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    • 26. 发明申请
    • TARGETED NANODROPLET EMULSIONS FOR TREATING CANCER
    • 靶向纳米颗粒乳剂治疗癌症
    • WO2018026958A1
    • 2018-02-08
    • PCT/US2017/045169
    • 2017-08-02
    • THE UNIVERSITY OF LOUISVILLE RESEARCH FOUNDATION, INC.
    • MALIK, Mohammad, TariqKOPECHEK, Jonathan, A.BATES, Paula
    • A61K47/54A61K47/69A61P35/00
    • A micelle, comprises a first phospholipid, a second phospholipid, a targeting agent, conjugated to the first phospholipid, a perfluorocarbon, and a therapeutically active compound. The first phospholipid and the second phospholipid form a shell enclosing the perfluorocarbon and the therapeutically active compound. The targeting agent comprises an anti-nucleolin agent, and the therapeutically active compound comprises a chemotherapeutic agent and/or a cytotoxic agent. An emulsion may be formed, comprising a plurality of the micelles, and continuous aqueous phase. A pharmaceutical composition for treating cancer may be prepared, comprising the emulsion, and a pharmaceutically acceptable carrier. A method of treating cancer includes administering an effective amount of the pharmaceutical composition to a patient in need thereof.
    • 胶束包含第一磷脂,第二磷脂,与第一磷脂缀合的靶向剂,全氟化碳和治疗活性化合物。 第一种磷脂和第二种磷脂形成包封全氟化碳和治疗活性化合物的壳。 靶向剂包含抗核素剂,并且治疗活性化合物包含化学治疗剂和/或细胞毒性剂。 可形成包含多个胶束和连续水相的乳液。 可以制备用于治疗癌症的药物组合物,其包含乳剂和药学上可接受的载体。 治疗癌症的方法包括给有此需要的患者施用有效量的药物组合物。
    • 27. 发明申请
    • ISOMOTIVE DIELECTROPHORESIS FOR DIELECTRIC ANALYSIS OF PARTICLE SUB-POPULATIONS
    • 用于粒子亚群的介电分析的等离子体电泳
    • WO2018009892A1
    • 2018-01-11
    • PCT/US2017/041238
    • 2017-07-07
    • UNIVERSITY OF LOUISVILLE RESEARCH FOUNDATION, INC
    • WILLIAMS, Stuart J.
    • B03C5/00B03C5/02
    • Provided herein are a methods of analyzing particles and isomotive dielectrophoresis devices, and methods of forming dielectrophoresis devices. The method of analyzing particles includes providing an isomotive dielectrophoresis device; positioning a sample within the device, the sample including at least one particle; applying an electric field to the device, the electric field inducing a constant dielectrophoresis force on the at least one particle of the sample; and monitoring a translation of the at least one particle. One isomotive dielectrophoresis device includes a first electrode having a first surface geometry; a second electrode having a second surface geometry; and an electrically insulating material at least partially surrounding the first electrode and the second electrode.
    • 本文提供了分析颗粒和流体介电泳装置的方法以及形成介电泳装置的方法。 分析颗粒的方法包括提供一个驱动式介电电泳装置; 将样品定位在所述装置内,所述样品包括至少一个颗粒; 向器件施加电场,电场在样品的至少一个颗粒上引起恒定的介电泳力; 并监测至少一个粒子的平移。 一种汽车介电电泳装置包括具有第一表面几何形状的第一电极; 具有第二表面几何形状的第二电极; 以及至少部分围绕第一电极和第二电极的电绝缘材料。
    • 28. 发明申请
    • METHODS AND COMPOSITIONS FOR EX VIVO EXPANSION OF VERY SMALL EMBRYONIC-LIKE STEM CELLS (VSELS)
    • 用于EXVIVO扩增非常小的胚胎样干细胞(VSELS)的方法和组合物
    • WO2017152073A1
    • 2017-09-08
    • PCT/US2017/020696
    • 2017-03-03
    • UNIVERSITY OF LOUISVILLE RESEARCH FOUNDATION, INC.
    • RATAJCZAK, Mariusz ZRATAJCZAK, JaninaKUCIA, MagdalenaMILLER, Donald
    • C12N5/0735A61K35/12
    • Methods for ex vivo expansion of very small embryonic like stem cells in the absence of feeder cells are provided. In some embodiments the methods include providing a plurality of VSELs; and growing the VSELs in a culture medium that includes a histone deacetylase inhibitor, luteinizing hormone, follicle-stimulating hormone, and optionally transforming growth factor beta in an amount that is sufficient to overcome quiescence of the VSELs. Also provided are feeder cell-free cell cultures, ex vivo expanded VSELs, pharmaceutical compositions that include the disclosed ex vivo expanded VSELs, methods for overcoming quiescence in VSELs, methods for re-establishing imprinting in VSELs, method for treating injuries to tissues in subjects, methods for repopulating cell types in subjects, methods for bone marrow transplantation, methods for treating radiation exposure in subjects, and methods that relate to regenerative medicine.
    • 提供了在不存在饲养细胞的情况下体外扩增非常小的胚胎样干细胞的方法。 在一些实施例中,该方法包括提供多个VSEL; 以及在包含组蛋白脱乙酰酶抑制剂,黄体生成素,促卵泡激素和任选转化生长因子β的培养基中生长VSEL,其量足以克服VSEL的静止。 还提供了无饲养细胞的细胞培养物,离体扩增的VSEL,包括公开的离体扩增VSEL的药物组合物,用于克服VSEL中的静止的方法,用于在VSEL中重建印记的方法,用于治疗受试者组织的损伤的方法 ,用于在受试者中重建细胞类型的方法,用于骨髓移植的方法,用于治疗受试者中的辐射暴露的方法以及涉及再生医学的方法。