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    • 1. 发明授权
    • Polymer composite for controlled release or membrane formation
    • 用于控制释放或膜形成的聚合物复合材料
    • US4898734A
    • 1990-02-06
    • US162161
    • 1988-02-29
    • Edith MathiowitzRobert S. LangerAbraham WarshawskyElazar Edelman
    • Edith MathiowitzRobert S. LangerAbraham WarshawskyElazar Edelman
    • A01N25/34A61K9/16A61K9/20A61K9/70B01J13/02
    • A01N25/34A61K9/1641A61K9/1647A61K9/2077A61K9/2081A61K9/7023B01J13/025
    • The present invention is a method to produce novel composites based on microcapsules or microspheres embedded in contiuous polymeric matrices. Both non-bioerodible and erodible polymers can be used. Material can be incorporated into the microcapsules or microspheres for subsequent release. In one embodiment of the present invention, spheres are homogeneously dispersed in a polymer matrix and then forced to release their contents by exposure to temperature, light or ultrasound. Alternatively, polymers which degrade as a function of time or hydrolysis can be used for controlled releases. The polymer composites have completely different properties from either a continuous polymer matrix or microcapsules or microspheres and are therefore useful for a wide variety of applications. When carbon tetrachloride is the incorporated material, the film is useful as a flame retarding device. When foaming agents are used, especially UV or heat sensitive materials, gas can be evolved inside each capsulThe Government has rights in this invention pursuant to Grant Number 5-R01-GM26698 awarded by the Department of Health and Human Services.
    • 本发明是一种基于嵌入在连续聚合物基质中的微胶囊或微球体生产新型复合材料的方法。 可以使用非生物可腐蚀和可侵蚀的聚合物。 可以将材料并入微胶囊或微球体中用于随后的释放。 在本发明的一个实施方案中,球体均匀地分散在聚合物基质中,然后通过暴露于温度,光或超声波被迫释放其内容物。 或者,作为时间或水解的函数降解的聚合物可用于受控释放。 聚合物复合材料与连续聚合物基质或微胶囊或微球具有完全不同的性质,因此可用于各种应用。 当四氯化碳是引入的材料时,该膜可用作阻燃装置。 当使用发泡剂,特别是UV或热敏材料时,可在每个胶囊内放出气体,以在聚合物中形成气泡。 当药物或其他生物活性剂掺入球体并用聚合物包封时,仅通过侵蚀或破裂的球体释放。 与从包封的微胶囊的释放相反,从聚合物复合材料的释放大约是随时间线性的。 聚合物球体的侵蚀也可用于产生多孔聚合物结构。 这种装置可用于透皮药物递送,血管移植物,伤口愈合膜或作为聚合物多孔膜。
    • 2. 发明授权
    • Preparation of multiwall polymeric microcapsules
    • 多壁聚合物微胶囊的制备
    • US4861627A
    • 1989-08-29
    • US45840
    • 1987-05-01
    • Edith MathiowitzRobert S. Langer
    • Edith MathiowitzRobert S. Langer
    • A01N25/28A61K8/00A61K8/18A61K8/87A61K8/88A61K9/16A61K9/50A61K9/56A61K9/58A61Q13/00B01J13/14C05G3/00C09B67/08C11B9/00
    • A61K9/5089A61K9/1694Y10S514/963Y10T428/2987Y10T428/2989
    • A single step method for preparation of multi-layer polymeric delivery systems. Any two or three different degradable or non-degradable polymers which are not soluble in each other at a particular concentration, as dictated by their phase diagram, can be used. The multi-layer microcapsules produced by the method are distinguished by extremely uniform dimensioned layers of polymer and actual incorporation of the substance to be delivered into the polymer layers.In the preferred embodiment of the method, two polymers are dissolved in a volatile organic solvent, the substance to be encapsulated is dispersed or dissolved in the polymer solution, the mixture is suspended in an aqueous solution and stirred, and the solvent is slowly evaporated, creating microspheres with an inner core formed by one polymer and an outer layer formed by the second polymer. In another embodiment one polymer may be formed within a layer of the other polymer by increasing the rate of evaporation of the volatile solvent.
    • 用于制备多层聚合物递送系统的单步法。 可以使用任何两种或三种不同的可降解或不可降解的聚合物,其特定浓度彼此不溶,如其相图所示。 通过该方法制备的多层微胶囊通过聚合物的非常均匀的尺寸层和实际掺入待递送到聚合物层中的物质来区分。 在该方法的优选实施方案中,将两种聚合物溶解在挥发性有机溶剂中,待包封的物质分散或溶解在聚合物溶液中,将混合物悬浮在水溶液中并搅拌,并将溶剂缓慢蒸发, 产生具有由一种聚合物形成的内芯和由第二聚合物形成的外层的微球。 在另一个实施方案中,通过增加挥发性溶剂的蒸发速率,可以在其它聚合物的层内形成一种聚合物。
    • 5. 发明授权
    • Multiwall polymeric microspheres
    • 多壁聚合物微球
    • US5912017A
    • 1999-06-15
    • US906403
    • 1992-07-01
    • Edith MathiowitzRobert S. Langer
    • Edith MathiowitzRobert S. Langer
    • A61K9/16A61K9/50A61K9/52B01J13/12
    • A61K9/1694A61K9/5089Y10S514/963Y10S514/965Y10T428/2987Y10T428/2989
    • A method for preparation of multi-layer polymeric microspheres formed from any degradable or non-degradable polymers which are not soluble in each other at a particular concentration, but which have a positive spreading coefficient in solution. The multi-layer microspheres produced by the method are distinguished by extremely uniform dimensioned layers of polymer and actual incorporation of the substance to be delivered into the polymer layers. In the preferred embodiment of the method, two polymers are dissolved in a volatile organic solvent, the substance to be incorporated is dispersed or dissolved in the polymer solution, the mixture is suspended in an aqueous solution and stirred, and the solvent is slowly evaporated, creating microspheres with an inner core formed by one polymer and an outer layer formed by the second polymer. In another embodiment, solvent is removed by spray drying. In still another embodiment, polymers are melted and combined with the substance to be incorporated, then cooled to form layered microspheres.
    • 一种由任何可溶解或不可降解的聚合物制备的多层聚合物微球的方法,它们在特定浓度下彼此不溶,但在溶液中具有正扩散系数。 通过该方法制备的多层微球的特征在于聚合物尺寸非常均匀,并且实际掺入待递送到聚合物层中的物质。 在该方法的优选实施方案中,将两种聚合物溶解在挥发性有机溶剂中,将待引入的物质分散或溶解在聚合物溶液中,将混合物悬浮在水溶液中并搅拌,并将溶剂缓慢蒸发, 产生具有由一种聚合物形成的内芯和由第二聚合物形成的外层的微球。 在另一个实施方案中,通过喷雾干燥除去溶剂。 在另一个实施方案中,将聚合物熔化并与待掺入的物质组合,然后冷却形成层状微球。
    • 6. 发明授权
    • Microspheres comprising polymer and drug dispersed there within
    • 包含分散在其中的聚合物和药物的微球
    • US5718921A
    • 1998-02-17
    • US691874
    • 1996-08-02
    • Edith MathiowitzClaudy J.P. MullonAbraham J. DombRobert S. Langer
    • Edith MathiowitzClaudy J.P. MullonAbraham J. DombRobert S. Langer
    • A61K9/50B01J13/02A61K9/52B01J13/12
    • B01J13/02A61K9/5031Y10S514/866Y10S514/963Y10S514/965
    • A method for preparation of biodegradable polymeric drug delivery devices using relatively low temperatures and non-aqueous solutions which is particularly useful with polyanhydrides, thermolabile drugs, and in forming multi-layered devices. In a first embodiment, the polymer is dissolved in a volatile organic solvent, the drug is dispersed or dissolved in the polymer solution, the mixture is suspended in an organic oil, and the organic solvent is extracted into the oil, creating microspheres. The preferred polymers are polyanhydrides since they are biodegradable and have been proven to be useful in vivo. In a second embodiment, the polymer is dissolved in organic solvent with or without the drug, and the mixture is suspended in glycerol. The suspension is frozen and the organic solvent slowly evaporated. Using these embodiments, alone or in combination with other methods including the "hot melt" technique, multi-walled microspheres having each wall degrading at a different rate or containing different drugs can be manufactured.
    • 一种使用相对较低温度制备可生物降解的聚合物药物递送装置的方法以及非常适用于聚酐,不耐热药物和形成多层装置的非水溶液。 在第一实施方案中,将聚合物溶解在挥发性有机溶剂中,将药物分散或溶解在聚合物溶液中,将混合物悬浮在有机油中,并将有机溶剂萃取到油中,形成微球体。 优选的聚合物是聚酐,因为它们是可生物降解的并且已被证明在体内是有用的。 在第二个实施方案中,将聚合物溶解在有或者没有药物的有机溶剂中,并将混合物悬浮在甘油中。 将悬浮液冷冻并缓慢蒸发有机溶剂。 使用这些实施方案,可单独使用或与包括“热熔融”技术在一起的其它方法结合使用,可以制造具有以不同速率降解或含有不同药物的各壁的多壁微球体。
    • 7. 发明授权
    • Pure polyanhydride from dicarboxylic acid and coupling agent
    • 来自二羧酸和偶联剂的纯聚酐
    • US4916204A
    • 1990-04-10
    • US80332
    • 1987-07-31
    • Abraham J. DombRobert S. LangerEyal RonSteven GiannosRohit KothariEdith Mathiowitz
    • Abraham J. DombRobert S. LangerEyal RonSteven GiannosRohit KothariEdith Mathiowitz
    • A61K31/335A61K31/365A61K31/39C08G67/04C08G69/08C08G69/10
    • A61K31/335A61K31/365A61K31/39C08G67/04C08G69/08C08G69/10Y10S514/863
    • A method for synthesizing polyanhydrides in solution using coupling agents and a removable acid acceptor to effect a one-step polymerization of dicarboxylic acids. As used in the method, these coupling agents include phosgene, diphosgene, and acid chlorides. Insoluble acid acceptors include insoluble polyamines and crosslinked polyamines such as polyethyleneimine and polyvinylpyridine and inorganic bases such as K.sub.2 CO.sub.3, Na.sub.2 CO.sub.3, NaHCO.sub.3, and CaCO.sub.3. The only byproduct formed is a removable hydrochloric acid-acid acceptor.Examples are provided of the polymerization of highly pure polyanhydrides using phosgene, diphosgene or an acid chloride as the coupling agent, in combination with either an insoluble acid acceptor or a soluble acid acceptor in a solvent wherein the polymerization byproduct or polymer is insoluble.A particularly important application of these polyanhydrides is in the formation of drug delivery devices containing bioactive compounds. The method is also useful in the polymerization of dicarboxylic acids including heat liable dipeptides of glutamic or aspartic acid.
    • 使用偶联剂和可除去的酸受体在溶液中合成聚酐以进行二羧酸的一步聚合的方法。 如该方法所用,这些偶联剂包括光气,双光气和酰氯。 不溶性酸受体包括不溶性多胺和交联聚胺如聚乙烯亚胺和聚乙烯吡啶以及无机碱如K 2 CO 3,Na 2 CO 3,NaHCO 3和CaCO 3。 形成的唯一副产物是可除去的盐酸酸受体。 提供了使用光气,双极光或酰氯作为偶联剂的高纯度聚酐与在溶剂中的不溶性酸受体或可溶性酸受体组合的聚合反应,其中聚合副产物或聚合物是不溶的。 这些多酸酐的特别重要的应用是形成含有生物活性化合物的药物递送装置。 该方法也可用于二羧酸的聚合,包括谷氨酸或天冬氨酸的热应答二肽。
    • 9. 发明授权
    • One step preparation of poly(amide-anhydride)
    • 聚(酰胺 - 酐)一步法制备
    • US4933431A
    • 1990-06-12
    • US269448
    • 1988-11-09
    • Abraham J. DombRobert S. LangerEyal RonSteven GiannosRohit KothariEdith Mathiowitz
    • Abraham J. DombRobert S. LangerEyal RonSteven GiannosRohit KothariEdith Mathiowitz
    • C08G67/04C08G69/08C08G69/10
    • C08G69/08C08G67/04C08G69/10
    • A method for synthetizing polyanhydrides in solution using coupling agents and a removable acid acceptor to effect a one-step polymerization of dicarboxylic acids. As used in the method, these coupling agents include phosgene, diphosgene, and acid chlorides. Insoluble acid acceptors include insoluble polyamines and crosslinked polyamines such as polyethyleneimine and polyvinylpyridine and inorganic bases such as K.sub.2 CO.sub.3, Na.sub.2 CO.sub.3, NaHCO.sub.3, and CaCO.sub.3. The only byproduct formed is a removable hydrochloric acid-acid acceptor.Examples are provided of the polymerization of highly pure polyanhydrides using phosgene, diphosgene or an acid chloride as the coupling agent, in combination with either an insoluble acid acceptor or a soluble acid acceptor in a solvent wherein the polymerizaiton byproduct or polymer is insoluble.A particularly important application of these polyanhydrides is in the formation of drug delivery devices containing bioactive compounds. The method is also useful in the polymerization of dicarboxylic acids including heat liable dipeptides of glutamic or aspartic acid.
    • 使用偶联剂和可除去的酸受体在溶液中合成聚酐以实现二羧​​酸的一步聚合的方法。 如该方法所用,这些偶联剂包括光气,双光气和酰氯。 不溶性酸受体包括不溶性多胺和交联聚胺如聚乙烯亚胺和聚乙烯吡啶以及无机碱如K 2 CO 3,Na 2 CO 3,NaHCO 3和CaCO 3。 形成的唯一副产物是可除去的盐酸酸受体。 提供了使用光气,双光气或酰氯作为偶联剂的高纯度聚酐与在溶剂中的不溶性酸受体或可溶性酸受体组合的聚合反应,其中聚合物副产物或聚合物是不溶的。 这些多酸酐的特别重要的应用是形成含有生物活性化合物的药物递送装置。 该方法也可用于二羧酸的聚合,包括谷氨酸或天冬氨酸的热应答二肽。