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公开(公告)号:US11701437B2
公开(公告)日:2023-07-18
申请号:US16612648
申请日:2018-05-14
Applicant: President and Fellows of Harvard College , Massachusetts Institute of Technology , The Brigham and Women's Hospital, Inc. , The General Hospital Corporation
Inventor: Denitsa M. Milanova , George M. Church , Noah Davidsohn , Carl Schoellhammer , Robert S. Langer , Anna I. Mandinova , Carlo Giovanni Traverso
CPC classification number: A61K48/0075 , A61K47/6901 , A61N7/00 , C12N15/86 , A61K9/7023 , C12N2750/14143 , C12N2750/14145 , C12N2750/14151 , C12N2810/859
Abstract: A method for the systemic delivery of a polypeptide within a subject is provided by creating genetically modified skin cells via topical introduction of a genetically engineered virus which delivers a nucleic acid encoding a therapeutic polypeptide for expression by the skin cells, wherein the expressed therapeutic polypeptide is secreted by the skin cells and is introduced into the circulatory system of the subject.
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公开(公告)号:US11672864B2
公开(公告)日:2023-06-13
申请号:US16895638
申请日:2020-06-08
Inventor: Jeffrey M. Karp , Praveen Kumar Vemula , Nathaniel R. Campbell , Abdullah M. Syed , Sufeng Zhang , Omid C. Farokhzad , Robert S. Langer
IPC: A61K47/22 , A61K9/00 , A61K9/06 , A61K9/107 , A61K31/166 , A61K31/405 , A61K31/4188 , A61K31/4745 , A61K31/58 , A61K31/573 , A61K47/26 , A61K47/28 , A61K47/14 , A61K31/713 , A61K38/28
CPC classification number: A61K47/22 , A61K9/0019 , A61K9/06 , A61K9/1075 , A61K31/166 , A61K31/405 , A61K31/4188 , A61K31/4745 , A61K31/573 , A61K31/58 , A61K31/713 , A61K38/28 , A61K47/14 , A61K47/26 , A61K47/28
Abstract: Self-assembled gel compositions including a gelator, e.g., an enzyme-cleavable gelator, e.g., having a molecular weight of 2500 or less, are described. The self-assembled gel compositions can encapsulate one or more agents. Methods of making the self-assembled gel compositions, and methods of drug delivery using the self-assembled gel compositions are also described.
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公开(公告)号:US20230072606A1
公开(公告)日:2023-03-09
申请号:US17903586
申请日:2022-09-06
Applicant: Massachusetts Institute of Technology
Inventor: Robert S. Langer , Ana Jaklenec , Joseph Collins , Morteza Sarmadi , Aurelien vander Straeten , Maria Kanelli , John Daristotle
Abstract: Disclosed are compositions that stabilize (e.g., thermo-stabilize) biological agents, such as mRNA. Also disclosed are methods of administering and using said compositions.
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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
Inventor: 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: 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
Abstract: 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:US11491228B2
公开(公告)日:2022-11-08
申请号:US16502551
申请日:2019-07-03
Applicant: Massachusetts Institute of Technology
Inventor: Robert S. Langer , Owen Shea Fenton , Jason Andresen , Marion Paolini
Abstract: Provided herein are polymers of Formula (I), and pharmaceutically acceptable salts, co-crystals, tautomers, stereoisomers, and isotopically labeled derivatives thereof, compositions, and formulations thereof. The polymers described herein are biocompatible, non-toxic, water compatible, and operationally simple to formulate. Also provided are methods and kits involving the polymers described herein (e.g., methods of using polymers described herein for delivering agents (e.g., for therapeutic, diagnostic, prophylactic, imaging, ophthalmic, intraoperative, or cosmetic use) to a subject, cell, tissue, or biological sample, as part of materials (e.g., biodegradable materials, biocompatible materials, wound dressing (e.g., bandages), drug depots, coatings), or as scaffolds for tissue engineering. Provided are methods for synthesizing the polymers described herein, and polymers described herein synthesized by the synthetic methods described herein.
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公开(公告)号:US11414393B2
公开(公告)日:2022-08-16
申请号:US17070486
申请日:2020-10-14
Applicant: Massachusetts Institute of Technology
Inventor: Kerry Peter Mahon , Kevin Thomas Love , Christopher G. Levins , Kathryn Ann Whitehead , Robert S. Langer , Daniel Griffith Anderson
IPC: C07D295/13 , A61K9/127 , A61K9/51 , A61K47/16 , A61K48/00 , C07C215/14 , C12N15/11 , C12N15/88 , A61K47/54 , C07C217/08 , A61K31/7088 , A61K38/02 , A61K9/107 , C12N15/113
Abstract: Aminoalcohol lipidoids are prepared by reacting an amine with an epoxide-terminated compound are described. Methods of preparing aminoalcohol lipidoids from commercially available starting materials are also provided. Aminoalcohol lipidoids may be prepared from racemic or stereochemically pure epoxides. Aminoalcohol lipidoids or salts forms thereof are preferably biodegradable and biocompatible and may be used in a variety of drug delivery systems. Given the amino moiety of these aminoalcohol lipidoid compounds, they are particularly suited for the delivery of polynucleotides. Complexes, micelles, liposomes or particles containing the inventive lipidoids and polynucleotide have been prepared. The inventive lipidoids may also be used in preparing microparticles for drug delivery. They are particularly useful in delivering labile agents given their ability to buffer the pH of their surroundings.
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公开(公告)号:US11318231B2
公开(公告)日:2022-05-03
申请号:US16182307
申请日:2018-11-06
Inventor: Omid Veiseh , Robert S. Langer , Daniel G. Anderson , William Shain , Brian W. Hanak , Samuel R. Browd , Robert F. Hevner
IPC: A61K31/192 , A61L29/08 , A61L29/16 , G01N33/68 , A61L31/06 , A61L27/34 , A61L29/06 , A61L31/10 , A61L31/16 , A61L27/18 , A61L27/54 , A61M27/00
Abstract: Neurological implants whose surfaces have been chemically and covalently modified to impart beneficial properties to the neurological implants are described. The neurological implants possess improved biocompatibility compared to a corresponding neurological implant that lacks the chemical modification. Following implantation in a subject, the surface-modified neurological implants induce a lower-foreign body response, compared to a corresponding unmodified product.
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公开(公告)号:US20220080115A1
公开(公告)日:2022-03-17
申请号:US16614229
申请日:2018-05-17
Inventor: Carlo Giovanni Traverso , Alex G. Abramson , Ester Caffarel Salvador , Niclas Roxhed , Minsoo Khang , Taylor Bensel , Robert S. Langer
Abstract: 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:US11266606B2
公开(公告)日:2022-03-08
申请号:US16584170
申请日:2019-09-26
Inventor: Arturo J. Vegas , Joshua C. Doloff , Omid Veiseh , Minglin Ma , Robert S. Langer , Daniel G. Anderson
IPC: A61K35/39 , A61K9/00 , A61K9/50 , A61L29/08 , A61L31/10 , C08B37/00 , C12N5/00 , C12N5/071 , A61L33/08
Abstract: Covalently modified alginate polymers, possessing enhanced biocompatibility and tailored physiochemical properties, as well as methods of making and use thereof, are disclosed herein. The covalently modified alginates are useful as a matrix for coating of any material where reduced fibrosis is desired, such as encapsulated cells for transplantation and medical devices implanted or used in the body.
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公开(公告)号:US20220064584A1
公开(公告)日:2022-03-03
申请号:US17394125
申请日:2021-08-04
Inventor: Armon R. Sharei , Shirley Mao , George Hartoularos , Sophia Liu , Megan Heimann , Pamela Basto , Gregory Szeto , Siddharth Jhunjhunwala , Darrell J. Irvine , Robert S. Langer , Klavs F. Jensen , Ulrich H. Von Andrian
IPC: C12M1/42 , C12N15/87 , A61K39/00 , A61K45/06 , A61K49/00 , C12M3/06 , C12N5/0781 , C12N5/0783 , C12N5/0784 , G01N33/50
Abstract: A method and device for preferentially delivering a compound such as an antigen to the cytosol of an immune cell. The method comprises passing a cell suspension comprising the target immune cell through a microfluidic device and contacting the suspension with the compound(s) or payload to be delivered.
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