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    • 33. 发明授权
    • Adhesive compositions for the treatment of xerostomia
    • 用于治疗口腔干燥症的粘合剂组合物
    • US09161909B2
    • 2015-10-20
    • US12757508
    • 2010-04-09
    • Abraham J. DombBenny BramaBoaz Mizrahi
    • Abraham J. DombBenny BramaBoaz Mizrahi
    • A61K9/20A61K9/00A61K31/22
    • A61K9/006A61K9/2086A61K31/22
    • Compositions for the treatment of xerostomia, and methods of making and using thereof are disclosed herein. The compositions are typically in the form of a film or tablet, such as a double layer sticker tablet. The compositions adhere to a buccal surface or mucosal surface in the oral cavity for at least 15 minutes, preferably for at least 30 minutes. The compositions themselves are able to increase the levels of saliva in the mouth without the need for active agents, such sialogogic agents. The compositions optionally contain a non-lipid lubricant, a flavoring agent, and/or a buffering agent. The composition is generally effective at treating or ameliorating the effects of xerostomia for a time period ranging from at least 30 minutes up to eight hours following administration to the buccal or oral mucosa.
    • 本文公开了用于治疗口干燥症的组合物及其制备和使用方法。 组合物通常为薄膜或片剂的形式,例如双层贴片片剂。 组合物粘附在口腔中的口腔表面或粘膜表面至少15分钟,优选至少30分钟。 组合物本身能够增加口中唾液的水平,而不需要活性剂,例如唾液酸剂。 组合物任选地含有非脂润滑剂,调味剂和/或缓冲剂。 组合物通常有效地治疗或改善口腔干燥症的作用在给药至颊或口腔粘膜后至少30分钟至8小时的时间段内。
    • 36. 发明申请
    • INJECTABLE BIODEGRADABLE POLYMER COMPOSITIONS FOR SOFT TISSUE REPAIR AND AUGMENTATION
    • 用于软组织修复和补充的可注射的生物可降解聚合物组合物
    • US20100260703A1
    • 2010-10-14
    • US12678492
    • 2008-10-05
    • Lior YankelsonAbraham J. Domb
    • Lior YankelsonAbraham J. Domb
    • A61K31/765A61P13/00A61P17/00A61F2/02
    • A61L27/58A61L27/18A61L27/50A61L2400/06C08L67/04
    • Methods for soft tissue repair and/or augmentation using injectable, biodegradable polymers are described herein. In one embodiment, the polymer compositions are liquid or pastes at room temperature. In a preferred embodiment, the polymer composition contains liquid or pasty hydroxy fatty acid-based copolyesters, polyester-anhydrides, or combinations thereof. The viscosity of the polymers increases upon contact with bodily fluid to form a solid or semisolid implant suitable for soft tissue repair and/or augmentation. In another embodiment, the polymer composition contains particles of a polymer stereocomplex. One or more active agents may be incorporated into the polymer compositions. Suitable classes of active agents include local anesthetics, anti-inflammatory agents, antibiotics, analgesics, growth factors and agents that induce and/or enhance growth of tissue within the filled cavity or control the growth of a certain type of tissue, and combinations thereof. The polymer compositions may also contain one or more additives or excipients that modify the physical and/or mechanical properties of the polymer. The polymer compositions are typically administered by injection. The injectable polymers can be used for a variety of soft tissue repair and augmentation procedures.
    • 本文描述了使用可注射的可生物降解的聚合物进行软组织修复和/或增加的方法。 在一个实施方案中,聚合物组合物在室温下为液体或糊状物。 在优选的实施方案中,聚合物组合物含有液体或糊状羟基脂肪酸基共聚酯,聚酯酸酐或其组合。 当与体液接触时,聚合物的粘度增加,以形成适于软组织修复和/或增加的固体或半固体植入物。 在另一个实施方案中,聚合物组合物含有聚合物立体络合物的颗粒。 一种或多种活性剂可以并入聚合物组合物中。 合适类别的活性剂包括局部麻醉剂,抗炎剂,抗生素,止痛剂,生长因子和诱导和/或增强填充腔内组织生长或控制某种类型组织生长的试剂及其组合。 聚合物组合物还可以含有改变聚合物的物理和/或机械性能的一种或多种添加剂或赋形剂。 聚合物组合物通常通过注射施用。 可注射聚合物可用于各种软组织修复和增强程序。
    • 39. 发明授权
    • Dispersible concentrate for the delivery of cyclosprin
    • 可分散浓缩物用于递送环糊精
    • US07026290B1
    • 2006-04-11
    • US09869519
    • 1999-12-30
    • Abraham J. Domb
    • Abraham J. Domb
    • A61K38/13
    • A61K9/1075
    • A formulation for the administration of a cyclosporin. This formulation features a hydrophilic solvent which is characterized by being a lower alkyl ester of hydroxyalkanoic acid; and a surfactant, preferably a combination of a surfactant with a high HLB (hydrophilic/lipophilic balance) of at least about 8 and a surfactant with a low HLB of less than about 5. Other ingredients are optional, such as a fatty acid ester such as tricaprin, a phospholipid, and an ethoxylated fat such as Cremophor or another similar substance. Optionally, the ethoxylated fat is substituted for the surfactant. The preferred particle size of the resultant formulation is less than about 100 nm, more preferably less than about 60 nm, and most preferably from about 5 nm to about 50 nm. The formulation of the present invention is characterized by having high bioavailability.
    • 用于施用环孢菌素的制剂。 该制剂具有亲水性溶剂,其特征在于羟基链烷酸的低级烷基酯; 和表面活性剂,优选具有至少约8的高HLB(亲水/亲油平衡)的表面活性剂和低HLB小于约5的表面活性剂的组合。其它成分是任选的,例如脂肪酸酯如 作为三萜皂苷,磷脂和乙氧基化脂肪如Cremophor或其它类似物质。 任选地,用乙氧基化脂肪代替表面活性剂。 所得制剂的优选粒度小于约100nm,更优选小于约60nm,最优选约5nm至约50nm。 本发明的制剂的特征在于具有高的生物利用度。