a high megakaryocyte blocking rate and a high platelet permeation rate, and a cell separation filter and a method for producing a platelet which use the same. The separation substrate of the present invention is a separation substrate including a porous membrane for separating a platelet from a cell suspension containing a megakaryocyte and the platelet, in which an average pore diameter of the separation substrate is 2.0 μm to 12.0 μm, and the separation substrate is formed of at least one resin selected from the group consisting of a polysulfone resin and a polyvinylidene fluoride resin.
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6.
公开(公告)号:US20200002675A1
公开(公告)日:2020-01-02
申请号:US16570626
申请日:2019-09-13
Applicant: FUJIFILM Corporation
Inventor: Toshiki TAKEI , Tadanori YAMADA
Abstract: An object of the present invention is to provide a method for efficiently separating megakaryocytes and platelets produced from the megakaryocytes, and an instrument for efficiently separating megakaryocytes and platelets produced from the megakaryocytes. According to the present invention, a method for separating megakaryocytes and platelets, including a contact step of bringing a culture solution that contains at least megakaryocytes into contact with a substrate coated with a biocompatible polymer that adheres to the megakaryocytes via at least one of a VLA-4 integrin or a VLA-5 integrin; a culture step of culturing the megakaryocytes to produce platelets before and/or after the contact step; and a recovery step of recovering the culture solution after the contact step and the culture step is provided.
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