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    • 1. 发明授权
    • Gas-filled microvesicles composition for contrast imaging
    • 用于对比成像的充气微泡组合物
    • US09248204B2
    • 2016-02-02
    • US11660188
    • 2005-08-17
    • Philippe BussatPeter FrinkingChristian GuillotMichel Schneider
    • Philippe BussatPeter FrinkingChristian GuillotMichel Schneider
    • A61K49/22A61K49/04
    • A61K49/223
    • The present invention relates to a new composition comprising gas-filled microvesicles for contrast imaging which are particularly suitable for providing an effective echo response to at least two selected ultrasound waves having different frequencies. Said composition preferably comprises at least two different preparations of gas-filled microvesicles having respective peaks of non-liner echographic response differing by at least 2 MHz to each other, and preferably have respective size distributions with different mean sizes. In particular, said preparations preferably have size distributions with respective DV50 values differing from each other by at least 0.5 μm, more preferably at least 1.0 μm. Alternatively, said composition has a volume size distribution showing a value of Bowley skewness of 0.16 or higher. According to a preferred embodiment, at least 95% of the total volume of gas contained in said microvesicles, calculated on the population of microvesicles up to a diameter of 10 μm, is contained in microvesicles having a diameter of 8 micron or less.
    • 本发明涉及一种新的组合物,其包括用于对比成像的气体填充微泡,其特别适合于向至少两个具有不同频率的选定超声波提供有效的回波响应。 所述组合物优选包含气相填充微泡的至少两种不同制剂,其具有彼此相差至少2MHz的非线性回波影响响应的各个峰,并且优选具有不同平均尺寸的相应尺寸分布。 特别地,所述制剂优选具有各自的DV50值彼此相差至少0.5μm,更优选至少1.0μm的尺寸分布。 或者,所述组合物具有显示Bowley偏度值为0.16或更高的体积大小分布。 根据一个优选实施方案,所述微泡中包含的气体的总体积的至少95%是以直径为10μm的微泡总体计​​算的,包含在直径为8微米或更小的微泡中。
    • 5. 发明授权
    • Liposomes with enhanced entrapment capacity, method and use
    • 具有增强的捕获能力,方法和用途的脂质体
    • US5702722A
    • 1997-12-30
    • US527087
    • 1995-09-12
    • Herve TournierMichel SchneiderChristian Guillot
    • Herve TournierMichel SchneiderChristian Guillot
    • A61K9/127A61K49/04B01J13/02
    • A61K9/1277Y10S514/945Y10T428/2984
    • The invention relates to a dry deposit as a precursor to liposome vesicles, the precursor being a three dimensional expanded structure with bulk density between 0.01 and 0.001 g/cm.sup.3. The invention also concerns a method of making liposome vesicles with an enhanced entrapment capacity by dissolving one or more film forming lipids in at least one organic solvent to form a solution in a reaction vessel, evaporating the solvent to form an expanded three dimensional porous lipid structure, contacting the lipid deposit with an aqueous carrier phase, and producing liposome vesicles entrapping the carrier phase as well as an apparatus comprising an array of tubing or an inert packing which serves as a material support or a matrix surface for the deposition of lipids produced according to the method.
    • 本发明涉及作为脂质体囊泡前体的干沉积物,该前体是体积密度在0.01至0.001g / cm 3之间的三维膨胀结构。 本发明还涉及通过将一种或多种成膜脂质溶解在至少一种有机溶剂中以形成溶液在反应容器中,使溶剂蒸发以形成扩展的三维多孔脂质结构,从而制备具有增强的捕获能力的脂质体囊泡的方法 使脂质沉积物与水性载体相接触,并产生包裹载体相的脂质体囊泡,以及包含管阵列或惰性填料的装置,其用作材料载体或基质表面,用于沉积根据 的方法。
    • 7. 发明授权
    • Composition for binding bioactive substances
    • 用于结合生物活性物质的组合物
    • US4451568A
    • 1984-05-29
    • US285182
    • 1981-07-13
    • Michel SchneiderPierre ChevreuxChristian Guillot
    • Michel SchneiderPierre ChevreuxChristian Guillot
    • C08F2/50C12N11/08C12N11/06
    • C12N11/08Y10T428/31536
    • An acrylic-acid- based photopolymerizable composition is prepared which is capable of binding bioactive substances after being photopolymerized. The composition may be applied as a coating on a carrier substrate, photopolymerized and a bioactive substance fixed thereto. The composition adheres well to any usual carrier substrates, and its degree of hydrophilicity and permeability can be adapted to needs. The composition contains acrylic acid, a photoinitiator which is an aromatic ketone compound, a photopolymerization activator and adhesion promotor which is an amino-alcohol, acrylate or methacrylate, and a copolymerizable olefinic monomer which contains a reactive functional group capable of binding bioactive substances. The olefinic monomer is preferably N-hydroxysuccinimide acrylate, N-hydroxysuccinninimde amidocaproate, epoxypropyl acrylate or 2-isocyanato-ethyl acrylate.
    • PCT No.PCT / CH80 / 00138 Sec。 371日期1981年7月13日 102(e)日期1981年7月13日PCT提交1980年11月13日PCT公布。 出版物WO81 / 0141200 日期:1981年5月28日。制备能够在光聚合后结合生物活性物质的丙烯酸类光聚合组合物。 组合物可以涂覆在载体基材上,光聚合和固定在其上的生物活性物质。 该组合物很好地粘附到任何通常的载体基底上,并且其亲水性和渗透性的程度可以适应需要。 该组合物含有丙烯酸,作为芳族酮化合物的光引发剂,光聚合活化剂和作为氨基醇,丙烯酸酯或甲基丙烯酸酯的粘合促进剂和含有能够结合生物活性物质的反应性官能团的可共聚烯烃单体。 烯属单体优选为N-羟基琥珀酰亚胺丙烯酸酯,N-羟基琥珀酰亚胺酰胺,丙烯酸环氧丙酯或丙烯酸-2-异氰酸酯基乙酯。
    • 9. 发明授权
    • Compressive hemostatic device
    • 压缩式止血装置
    • US09107671B2
    • 2015-08-18
    • US13387516
    • 2010-07-26
    • Romain Christian Guillot
    • Romain Christian Guillot
    • A61B17/00A61B17/132
    • A61B17/1325A61B17/1327
    • The invention relates to a device capable of stopping the bleeding caused by the withdrawal of an introducer stuck into an introduction area of a patient. The device comprises: a base; a supporting means capable of temporarily attaching the base to the patient; an applicator supported by the base and provided with a transparent pad; and a screw-and-nut adjustment means capable of moving the applicator toward the introduction area so that the applicator moves to a position where the pad exerts pressure on the introduction area. The screw-and-nut system is located completely outside the diameter of the transparent pad. The invention can be used for angiography and angioplasty operations.
    • 本发明涉及一种能够阻止引入器抽出而导致的渗血的装置,该导引器卡在病人的导入区域中。 该装置包括:基座; 支撑装置,能够临时将基座附接到病人身上; 由基座支撑并具有透明垫的施加器; 以及螺旋螺母调节装置,其能够将施加器移动到引入区域,使得施加器移动到垫在引入区域上施加压力的位置。 螺母和螺母系统完全位于透明垫的直径之外。 本发明可用于血管造影和血管成形术操作。
    • 10. 发明授权
    • Liposomes with enhanced entrapment capacity and their use in imaging
    • 具有增强的捕获能力的脂质体及其在成像中的应用
    • US5980937A
    • 1999-11-09
    • US909827
    • 1997-08-12
    • Herve TournierMichel SchneiderChristian Guillot
    • Herve TournierMichel SchneiderChristian Guillot
    • A61K9/127A61K49/04B01J13/02
    • A61K9/1277Y10S514/945Y10T428/2984
    • The invention relates to a dry deposit as a precursor to liposome vesicles, the precursor being a three dimensional expanded structure with bulk density between 0.01 and 0.001 g/cm.sup.3. The invention also concerns a method of making liposome vesicles with an enhanced entrapment capacity by dissolving one or more film forming lipids in at least one organic solvent to form a solution in a reaction vessel, evaporating the solvent to form an expanded three dimensional porous lipid structure, contacting the lipid deposit with an aqueous carrier phase, and producing liposome vesicles entrapping the carrier phase as well as an apparatus comprising an array of tubing or an inert packing which serves as a material support or a matrix surface for the deposition of lipids produced according to the method.
    • 本发明涉及作为脂质体囊泡前体的干沉积物,该前体是体积密度在0.01至0.001g / cm 3之间的三维膨胀结构。 本发明还涉及通过将一种或多种成膜脂质溶解在至少一种有机溶剂中以形成溶液在反应容器中,使溶剂蒸发以形成扩展的三维多孔脂质结构,从而制备具有增强的捕获能力的脂质体囊泡的方法 使脂质沉积物与水性载体相接触,并产生包裹载体相的脂质体囊泡,以及包含管阵列或惰性填料的装置,其用作材料载体或基质表面,用于沉积根据 的方法。