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    • 3. 发明授权
    • Voltage modulation of advanced electrochemical delivery system
    • 先进的电化学传递系统的电压调制
    • US06872292B2
    • 2005-03-29
    • US10353770
    • 2003-01-28
    • Felix TheeuwesJeremy Corwin Wright
    • Felix TheeuwesJeremy Corwin Wright
    • A61M5/142A61M5/145B01D61/42B01D61/44A61N1/30
    • B01D61/427A61M5/14276A61M2005/14513
    • An electro-osmotic cell capable of substantially reducing zero-current transport is disclosed, wherein the cell includes a cell housing having a first half cell and a second half cell, with an ion selective membrane therebetween, a first electrode positioned within the first half cell, a second electrode positioned within the second half cell, an electrolyte in electrical communication with the first electrode and the second electrode, and a wiring apparatus electrically connecting the first electrode and the second electrode, wherein the wiring apparatus has one or more structures used for counteracting salt concentration increases within the electro-osmotic cell. Such a cell may be used within an electro-osmotic fluid delivery device, along with a fluid inlet, a piston member adjacent the electro osmotic cell, and a drug reservoir adjacent the piston member, wherein the drug reservoir includes a sealed compartment having an exit port. A method for using such a device is similarly disclosed.
    • 公开了能够显着减少零电流输送的电渗透电池,其中电池包括具有第一半电池和第二半电池的电池壳体,其间具有离子选择性膜,位于第一半电池内的第一电极 位于所述第二半单元内的第二电极,与所述第一电极和所述第二电极电连通的电解质,以及电连接所述第一电极和所述第二电极的布线装置,其中所述布线装置具有用于 在电渗透细胞内抵消盐浓度增加。 这样的细胞可以与电渗透流体递送装置一起使用,以及流体入口,邻近电渗透细胞的活塞构件和邻近活塞构件的药物储存器,其中药物储存器包括密封隔室,其具有出口 港口。 类似地公开了使用这种装置的方法。
    • 4. 发明申请
    • Transdermal Delivery Systems for Sufentanil
    • 舒芬太尼透皮给药系统
    • US20130028953A1
    • 2013-01-31
    • US13486711
    • 2012-06-01
    • Su II YumFelix Theeuwes
    • Su II YumFelix Theeuwes
    • A61K9/70A61P29/00A61K31/4535
    • A61K9/703A61F2013/0296A61K9/7053A61K9/7061A61K9/7084A61K31/445A61K31/4535A61M35/00
    • Transdermal delivery systems for administering sufentanil through the skin are provided. The systems contain a sufficient amount of sufentanil to induce and maintain a constant state of analgesia when applied to a subject. The systems are characterized as having one or more features including a high degree of dosage form rate control over flux of sufentanil from the system, a high net flux of sufentanil from the system through the skin, lack of a permeation enhancer, an adhesive member demonstrating superior shear time, a low coefficient of variation in the net flux of sufentanil from the system, a high delivery efficiency, and a substantially constant steady state net flux of sufentanil from the system. Methods of using the transdermal delivery systems to administer a sufficient amount of sufentanil to induce and maintain analgesia for extended periods when applied to a subject are also provided.
    • 提供了通过皮肤施用舒芬太尼的透皮递送系统。 当施用于受试者时,该系统含有足量的舒芬太尼以诱导和保持恒定的止痛状态。 该系统的特征在于具有一个或多个特征,其包括对来自系统的舒芬太尼的通量的高剂量形式速率控制,来自系统通过皮肤的舒芬太尼的高净通量,缺乏渗透促进剂, 优异的剪切时间,来自系统的舒芬太尼的净通量的低变异系数,高的输送效率和来自系统的舒芬太尼的稳定的稳态净通量。 还提供了使用透皮递送系统施用足够量的舒芬太尼以在施用于受试者时延长期间诱导和维持止痛的方法。
    • 5. 发明授权
    • Transdermal delivery systems
    • 透皮递送系统
    • US08246977B2
    • 2012-08-21
    • US11665813
    • 2005-10-21
    • Su Il YumFelix Theeuwes
    • Su Il YumFelix Theeuwes
    • A61K9/70A61K31/445
    • A61K9/703A61F2013/0296A61K9/7053A61K9/7061A61K9/7084A61K31/445A61K31/4535A61M35/00
    • Transdermal delivery systems for administering sufentanil through the skin are provided. The systems contain a sufficient amount of sufentanil to induce and maintain a constant state of analgesia when applied to a subject. The systems are characterized as having one or more features including a high degree of dosage form rate control over flux of sufentanil from the system, a high net flux of sufentanil from the system through the skin, lack of a permeation enhancer, an adhesive member demonstrating superior shear time, a low coefficient of variation in the net flux of sufentanil from the system, a high delivery efficiency, and a substantially constant steady state net flux of sufentanil from the system. Methods of using the transdermal delivery systems to administer a sufficient amount of sufentanil to induce and maintain analgesia for extended periods when applied to a subject are also provided.
    • 提供了通过皮肤施用舒芬太尼的透皮递送系统。 当施用于受试者时,该系统含有足量的舒芬太尼以诱导和保持恒定的止痛状态。 该系统的特征在于具有一个或多个特征,其包括对来自系统的舒芬太尼的通量的高剂量形式速率控制,来自系统通过皮肤的舒芬太尼的高净通量,缺乏渗透促进剂, 优异的剪切时间,来自系统的舒芬太尼的净通量的低变异系数,高的输送效率和来自系统的舒芬太尼的稳定的稳态净通量。 还提供了使用透皮递送系统施用足够量的舒芬太尼以在施用于受试者时延长期间诱导和维持止痛的方法。
    • 6. 发明申请
    • Pharmaceutical compositions for administraton to a sinus
    • 用于给鼻窦的药物组合物
    • US20100016267A1
    • 2010-01-21
    • US10592886
    • 2005-03-15
    • Felix TheeuwesArthur J. Tipton
    • Felix TheeuwesArthur J. Tipton
    • A61K31/58A61P27/00
    • A61K9/0043
    • Pharmaceutical compositions for delivering a drug to a sinus in a subject are provided. The compositions are formed by the combination of a carrier material and a drug and are specially adapted for delivery to a sinus. The compositions have no fixed shape, and the carrier material serves to increase the viscosity or specific volume of the composition after introduction of the composition into the sinus. Also provided are methods for delivering a drug to a subject. The methods entail administering a pharmaceutical composition according to the present invention directly to a sinus. The drug is then released from the composition to the sinus. The pharmaceutical compositions can be administered to a sinus in liquid form, for example, as a suspension or solution using standard techniques. Also provided is the use of a carrier material in the manufacture of a drug delivery composition. The drug delivery composition is for delivering a drug to a sinus in a subject. The composition comprises the carrier material combined with the drug to be delivered, and has no fixed shape. After the composition is introduced into a sinus, the carrier material serves to increase the viscosity or specific volume of the composition.
    • 提供用于将药物递送至受试者的窦的药物组合物。 组合物通过载体材料和药物的组合形成,并且特别适于递送至窦。 组合物没有固定的形状,并且载体材料用于在将组合物引入窦内后增加组合物的粘度或比体积。 还提供了将药物递送到受试者的方法。 所述方法需要将根据本发明的药物组合物直接给予鼻窦。 然后将药物从组合物释放到窦。 药物组合物可以以液体形式施用于窦,例如使用标准技术作为悬浮液或溶液施用。 还提供了载体材料在制备药物递送组合物中的用途。 药物递送组合物用于将药物递送至受试者的窦。 该组合物包含与待输送药物结合的载体材料,并且不具有固定形状。 在将组合物引入窦中之后,载体材料用于增加组合物的粘度或比体积。
    • 7. 发明申请
    • Transdermal delivery systems
    • 透皮递送系统
    • US20080260811A1
    • 2008-10-23
    • US11888661
    • 2007-07-31
    • Su Il YumFelix Theeuwes
    • Su Il YumFelix Theeuwes
    • A61K31/4436A61K9/70A61P43/00
    • A61K31/4535A61F2013/0296A61K9/7053A61K9/7061A61K9/7084
    • Transdermal delivery systems for administering sufentanil through the skin are provided. The systems contain a sufficient amount of sufentanil to induce and maintain a constant state of analgesia when applied to a subject. The systems are characterized as having one or more features including a high degree of dosage form rate control over flux of sufentanil from the system, a high net flux of sufentanil from the system through the skin, lack of a permeation enhancer, an adhesive member demonstrating superior shear time, a low coefficient of variation in the net flux of sufentanil from the system, a high delivery efficiency, and a substantially constant steady state net flux of sufentanil from the system. Methods of using the transdermal delivery systems to administer a sufficient amount of sufentanil to induce and maintain analgesia for extended periods when applied to a subject are also provided.
    • 提供了通过皮肤施用舒芬太尼的透皮递送系统。 当施用于受试者时,该系统含有足量的舒芬太尼以诱导和保持恒定的止痛状态。 该系统的特征在于具有一个或多个特征,其包括对来自系统的舒芬太尼的通量的高剂量形式速率控制,来自系统通过皮肤的舒芬太尼的高净通量,缺乏渗透促进剂, 优异的剪切时间,来自系统的舒芬太尼的净通量的低变异系数,高的输送效率和来自系统的舒芬太尼的稳定的稳态净通量。 还提供了使用透皮递送系统施用足够量的舒芬太尼以在施用于受试者时延长期间诱导和维持止痛的方法。
    • 9. 发明申请
    • Local concentration management system
    • 本地集中管理制度
    • US20070167932A1
    • 2007-07-19
    • US11726517
    • 2007-03-21
    • Felix TheeuwesSu Yum
    • Felix TheeuwesSu Yum
    • A61K9/22
    • A61M25/00A61M25/0043A61M2025/0057A61M2025/105A61M2025/1086
    • The invention provides a local concentration management system (LCMS) for delivery of highly concentrated therapeutic agent formulations. The LCMS comprises a device comprising an elongate body defining a lumen between its proximal and distal ends, and a diffuser element, a dilutor element, or both. The diffuser element, which is selectively permeable to the agent, is operatively associated with the elongate body so that agent flows through the elongate body, and into and through the diffuser element to exit the system. The dilutor element can be operatively associated with the system to be in fluid communication with the elongate body lumen, a diffusion space defined by a diffuser element inner wall, or both. The dilutor element is selectively water permeable, but substantially impermeable to agent, to provide for dilution of the agent during transit through the system. The LCMS system is designed to disperse and/or dilute the drug delivery stream.
    • 本发明提供了用于递送高度浓缩的治疗剂制剂的局部浓度管理系统(LCMS)。 LCMS包括装置,其包括在其近端和远端之间限定内腔的细长主体,以及扩散器元件,稀释元件或两者。 对试剂选择性渗透的扩散器元件可与细长体可操作地连接,使得试剂流过细长体并进入并通过扩散器元件以离开系统。 稀释元件可以与系统可操作地相关联以与细长体腔流体连通,由扩散器元件内壁或两者限定的扩散空间。 稀释剂元件选择性地是水可渗透的,但是对试剂基本上是不可渗透的,以便在通过系统运输期间提供试剂的稀释。 LCMS系统被设计成分散和/或稀释药物输送流。