CA2401385C - Materiaux de matrice proteique, dispositifs correspondants et procedes pour leur production et leur utilisation - Google Patents
Materiaux de matrice proteique, dispositifs correspondants et procedes pour leur production et leur utilisation Download PDFInfo
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- CA2401385C CA2401385C CA2401385A CA2401385A CA2401385C CA 2401385 C CA2401385 C CA 2401385C CA 2401385 A CA2401385 A CA 2401385A CA 2401385 A CA2401385 A CA 2401385A CA 2401385 C CA2401385 C CA 2401385C
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
- A61P5/46—Drugs for disorders of the endocrine system of the suprarenal hormones for decreasing, blocking or antagonising the activity of glucocorticosteroids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0002—Galenical forms characterised by the drug release technique; Application systems commanded by energy
- A61K9/0009—Galenical forms characterised by the drug release technique; Application systems commanded by energy involving or responsive to electricity, magnetism or acoustic waves; Galenical aspects of sonophoresis, iontophoresis, electroporation or electroosmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
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- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- Epidemiology (AREA)
- Neurosurgery (AREA)
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- Neurology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Addiction (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Psychiatry (AREA)
- Reproductive Health (AREA)
- Anesthesiology (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Gynecology & Obstetrics (AREA)
- Obesity (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Plastic & Reconstructive Surgery (AREA)
Abstract
L'invention concerne des matériaux de matrice protéique, des dispositifs correspondants, ainsi que des procédés pour leur production et leur utilisation. Elle concerne plus particulièrement des matériaux de matrice protéique et des dispositifs correspondants pouvant être utilisés pour diverses applications médicales comprenant, de manière non exhaustive, des dispositifs d'administration de médicaments pour la libération contrôlée de principes actifs pharmacologiques, des dispositifs de type stents encapsulés ou enrobés, des vaisseaux, des greffes tubulaires, des greffes vasculaires, des dispositifs de cicatrisation comprenant le matériau de suture et des maillages à base de matrice protéique, des greffes de peau/d'os/de tissus, des matrices électroconductrices biocompatibles, des matrices de protéines transparentes, des barrières servant à empêcher l'adhérence de la matrice protéique, des squelettes cellulaires et autres dispositifs à matrices protéiques biocompatibles. L'invention concerne en outre des matériaux de matrice protéique et des dispositifs correspondants obtenus par formation d'un film comprenant un ou plusieurs matériaux de matrice protéique biodégradables, un ou plusieurs solvants biodégradables et éventuellement un ou plusieurs principes actifs pharmacologiques. Ce film est ensuite partiellement séché, enroulé ou façonné d'une autre manière, puis comprimé pour former le dispositif à matrice protéique voulu.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18542000P | 2000-02-28 | 2000-02-28 | |
| US60/185,420 | 2000-02-28 | ||
| US22276200P | 2000-08-03 | 2000-08-03 | |
| US60/222,762 | 2000-08-03 | ||
| PCT/US2001/006502 WO2001087267A1 (fr) | 2000-02-28 | 2001-02-28 | Materiaux de matrice proteique, dispositifs correspondants et procedes pour leur production et leur utilisation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2401385A1 CA2401385A1 (fr) | 2001-11-22 |
| CA2401385C true CA2401385C (fr) | 2011-05-17 |
Family
ID=26881122
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2401385A Expired - Fee Related CA2401385C (fr) | 2000-02-28 | 2001-02-28 | Materiaux de matrice proteique, dispositifs correspondants et procedes pour leur production et leur utilisation |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1259223A4 (fr) |
| JP (1) | JP2003533468A (fr) |
| AU (2) | AU2001249079B2 (fr) |
| CA (1) | CA2401385C (fr) |
| WO (1) | WO2001087267A1 (fr) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6890546B2 (en) | 1998-09-24 | 2005-05-10 | Abbott Laboratories | Medical devices containing rapamycin analogs |
| US20050147690A1 (en) * | 1998-09-25 | 2005-07-07 | Masters David B. | Biocompatible protein particles, particle devices and methods thereof |
| US20030007991A1 (en) * | 1998-09-25 | 2003-01-09 | Masters David B. | Devices including protein matrix materials and methods of making and using thereof |
| US7662409B2 (en) | 1998-09-25 | 2010-02-16 | Gel-Del Technologies, Inc. | Protein matrix materials, devices and methods of making and using thereof |
| US20020156437A1 (en) * | 2000-12-22 | 2002-10-24 | Kimberly-Clark Worldwide, Inc. | Removal of targeted proteases with proteinaceous wound dressings containing growth factors |
| US6444222B1 (en) * | 2001-05-08 | 2002-09-03 | Verigen Transplantation Services International Ag | Reinforced matrices |
| MXPA04003162A (es) | 2001-10-05 | 2005-01-25 | Surmodics Inc | Recubrimientos de particulas inmovilizadas y usos de los mismos. |
| US6902932B2 (en) * | 2001-11-16 | 2005-06-07 | Tissue Regeneration, Inc. | Helically organized silk fibroin fiber bundles for matrices in tissue engineering |
| ES2251623T3 (es) * | 2001-12-21 | 2006-05-01 | Coloplast A/S | Dispositivo de cuidado de heridas. |
| AU2003225212A1 (en) | 2002-04-29 | 2003-11-17 | Gel-Del Technologies, Inc. | Biomatrix structural containment and fixation systems and methods of use thereof |
| WO2004012676A2 (fr) * | 2002-08-02 | 2004-02-12 | Gp Medical | Materiau biologique charge de medicament traite chimiquement par la genipine |
| JP2006505562A (ja) * | 2002-10-17 | 2006-02-16 | アルカーメス コントロールド セラピューティクス,インコーポレイテッド | 持続放出組成物の放出プロフィールの調節方法 |
| CA2505576A1 (fr) * | 2002-11-08 | 2004-05-27 | Conor Medsystems, Inc. | Dispositif medical extensible et procede de traitement d'occlusions totales chroniques par administration locale d'un facteur angiogenique |
| US7517954B2 (en) * | 2003-03-28 | 2009-04-14 | Fuji Film Manufacturing Europe B.V. | RGD-enriched gelatine-like proteins with enhanced cell binding |
| EP1624864B1 (fr) * | 2003-05-14 | 2014-11-26 | Danisco US Inc. | Liberation controlee d'agents actifs a l'aide de polymeres proteiques a sequences repetees |
| US8465537B2 (en) | 2003-06-17 | 2013-06-18 | Gel-Del Technologies, Inc. | Encapsulated or coated stent systems |
| US8734421B2 (en) | 2003-06-30 | 2014-05-27 | Johnson & Johnson Consumer Companies, Inc. | Methods of treating pores on the skin with electricity |
| US8153591B2 (en) | 2003-08-26 | 2012-04-10 | Gel-Del Technologies, Inc. | Protein biomaterials and biocoacervates and methods of making and using thereof |
| CA2548822C (fr) | 2003-12-08 | 2015-08-11 | Gel-Del Technologies, Inc. | Dispositifs d'administration de medicaments mucoadhesifs et procedes de fabrication et d'utilisation associes |
| JP2007518811A (ja) * | 2004-01-23 | 2007-07-12 | カリフォルニア インスティチュート オブ テクノロジー | 操作されたタンパク質、ならびに作製方法および使用方法 |
| CA2608862C (fr) | 2004-06-11 | 2020-05-05 | Trustees Of Tufts College | Systeme d'administration de medicament a base de soie |
| US20060067971A1 (en) * | 2004-09-27 | 2006-03-30 | Story Brooks J | Bone void filler |
| US20090246283A1 (en) * | 2006-02-23 | 2009-10-01 | Danisco Us Inc., Genecor Division | Repeat Sequence Protein Polymer Nanoparticles Optionally Containing Active Agents and Their Preparation |
| US8267918B2 (en) * | 2006-03-14 | 2012-09-18 | Kci Licensing, Inc. | System and method for percutaneously administering reduced pressure treatment using a flowable manifold |
| AU2008345047A1 (en) | 2007-12-26 | 2009-07-09 | Gel-Del Technologies, Inc. | Biocompatible protein particles, particle devices and methods thereof |
| CN101221180B (zh) * | 2008-01-25 | 2011-11-30 | 马义才 | 一种便携式多种肿瘤标志物快速联检装置 |
| WO2010026760A1 (fr) * | 2008-09-03 | 2010-03-11 | 富士フイルム株式会社 | Compositions dans lesquelles des composants bioactifs sont operculés de façon stable |
| US10016534B2 (en) | 2008-11-17 | 2018-07-10 | Gel-Del Technologies, Inc. | Protein biomaterial and biocoacervate vessel graft systems and methods of making and using thereof |
| US9308070B2 (en) | 2008-12-15 | 2016-04-12 | Allergan, Inc. | Pliable silk medical device |
| US20110060419A1 (en) * | 2009-03-27 | 2011-03-10 | Jennifer Hagyoung Kang Choi | Medical devices with galvanic particulates |
| PL2435102T3 (pl) * | 2009-05-28 | 2021-01-11 | Addbio Ab | Wielowarstwowe folie białkowe, sposoby ich wytwarzania, urządzenia do podawania leku oraz implanty biomedyczne wykorzystujące folie |
| MX2014005704A (es) * | 2011-11-09 | 2015-02-17 | Tufts College | Espumas de fibroina de seda inyectables y sus usos. |
| HK1205953A1 (en) * | 2012-03-20 | 2015-12-31 | Trustees Of Tufts College | Silk reservoirs for drug delivery |
| BR112014024131A2 (pt) | 2012-03-29 | 2017-07-25 | Shire Human Genetic Therapies | lipídios catiônicos ionizáveis |
| US8691915B2 (en) | 2012-04-23 | 2014-04-08 | Sabic Innovative Plastics Ip B.V. | Copolymers and polymer blends having improved refractive indices |
| WO2018081815A2 (fr) | 2016-10-31 | 2018-05-03 | Sofregen Medical, Inc. | Compositions comprenant des particules de fibroïne de soie et leurs utilisations |
| CN108310455B (zh) * | 2018-03-20 | 2021-07-30 | 嘉兴尔云信息科技有限公司 | 纳米羟基磷灰石、pgs-m复合骨修复材料及其制备方法 |
| CN108926744A (zh) * | 2018-09-13 | 2018-12-04 | 广州贝奥吉因生物科技有限公司 | 一种用于软骨修复的复合支架及其制备方法 |
| US11738174B2 (en) | 2019-10-15 | 2023-08-29 | Sofregen Medical, Inc. | Delivery devices for delivering and methods of delivering compositions |
| TWI763265B (zh) | 2021-01-20 | 2022-05-01 | 巴斯特製藥科技顧問股份有限公司 | 一種結構性蛋白器官修補膜及其處理方法與處理劑 |
| CN114354585B (zh) * | 2021-11-09 | 2023-09-26 | 北京航空航天大学 | 一种辣根过氧化酶复合凝胶光子晶体传感器和方法 |
| CN114505070B (zh) * | 2022-04-02 | 2024-02-02 | 陕西师范大学 | 多孔纳米酶、多孔纳米酶晶体及其制备方法和应用 |
| PL446675A1 (pl) | 2023-11-08 | 2025-05-12 | Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie | Sposób otrzymywania jednorodnej zawiesiny kolagenu, zastosowanie jednorodnej zawiesiny kolagenu, sposób otrzymywania hydrożelowych materiałów na bazie kolagenu, sposób otrzymywania kolagenowej folii i/lub warstwy i/lub podłoża do hodowli, sposób otrzymywania kolagenowych wydruków oraz sposoby otrzymywania porowatych kształtek kolagenowych |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4718433A (en) * | 1983-01-27 | 1988-01-12 | Feinstein Steven B | Contrast agents for ultrasonic imaging |
| JPS6253919A (ja) * | 1985-05-30 | 1987-03-09 | Showa Yakuhin Kako Kk | 放出制御薬剤 |
| JPH0759522B2 (ja) * | 1985-12-27 | 1995-06-28 | 住友製薬株式会社 | 徐放性製剤の製造法 |
| AU8702491A (en) * | 1990-11-08 | 1992-05-14 | Matrix Pharmaceutical, Inc. | Fibrin/collagen membrane material for biomedical use |
| JPH06500802A (ja) * | 1991-06-14 | 1994-01-27 | アムジエン・インコーポレーテツド | コラーゲンフィルムによるタンパクのドラッグ・デリバリー |
| JPH0543453A (ja) * | 1991-08-20 | 1993-02-23 | Sumitomo Pharmaceut Co Ltd | 創傷治癒促進用局所用徐放性製剤 |
| AU3972793A (en) * | 1992-04-10 | 1993-11-18 | General Hospital Corporation, The | Cartilage matrix protein and methods for use |
| AU7568394A (en) * | 1993-08-19 | 1995-03-14 | Cygnus Therapeutic Systems | Water-soluble pressure-sensitive mucoadhesive and devices provided therewith for emplacement in a mucosa-lined body cavity |
| US5783214A (en) * | 1994-06-13 | 1998-07-21 | Buford Biomedical, Inc. | Bio-erodible matrix for the controlled release of medicinals |
| CN1052915C (zh) * | 1995-11-27 | 2000-05-31 | 中国医学科学院生物医学工程研究所 | 用于携载基因的蛋白质涂层医用载体及其制作方法 |
| WO1997041899A1 (fr) * | 1996-05-03 | 1997-11-13 | Innogenetics N.V. | Nouveaux medicaments contenant de la gelatine reticulee avec des polysaccharides oxydes |
| US6221425B1 (en) * | 1998-01-30 | 2001-04-24 | Advanced Cardiovascular Systems, Inc. | Lubricious hydrophilic coating for an intracorporeal medical device |
| GB9806966D0 (en) * | 1998-03-31 | 1998-06-03 | Ppl Therapeutics Scotland Ltd | Bioloically modified device |
| US6544548B1 (en) * | 1999-09-13 | 2003-04-08 | Keraplast Technologies, Ltd. | Keratin-based powders and hydrogel for pharmaceutical applications |
| JP4332660B2 (ja) * | 1999-10-01 | 2009-09-16 | Oci株式会社 | 口中清涼フィルム |
-
2001
- 2001-02-28 CA CA2401385A patent/CA2401385C/fr not_active Expired - Fee Related
- 2001-02-28 JP JP2001583736A patent/JP2003533468A/ja active Pending
- 2001-02-28 WO PCT/US2001/006502 patent/WO2001087267A1/fr not_active Ceased
- 2001-02-28 AU AU2001249079A patent/AU2001249079B2/en not_active Ceased
- 2001-02-28 EP EP01922258A patent/EP1259223A4/fr not_active Ceased
- 2001-02-28 AU AU4907901A patent/AU4907901A/xx active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001087267A1 (fr) | 2001-11-22 |
| AU4907901A (en) | 2001-11-26 |
| JP2003533468A (ja) | 2003-11-11 |
| CA2401385A1 (fr) | 2001-11-22 |
| EP1259223A1 (fr) | 2002-11-27 |
| AU2001249079B2 (en) | 2005-11-03 |
| EP1259223A4 (fr) | 2006-11-29 |
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