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公开(公告)号:US10752673B2
公开(公告)日:2020-08-25
申请号:US15619835
申请日:2017-06-12
Applicant: Academia Sinica
Inventor: An-Suei Yang , Hong-Sen Chen , Chung-Ming Yu , Shin-Chen Hou , Wei-Ying Kuo , Yi-Kai Chiu , Yueh-Liang Tsou , Hung-Ju Hsu , Hwei-Jiung Wang , Shih-Hsien Chuang , Chao-Pin Lee
Abstract: Disclosed herein are methods for high-throughput screening of a functional antibody fragment for an immunoconjugate that targets a protein antigen. The method combines a phage-displayed synthetic antibody library and high-throughput cytotoxicity screening of non-covalently assembled immunotoxins or cytotoxic drug to identify highly functional synthetic antibody fragments for delivering toxin payloads.
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822.
公开(公告)号:US10752657B2
公开(公告)日:2020-08-25
申请号:US16258115
申请日:2019-01-25
Applicant: Academia Sinica
Inventor: Chiaho Shih , Heng-Li Chen , Pei-Yi Su
IPC: C07K14/005 , A61K39/12 , A61K39/29 , C12N7/00 , A61K38/00
Abstract: A pharmaceutical composition comprising: (a) an isolated peptide, wherein the peptide includes three or four arginine-rich domains (ARDs) from the carboxy-terminal region of hepatitis B virus core protein (HBc) and exhibits an anti-microbial activity; and (b) a pharmaceutically acceptable carrier.
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公开(公告)号:US20200161110A1
公开(公告)日:2020-05-21
申请号:US16686203
申请日:2019-11-17
Applicant: Academia Sinica
Inventor: Abdil OZDEMIR , Jung-Lee LIN , Chung-Hsuan CHEN
Abstract: Disclosed herein is a device for characterizing a biological sample or an airborne sample. According to embodiments of the present disclosure, the device comprises an electrospray source, a mass analyzer, a charge detector, and optionally, an ion guide. The present device is useful in analyzing the particle population in the biological or airborne sample based on the mass to charge (m/z) ratio and the charge (z) of each particle. Also disclosed herein are the methods of making a diagnosis of cancer by use of the present device, and methods of determining the mass distribution of particles in an airborne sample.
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公开(公告)号:US10584341B2
公开(公告)日:2020-03-10
申请号:US15755958
申请日:2016-08-31
Applicant: Academia Sinica , National Taiwan University
Inventor: Pan-Chyr Yang , Wei-Yun Lai , Bo-Tsang Huang
IPC: C12N15/11 , C12N15/115 , A61K31/711 , A61P35/00
Abstract: Aptamers that bind to and antagonize PDL1 and uses thereof in enhancing immune activity (e.g., promoting T cell proliferation), treating cancer, and/or infectious diseases such as infections caused by enterovirus, HBV, or HCV infection.
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825.
公开(公告)号:US10584120B1
公开(公告)日:2020-03-10
申请号:US16552554
申请日:2019-08-27
Applicant: National Health Research Institutes , Academia Sinica
Inventor: Chih-Hao Chen , Chuan Shih , Chiung-Tong Chen , Hwei-Jiung Wang , Kai-Fa Huang
IPC: C07D417/14 , C07D403/14 , C07D413/14 , A61P25/28 , C07D409/14 , A61K45/06
Abstract: Benzimidazole compounds of formula (I), shown below, are disclosed. The compounds are potent human glutaminyl cyclase inhibitors. Also disclosed is a pharmaceutical composition containing one of these compounds and a pharmaceutical acceptable carrier, as well as a method of treating Alzheimer's disease or Huntington's disease by administering to a subject in need thereof an effective amount of such a compound.
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公开(公告)号:US10568897B2
公开(公告)日:2020-02-25
申请号:US15589963
申请日:2017-05-08
Applicant: ACADEMIA SINICA
Inventor: Wen-Chin Yang , Lee-Tian Chang
IPC: A61K36/00 , A61K31/7028 , A23K20/163 , A23K20/10 , A23K50/75 , A61K36/28 , A23K10/30 , A23K50/70 , A23K20/00 , A23K50/80 , A23K20/195
Abstract: A composition for use in prevention, inhibition and/or treatment of coccidiosis in an animal is disclosed. The composition comprises an effective amount of Bidens pilosa, an active constituent thereof, or an active compound isolated therefrom. In another aspect, a composition for use in enhancing growth in an animal is disclosed. The composition comprising an animal feed and an effective amount of Bidens pilosa, or an isolated active constituent comprising a polyacetylenic compound.
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公开(公告)号:US10533179B2
公开(公告)日:2020-01-14
申请号:US15500345
申请日:2015-07-31
Applicant: Academia Sinica , National Taiwan University , Taipei Medical University
Inventor: Konan Peck , Pan-Chyr Yang , Yi-Chung Chang , Bo-Tsang Huang , Shauh-Der Yeh
IPC: C12N15/115 , C12N15/113 , A61K31/711 , A61K9/00 , A61K31/713 , A61K47/60
Abstract: Aptamers that bind to and inhibit CTLA-4 and uses thereof in enhancing immune activities, and treating cancer and HIV infection are provided.
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公开(公告)号:US10533034B2
公开(公告)日:2020-01-14
申请号:US15866378
申请日:2018-01-09
Applicant: ACADEMIA SINICA
Inventor: Chi-Huey Wong , Alice L. Yu , Kun-Hsien Lin , Tai-Na Wu
Abstract: Glycosphingolipids (GSLs) compositions and methods for iNKT-independent induction of chemokines are disclosed.
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公开(公告)号:US10532097B2
公开(公告)日:2020-01-14
申请号:US15325346
申请日:2015-07-10
Applicant: Academia Sinica
Inventor: Patrick C. H. Hsieh , Pei-Jung Wu , Steve Roffler , Bill Cheng
IPC: A61K39/395 , C07K16/44 , A61K9/00 , A61K47/36 , A61K47/42 , A61K9/06 , A61K47/60 , A61K47/68 , A61K38/00
Abstract: Disclosed herein is a multiple drugs delivery system and its uses in treating diseases. The multiple drugs delivery system includes, an anti-PEG antibody for directing the PEGylated therapeutic to the treatment site; and a hydrogel for retaining the anti-PEG antibody and/or the PEGylated therapeutic at the treatment site for at least 3 days. The hydrogel is selected from the group consisting of hyaluronan (HA) or a derivative of HA, collagen, gelatin, fibronectin, fibrinogen, alginate, chitosan, and a synthetic biocompatible polymer. The anti-PEG antibody and the hydrogel are present in the mixture in a ratio from about 1:1 (v/v) to 1:100 (v/v). At least two dosages of the PEGylated therapeutic, which may be the same or different, are administered to the subject, with each dosage being given at about 1 hour to about 1 week apart. Accordingly, a novel method of treating a subject having cancer or ischemic disease is also provided.
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公开(公告)号:US20200000722A1
公开(公告)日:2020-01-02
申请号:US16455800
申请日:2019-06-28
Applicant: Academia Sinica
Inventor: Hsien-Ming LEE , Hua-De GAO , Jia-Lin HONG , Chih-Yu KUO , Cheng-Bang JIAN
Abstract: Disclosed herein are novel synthetic polypeptides and uses thereof in the preparation of liposomes. According to embodiments of the present disclosure, the synthetic polypeptide comprises a membrane lytic motif, a masking motif, and a linker configured to link the membrane lytic motif and the masking motif. The linker is cleavable by a stimulus, such as, light, protease, or phosphatase. Once being coupled to a liposome, the exposure to the stimulus cleaves the linker that results in the separation of the masking motif from the membrane lytic motif, which in turn exerts membrane lytic activity on the liposome that leads to the collapse of the intact structure of the liposome, and releases the agent encapsulated in the liposome to the target site. Also disclosed herein are methods of diagnosing or treating a disease in a subject by use of the present liposomes.
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