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    • 4. 发明申请
    • LIPID-DRUG COMPLEXES IN REVERSED LIQUID AND LIQUID CRYSTALLINE PHASES
    • 反相液相和液晶相中的脂质 - 药物复合物
    • WO2004012680A2
    • 2004-02-12
    • PCT/US2003/024512
    • 2003-08-06
    • LYOTROPIC THERAPEUTICS, INC.
    • ANDERSON, David, M.
    • A61K
    • A61K9/1274A61K47/541A61K47/55
    • A pharmaceutical is formulated to enable enhanced delivery across membrane barriers, permit solubilization, protect compounds from deactivation by thiol containing compounds in the body, and allow retention of the drug during transport to a desired site of activity. The pharmaceutical includes a complex of two moieties where at least one is pharmaceutically active and is larger than a single atom in size, and the second moiety, when combined with a cationic or anionic counterion forms either a pharmaceutically acceptable anionic or cationic surfactant or a pharmaceutically acceptable salt that has an octanol water partition coefficient of greater than about 100.
    • 配制药物以增强穿过膜屏障的递送,允许溶解,保护化合物免受体内含硫醇化合物的失活,并允许药物在运输至期望的活性部位期间保留。 药物包括两个部分的复合物,其中至少一个具有药学活性并且大于单个原子的大小,并且当第二部分与阳离子或阴离子平衡离子结合时形成药学上可接受的阴离子或阳离子表面活性剂或药学上可接受的 辛醇水分配系数大于约100的可接受盐。
    • 5. 发明申请
    • A NANOPOROUS PARTICLE WITH A RETAINED TARGET
    • 具有保留目标的纳米颗粒
    • WO2003106589A1
    • 2003-12-24
    • PCT/US2002/018657
    • 2002-06-13
    • LYOTROPIC THERAPEUTICS, INC.
    • ANDERSON, David, M.
    • C09K19/00
    • B82Y5/00C09K19/00C12Q1/68G01N33/5436C12Q2565/629
    • Porous nanostructured materials, such as porous nanostructured liquid and liquid crystalline particles or materials, incorporate a target substantially within the material which selectively binds a chemical of interest which can diffusion within the porous nanostructured material and be bound by the target. The porous nanostructured materials can be dispersed as particles in a medium in which said chemical of interest is located with low turbidity. Markers which detect binding of said chemical of interest can be maintained in the medium separate and apart from the target, and any active compound (e.g., an enzyme) associated therewith by the porous nanostructured material, such that detectable changes in the maker only result when the active compounds diffuse out of the porous nanostructured materials after the chemical of interest binds to the target.
    • 多孔纳米结构材料,例如多孔纳米结构化液体和液晶颗粒或材料,将基本上在目标物质内的目标物结合的材料中,靶材料选择性地结合目的化学物质,其可在多孔纳米结构化材料内扩散。 多孔纳米结构材料可以作为颗粒分散在所述感兴趣的化学物质位于低浊度的介质中。 检测所述化学物质的结合的标记物可以在分离和分离靶的培养基以及与多孔纳米结构材料相关联的任何活性化合物(例如,酶)中保持,使得制造商的可检测变化仅在 感兴趣的化学物质结合靶之后,活性化合物从多孔纳米结构材料中扩散出来。
    • 6. 发明申请
    • TREATMENT USING DANTROLENE
    • 使用DANTROLENE治疗
    • WO2005013919A3
    • 2006-05-18
    • PCT/US2004006135
    • 2004-03-01
    • LYOTROPIC THERAPEUTICS INC
    • ANDERSON DAVIDCAMERANSI BENJAMIN GCONKLIN VINCENT M
    • A61K20060101A61K6/00A61K9/127A61K9/14A61K31/4166A61K31/415
    • A61K31/415A61K9/0019A61K9/145A61K9/146A61K31/4166A61K47/10A61K47/16A61K47/186
    • Low volume safe for injection formulations of dantrolene yield significant advantages over the currently approved and marketed dantrolene for MH threatening anesthetic crisis. Once dantrolene can be made immediately available to patients triggered of MH, the anesthesiologist will be able to focus exclusively on the management of the patient's physiologic status in this complex and evolving crisis, not on the laborious and time consuming reconstitution process of the rescue agent. Additionally, a safe for injection low volume formulation of dantrolene can be made widely available to non-anesthesiologist practitioners who have occasion to use dantrolene intravenously in the treatment of other potentially life threatening conditions, including in the field. The low volume, safe for injection formulations of dantrolene, as well as other formulations of dantrolene, have significant advantages over currently used approaches to the prevention and treatment of pumphead, and other neurological, cognitive and motor dysfunction incident to iatrogenically or trauma induced situations of altered blood flow, including those incurred during surgical procedures involving CPB or related procedures, as well as those incurred during non-normothermic episodes caused iatrogenically or by disease.
    • 低剂量安非他酮注射剂配方,与目前批准和上市的丹曲林相比,具有威胁麻醉危险的MH。 一旦丹培罗林可以立即提供给触发MH的患者立即使用,麻醉师将能够专注于在这个复杂而不断演变的危机中对患者生理状况的管理,而不是在救援人员的费力和耗时的重建过程中。 另外,可以广泛使用非麻醉医师从事静脉内使用丹曲罗治疗其他潜在危及生命的疾病,包括在现场的非麻醉医师。 对于预防和治疗泵头以及其他神经系统,认知和运动功能障碍,医源性或创伤性诱发的情况,丹那罗林的低体积,安全注射剂型以及其他丹曲林制剂具有显着优点。 改变的血液流量,包括涉及CPB或相关手术的手术过程中发生的血流量以及在医源性或疾病引起的非正常体温发作期间发生的血流量。