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    • 2. 发明申请
    • Devices and methods for pain management
    • 疼痛管理的设备和方法
    • US20080161357A1
    • 2008-07-03
    • US11888654
    • 2007-07-31
    • Randolph Mellus JohnsonFelix Theeuwes
    • Randolph Mellus JohnsonFelix Theeuwes
    • A61K31/4535A61P25/00
    • A61M37/0069A61K9/0004A61K9/0014A61K9/0019A61K9/0024A61K31/4468A61K31/4535A61K47/10A61K47/14A61K47/26
    • The invention features devices and methods for the systemic delivery of fentanyl or a fentanyl congener (e.g., sufentanil) to treat pain. In the present invention, a drug formulation comprising fentanyl or a fentanyl congener is stored within a drug delivery device (e.g., contained in a reservoir or impregnated within a matrix within the controlled drug delivery device). The drug formulation comprises an amount of drug sufficient for treatment and is stable at body temperatures (i.e., no unacceptable degradation) for the entire pre-selected treatment period. The drug delivery devices store the drug formulation safely (e.g., without dose dumping), provide sufficient protection from bodily processes to prevent unacceptable degradation of the formulation, and release the drug formulation in a controlled fashion at a therapeutically effective rate to treat pain. In use, the drug delivery device is implanted in the subject's body at an implantation site, and the drug formulation is released from the drug delivery device to a delivery site. The delivery site may be the same as, near, or distant from the implantation site. Once released at the delivery site, the drug formulation enters the systemic circulation and is transported to the site of action in the body to modulate the pain response (e.g., the brain or other pain sensory location).
    • 本发明的特征在于用于系统递送芬太尼或芬太尼(例如舒芬太尼)以治疗疼痛的装置和方法。 在本发明中,包含芬太尼或芬太尼同系物的药物制剂储存在药物递送装置内(例如,包含在储存器中或浸入受控药物递送装置内的基质内)。 药物制剂包含一定量的用于治疗的药物,并且在整个预选治疗期间在体温下稳定(即,不可接受的降解)。 药物递送装置安全地存储药物制剂(例如,没有剂量倾倒),提供足够的保护以防止身体过程以防止制剂的不可接受的降解,并以治疗有效的速率以受控的方式释放药物制剂以治疗疼痛。 在使用中,将药物递送装置植入到受试者的身体中的植入部位,并且药物制剂从药物递送装置释放到递送部位。 输送部位可以与植入部位相同,接近或远离植入部位。 一旦在递送部位释放,药物制剂进入体循环并被运送到身体中的作用部位以调节疼痛反应(例如,脑或其它疼痛感觉位置)。
    • 5. 发明授权
    • Devices and methods for pain management
    • 疼痛管理的设备和方法
    • US06541021B1
    • 2003-04-01
    • US09522535
    • 2000-03-10
    • Randolph Mellus JohnsonFelix Theeuwes
    • Randolph Mellus JohnsonFelix Theeuwes
    • A61F1300
    • A61M37/0069A61K9/0004A61K9/0014A61K9/0019A61K9/0024A61K31/4468A61K31/4535A61K47/10A61K47/14A61K47/26
    • The invention features devices and methods for the systemic delivery of fentanyl or a fentanyl congener (e.g., sufentanil) to treat pain. In the present invention, a drug formulation comprising fentanyl or a fentanyl congener is stored within a drug delivery device (e.g., contained in a reservoir or impregnated within a matrix within the controlled drug delivery device). The drug formulation comprises an amount of drug sufficient for treatment and is stable at body temperatures (i.e., no unacceptable degradation) for the entire pre-selected treatment period. The drug delivery devices store the drug formulation safely (e.g., without dose dumping), provide sufficient protection from bodily processes to prevent unacceptable degradation of the formulation, and release the drug formulation in a controlled fashion at a therapeutically effective rate to treat pain. In use, the drug delivery device is implanted in the subject's body at an implantation site, and the drug formulation is released from the drug delivery device to a delivery site. The delivery site may be the same as, near, or distant from the implantation site. Once released at the delivery site, the drug formulation enters the systemic circulation and is transported to the site of action in the body to modulate the pain response (e.g., the brain or other pain sensory location).
    • 本发明的特征在于用于系统递送芬太尼或芬太尼(例如舒芬太尼)以治疗疼痛的装置和方法。 在本发明中,包含芬太尼或芬太尼同系物的药物制剂储存在药物递送装置内(例如,包含在储存器中或浸入受控药物递送装置内的基质内)。 药物制剂包含一定量的用于治疗的药物,并且在整个预选治疗期间在体温下稳定(即,不可接受的降解)。 药物递送装置安全地存储药物制剂(例如,没有剂量倾倒),提供足够的保护以防止身体过程以防止制剂的不可接受的降解,并以治疗有效的速率以受控的方式释放药物制剂以治疗疼痛。 在使用中,将药物递送装置植入到受试者的身体中的植入部位,并且药物制剂从药物递送装置释放到递送部位。 输送部位可以与植入部位相同,接近或远离植入部位。 一旦在递送部位释放,药物制剂进入体循环并被运送到身体中的作用部位以调节疼痛反应(例如,脑或其它疼痛感觉位置)。
    • 6. 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。
    • 7. 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。
    • 8. 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。
    • 9. 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。