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公开(公告)号:US11623960B2
公开(公告)日:2023-04-11
申请号:US16982361
申请日:2019-03-20
发明人: Neng-yao Shih , Ko-jiunn Liu , Li-tzong Chen , Wen-chun Hung , Yun-chang Chen , Kuan-chung Hsiao , San-tai Shen
IPC分类号: A61K39/395 , C07K16/28 , A61P35/00 , A61K39/00
摘要: An isolated antibody, comprising heavy chain complementary determining regions CDR1, CDR2, and CDR3 from a heavy chain variable region sequence having SEQ ID NO: 1 or 3; light chain complementary determining regions CDR1, CDR2, and CDR3 from a light chain variable region sequence having SEQ ID NO: 2 or 4; wherein the antibody binds specifically to both vascular endothelial growth factor receptor-2 (VEGFR2) and vascular endothelial growth factor receptor-3 (VEGFR3).
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公开(公告)号:US20230100367A1
公开(公告)日:2023-03-30
申请号:US17894333
申请日:2022-08-24
申请人: National Yang Ming Chiao Tung University , National Health Research Institutes , Chang Gung Medical Foundation, Chang Gung Memorial Hospital, Linkou
发明人: Ting-Fen Tsai , Jinq-Chyi Lee , Hui-Yi Shiao , Chi-Hsiao Yeh
IPC分类号: C07D333/36 , C07D417/12 , A61P9/00
摘要: A method of treating a Cisd2 insufficiency-associated disorder. The method includes administering to a subject in need a compound of formula (I). Also disclosed is a method of increasing Cisd2 gene expression.
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公开(公告)号:US20230031385A1
公开(公告)日:2023-02-02
申请号:US17380474
申请日:2021-07-20
发明人: Feng-Huei LIN , Yu-Chun CHEN , Wen-Yu SU , Yen-Hsien LEE , Ko-Hua CHEN
摘要: A corneal storage composition is disclosed. The composition comprises a buffered, balanced, nutrient and electrolyte aqueous solution; γ-PGA; and ferulic acid, in amounts effective to maintain cell integrity and viability of the corneal tissue for a period of greater than 14 days.
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公开(公告)号:US20220267301A1
公开(公告)日:2022-08-25
申请号:US17736924
申请日:2022-05-04
申请人: Yufeng Jane TSENG , NATIONAL TAIWAN UNIVERSITY , NATIONAL YANG MING CHIAO TUNG UNIVERSITY , NATIONAL HEALTH RESEARCH INSTITUTES
发明人: Yufeng Jane TSENG , Yu-Li LIU , Chung-Ming SUN , Wen-Sung LAI , Chih-Min LIU , Hai-Gwo HWU
IPC分类号: C07D401/12 , A61P25/18 , C07D401/14 , C07D405/14 , C07D409/14 , C07D413/14
摘要: The present invention provides novel substituted benzimidazole derivatives used as DAAO inhibitors and for treatment and/or prevention of neurological disorders.
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公开(公告)号:US11384326B2
公开(公告)日:2022-07-12
申请号:US15777501
申请日:2016-11-18
摘要: A target particle transferring device is disclosed, which comprises: (a) a substrate with a thickness of T and a width of W, having top and bottom portions, the top portion having a top surface and the bottom portion having a bottom surface; (b) a notch structure formed in the bottom portion of the substrate, comprising: a groove with a width of W1, located at a distance oft below the top surface of the substrate, wherein the groove is formed in the bottom portion from the bottom surface extending toward the top portion; and (c) a target substrate portion with a width of W2 and a thickness of T, located in the top and bottom portions of the substrate and being surrounded by the groove. Methods of transferring a target particle from one device to another is also disclosed.
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公开(公告)号:US20220152090A1
公开(公告)日:2022-05-19
申请号:US17454748
申请日:2021-11-12
发明人: Shu-Yi LIN , Jyh-Lyh JUANG , Jinq-Chyi LEE
IPC分类号: A61K31/739 , C07H13/06 , A61K31/7024 , A61P25/28
摘要: The present disclosure relates to a method for treating or preventing or delaying the onset or progression of an amyloidogenic disease in a subject in need, comprising administering a pharmaceutical composition comprising a therapeutically effective amount of amphiphilic liposaccharide to the subject. The present disclosure also relates to a method for selecting an agent for treating or preventing or delaying the onset or progression of an amyloidogenic disease and a novel liposaccharide.
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公开(公告)号:US20220152036A1
公开(公告)日:2022-05-19
申请号:US17439630
申请日:2020-03-25
IPC分类号: A61K31/52 , A61P7/06 , C07D473/16 , C07D473/18 , A61K31/5377
摘要: Provided herein are compounds of Formula (I). The compounds described herein are useful in treating a disease associated with the expression of endogenous embryonic/fetal globin (e.g., γ globin) in erythrocytes (e.g., treating β-thalassemia and/or sickle cell disease through at least the induction of the globin gene expression in erythrocytes), and/or anemia (β-thalassemia and/or sickle cell anemia). The compounds described herein are useful in treating, delaying, and/or preventing the adverse effects of β-thalassemia and/or sickle cell disease, inducing γ globin production, and/or inducing the expression of embryonic/fetal globin genes in a subject, cell, tissue, or biological sample. Also provided in the present disclosure are pharmaceutical compositions, kits, and methods of using the compounds for inducing γ globin production described herein and for treating any of the target diseases described herein.
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公开(公告)号:US20220143595A1
公开(公告)日:2022-05-12
申请号:US17523542
申请日:2021-11-10
发明人: Chia-Hsien HSU , Chuan-Feng YEH
摘要: This invention provides a high-efficient single-cell collection method using a specially designed collection well and collection pipet tip for particle/cell collection from the collection well. The structures of the collection well and pipet tip eliminate fluidic dead volume in the collection, resulting in all (or most) of the particles/cells can be brought into the collection pipette tip with the flow. The advantages of this invention in cell manipulation include high cell collection efficiency, low cell damage and easy operation procedure.
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公开(公告)号:US11160862B2
公开(公告)日:2021-11-02
申请号:US16172207
申请日:2018-10-26
摘要: The invention provides a nanoemulsion adjuvant and a preparation method thereof, which are composed of the following components: a continuous aqueous phase containing H2O molecules, an oil phase material containing fats and oils, and an emulsion system for stabilizing the interface between the continuous aqueous phase and the oil phase, and the emulsion system is an emulsifier mixture. The adjuvant is characterized in that the emulsion system does not contain an ionic emulsifier and the particle size of the emulsion is between 20 and 200 nanometers. The use of the nanoemulsion adjuvant can prevent toxicity and possible harm of ionic emulsifiers to human cells, and provide a vaccine preparation capable of eliciting a high degree of immune response.
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10.
公开(公告)号:US20210077526A1
公开(公告)日:2021-03-18
申请号:US17041653
申请日:2018-03-27
发明人: Shu Yi LIN
IPC分类号: A61K33/242 , C09D179/02
摘要: A sub-nanometer gold sticker for blocking efficiently endotoxin activity to protect against sepsis is disclosed. The sub-nanometer gold sticker comprises a gold nanocluster that serves as a flake-like substrate and a coating of short alkyl motifs that act as an adhesive, allowing the sub-nanometer gold sticker to dock with LPS by compacting the intramolecular hydrocarbon chain-chain distance (d-spacing) of lipid A, an endotoxicity active site that can cause overwhelming cytokine induction resulting in sepsis progression. Methods of blocking endotoxin activity, and suppressing pro-inflammatory cytokines are also disclosed. Also disclosed is a method of protecting against endotoxin-induced sepsis via increasing critical micelle concentration for the inhibition of LPS non-lamellar aggregation.
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