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公开(公告)号:US20180371149A1
公开(公告)日:2018-12-27
申请号:US16024560
申请日:2018-06-29
申请人: Massachusetts Institute of Technology , The Brigham and Women's Hospital, Inc. , Biocant-Center of Innovation and Biotechnology
发明人: Robert S. Langer , Jeffrey M. Karp , Maria Jose Maio Nunes-Pereira , Ben Ouyang , Lino da Silva Ferreira , Debanjan Sarkar
摘要: Among other things, the present disclosure provides compositions and methods for an elastomeric cross-linked polyester material. Such an elastomeric cross-linked polyester material, in sonic embodiments, comprises a plurality of polymeric units of the general formula (-A-B-)p, wherein p is an integer greater than 1; and a plurality of urethane cross-links each of which covalently links two polymeric units to one another, which two linked polymeric unit each had at least one free hydroxyl or amino group prior to formation of the crosslink.
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公开(公告)号:US20210230343A1
公开(公告)日:2021-07-29
申请号:US17185528
申请日:2021-02-25
申请人: Massachusetts Institute of Technology , The Brigham and Women's Hospital, Inc. , Biocant-Center of Innovation and Biotechnology
发明人: Robert S. Langer , Jeffrey M. Karp , Maria Jose Maio Nunes-Pereira , Ben Ouyang , Lino da Silva Ferreira , Debanjan Sarkar
摘要: Among other things, the present disclosure provides compositions and methods for an elastomeric cross-linked polyester material. Such an elastomeric cross-linked polyester material, in some embodiments, comprises a plurality of polymeric units of the general formula (-A-B-)p, wherein p is an integer greater than 1; and a plurality of urethane cross-links each of which covalently links two polymeric units to one another, which two linked polymeric unit each had at least one free hydroxyl or amino group prior to formation of the crosslink.
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公开(公告)号:US11254781B2
公开(公告)日:2022-02-22
申请号:US17185528
申请日:2021-02-25
申请人: Massachusetts Institute of Technology , The Brigham and Women's Hospital, Inc. , Biocant-Center of Innovation and Biotechnology
发明人: Robert S. Langer , Jeffrey M. Karp , Maria Jose Maio Nunes-Pereira , Ben Ouyang , Lino da Silva Ferreira , Debanjan Sarkar
摘要: Among other things, the present disclosure provides compositions and methods for an elastomeric cross-linked polyester material. Such an elastomeric cross-linked polyester material, in some embodiments, comprises a plurality of polymeric units of the general formula (-A-B-)p, wherein p is an integer greater than 1; and a plurality of urethane cross-links each of which covalently links two polymeric units to one another, which two linked polymeric unit each had at least one free hydroxyl or amino group prior to formation of the crosslink.
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公开(公告)号:US10982038B2
公开(公告)日:2021-04-20
申请号:US16024560
申请日:2018-06-29
申请人: Massachusetts Institute of Technology , The Brigham and Women's Hospital, Inc. , Biocant-Center of Innovation and Biotechnology
发明人: Robert S. Langer , Jeffrey M. Karp , Maria Jose Maio Nunes-Pereira , Ben Ouyang , Lino da Silva Ferreira , Debanjan Sarkar
摘要: Among other things, the present disclosure provides compositions and methods for an elastomeric cross-linked polyester material. Such an elastomeric cross-linked polyester material, in some embodiments, comprises a plurality of polymeric units of the general formula (-A-B—)p, wherein p is an integer greater than 1; and a plurality of urethane cross-links each of which covalently links two polymeric units to one another, which two linked polymeric unit each had at least one free hydroxyl or amino group prior to formation of the crosslink.
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公开(公告)号:US20220213252A1
公开(公告)日:2022-07-07
申请号:US17573414
申请日:2022-01-11
申请人: Massachusetts Institute of Technology , The Brigham and Women's Hospital, Inc. , Biocant-Center of Innovation and Biotechnology
发明人: Robert S. Langer , Jeffrey M. Karp , Maria Jose Maio Nunes-Pereira , Ben Ouyang , Lino da Silva Ferreira , Debanjan Sarkar
摘要: Among other things, the present disclosure provides compositions and methods for an elastomeric cross-linked polyester material. Such an elastomeric cross-linked polyester material, in some embodiments, comprises a plurality of polymeric units of the general formula (-A-B-)p, wherein p is an integer greater than 1; and a plurality of urethane cross-links each of which covalently links two polymeric units to one another, which two linked polymeric unit each had at least one free hydroxyl or amino group prior to formation of the crosslink.
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公开(公告)号:US20230039421A1
公开(公告)日:2023-02-09
申请号:US17836972
申请日:2022-06-09
发明人: Andrew Bellinger , Shiyi Zhang , Carlo Giovanni Traverso , Robert S. Langer , Stacy Mo , Tyler Grant , Mousa Jafari , Dean Liang Glettig , Angela DiCiccio , Lowell L. Wood, JR. , Philip A. Eckhoff
IPC分类号: A61K9/00 , C08G18/73 , C08G63/08 , C08G18/42 , A61K47/58 , A61K47/69 , A61K9/48 , A61K31/357 , A61K31/65 , A61K31/7048 , C08G83/00 , A61K47/32 , C08L33/02 , C08L33/08 , C08L33/14 , A61K47/10 , A61K47/34 , A61K47/40 , A61K47/42 , A61M31/00
摘要: Residence structures, systems, and related methods are generally provided. Certain embodiments comprise administering (e.g., orally) a residence structure to a subject (e.g., a patient) such that the residence structure is retained at a location internal to the subject for a particular amount of time (e.g., at least about 24 hours) before being released. The residence structure may be, in some cases, a gastric residence structure. In some embodiments, the structures and systems described herein comprise one or more materials configured for high levels of active substances (e.g., a therapeutic agent) loading, high active substance and/or structure stability in acidic environments, mechanical flexibility and strength in an internal orifice (e.g., gastric cavity), easy passage through the GI tract until delivery to at a desired internal orifice (e.g., gastric cavity), and/or rapid dissolution/degradation in a physiological environment (e.g., intestinal environment) and/or in response to a chemical stimulant (e.g., ingestion of a solution that induces rapid dissolution/degradation). In certain embodiments, the structure has a modular design, combining a material configured for controlled release of therapeutic, diagnostic, and/or enhancement agents with a structural material necessary for gastric residence but configured for controlled and/or tunable degradation/dissolution to determine the time at which retention shape integrity is lost and the structure passes out of the gastric cavity. For example, in certain embodiments, the residence structure comprises a first elastic component, a second component configured to release an active substance (e.g., a therapeutic agent), and, optionally, a linker. In some such embodiments, the linker may be configured to degrade such that the residence structure breaks apart and is released from the location internally of the subject after a predetermined amount of time.
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公开(公告)号:US20220001159A1
公开(公告)日:2022-01-06
申请号:US17293968
申请日:2019-05-17
发明人: Robert S. Langer , Carlo Giovanni Traverso , Daniel Minahan , Alex G. Abramson , Ester Caffarel Salvador , Vance Soares
摘要: Actuating components and related methods are generally disclosed. Certain embodiments comprise an actuating component associated with a plurality of microneedles (e.g., for administering a therapeutic agent to a subject). In some embodiments, the actuating component may be administered to a subject such that the plurality of microneedles are deployed at a location internal to the subject (e.g., in the gastrointestinal tract). The actuating component may be contained within, in some embodiments, a capsule (e.g., for oral administration to a subject). In some embodiments, the actuating component has a pre-deployment configuration in which the plurality of microneedles have a first orientation and a deployed configuration in which the plurality of microneedles have a second orientation, different than the first orientation.
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公开(公告)号:US11207272B2
公开(公告)日:2021-12-28
申请号:US16614299
申请日:2018-05-17
发明人: Carlo Giovanni Traverso , Alex G. Abramson , Ester Caffarel Salvador , Niclas Roxhed , Minsoo Khang , Taylor Bensel , David Dellal , Robert S. Langer
IPC分类号: A61K9/48 , A61J3/07 , A61K9/00 , A61B5/145 , A61B10/02 , A61M5/142 , A61M37/00 , A61N1/32 , A61N1/36 , A61M5/20 , A61M5/32 , A61M31/00 , A61K38/28 , A61M5/158 , A61N1/05
摘要: Self-righting articles, such as self-righting capsules for administration to a subject, are generally provided. In some embodiments, the self-righting article may be configured such that the article may orient itself relative to a surface (e.g., a surface of a tissue of a subject). The self-righting articles described herein may comprise one or more tissue engaging surfaces configured to engage (e.g., interface with, inject into, anchor) with a surface (e.g., a surface of a tissue of a subject). In some embodiments, the self-righting article may have a particular shape and/or distribution of density (or mass) which, for example, enables the self-righting behavior of the article. In some embodiments, the self-righting article may comprise a tissue interfacing component and/or a pharmaceutical agent (e.g., for delivery of the active pharmaceutical agent to a location internal of the subject). In some cases, upon contact of the tissue with the tissue engaging surface of the article, the self-righting article may be configured to release one or more tissue interfacing components. In some cases, the tissue interfacing component is associated with a self-actuating component. For example, the self-righting article may comprise a self-actuating component configured, upon exposure to a fluid, to release the tissue interfacing component from the self-righting article. In some cases, the tissue interfacing component may comprise and/or be associated with the pharmaceutical agent (e.g., for delivery to a location internal to a subject).
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公开(公告)号:US20210353174A1
公开(公告)日:2021-11-18
申请号:US17318040
申请日:2021-05-12
申请人: Massachusetts Institute of Technology , The Brigham and Women's Hospital, Inc. , The General Hospital Corporation
发明人: Robert S. Langer , Carlo Giovanni Traverso , Malvika Verma , Feyisope Eweje , Christoph Winfried Johannes Steiger , Junwei Li , Nhi Phan , Hen-Wei Huang , Jacqueline Chu , John Ashraf Fou Salama
摘要: Drug delivery articles, resident articles, and retrieval systems e.g., for gram-level dosing, are generally provided. In some embodiments, the residence articles are configured for transesophageal administration, transesophageal retrieval, and/or gastric retention to/in a subject. In certain embodiments, the residence article includes dimensions configured for transesophageal administration with a gastric resident system. In some cases, the residence article may be configured to control drug release e.g., with zero-order drug kinetics with no potential for burst release for weeks to months. In some embodiments, the residence articles described herein comprise biocompatible materials and/or are safe for gastric retention. In certain embodiments, the residence article includes dimensions configured for transesophageal retrieval. In some cases, the residence articles described herein may comprise relatively large doses of drug (e.g., greater than or equal to 1 gram).
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公开(公告)号:US20210046011A1
公开(公告)日:2021-02-18
申请号:US16991536
申请日:2020-08-12
发明人: Carlo Giovanni Traverso , Joshua Korzenik , Robert S. Langer , Christoph Winfried Johannes Steiger
摘要: Articles and methods for delivering a therapeutic agent to a subject are described. These articles and methods may be useful, in some cases, for the delivery of therapeutic agents to the colon of a subject. In some embodiments, an article is configured to release a secretion inducing agent e.g., to stimulate the release of intestinal fluids. The article, in some embodiments, comprises a therapeutic agent such that the stimulated release of intestinal fluid increases the amount of therapeutic agent available for absorption by the colon. For example, in some embodiments, the articles and methods described herein advantageously promote increased absorption of therapeutic agents in subjects as compared to traditionally administered therapeutic agents without additional components such as a secretion inducing agent. In some embodiments, articles and methods described herein may increase the motility of the colon of a subject. The increase in contractions and movement of fluidic in the colon caused by increase motility may advantageously facilitate the dissolution or absorption of the therapeutic agent.
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