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公开(公告)号:US20240342125A1
公开(公告)日:2024-10-17
申请号:US18683376
申请日:2022-09-21
Applicant: HISAMITSU PHARMACEUTICAL CO., INC.
Inventor: Naoko FUJITA , Nao IWAMOTO , Kazuyuki HIROSE , Naoyuki UCHIDA
IPC: A61K31/196 , A61K9/70
CPC classification number: A61K31/196 , A61K9/7061 , A61K9/7069
Abstract: A method for inhibiting the generation of diclofenac indolinones in an adhesive patch is provided. This adhesive patch comprises a support body layer and an adhesive layer that is layered on the support body layer. The aforementioned method includes a step for mixing a diclofenac free acid and an adhesive base to acquire an adhesive composition, and a step for shaping the adhesive composition to obtain an adhesive patch. The content of the diclofenac free acid is 0.5-8 mass % on the basis of the total mass of the adhesive layer.
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公开(公告)号:US20230414530A1
公开(公告)日:2023-12-28
申请号:US18035951
申请日:2021-11-08
Applicant: HISAMITSU PHARMACEUTICAL CO., INC.
Inventor: Yuka TAKAGI , Nao IWAMOTO
IPC: A61K9/70 , A61K47/18 , A61K31/407
CPC classification number: A61K9/7046 , A61K47/18 , A61K31/407
Abstract: Disclosed is a method for inhibiting degradation of asenapine or a pharmaceutically acceptable salt thereof in a patch. The patch comprises an adhesive layer on a base, and the adhesive layer contains an adhesive base and asenapine or a pharmaceutically acceptable salt thereof. The method includes incorporating at least one amine compound selected from the group consisting of monoethanolamine, diethanolamine, diisopropanolamine, isopropanolamine, triethanolamine and meglumine in the adhesive layer.
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公开(公告)号:US20230310340A1
公开(公告)日:2023-10-05
申请号:US18036203
申请日:2021-11-08
Applicant: HISAMITSU PHARMACEUTICAL CO., INC.
Inventor: Yuka TAKAGI , Nao IWAMOTO
IPC: A61K9/70 , A61K31/407 , A61K47/18
CPC classification number: A61K9/7069 , A61K31/407 , A61K47/183
Abstract: Disclosed is a patch in which degradation of asenapine or a pharmaceutically acceptable salt thereof is inhibited. The patch comprises an adhesive layer on a base, wherein the adhesive layer contains an adhesive base, asenapine or a pharmaceutically acceptable salt thereof, and at least one basic amino acid selected from the group consisting of lysine, arginine and histidine, or a pharmaceutically acceptable salt of said basic amino acid.
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