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    • 31. 发明授权
    • Methods of imaging and treatment
    • 成像和治疗方法
    • US07329402B2
    • 2008-02-12
    • US10341167
    • 2003-01-13
    • Evan C. UngerYunqiu Wu
    • Evan C. UngerYunqiu Wu
    • A61B8/00A61R9/127A61R38/00A61R38/04
    • A61K49/225A61K49/223A61K49/227A61K49/228B82Y5/00
    • Novel ultrasound methods comprising administering to a patient a targeted vesicle composition which comprises vesicles comprising a lipid, protein or polymer, encapsulating a gas, in combination with a targeting ligand, and scanning the patient using ultrasound. The scanning may comprise exposing the patient to a first type of ultrasound energy and then interrogating the patient using a second type of ultrasound energy. The targeting ligand preferably targets tissues, cells or receptors, including myocardial cells, endothelial cells, epithelial cells, tumor cells and the glycoprotein GPIIbIIIa receptor. The methods may be used to detect a thrombus, enhancement of an old or echogenic thrombus, low concentrations of vesicles and vesicles targeted to tissues, cells or receptors.
    • 新型超声方法包括向患者施用靶向囊泡组合物,其包含包含脂质,蛋白质或聚合物的囊泡,包封气体,与靶向配体组合,以及使用超声波扫描患者。 扫描可以包括将患者暴露于第一类型的超声能量,然后使用第二类型的超声能量询问患者。 靶向配体优选靶向组织,细胞或受体,包括心肌细胞,内皮细胞,上皮细胞,肿瘤细胞和糖蛋白GPIIbIIIa受体。 该方法可用于检测血栓,老化或回声血栓的增强,靶向组织,细胞或受体的低浓度囊泡和囊泡。
    • 32. 发明授权
    • Acoustically active drug delivery systems
    • 声学活性药物输送系统
    • US06416740B1
    • 2002-07-09
    • US09075343
    • 1998-05-11
    • Evan C. Unger
    • Evan C. Unger
    • A61B800
    • A61K9/5123A61K9/0009A61K9/1075A61K9/127A61K9/1271A61K9/1272A61K9/145A61K9/146A61K41/0028A61K47/62A61K47/6925A61K49/223B82Y5/00
    • The present invention is directed to targeted therapeutic delivery systems comprising a gas or gaseous precursor filled microsphere wherein said gas or gaseous precursor filled microsphere comprises an oil, a surfactant, and a therapeutic compound. Methods of preparing the targeted therapeutic delivery systems are also embodied by the present invention which comprise processing a solution comprising an oil and a surfactant in the presence of a gaseous precursor, at a temperature below the gel to liquid crystalline phase transition temperature of the surfactant to form gas or gaseous precursor filled microsphere, and adding to said microspheres a therapeutic compound resulting in a targeted therapeutic delivery system, wherein said processing is selected from the group consisting of controlled agitation, controlled drying, and a combination thereof.
    • 本发明涉及包含气体或气体前体填充的微球体的靶向治疗递送系统,其中所述气体或气体前体填充的微球体包含油,表面活性剂和治疗化合物。 制备靶向治疗递送系统的方法也由本发明体现,其包括在气态前体存在下,在低于表面活性剂的凝胶至液晶相转变温度的温度下处理包含油和表面活性剂的溶液, 形成气体或气体前体填充微球体,并向所述微球体加入导致靶向治疗递送系统的治疗化合物,其中所述加工选自受控搅拌,受控干燥及其组合。