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    • 72. 发明申请
    • Monochromatic fluid treatment systems
    • 单色液体处理系统
    • US20040121302A1
    • 2004-06-24
    • US10660930
    • 2003-09-12
    • John Coogan
    • A01N001/02H01K001/50
    • H01J61/125A61M1/3681A61M1/3683C12N13/00
    • Methods, systems and apparatus for photo-processing of fluids, particularly complex fluids, such as blood products, pharmaceuticals, injectables and vaccines, are provided. The disclosed methods and systems employ non-laser light source(s) to generate monochromatic light energy, preferably in the range of 260 nm to 310 nm, for fluid treatment. Advantageous processing regimens and/or adjunct additives and/or agents may also be used to achieve desired and/or enhanced results, e.g., inactivation of pathogens, bacteria and/or viruses, modulation of immune response, and/or leukoreduction. Particularly preferred embodiments include specific wavelengths, novel temperature control systems and geometric/structural arrangements that provide enhanced processing results and/or efficiencies. The disclosed methods, systems and apparatus achieve desirable results in a broad range of diagnostic, therapeutic and treatment applications, and generally provide enhanced operating efficiencies and/or processing results in application modalities that employ a broad range of photo-activated and/or photo-responsive materials and/or compounds.
    • 提供了用于流体,特别是复杂流体如血液制品,药物,注射剂和疫苗的光加工的方法,系统和装置。 所公开的方法和系统使用非激光光源来产生单色光能,优选在260nm至310nm的范围内用于流体处理。 还可以使用有利的加工方案和/或辅助添加剂和/或试剂来实现期望和/或增强的结果,例如病原体,细菌和/或病毒的失活,免疫应答的调节和/或白细胞减退。 特别优选的实施方案包括特定的波长,新的温度控制系统和提供增强的处理结果和/或效率的几何/结构布置。 公开的方法,系统和装置在广泛的诊断,治疗和治疗应用中实现期望的结果,并且通常在应用模式中提供增强的操作效率和/或处理结果,其应用范围广泛的光激活和/ 响应材料和/或化合物。
    • 73. 发明申请
    • Monochromatic fluid treatment systems
    • US20040115612A1
    • 2004-06-17
    • US10661262
    • 2003-09-12
    • John CooganBarry Ressler
    • A01N001/02A61N001/30
    • H01J61/125A61M1/3681A61M1/3683C12N13/00
    • Methods, systems and apparatus for photo-processing of fluids, particularly complex fluids, such as blood products, pharmaceuticals, injectables and vaccines, are provided. The disclosed methods and systems employ non-laser light source(s) to generate monochromatic light energy, preferably in the range of 260 nm to 310 nm, for fluid treatment. Advantageous processing regimens and/or adjunct additives and/or agents may also be used to achieve desired and/or enhanced results, e.g., inactivation of pathogens, bacteria and/or viruses, modulation of immune response, and/or leukoreduction. Particularly preferred embodiments include specific wavelengths, novel temperature control systems and geometric/structural arrangements that provide enhanced processing results and/or efficiencies. The disclosed methods, systems and apparatus achieve desirable results in a broad range of diagnostic, therapeutic and treatment applications, and generally provide enhanced operating efficiencies and/or processing results in application modalities that employ a broad range of photo-activated and/or photo-responsive materials and/or compounds.
    • 74. 发明申请
    • Organ preservation apparatus and methods
    • 器官保存仪器及方法
    • US20040082057A1
    • 2004-04-29
    • US10692394
    • 2003-10-23
    • Martin L. AlfordRobert M. Dowben
    • A01N001/02
    • A01N1/0247A01N1/02A01N1/0273
    • This invention is a transportable organ preservation system that substantially increases the time during which the organ can be maintained viable for successful implantation into a human recipient. A chilled oxygenated nutrient solution is pumped through the vascular bed of the organ after excision of the organ from the donor and during transport. The device of the present invention uses flexible permeable tubing to oxygenate the perfusion fluid while the CO2 produced by the organ diffuses out of the perfusion fluid. One pressurized two liter nullCnull cylinder that contains 255 liters of oxygen at standard temperature and pressure can supply oxygen for up to 34 hours of perfusion time. The device uses a simple electric pump driven by a storage battery to circulate the perfusion fluid through the organ being transported. The vessel containing the organ to be transported is held at 4null C. by coolant blocks.
    • 本发明是一种可运输的器官保存系统,其大大增加了器官可以维持生存以便成功植入人类接受者的时间。 将冷冻的含氧营养液从供体切除并在运输过程中抽出器官的血管床。 本发明的装置使用柔性可渗透管来对灌注流体进行氧化,同时由器官产生的CO 2从灌注液中扩散出来。 在标准温度和压力下包含255升氧气的一个加压的两升“C”气瓶可以供给氧气长达34小时的灌注时间。 该装置使用由蓄电池驱动的简单的电动泵来使灌注流体循环通过被运送的器官。 装有运输器官的容器由冷却剂块保持在4℃。
    • 79. 发明申请
    • Assay for low molecular weight heparin
    • 测定低分子量肝素
    • US20040033551A1
    • 2004-02-19
    • US10222345
    • 2002-08-16
    • Ted C. K. LeeAmanda B. McBrideFrank M. LaDuca
    • A01N001/02C12Q001/56
    • C12Q1/56G01N33/86G01N2405/04
    • A prothrombin time reagent for determination of low molecular weight heparin in fresh whole blood and in anti-coagulant treated blood is provided. The reagent is composed of recombinant animal tissue factor, and a mixture of synthetic phospholipids, which mixture includes a phosphatidylalcohol. A formulation buffer which includes a sensitivity adjuster is used in formulating the reagent. The recombinant animal tissue factor includes rabbit brain. The synthetic phospholipids of the mixture include palmitoyloleoylphosphatidylcholine (POPC), palmitoyloleoyl-phosphatidylserine (POPS), and a phosphatidylalcohol. The phosphatidyl alcohol includes dioleoylphosphatidylethanol, dioleoylphosphatidylmethanol, dioleoylphosphatidylpropanol, dioleoylphosphatidylbutanol, and dioleoylphosphatidylinositol. The sensitivity adjuster included in the formulation buffer is null-Cyclodextrin. The formulated reagent is air-dried and remains stable for at least 3 weeks at 37null C.
    • 提供了一种用于测定新鲜全血和抗凝血剂处理血液中低分子量肝素的凝血酶原时间试剂。 试剂由重组动物组织因子和合成磷脂的混合物组成,该混合物包含磷脂酰醇。 在配制试剂时使用包含灵敏度调节剂的制剂缓冲液。 重组动物组织因子包括兔脑。 该混合物的合成磷脂包括棕榈酰胆碱磷脂酰胆碱(POPC),棕榈酰叶酰磷脂酰丝氨酸(POPS)和磷脂酰醇。 磷脂酰胆固醇包括二油酰磷脂酰乙醇,二油酰磷脂酰基甲醇,二油酰磷脂酰丙醇,二油酰磷脂酰丁醇和二油酰磷脂酰肌醇。 制剂缓冲液中的灵敏度调节剂是γ-环糊精。 将配制的试剂空气干燥,并在37℃下保持稳定至少3周。