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    • 13. 发明申请
    • MICROPARTICLES AND A SYSTEM AND METHOD FOR THE SYNTHESIS OF MICROPARTICLES
    • 微量元素和微生物合成的系统和方法
    • WO2013178802A3
    • 2014-02-27
    • PCT/EP2013061302
    • 2013-05-31
    • UNIV DUBLIN
    • LEE GILO'MAHONY JAMESPLATT MARK
    • A61K9/50B01J13/04
    • C01G49/02A61B5/055A61K9/5094B01F3/0811B01F3/0853B01F3/223B01F7/00B01F15/0203B01F2015/062B01J13/043B01J13/125C01P2004/61C01P2006/42H01F1/0054
    • There is provided a method of producing microparticles using an emulsion based synthesis route including: Providing a first fluid phase and a second fluid phase, wherein the first fluid phase is a continuous phase and the second fluid phase is a dispersed phase comprising a dispersed material, wherein the continuous phase is immiscible with the dispersed phase; Mixing the first continuous phase and the second dispersed phase in the presence of a surfactant in a shear device to form an emulsion of droplets of controllable size and having a narrow drop size distribution; Drying the emulsion to form microparticles of controllable size and having narrow size distribution, and wherein the microparticles may comprise spherical, crumpled, dimpled, porous or hollow microparticles morphology. Also provided is a system including shear device and drying arrangement. Also provided are microparticles of controllable size and morphology formed by the method.
    • 提供了使用基于乳液的合成途径制备微粒的方法,包括:提供第一流体相和第二流体相,其中第一流体相是连续相,第二流体相是包含分散材料的分散相, 其中连续相与分散相不混溶; 在剪切装置中在存在表面活性剂的情况下将第一连续相和第二分散相混合以形成可控尺寸并具有窄液滴尺寸分布的液滴的乳液; 干燥乳液以形成可控尺寸并且具有窄尺寸分布的微粒,并且其中微粒可以包含球形,皱缩的,凹陷的,多孔的或中空的微粒形态。 还提供了包括剪切装置和干燥装置的系统。 还提供了通过该方法形成的可控尺寸和形态的微粒。
    • 16. 发明申请
    • EMULSION-BASED PROCESSES FOR MAKING MICROPARTICLES
    • 基于乳液的微粒制备工艺
    • WO0066087A9
    • 2001-07-12
    • PCT/US0011781
    • 2000-05-02
    • SOUTHERN BIOSYSTEMS INCGIBSON JOHN WHOLL RICHARD JTIPTON ARTHUR J
    • GIBSON JOHN WHOLL RICHARD JTIPTON ARTHUR J
    • A61K9/16B01J13/12
    • B01J13/125A61K9/1647A61K9/1694Y10T428/2984Y10T428/2985
    • Processes for making microparticles, preferably containing an active agent, are provided. In a preferred embodiment, the process involves preparing (1) a dispersed phase containing an agent in a solution of polymer and a first solvent; (2) a continuous phase containing a surfactant, a second solvent that is totally or partially immiscible with the first solvent, and sufficient first solvent to saturate the continuous phase; and (3) an extraction phase that is a nonsolvent for the polymer, a solvent for the continuous phase components, and a solvent for the first solvent, wherein the first solvent has solubility in the extraction phase of between about 0,1 % and 25 % by weight. Then, the dispersed phase and the continuous phase are mixed to form an emulsion, and the emulsion is then briefly mixed with a suitable quantity of extraction phase to induce skin formation at the interface of the dispersed and continuous phases. Remaining solvent is removed by an evaporation process step. The emulsification and solvent removal steps are preferably conducted in a continuous process. The brief extraction step prior to evaporation minimizes the loss of active agent from the microparticles, and reduces the required volume of extraction phase as compared to other extraction-based processes. Alternate emulsification methods and solvent removal methods, such as incremental extraction, cryogenic extraction, or membrane separation, also are provided, and can be used in various combinations to make microparticles.
    • 提供了制造优选含有活性剂的微粒的方法。 在一个优选的实施方案中,该方法涉及制备(1)在聚合物和第一溶剂的溶液中含有试剂的分散相; (2)含有表面活性剂,与第一溶剂完全或部分不混溶的第二溶剂和足以使连续相饱和的第一溶剂的连续相; 和(3)作为聚合物的非溶剂的萃取相,连续相组分的溶剂和第一溶剂的溶剂,其中第一溶剂在萃取相中的溶解度为约0.1%至25% 重量%。 然后,将分散相和连续相混合形成乳液,然后将乳液与适量的萃取相短暂混合,以在分散相和连续相的界面处诱导皮肤形成。 剩余溶剂通过蒸发工艺步骤除去。 乳化和溶剂去除步骤优选以连续方法进行。 与其他基于提取的方法相比,在蒸发之前的简单提取步骤使来自微粒的活性剂的损失最小化,并且减少了所需的提取相体积。 还提供了替代乳化方法和溶剂去除方法,如增量提取,深冷提取或膜分离,并且可以以各种组合使用以制造微粒。