SYNTHETIC COLLAGEN ORTHOPAEDIC STRUCTURES SUCH AS GRAFTS, TENDONS AND OTHER STRUCTURES
    82.
    发明申请
    SYNTHETIC COLLAGEN ORTHOPAEDIC STRUCTURES SUCH AS GRAFTS, TENDONS AND OTHER STRUCTURES 审中-公开
    合成胶原蛋白结构如花束,腱和其他结构

    公开(公告)号:WO1996014095A1

    公开(公告)日:1996-05-17

    申请号:PCT/US1995014308

    申请日:1995-11-07

    Abstract: An improved biodegradable and biocompatible reconstituted monofilament collagen fiber having increased strength and elasticity is disclosed. The method of manufacture of the fiber, comprising a water bath step following a dehydration step, is also disclosed. Several embodiments of the collagen fiber are disclosed, including grafts, prosthetic devices, bundles of the fibers where the fibers of the bundle are tensioned and fail substantially in unison, and methods thereof. The fibers of the invention, or the embodiments of the fibers, may be coated or embedded in a polymer to protect the fibers and to bind them together. Additionally, proteoglycans may be incorporated into the fibers to enhance the ultimate tensile strength of the fibers.

    Abstract translation: 公开了具有增强的强度和弹性的改进的可生物降解和生物相容性重建单丝胶原纤维。 还公开了包含脱水步骤后的水浴步骤的纤维的制造方法。 公开了胶原纤维的几个实施方案,包括移植物,假体装置,纤维束,其中束的纤维被张紧并且基本上一致地失效,以及其方法。 本发明的纤维或纤维的实施方案可以被涂覆或嵌入聚合物中以保护纤维并将它们结合在一起。 此外,蛋白多糖可以并入纤维中以增强纤维的极限拉伸强度。

    ANALOGS OF GLYCOPROTEIN HORMONE RECEPTORS WHICH BIND CHORIOGONADOTROPHINS, LEUTROPHINS, AND FOLLITROPHINS AND METHODS FOR PREPARING AND USING SAME
    83.
    发明申请
    ANALOGS OF GLYCOPROTEIN HORMONE RECEPTORS WHICH BIND CHORIOGONADOTROPHINS, LEUTROPHINS, AND FOLLITROPHINS AND METHODS FOR PREPARING AND USING SAME 审中-公开
    含有氯霉素酮的胆碱蛋白激素受体的模拟物,光合作用和焦虑症及其制备和使用方法

    公开(公告)号:WO1992022667A1

    公开(公告)日:1992-12-23

    申请号:PCT/US1992004987

    申请日:1992-06-12

    CPC classification number: C07K14/723 C07K2319/00 C07K2319/033 C07K2319/32

    Abstract: In one embodiment, the present invention pertains to a protein having binding affinity to human chorionic gonadotrophin (hCG), luteinizing hormone (LH), and follicle stimulating hormone (FSH), comprising an amino acid sequence of 341 amino acids, wherein the protein is a chimera having an amino acid sequence homologous to the amino acid sequence of residues 1-92 of FSHR, an amino acid sequence homologous to the amino acid sequence of residues 93-170 of LHR, and an amino acid sequence homologous to the amino acid sequence of residues 171-341 of FSHR, wherein the protein is a chain of amino acids that is not naturally occurring as a binding protein. (LH numbering system). In another embodiment, the present invention pertains to a glycoprotein hormone receptor having binding affinity to human chorionic gonadotrophin (hCG), luteinizing hormone (LH), and follicle stimulating hormone (FSH), wherein the receptor comprises a transmembrane region and an extracellular N-terminus region, wherein the N-terminus region is a chimera containing an amino acid sequence of 341 amino acids comprising an amino acid sequence homologous to the amino acid sequence of residues 1-92 of FSHR, an amino acid sequence homologous to the amino acid sequence of residues 93-170 of LHR, and an amino acid sequence homologous to the amino acid sequence of residues 171-341 of FSHR, wherein the receptor is a chain of amino acids that is not naturally occurring as a receptor. (LH nmbering system).

    Abstract translation: 在一个实施方案中,本发明涉及对人绒毛膜促性腺激素(hCG),黄体生成激素(LH)和促卵泡激素(FSH))具有结合亲和力的蛋白质,其包含341个氨基酸的氨基酸序列,其中所述蛋白质是 具有与FSHR的残基1-92的氨基酸序列同源的氨基酸序列的嵌合体,与LHR的残基93-170的氨基酸序列同源的氨基酸序列和与氨基酸序列同源的氨基酸序列 的FSHR的残基171-341,其中所述蛋白质是不是天然存在的结合蛋白质的氨基酸链。 (LH编号系统)。 在另一个实施方案中,本发明涉及对人绒毛膜促性腺激素(hCG),黄体生成激素(LH)和促卵泡激素(FSH)具有结合亲和力的糖蛋白激素受体,其中所述受体包含跨膜区和细胞外N- 其中所述N末端区域是包含341个氨基酸的氨基酸序列的嵌合体,其包含与FSHR的残基1-92的氨基酸序列同源的氨基酸序列,与氨基酸序列同源的氨基酸序列 的LHR的残基93-170和与FSHR的残基171-341的氨基酸序列同源的氨基酸序列,其中受体是不天然存在的受体的氨基酸链。 (LH nmbering系统)。

    BIODEGRADABLE MATRIX AND METHODS FOR PRODUCING SAME
    84.
    发明申请
    BIODEGRADABLE MATRIX AND METHODS FOR PRODUCING SAME 审中-公开
    生物可降解矩阵及其生产方法

    公开(公告)号:WO1985004413A1

    公开(公告)日:1985-10-10

    申请号:PCT/US1985000504

    申请日:1985-03-27

    Abstract: Processes for preparaing biodegradable collagen-based matrices in sponge or sheet form wherein in one embodiment a collagen-based material including a collagen selected from the group consisting of types I, II and III collagens is freeze dried to form a collagen-based sponge which is contacted with a crosslinking agent selected from the group consisting of a carbodiimide or a succinimidyl active ester to form an intermediate collagen-based matrix which is subsequently subjected to conditions of severe dehydration to form the collagen-based matrix in sponge or sheet form. In another embodiment, a collagen-based sponge or sheet is first subjected to conditions of severe dehydration followed by contacting the thus formed intermediate collagen-based matrix with a carbodiimide crosslinking compound to form the collagen-based matrix in sponge or sheet form. In still another embodiment of the present invention the cross-linking agent is admixed with the collagen-based material prior to formation of the collagen-based sponge or sheet followed by processing steps of severe dehydration. In a paticularly preferred form of the invention, a carrier compound is incorporated during processing to form a collagen-based matrix in sponge or sheet form impregnated with a carrier compound wherein the carrier compound is selected from the group consisting of types IV and V collagen, fibronecting, laminin, hyaluronate, proteoglycan, epidermal growth factor, platelet derived growth factor, angiogenesis factor, antibiotic, antifungal agent, spermacidal agent, enzyme and enzyme inhibitor.

    Abstract translation: 以海绵或片状形式制备可生物降解的胶原基质的方法,其中在一个实施方案中,将包含选自I,II和III型胶原蛋白的胶原蛋白的胶原基材料冷冻干燥以形成基于胶原的海绵, 与选自碳二亚胺或琥珀酰亚胺基活性酯的交联剂接触以形成中间胶原基质,随后经历严重脱水的条件以形成海绵或片状形式的基于胶原的基质。 在另一个实施方案中,基于胶原的海绵或片材首先经受严重脱水的条件,然后使由此形成的中间胶原基质与碳二亚胺交联化合物接触以形成海绵或片状形式的基于胶原的基质。 在本发明的另一个实施方案中,在形成基于胶原的海绵或片材之前将交联剂与基于胶原的材料混合,然后进行严重脱水的加工步骤。 在本发明的特别优选形式中,在加工过程中加入载体化合物以形成浸渍有载体化合物的海绵或片状形式的基于胶原的基质,其中载体化合物选自IV型和V型胶原, 纤连蛋白,层粘连蛋白,透明质酸,蛋白多糖,表皮生长因子,血小板衍生生长因子,血管生成因子,抗生素,抗真菌剂,精子拮抗剂,酶和酶抑制剂。

    METHOD OF TREATING DYSKINESIA
    89.
    发明申请
    METHOD OF TREATING DYSKINESIA 审中-公开
    治疗DYSKINESIA的方法

    公开(公告)号:WO2012149113A1

    公开(公告)日:2012-11-01

    申请号:PCT/US2012/035129

    申请日:2012-04-26

    CPC classification number: A61K31/485 A61K31/197 A61K45/06

    Abstract: Methods of treating patients with dyskinesias, by administering a therapeutically effective amount of a dual-action mu-opioid receptor antagonist/kappa-opioid receptor agonist or prodrug thereof to a subject in need thereof, sufficient to mitigate the dyskinesia. Alternatively, a combination of both a mu-opioid receptor antagonist or prodrug thereof, and a kappa-opioid receptor agonist or prodrug thereof can be administered, either together or separately.

    Abstract translation: 通过向有需要的受试者施用足以减轻运动障碍的治疗有效量的双重作用的μ-阿片样物质受体拮抗剂/κ-阿片受体激动剂或其前体药物来治疗运动障碍患者的方法。 或者,可以一起或分开施用μ-阿片受体拮抗剂或其前药和κ-阿片受体激动剂或其前药的组合。

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